让杀菌光照进来:这款500美元灯具或可阻止下一场大流行病——来自《Complex Systems》
Patrick McKenzie × Misha Gurevich × Vivian Belenky × Nathan Labenz
- AeroLamp目前以约500美元的价格提供222纳米远UVC灯具。 Vivian Belenky将其杀菌效果比作约30–50次等效换气,Misha Gurevich则称发射器的输出功率约为100毫瓦。单盏灯可覆盖约250平方英尺,因此一间教室通常需要2至3盏,较大的房间可能需要4盏。专业安装费用大致与灯具本身相当;灯泡额定可在保持70%输出的情况下运行至少10,000小时,按每个工作日运行8小时计算,相当于约5至6年。
- 这个市场仍然极小:Vivian估计全球年销量可能只有几百盏。 可比灯具的售价约为2,000–3,500美元,而AeroLamp正在提供500美元的产品。Vivian认为,即使没有技术创新,未来几年价格也可能降至约100美元,不过对于大型安装项目而言,当前价格仍然构成实际约束。
- 其安全机制主要是机械性的。 远UVC会被病原体的DNA、RNA和蛋白质吸收;厚约20微米、富含蛋白质的死皮细胞层几乎可以吸收全部200–235纳米光线,其中以222纳米为主。眼睛更脆弱:泪液层只能吸收约15%,安全眼部剂量低于安全皮肤剂量,且长期研究仍然有限。Vivian称,日本正在开展1年期和3年期眼部安全研究,但行业具体剂量上限仍存在一定不确定性。
- 目前讨论中最有实地相关性的初步证据,来自一项南非结核病研究:在豚鼠只能通过空气接触人类的动物实验中,传播被抑制了90%。 Vivian指出,结核病相对更难被远UVC灭活——可能比典型呼吸道病毒难约10倍——因此结果令人鼓舞,但并不能直接证明流感或冠状病毒的传播也会受到同样影响。
- 最早可能部署的场景包括长期护理机构和老年中心、结核病高发地、医院候诊室、大学、交通枢纽、寄宿学校,最终才是普通学校。 Vivian认为,小学和初中可能受益最大,因为通风条件较差、儿童也更容易感染,但预计家长和学校的保守态度会推迟这类部署。随机试验很难开展,早期安装的收益也可能低于线性增长,直到覆盖率扩大。
- 远UVC对防范大流行病的价值,高于对普通感冒的价值。 Vivian不确定远UVC能在多大程度上阻止近距离传播的感冒,但更确信它有能力压制未来高度传染性的呼吸道大流行病。她提到,传统254纳米UVC历史上曾用于控制麻疹;她估计麻疹的基本再生数约为20,而COVID-19在最严重时是“一点几”(“one point something”)。
- 看空逻辑的核心是传播动力学,而不是技术能否实现。 Speaker 2警告,如果常见空气传播疾病主要通过短距离、高剂量接触传播,那么即使远UVC仍是重要的大流行病基础设施,日常商业价值也可能很有限。Vivian估算,典型安装每2分钟提供1次等效换气,8分钟可使空气中的冠状病毒或流感病毒减少约90%,约15分钟减少99%;但要打断近距离2英尺交谈造成的暴露则更难。她认为完全没有收益的可能性很低。
- 采用受限于认知、证据、价格和供应链规模,而不是某一个决定性的监管障碍。 Gurevich强调信息传播和公众认知的重要性;Vivian则更倾向于通过试点部署建立信心。当前最好的氯化氪发射器来自一家日本公司,并需要使用氟化氢气体;固态远紫外发射器仍属于未来选项。远UVC可以叠加在通风和过滤之上,雇主也可能有直接的商业动机,因为疾病和照护缺勤的成本由雇主承担。一位嘉宾认为,对大多数家庭而言,500美元的家用部署并不经济;Vivian则认为,婴儿或免疫功能低下者等特殊情况足以支撑这笔支出。
1. 机制:蛋白质吸收既是其有效之处,也是其更安全的原因
Vivian Belenky解释称,远UVC会被病原体的DNA和RNA吸收,也会被几乎所有蛋白质吸收。正是这种蛋白质吸收机制,使它比波长更长的杀菌紫外线更安全。病原体在照射后仍然留在空气中,但已经失去复制能力,而且这一效果来得很快。
她用一种极强的空气净化器来作比喻:普通设备可能只能为一个空间增加1至2次换气,而远UVC可以提供约30–50次等效换气。
Patrick McKenzie最初以为,这种波长存在于阳光中。Belenky纠正了他:阳光主要由UVA和UVB构成,而UVC会被臭氧层完全阻挡。阳光仍有轻微杀菌作用,只是依靠更大的总光量来弥补单个光子的杀菌效果较弱;这也引出了McKenzie的插话:Oliver Wendell Holmes从经验上看已经被科学证伪。
2. 安全性是一个机械问题,眼睛是更棘手的部位
Belenky称,这项技术的安全机制“更多是机械性的,而不是化学或生物学机制”。人体拥有一层约20微米厚的死皮细胞,即角质层,其中富含蛋白质,能够吸收几乎全部远UVC。这一特性针对的是更短的200–235纳米波长,主要是222纳米。
254纳米和265纳米等更长波长的UVC被用于水消毒,但并不具备同等程度的蛋白质吸收能力。Belenky不愿断言这些波长会致癌,但表示人体暴露在其中并不舒服,而且普遍认为其致癌性低于UVB。
眼睛更脆弱,因为没有对应的死细胞保护层。泪液层只能吸收入射远UVC的约15%,其余部分会被上皮吸收。因此,较低剂量就可能引发眼痛或不适。眼睑、睫毛、眉毛和眉弓能够降低正常暴露,但眼睛的安全有效剂量仍低于皮肤。
Belenky表示,这项技术存在的时间还不够长,无法完成极长期的研究。她提到,日本正在开展一项1年期和一项3年期的眼部安全研究,但加上了“我想是这样”的限定。她还说,最可能的失效模式更像是盯着强光看,而不是直视红外激光:疼痛会促使人停止注视,而不是让人在没有察觉的情况下遭受致盲性暴露。剩下的不确定性,在于如何把安全性证据转化为行业实践。
3. 安装在墙角的设备只是可行性证明,并非最终形态
AeroLamp目前的设备通常安装在房间角落,因为灯具的光束角较窄。将灯从一个角落朝向对角,可以最大化光束路径长度,从而提高整个房间的平均剂量。
Belenky最终期待看到的是普通的顶灯——“就是一款无聊的天花板灯具”,和其他常规建筑基础设施没有区别——进入办公室、医院和学校。目前的设计更容易安装,也证明客户可以购买设备后立即使用。
Gurevich将当前灯具称为这项技术的“存在性证明”(“existence proof”)。他说,不存在无法克服的技术或物流障碍,但也承认经营一家高科技企业本身有各种普通的困难。这类产品并不只供秘密政府实验室使用,也不需要进行10,000美元级别的安装。
相较旧式UVC系统,这种安装方式的优势在于安全性。采用旧波长的上层空间系统必须谨慎安装,因为安装不当可能迅速造成眼部损伤。Gurevich称,222纳米系统本质上更安全,普通电工就可以完成安装。对基础部署而言,McKenzie认为,这只是安装一款稍显特殊的灯具,而不是解决一个尚未解决的材料科学问题。
4. 单位经济性与部署规模
Gurevich估计,单盏灯的覆盖面积约为250平方英尺。一间普通教室需要2至3盏,较大的教室可能需要4盏。一栋小型建筑可能需要投入4位数至5位数的灯具成本;大学这样的大型机构可能需要数百盏灯,仅灯具成本就达到6位数。专业安装费用可能与灯具本身相当,而自行安装几乎不产生额外费用:设备可以固定在墙上并插入电源插座,约10分钟即可完成。
Belenky称,在面向大规模部署做预算时,按照灯具成本的同等金额预留安装费用,是一个偏保守的经验法则。实际金额取决于电气系统和天花板类型。
制造商给当前灯泡的额定寿命是至少10,000小时,同时保持70%的输出功率。Belenky见过一些数据,认为13,000–14,000小时或许也能实现。按工作日每天运行8小时计算,寿命约为5至6年;如果连续24/7运行,则约为1年半。
McKenzie的结构性论点是,这种产品可以装进一个集装箱,因此随着生产规模扩大,成本应当下降。他将其与需要大量人工的医疗干预相比较,后者的成本可能长期维持在高位;而医院照明很少会以同样的方式变得无法负担。
5. 首批证据和部署可能出现在哪里
Belenky认为,小学和初中可能产生最大的收益,因为这些场所往往通风不良,儿童在免疫学上也更缺乏既往暴露经验。不过,她不确定现有安全证据是否足以让大多数家长欢迎一项相对较新的学校技术。她预计,私立学校或特色学校会早于公立学校采用。
她还将长期护理中心和医院候诊室列为高价值场景。在候诊室,整体人员占用率很高,但每位访客停留时间相对短,这既降低了单个人接受可能令人担忧的累积剂量的概率,又能实现较大范围的人群暴露。
Gurevich对专门场景中的早期证据更加乐观,这些场景往往社交混合有限,或存在特别易感的病原体。他重点提到结核病高发地,以及长期护理机构和老年中心,并预计这些场所很快就能看到明显的传播下降。大学也可能成为早期采用者,因为大学面对的是成年学生,而不是儿童。
南非的结核病研究被视为初步证据。Belenky称,该研究报告结核病病房中的传播抑制率达到90%,但随后澄清这是一项动物实验:豚鼠只能通过空气接触人类,研究人员观察有多少豚鼠最终感染结核病。
她同时提醒,结核病对远UVC相对更耐受——可能比流感或冠状病毒等典型呼吸道病毒难灭活约10倍——而且结核病未必以完全相同的方式通过空气传播。这个结果令人鼓舞,但并没有解决更广泛的问题。
6. 大流行病防控逻辑与建筑规范的作用
Belenky称,防范大流行病“远远是远UVC最令人兴奋的部分”,但在与普通客户交流时,她会避免过度强调大流行病,因为人们仍然受到COVID-19的创伤影响。
她对普通感冒的判断没有那么确定,因为感冒可能需要长时间的近距离互动;但对于压制未来的呼吸道大流行病,她更有信心。她的理由是,高度传染性的病原体提供了更多传播机会,也就给环境干预留下了更多打断传播的机会。她提到,传统254纳米UVC曾用于控制麻疹;她估计麻疹的基本再生数约为20,而COVID-19在最严重时是“一点几”。
McKenzie强调了协调优势。疫苗接种和口罩佩戴需要大量个人决策,而建筑物所有者可以单方面安装环境干预设施。Gurevich补充称,感染防控要求最终可能被纳入建筑规范,然后随着正常的商业翻新周期自然部署。
他指出,ASHRAE 241是当前的感染防控标准,但仍在制定过程中,且尚未被拥有管辖权的主管部门广泛采用。如果建筑规范要求达到特定程度的感染防控,而UVC是实现这一目标最便宜、最容易的方式,他预计建筑物就会采用UVC。
7. 远UVC是通风和过滤的补充
Belenky并没有把远UVC描述为其他洁净空气措施的替代品。建筑物应增加室外空气引入量、增加经过过滤的回风,并使用室内空气净化器。她称,MERV 13便携式空气过滤器可以达到与更高等级过滤器相当的效果,同时噪音更低。
即使与UVC并用,过滤仍然有价值,因为空气中的污染物不只有病原体。灰尘、过敏原、颗粒物和化学污染物仍需要其他干预措施。远UVC通过吸收蛋白质,对过敏原有一定作用,但效果远弱于传统过滤。
不过对于病原体,Belenky认为,在礼堂、阶梯教室和体育馆等空间大、人员密集的场所,单纯移动空气可能不够。如果不使用UVC,许多建筑物要达到洁净空气标准的成本可能高得难以承受。
McKenzie认为,远UVC可以与疫苗、过滤器、通风以及其他干预措施叠加。它通过降低空气中的病原体浓度,可能让现有措施更加有效,同时比疫苗接种或戴口罩更少依赖个人协调。
8. 采用是一个社会扩散问题,但当前价格和供应也很重要
Vivian估计,全球每年的灯具销量可能只有几百盏,而且她不确定这个数字是否正在增长。如果采用能够成为社会常态,她会以LED照明作为参照;但她预计,即使技术真正起飞,广泛部署也至少需要10年,因为商业建筑大致每10年才翻新一次。
她说,市场上没有一个决定性障碍,这一点令人沮丧。安全性和其他研究仍有大量工作要做,但她看不到一项必须完成、否则部署就无法开始的关键研究,也看不到重大的监管障碍。她将其描述为一个“社会扩散问题”:这个想法如何变成一种人们知道自己可以、也应该去做的事情?
Gurevich认为,广泛的信息传播和公众认知是主要瓶颈。Belenky则愿意把大量资源投入试点部署,因为她认为正式证据可能是建立认知的更稳健方式。她还警告,过早获得过多关注可能产生“IFSR效应”,因此公司希望以负责任的方式扩大规模。
9. 供应链与价格阶梯
Gurevich称,当前最好的发射器由一家日本公司生产,该公司的业务集中在高端、高毛利产品。即使扣除这部分利润,发射器成本仍约为每个15–20美元。制造过程还需要氟化氢气体,工艺不如LED生产直接,但他不认为其在根本上无法扩大规模。
Belenky反驳了与LED进行简单类比的做法。LED芯片本身也高度复杂且资本密集,但一旦完成资本投入,产能就可以非常有效地扩大。氯化氪准分子灯目前处于不那么激进的成本下降曲线上,可能无法达到白光LED的经济性。固态、芯片式远紫外发射器最终或许能改善成本结构,但这些技术仍然距离成熟很远。
当前灯具的售价不只是发射器成本的反映。Gurevich称,许多产品售价约为2,000美元,另有一笔已知成交价达到3,500美元。他区分了价格和成本:当前价格反映的是一个极小型行业需要依靠高毛利来生存,而不是某个不可突破的根本成本底线。
Vivian表示,这正是AeroLamp推出500美元灯具的原因;她认为,未来几年价格可能降至约100美元,甚至更快,而且不需要重大技术创新。同时,若一项大型安装需要100盏灯,当前价格仍然会形成明显的投入门槛。
10. 看空逻辑是传播动力学
当McKenzie询问什么情况可能导致这一论点失败时,Speaker 2指出,关键不确定性在于空气传播的实际结构。如果普通感冒和流感中有很大一部分是在近距离传播的,即一个人直接向另一个人传递大剂量病毒,那么远UVC能够拦截的远距离传播可能并不多。
这会产生一个尴尬结果:远UVC可能仍是关键的大流行病基础设施,却缺乏近期商业价值。如果收益是10年或20年后才可能出现、且结果不确定的大流行病防控,而不是未来1年内可以减少的疾病或缺勤,就很难销售这类预防措施。
Vivian将环境干预的效果量化为每2分钟约1次等效换气。在共享空气的传播模型下,8分钟可使冠状病毒或流感病毒减少约90%,约15分钟减少99%。如果感染需要与患者共享空气30分钟或1小时,这种处理就可能显著降低风险;但如果感染来自一次近距离2英尺交谈中传递的大剂量病毒,环境处理的发挥空间就小得多。
她补充称,即使不能完全阻止感染,较低的病毒剂量仍可能降低疾病严重程度。她的结论是,远UVC带来的收益可能从边际改善一直延伸到改变社会的级别,但如果完全没有收益,她会非常意外。
11. 家庭、免疫发育与室内微生物群
家庭市场引发了分歧。一位嘉宾认为,对于疾病传播有限的大多数家庭来说,500美元的灯具并不具备成本效益;但对于富裕人群、极度重视避免生病的人,以及免疫功能低下者,计算结果会发生变化。Vivian则以自己生完孩子后的经历反驳:她在客厅里放了2盏灯,接待客人时会使用。
她认为,婴儿生病可能导致急诊就医、住院,甚至接受腰椎穿刺,因此对部分家庭而言,即使家用部署对社会整体的收益有限,预防价值仍然很高。对于广泛降低社会传播,她仍将学校、交通枢纽和其他共享环境视为更高优先级的场所。
针对“卫生假说”的反对意见,Vivian强烈反对儿童需要通过临床病毒感染来训练免疫系统的观点。她说,当前研究更强调环境细菌、共生菌以及其他微生物的作用。她引用一项研究称,儿童期接触RSV对未来疾病的影响为中性至负面;她还表示,麻疹可能破坏免疫记忆。
她的明确判断是,病毒性疾病只有伤害,免疫训练并不需要临床感染。如果孩子必须生病,她宁愿发生在10岁而不是5岁,发生在5岁而不是1岁,但最好完全不要生病。McKenzie开玩笑说,人们可以日后主动让自己感染;Belenky回应称,这项技术叫作疫苗。
室内微生物群仍缺乏充分研究。Belenky表示,远UVC对表面的效果远弱于对空气的效果,而表面细菌的耐受性极强,因此她的判断是,任何代价都可能很小。但她没有声称这一问题已经得到解决。McKenzie还指出,相比逆转一种生物干预,关掉灯是停止暴露的相对容易方式。
12. 商业切入口:洁净空气、雇主与认知
Gurevich最后呼吁的是提升公众对洁净空气技术的整体认知,而不只是让客户购买AeroLamp。他说,听说过紫外线消毒的人非常少,听说过222纳米的人更少。一旦人们理解了这个概念,他认为推介就很直接:一种近似科幻的技术,可以降低生病的风险。
关于最初100万美元应该如何使用,讨论再次出现分歧。Gurevich倾向于提升认知,但也承认试点部署可能是更好的选择。Belenky则倾向于试点,认为这是建立可信度更稳健的路径;她说,名人推广可能非常有效、非常糟糕,也可能完全没有效果。Gurevich假设中的名人选择是Paris Hilton,因为将洁净空气与高端酒店联系起来可能很有价值。
Belenky表示,正式研究特别容易遭遇“起哄者否决”:一个人的不适,就可能让机构审查委员会无法批准安装。由建筑物所有者自愿部署更容易;技术安装完成后,再研究其效果也更可行。在办公室里,她说员工通常比建筑管理者更支持,后者必须决定是否花这笔钱。
非政治性的商业逻辑来自雇主自己的资产负债表。一家拥有高薪员工的公司,需要承担员工生病的成本,也要承担父母因照顾生病孩子而缺勤的成本。Belenky称,她的经济分析发现,照护者缺勤是感冒成本中的重要组成部分。
创始人提到,一些金融公司在COVID-19早期就采用通风和过滤措施,因为它们看到了其中的商业逻辑。他们更广泛的论点是,洁净空气可以成为建筑基础设施的常规组成部分,由雇主、建筑物所有者、标准制定机构和公众认知共同推动,而不是只依赖个人的公共卫生选择。
Hi-de-ho, everyone. My name is Patrick McKenzie, better known as Patio11 on the internet. As longtime listeners of Complex Systems will know, I think that Far UVC is one of the sleeper picks for among the most important technologies being developed today. Far UVC is a wavelength of light that can deactivate viruses and other pathogens, and it is possible that we will be able to introduce this into our built environment, into our homes and offices, via specially made lamps for infection control.
I'm honored to be joined today by Misha, who is the CEO of AeroLamp, and Vivian Belenky, who is the chief scientist of AeroLamp and also a researcher at Columbia University. Thanks very much for coming on the program, guys.
Yeah. Good to meet you.
Good to meet you as well. So, for folks who haven't heard the Far UVC gospel yet, can we talk briefly about what this wavelength of light actually does, both on the chemistry and biology level and hopefully on the social and technology level?
1. Far UVC Targets Pathogens Safely
On a chemical and biological level, the special thing about Far UVC is that it is absorbed by the DNA and RNA of pathogens, as well as by essentially all proteins. This is very important because the fact that it's so heavily absorbed by proteins is what makes it much safer than other germicidal UV wavelengths.
Essentially, a pathogen or any microorganism—anything without significant protections like humans and animals—is going to be inactivated. It's still in the air, but it can no longer replicate, and this works extremely fast. It's essentially like having an extremely strong air purifier running in a space, except instead of maybe giving you an extra air change or 2 in your space, you can get the equivalent of 30 to 50.
And this is just a wavelength of light that happens to be invisible. It's something that we get in sunlight already, presumably, right?
No, actually. Sunlight is primarily UVA and UVB. UVB in particular is what we're most worried about when we're concerned about the risk of skin cancer and cataracts.
UVC is actually completely blocked by the ozone layer. This makes sense because UVC is quite efficient at inactivating microbial life. Probably the surface of our planet would look very different if it were present here on Earth.
There is no UVC in sunlight. Sunlight is germicidal, just like UVC, but to a much lesser extent. While sunlight does kill germs, it does so because there's just so much more sunlight than there is ever from any UVC lamp. Even though sunlight is only mildly germicidal per photon, it can still do the job.
The legal beagle in me has to say that Oliver Wendell Holmes was empirically disproven by the science. Sunlight is, in fact, not the best disinfectant.
This is an interesting wavelength of light. I personally have done a little bit of the reading and am relatively well-informed about the safety story, but I think that the typical member of the audience probably isn't. What is the chemical and biological reason that this is safe for us?
You've mentioned that it gets blocked by basically any proteins, so proteins in our skin and epidermal layer, presumably. But how is it safe to, for example, look at?
This is actually much more of a mechanical story than a chemical or biological story.
Okay.
Essentially, it's not good for living cells to be exposed to UVC of any wavelength. But the difference is that humans have a 20-micron-thick layer of dead skin cells that are chock-full of proteins that essentially absorb all Far UVC.
I should say this is unique to Far UVC—the wavelengths from 200 to 235 nanometers, principally 222 nanometers, which is what is most commercially viable right now. Longer UVC wavelengths, at 254 nanometers and 265 nanometers, which are used in water disinfection, do not have such significant protein absorption.
I'm not going to say they'll give you cancer. Relative to UVB, they're thought to be less carcinogenic, but they are not pleasant to be exposed to. So it's really something that is unique to the shorter wavelengths in Far UVC.
This high protein absorbance is due to the stratum corneum, the outer layer of the skin. It absorbs almost everything, and what is not absorbed is absorbed in only the very upper layers of the skin. Those skin layers generally slough off and become part of the stratum corneum within typically a couple of days.
I've never seen a study that showed any significant biological activity down at the basal skin cell layer, where you would start to worry about cancer if there were any damage to the DNA there.
Now, the story with the eyes is a little bit more complicated, and this is because there isn't a convenient dead skin cell layer—or dead eye cell layer, whatever that might mean—to protect us. But eyes are protected in the same way that they are protected from sunlight. We have eyelids, eyelashes, eyebrows, and a brow ridge. All of these things reduce the effective dose to the eye.
This does mean that, despite these mechanical protections, the eye is more vulnerable. There is the tear layer, which has some lipids and proteins, and that absorbs some of the Far UVC, but actually only about 15%. The rest of the incident dose would be absorbed in the epithelium, so a relatively lower dose might produce eye pain or discomfort.
The positive story there, though, is that even though these are living cells, they're still full of proteins, and the absorption is thought to essentially totally stop after the first few cell layers. So any chance of long-term damage is, in my opinion, fairly low, although this technology hasn't been around for long enough to do extremely long-running studies.
There have been a few long-run eye-safety studies. Actually, there's 1 1-year study and 1 3-year study going on, I think, in Japan. But it does mean that the safe, effective eye dose is lower than the safe, effective skin dose. We're still figuring out exactly what that is and exactly how to translate that into industry practice.
We are generally pretty conservative. But the good news is that it’s sort of like looking into a bright light, and not like looking into an infrared laser: if you feel any pain, that means you flinch away, and then you’re not really worrying about long-term damage. This is very different from, say, infrared lasers, where you could get a blinding dose and feel nothing. So thankfully, it’s nothing at all like that.
Yeah. If anyone has ever been in a lab that has lasers, the safety briefings are, first, terrifying, and second, if you feel anything, it’s far too late.
Yes. With far-UVC, if you feel something, stop looking at it. To clarify, it’s not that you might be sitting in the room and suddenly your eye starts hurting. It’s more like: did you accidentally climb up and stare right into it for a couple of minutes without turning it off? We’re talking more about accidents of that nature.
One of the big benefits of it being more effective than sunlight as a disinfectant is that you can actually use it at pretty low power levels. The emitters we’re using are putting out around 100 milliwatts, which is really not a lot. Over the distance of a room, it basically decreases to around 0, especially if you’re farther and farther away, right?
Yes. You need very little dose of this stuff to get a pretty rapid germicidal effect.
So we’re starting to see these emitters in the corners of rooms in more, let’s say, tech-forward places in the San Francisco Bay Area. I see your branded emitters more than most. Can you describe what the typical deployment of this would look like?
2. Building The First Installations
For now, we’re doing these corner-mounted units, mostly because it’s a little more cost-effective to mount them in the corner. This is because these lamps have a fairly narrow beam angle, which means that, to maximize the average dose in the room, you want to maximize the path length of that beam. Usually, that means mounting it in a corner and pointing it toward the opposite corner, which gets you a larger average dose over the space.
In the future, I think ultimately we’re looking at normal overhead ceiling lights: just a boring ceiling fixture, like a smoke alarm or any number of random pieces of building infrastructure in drop ceilings in offices, hospitals, and schools. We’re doing it this way right now because it’s a little easier to install. We wanted to emphasize that this is something you could just buy for your space and get on with it. Misha can talk a little more about that.
I basically see our current lamps we’re sending out as a very important existence proof that the technology is fundamentally ready to go. There aren’t any insurmountable technical difficulties, and there aren’t any insurmountable logistical difficulties to deploying it. There are still many difficulties, as there are in running any business, particularly any business that involves high-tech components.
But it’s not something where you can only get this for $10,000, or you can only get this if you’re a secret government lab. This is something that’s pretty much ready to be deployed.
One of the things that I like about this is that, as you mentioned, the tech is basically proven. We’ve done extensive lab studies about this, et cetera, et cetera. It is something that, bluntly, fits on a shipping container from China.
One of my theories about the world is that everything that fits on a shipping container from—without loss of generality—China craters in price over time, particularly as you scale up production a bit. While many of our other medically oriented interventions are consistently high-priced due to Baumol’s cost disease and other reasons, this is something that we should eventually be able to buy for not much more than the price of lighting. There are very few people or institutions that go, “Darn, we’re building out a hospital, but we just can’t afford the lights in it.”
So it’s largely a matter of will, I think, for deploying it, although you’ve probably had this conversation many more times than I have. Why does it not exist already in all of the hospitals?
Can you talk about what the research suggests with respect to this? As we’re prioritizing the rollout, where should we prioritize?
3. Choosing The Best Early Sites
Right. So this is a tough one. If I had to say where I think there would be the most benefit, I would say elementary schools, maybe middle schools, because they are often extremely poorly ventilated, and children are immunologically naive. One issue with doing airborne disease-transmission studies is that you’re using healthy adult volunteers.
It turns out that healthy adults generally don’t get the flu. You need a lot of shots on goal to successfully catch the flu. Children are a different story. It is a bit trickier, though, in that I am convinced on the strength of the safety evidence.
I don't know that we have a large enough pile of safety evidence that a large enough fraction of parents of children would be thrilled to try this relatively new technology in schools. I do expect schools to be relatively conservative, perhaps with the early rollouts happening in private or specialty schools. So I think ultimately occupational settings of some sort are going to see it earlier, even though I don't necessarily think that's where the very largest benefit is.
I think long-term care centers and hospital waiting rooms are big ones where the benefit is high, so any concern about photobiological risk is going to be more acceptable.
Presumptively, places that have a relatively transient population. So in a hospital bedroom, you might have a patient there for a relatively long time. But presumptively, people do not spend multiple days in the hospital waiting room. And so if you have some worry that there's some dose level that would be potentially inimical to a person, they are less likely to get that dose level in the waiting room than they are in other spaces.
Conversely, when you're not counting an individual human's dwell time in a space, the aggregate amount of dwell time in the waiting room is quite substantial. It's just spread over hundreds of patients. So I do think that it is likely to happen in private schools, maybe faster than public schools. And one reason is that, when I do the back-of-the-envelope numbers for it, it's something that a single parent could probably fund just by deciding to do it if they get the school on board.
Indeed, a few of my tech friends have discussed potentially doing that for the schools their children attend. Misha, can you talk a little bit about the economics of this, on a per-room and per-institution basis?
Yeah. So we usually say something like 250 square feet per lamp is how much coverage you would get. So for a standard classroom—this is sort of... I guess a standard classroom is a tough question because there are the standard classrooms as they actually exist, and then if you look into, say, California guidelines for a standard classroom, they're actually much bigger than standard classrooms tend to be. But that would be 2 to 3 lamps per classroom, maybe 4 for a bigger one.
And so for a lot of schools, you're looking at a lot of lamps, right? Dozens. For a really big institution, like a university, you're probably looking at hundreds of lamps. Universities are kind of a front-runner because, again, it's not children; it's older students, so it's a little easier to get installations set up.
One of our competitors recently set up a big installation in a Florida university. I haven't heard any details yet, but they're apparently collecting a lot of good data that way. This is the kind of thing where, on most small buildings, you're looking to spend maybe 4 to 5 figures if you want to outfit the whole building. And then once you're getting bigger, you're looking to spend maybe 6 figures purely on lamps, and then installation also.
Usually we say installation will cost you probably about what the lamps will cost you if you're hiring professionals to do it. If you're just doing it yourself, installation is basically free, right? It takes 10 minutes to stick one on the wall and plug it into an outlet. But if you're doing permanent installations, you're going to want to run wiring through the ceiling, that kind of thing, right?
Yeah. So the budget is as much for the installation as for the lamp itself. That's kind of just a rule of thumb, on average across all possible electrical systems and ceiling types. Even if this were happening on a mass level and we were hiring professionals to do all of it, I think for many typical scenarios it could be quite a bit cheaper. But just on average, when we're talking about mass-scale modeling, I think roughly double the cost for installation is a reasonable, conservative estimate.
And so at the moment, it's something like $500 a lamp. So if you need 2 of them for a room, that's $1,000, and then $1,000 for installation, and then multiply by the number of rooms that are at the top of your priority list. It's useful to point out that this is something electricians are very qualified to do already. You just say, “Hey, there is a weird light fixture that goes in the corner,” and they say, “Okay, I have done light fixtures before. That isn't an unsolved problem in materials science.”
One of the reasons that UV has not really been adopted more generally, even though it's been a known technology since the 1940s and 1950s, is that older wavelengths are more dangerous, so they have to be installed a lot more carefully. You can install UV in the upper part of a room where it's safe for people, but if they mess up an upper-room installation, then people are getting eye damage very quickly.
Whereas you can't really mess up a 222-nm installation that badly because it's innately a lot safer. And so the level of expertise is, like you said, any electrician can do it instead of needing an expert UV installer.
I'm familiar with standard lamps, although they changed a little bit in the LED era, where you have to go and replace the bulb every once in a while. What's the average lifetime of these installations?
Yeah, we think that the bulbs that we're using right now—the manufacturer will admit they'll last at least 10,000 hours while maintaining 70% output. I've seen some data that suggests it's actually a bit longer than that, maybe more like 13,000 to 14,000 hours.
If you are only using it in an occupational setting for 8 hours a day during your workweek, that's about 5 or 6 years of usage before you need to do any replacements. And if you're running them 24/7, which I don't know what scenario that would be most desirable in, that would be just about a year and a half.
I could imagine maybe a transportation scenario where you had them in, for example, a train station or an airport, where they would want to run them 24/7 or something pretty close to it. And I guess the big $64,000 question—or more now that a dollar is worth less than it used to be—is when will we start seeing the actual results in the physical universe?
When does the data start getting sort of undeniable? That's like, if you install this, then you win in terms of the amount of sick days you have and the clinical consequences.
4. Proving The Health Benefits
Yeah. So I think this is a really, really tough question. There are a number of reasons that these sorts of randomized controlled trials for an environmental disease-transmission intervention are quite hard to do. We're not entirely sure that we know how to design such a trial, but in principle, you should expect that this will roughly follow a sigmoidal shape.
The first few adopters are going to see sublinear benefits because maybe you install it in your office and nobody gives each other the flu in your office, but then your kid's school doesn't install anything and the flu goes around there, and then you just catch the flu from your kid. So there's going to be some critical coverage point within a community where the suppression really takes off, and we have modeling on this. But I think it's really, really uncertain.
I think I'm actually a lot more optimistic than that. I think a lot of specialized use cases are going to see fairly strong evidence, a lot faster and a lot more easily—basically, situations where people are not as social, not as mixed, or pathogens that are particularly susceptible. So there have been really good results on tuberculosis, for example.
This is not really something we think about day to day in America, but there are a lot of institutions and places that are tuberculosis hotspots that are also not doing a ton of social mixing. This is a big problem in a lot of countries that are not America. But even in America, there are places that have a lot of tuberculosis. And I think those places will see pretty noticeable drops in transmission fairly fast and pretty reliably.
I think that kind of thing will be forthcoming relatively quickly compared to if you put this in a school, in a community. We don't really know that fast. I also think long-term care centers and basically senior centers are another place where we're probably going to see results relatively faster because there's just not as much social mixing there with the rest of society.
I would agree with that. And also, I should point out that we have some really encouraging results on tuberculosis specifically. There's a trial going on in South Africa that already has preliminary results, and they're seeing 90% transmission suppression in these TB wards. This is an animal study, so the way it's set up is that there are guinea pigs that are exposed to the humans only through the air, and they're monitoring what percentage of the guinea pigs get tuberculosis.
But tuberculosis is actually not very sensitive to Far-UVC at all. It’s relatively resistant. I would say it’s about maybe 10 times more resistant than your typical respiratory virus, like flu or coronavirus. So are flu and coronavirus transmitted through the air in the exact same way as tuberculosis? No, probably not.
But there is, in fact, a lot of reason to be optimistic. I think Misha’s totally right about long-term care centers probably seeing much more immediate benefits than the school or office case, or perhaps boarding schools. I think boarding schools could be a relatively more immediate example.
I think this is going to be interesting because there are some institutions that require a stack of academic papers on this with confidence intervals, et cetera, et cetera. But when you’re talking about 90% decreases in infections, for example, the anecdotal evidence will pile up in certain communities extremely quickly.
It is just nakedly and obviously incentive-compatible for a case like a long-term care center. Regardless of who owns it, a PE firm or otherwise, they would strongly prefer that the residents not die. That is both the humanitarian mission for them, plus they get paid based on how many residents are still living at the moment.
You could imagine it having a high viral coefficient in that community of practice as soon as a chain installs it in one location and is able to check at the end of the month: “Well, we had 34 infections in the median of our locations, and in the one where we installed this, we had 3.” Then they could make the obvious decision very quickly after that.
Knock on wood, I hope that we will see evidence of the obvious decision getting made all over the place on a timeframe of months to a small number of years from now, followed by the broader societal rollout that this will likely take.
5. Preventing Future Pandemics
So we’ve talked about the decreasing-infections-locally case, but I think the huge societal upside here might be decreasing the total load of infections and, in particular, kneecapping future pandemics before they start. Can you talk about some of the pandemic math that we were unfortunately all forced to become experts on back in 2020, and what this does to the potential factors of virality and similar?
Yeah. I think the pandemic-prevention case is by far the most exciting element here. When you’re trying to market something to ordinary people in non-pandemic times, and when I talk to people about this, I really avoid mentioning the pandemic because people do not want to hear it. I think we’re all collectively traumatized, and we just don’t want to talk about it. So we’re talking about preventing colds and flus.
My honest assessment is that I’m much more uncertain about our ability to prevent the average cold, which is just not very contagious. Probably, if you’re getting someone’s cold, it’s because you spent an extended period of time interacting with them quite close. Can we prevent some colds in immunocompromised people and in some situations? Yeah, I think so.
But I’m actually much more confident that we could kneecap a future respiratory pandemic like COVID-19 or worse, just because, paradoxically, the more contagious something is, the more surface area there is to keep it from getting as bad as it could get. In fact, one of the earlier use cases for traditional germicidal UVC, which uses a different, more dangerous wavelength—the 254-nanometer wavelength—was to control measles.
Measles is just absurdly contagious. It is probably the extreme of how contagious a pathogen can even be. I think it has a reproduction number of 20, so each person who has it will, on average, infect 20 others. I believe that COVID-19 at its worst had a reproduction number of one point something. So UVC was able to successfully control measles outbreaks.
I think that makes me really optimistic that a relatively low level of coverage in key areas—transport hubs, for example, and other gathering places where people who aren’t actually in communities together are mixing—is where we can do pandemic suppression for relatively low cost.
No, I definitely think that’s a huge benefit. I also think that because it’s part of the built environment, you need a lot fewer people to be involved in the prevention process, right?
This is one of the big problems with COVID: vaccination requires a lot of people to opt into vaccination, and masking requires a lot of people to opt into masking. If you have whoever owns a building decide unilaterally, sometimes it’s just one person, and sometimes it’s a board of directors or something. But that takes way fewer people to reduce infections in an area than previous prevention methods, right?
Yeah. And if a certain amount of infection prevention gets written into building codes, and then these are broadly adopted by whatever the authority having jurisdiction is—that might be at the state level or the county level—these interventions just get built into buildings on a 10-year renovation cycle.
I think there is some potential here in going through building codes, because right now we only have one infection-prevention standard: ASHRAE 241. It’s an amazing standard that was put together very quickly, but it’s still under construction, and it’s not yet broadly adopted by any authorities having jurisdiction.
But if the standard says you need this much infection prevention in your building to be compliant, and UVC is the cheapest, easiest way to do that, people are going to do that. I do think that one really, really major advantage—maybe the advantage—of Far-UVC and UVC generally is that it is such a cost-effective way to get the required amount of infection prevention into an air-treatment space.
The sort of competing technologies—they’re not quite competing. Presumably, this is something that you could deploy in parallel, but your other options might include a huge upgrade to the HVAC system to cause more changes in the actual physical air in the room per hour, which requires upgrading both the central HVAC and also presumably all the vents, et cetera, and might be either impossible or extremely cost-ineffective for buildings that already physically exist.
Whereas this is, again, just: plop the light in the corner, and then you’re done.
Another comparison technology might be portable air filters, actually—not necessarily HEPA, but a lower rating can actually be just as effective and much quieter. So, just a MERV 13 portable air filter.
I do think these things are additive. We should absolutely be upgrading ventilation. We should be getting more outdoor air and more recirculated, filtered air. We should be using—you can call them portable filters, but you can also install them in the room. We can broadly call these in-room air cleaners.
I think these are some of the most cost-effective options. And for filter-based in-room air cleaners, you’re going to want them alongside UVC anyway, because pathogens are not the only airborne pollutant.
There's also chemical pollutants. There's particulate matter, dust, and allergens. Far-UVC actually does have a modest effect on allergens through the same protein-absorbance pathway, but it's much smaller than conventional filtration. So we should be doing all of these things.
But for pathogens specifically, just moving the air tends to be really, really insufficient, especially for very large spaces that are relatively densely occupied. In auditoriums, lecture halls, and gyms, it would be really, really difficult to meet the clean-air standard without UVC—essentially cost-prohibitive for most buildings.
This is one of a panoply of options we have with regard to infection control in our built spaces. I was about to say additive, but it's probably multiplicative, or better, if one actually does the math with regard to other non-pharmaceutical interventions—or pharmaceutical interventions, for that matter. If we have vaccines, they have some penetration rate in the community, et cetera, et cetera. The vaccine almost certainly doesn't become less effective just because there is less of the virus circulating around.
But given that this is easier to deploy and requires less coordination among people, there's also a political-economy question here that's dancing in the background. Hopefully, there will be less opposition to simply having light in the corner than to having needles deployed all over the place. It makes all of our existing and future technologies better to have this deployed alongside them.
Yeah, I think that's definitely true.
6. Breaking The Adoption Bottleneck
I once made a bet with someone that we would have broad deployment of this in the United States by 2030, and I think I'm going to lose that bet, unfortunately, because we're not moving at quite that speed. But if you were to put your finger to the wind, what does the curve look like for deployment of this over the next couple of years in maybe an optimistic scenario and then sort of a baseline scenario?
I think we're not exactly even on the curve. Worldwide, it might be as low as just a couple of hundred of these lamps sold per year. I don't even have a great sense for whether this is going up, but I think essentially it's a matter of, does this idea go viral? Har har. If it takes off and becomes, “Hey, this is a thing you can and should do,” then I think we can maybe look at the speed of deployment of LED lighting as a case.
We're still looking at at least a decade after it really takes off to get truly wide deployment. That 10-year renovation cycle for commercial buildings is going to play a role here. So it's really just a matter of when we get to that tipping point and how we get there.
This is something that really keeps me up at night because I talk to people, and people think there must be some good reason that this isn't getting going. There must be a regulatory barrier, a cost barrier, or a critical piece of safety research missing. Not that there isn't lots of safety research and other kinds of research still to do, but there's nothing supercritical where it's like, “Oh, we just need to know this and then we can get going.” There's not really any regulatory barrier either.
It's maybe just a social-diffusion question. Do we need a global awareness campaign? How do we get this out there? I've been in research for my entire career, so I'm not an expert in how to run a global awareness campaign or how to make one actually effective, and I certainly really wish I was.
Calling back to something that you said earlier, we're all somewhat traumatized by the pandemic, but implicitly we are racing the next pandemic. Hopefully, we have this up and running in as many spaces as possible prior to the somewhat inevitable crash efforts to again improve our physical spaces and other resilience that would be activated in the ordinary course during pandemic times. Ordinary course, to the extent that anything is ordinary during pandemic times.
It's a combination of frustrating and intellectually interesting that there is no barrier at the moment. It's a product that's commercially available. I guess we'll say a few words about scaling. This is presumptively manufactured in—without loss of generality—China. One thing we've learned from LEDs, among many other technologies, is that China and the industrial ecosystem there are very good at scaling up production of things for which there is a demand.
Is there any particular reason why this would be harder to scale than, for example, LEDs were?
There have been a few reasons, but they're not that major. The current manufacturing of the best emitters, which we think are the most cost-effective and have the best lifespan, is handled by only one company from Japan. They're generally in the business of making high-end, high-margin products. So even if we cut down all of their margin, we're still looking at a per-unit cost of $15 or $20 per emitter, which puts them in a different category than LEDs. They're not as easy to scale.
They require hydrogen fluoride gas as part of the manufacturing process. This is technically just a lot less simple than LEDs. It's still something that's very feasible to scale up. It's not something that's, on first principles, unscalable; it's just not as easy as LEDs.
I would push back that it's more complex than LEDs. The thing about LEDs is that it's extremely complex and capital-intensive to produce LED chips. But once you've made that capital investment, you can scale it very, very effectively. You put in tens of billions of dollars of capital, and if there's enough of a market, that makes sense to do.
Right now, these krypton chloride excimer lamps are on a different, less aggressive cost curve. I don't think they could get as cheap as the white LED. But there are hopes for some solid-state, chip-based solutions for far-UV emission. I just think that we're looking sufficiently far out that we're nowhere near the cost floor for even what we have here.
Once we're in this beautiful unicorn world where we're selling tens of millions of lamps and really rolling this out, how do we push the cost floor of a krypton chloride lamp even lower? How do we get solid-state, chip-based, scalable technologies online? I would love to have that problem. I would be so joyful if we had that problem.
Given that the cost doesn't seem to be the major barrier to deployment right now, and that, at least in the United States, you modeled 50% of the cost as labor, where that is very difficult to compress, I would assume that the cost drops as we scale production. That's generally how it goes in manufacturing.
But there isn't a radical step change in the likelihood of deployment or the ease of deployment as a function of reducing cost, it seems to me.
The existing industry is just so small, and as I said, it's kind of high-margin as a business model. So I think there is an—I don't know if I would call it a radical step change, but I think there's probably a pretty big inflection point at some point, because a lot of the lamps in this market are being sold for around $2,000. I recently heard someone sell their lamps for $3,500 each.
Once we're talking about installations where you need 100 for your building, that adds up really fast if you're spending $3,000 per lamp. So I do think that cost is probably a barrier in a lot of deployments.
But that cost is not fundamental to the industry. That cost is just an artifact of the fact that these are tiny companies that need to have high margins to survive. I think this is a very tractable thing if you're looking at it from the perspective of whether the world can throw money at this to get deployments a lot faster and cheaper. I think this is very feasible.
As we're talking about a total addressable market at the moment of hundreds of lamps per year transitioning to tens of millions or hundreds of millions, our priors should heavily be on the cost per unit going down pretty aggressively.
The cost per unit is really—I'm saying the cost per unit is not the cost, right? That's the price per unit.
I guess this was sort of our theory for offering a $500 lamp: that there is this inflection point. Our goal is to drop that even further.
I don't think there's any reason that in the near future, the next couple of years or so, or even sooner, the price couldn't be on the order of $100 per lamp. And that's with zero technological innovation of any sort.
And for the benefit of people who haven't seen your website, not to put too fine a point on it, this is a thing that you can literally go over to AeroLamp's website and buy right now. It comes in a box to your home or office, and then it is as easy to install as any other lighting fixture.
Actually, even easier. You just stick it on a tripod, put it on top of your bookshelf, or use a drywall anchor and stick it on your wall. Typical overhead lights can be quite a bit more annoying to install. I've done it in my home a couple of times.
And, full disclosure, I don't have it in my house yet, but I have considered it, and it exists in several commercial spaces I've been in in the San Francisco Bay Area, among others.
I get asked this question all the time: “Oh, should I get an AeroLamp?” But I think most private homes—the cost-benefit analysis is not really in favor of getting one, just because there's not that much disease transmission. Most people don't live in a big house with 20 people or anything, right? If it's you and your family, I don't think the benefits are going to be that high.
Although, obviously, this changes based on your own personal cost-benefit analysis, right? If you're particularly rich, particularly value not getting sick, or if you're immunocompromised, this sort of changes the balance. But for most people, having it in their home for $500 is not actually cost-effective. It doesn't actually price out very effectively. Maybe once they're down to $100, then yes.
I don't know. I would actually push back on that. I think there are quite a lot of families. I think the societal benefits are not particularly concentrated for individual homes. For individuals, in quite a lot of situations, it can be valuable.
For example, I had a baby 2 months ago, and babies essentially do not have immune systems. I quite valued having people over and around to help out postpartum, and I was using my lamps. I have 2 in my living room, and I turn them on when I have company. I turn them on when I host events and gatherings.
I think for individual homes, it's less something that you might have on all the time, but maybe something you like to have for home-health reasons. It's sort of like the ventilator in your kitchen. It is something that you quite like to have for home-health reasons. Maybe not at the $500 price point, though.
I think if you actually monetized the potential health benefits, it would look quite a bit better. Getting sick is very, very costly, so you don't need to prevent that many episodes of illness. Especially in tiny babies, where if a tiny baby gets a fever, you're looking at an emergency hospital trip, hospitalization, and potentially a spinal tap, and it's all deeply upsetting for everyone involved.
So I think you should rationally be extremely willing to pay to lower the probability of small babies and other immunocompromised people getting infections. But the societal benefits of homes are just kind of meh. That's not where I am most going to be pushing for this to go out. I think schools, transport hubs, and that sort of thing are where you'll see much broader social suppression.
When I was doing the back-of-the-envelope math—and I have not devoted the last couple of years to researching this—my thought was that the case for a home shaped like mine, where there are 4 occupants, 2 of whom are school-aged children, is not that great yet, except for the aesthetic benefit. Putting your chip on the table, this is something that I hope gets deployed widely in the future.
For special circumstances, sure. Also, given that most people who listen to Complex Systems are employed tech professionals or similar, the absolute number is probably not that big a barrier. But be that as it may, there is a question that we sometimes ask in investing, which I think is a clarifying one.
If it fails to work—if this doesn't achieve the societal-level benefits that we expect it to—why? What is the thing that we don't have confidence in, that we could potentially learn more about in the next couple of years in a way that would disappoint us negatively?
7. What Could Break The Thesis
For my part, it would be that it turns out that a huge chunk of airborne disease transmission is strongly short-range, and that there is actually very little long-range transmission of common pathogens like your typical cold or your typical flu. I think when it comes to pandemics, for something to be that contagious, it does sort of need to be more long-range.
I think it is imaginable that we end up in this uncomfortable world where we can't do very much for “normal” disease transmission, but it still is totally crucial anti-pandemic technology. But now there's not really a clear business case for deploying it because people hate paying for prevention.
It's a lot easier to sell someone something if you can tell them, “You're going to benefit from this in the next year,” and see your money back through prevented illnesses and prevented absences and so on, versus, “Hey, this is something that you install just in the event that there's going to be another mass pandemic in the next decade or two.” That's just a much tougher sell.
But I think it's the transmission dynamics and how these diseases actually transmit in real life, under what circumstances, and for what sort of people. I think that's our biggest question mark, and it's very challenging to study.
Yeah, needless to say, we're pretty optimistic, but if it fails, it'll be for reasons like that, right?
Yeah. You could imagine that we think that for a typical Far-UVC installation, you're looking at the equivalent of 1 air change happening every 2 minutes. That translates to 90% of coronavirus or influenza virus being reduced in about 8 minutes, and double that to get to 99%—so about 15 minutes for 99% reduction.
If the transmission dynamic is that you're sharing air with somebody who is ill and, after 30 minutes or an hour, you have inhaled enough infected air to, on average, produce an infection, Far-UVC will totally cut that down. If instead the transmission dynamic is that you talk to an infected person from 2 feet away and get a massive dose, and you are definitely, for sure, getting whatever it is that they have, then that's not really enough room for Far-UVC or any kind of environmental intervention to do much.
You can improve that a little bit by mixing the air and interrupting the airstream between people at that social distance, but it's definitely going to be more challenging. You might still reduce the severity of an infection just by reducing the viral dose. We saw this with COVID: even if you don't fully prevent an infection, if you get less virus in you, you're going to have a less severe infection. Probably quite a lot of diseases work this way as well.
But I think it would be quite unlikely that we would see no benefit at all, whether the benefits are relatively marginal—probably still worth it, especially at a lower price point—or whether the benefits are truly socially transformational, such that we can see vastly less airborne disease. That's the uncertainty. But I think no benefit at all is quite unlikely. I would be very surprised by that.
One hopes that, given numbers like 90% deactivation of pathogens, in an idealistic case, the amount of evidence, both formal and anecdotal, will pile up very quickly and lead to a high rate of diffusion in the built environment. I have heard one objection from people, and I think these interlocutors are overemphasizing the precautionary principle.
But ask the experts. We talked about children and infants being immunologically naïve, and the way you stop being immunologically naïve is to have time in the world, get exposed to pathogens, and have your immune system built up. Is it possibly the case that decreasing people's contact with pathogens is, on net, a bad thing?
I would push back on that quite strongly. The modern formulation of the hygiene hypothesis does not actually posit that you need to be exposed to pathogens to train your immune system.
We now think that the primary immune system training you get as you're growing up is with environmental and commensal bacteria and other microorganisms. There doesn't actually seem to be any benefit to having a clinical episode of illness. I was actually just looking at a couple of studies on this the other day. For example, there was one study on the effect of a child having RSV; it was a neutral-to-negative effect on future illness.
In the extreme case, catching measles wreaks total havoc on your immunological memory. It's purely bad for you. I think the emerging understanding is that all viruses are like this: it is purely bad to catch a virus and get sick. You might not be able to prevent it, but you would still rather it not happen to you at all. If it has to happen, you would rather it happen to you when you're older.
I would much rather my kid catch whatever it is that's going around at 10 than at 5, and I'd rather it happen at 5 than at 1. But I'd really rather it just not happen. There's just no benefit. The immune training comes from contact with the environment and with the world. The world is just teeming with microorganisms; there is absolutely no lack of immune training. So if we just totally ended viral infections, I think that is overwhelmingly good. No downside.
That is great to hear. A thing that I've told people is, if it turns out that there is some optimal level of viral infections that we have to have for a perfectly tweaked immune system, we can always intentionally infect ourselves in the future. If it's just, “Oh, man, my child just hasn't gotten sick enough in the last 9 years.”
I think this is actually called vaccines. I think intentionally exposing people to viruses—we have a technology for that.
Exactly true. On net, we deal with less disease load than we had in historical environments and haven't seen major impacts as a result of that. But we have engineering and pharmaceutical options to raise or lower the level if it turns out that we ever go below the optimal level of illness. Just putting a finger to the wind on how things likely are, I think it's very likely that we are above the optimal level, if there is indeed an optimal level of illness.
Yeah, I think people go too far with the hygiene hypothesis because we can look at the data, or at our lived experience of what it's like to be a human living in our society, and say, “Oh, asthma is up. Allergies are up.” The thing is, those are relatively trivial compared to childhood mortality, which is way down.
Yeah. I think there is just gathering evidence that increased allergies and asthma certainly have nothing to do with viral infections. There might be some question of whether widely deployed Far-UVC is going to mess with the indoor microbiome in a way that affects us. My answer is mostly no, just because microorganisms—bacteria especially, those living on surfaces and not in the air—are extremely hardy.
Far-UVC is generally much less effective on surfaces than in the air. This has not been explicitly studied: what the effects are on the indoor microbiome. But my bet is that if there's a cost, it's relatively minor. In the event that there is a substantive effect, you go outside, and there are going to be germs there. There's dirt, there's bugs; there's no lack of potential exposures.
Yeah. And not to say something spicy on the podcast for the sake of spiciness, but I think the precautionary principle ends up being a really rough way to live life. You can always argue that, in the multimillion-dimensional space that we live in, there is at least one dimension where a given technology would disimprove you, and therefore the precautionary principle says never do anything.
We know what the numbers are for infectious diseases in terms of deaths caused per year. They're horrific. If there is hypothetically a future in which there is a line in the history books—before the ending of flu and after the ending of flu—that will be a world-historical achievement. Again, we're not necessarily 100% expecting that to happen as a result of Far-UVC, but that is something that is possible in the solution set, or possible in the outcome set, given deployment of this. When you compare some percentage of that to some percentage of, “Well, it might subtly tweak the indoor microbiomes,” those are 2 very different numbers in terms of their impact on the human experience.
Absolutely. I'm not saying we shouldn't study it. We should absolutely study it. The space of things that we don't yet know and would really like to know is huge. But you always have to reason under uncertainty and reason about different risks.
This is what I tell people when they talk about photobiological safety: yes, we don't have long-term data; yes, it is reasonable to be cautious about these kinds of exposures; we haven't studied this in this specific population; and yes, there are unknown unknowns, and I cannot fully characterize this risk. But that is just massively underrating the risks from infectious disease.
I think there are also quite a lot of unknown unknowns regarding how bad episodes of viral illness are. I have a strong suspicion that long COVID, for example, is not special, in that quite a lot of viruses have long-term sequelae. I mentioned measles has long-term impacts on immunological memory. There's lots of stuff like this, like MHV virus. I might be saying that completely wrong. We don't necessarily fully capture the downside of an episode of clinical illness, even a relatively mild clinical illness.
It is possible that basically the entire population, for all of human history—or at least all of human history since, say, the move to cities—is suffering under the effects of long flu, and we don't have a word for it because we assume that getting the flu was just something you were resigned to. But in a future where, hypothetically, we are less resigned to that, there might just be far fewer long-term health impacts than there were previously.
Yeah. Some viruses can cause cancers. Personally, anytime I get a bad cold in the winter, half the time I'll be coughing like crazy for 2 months afterward. We don't even fully know everything that we're constantly passing to each other. So I think there are some unknown unknown downsides, and I think there are some unknown unknown upsides as well.
Mm-hmm. I will say, relative to other infection-prevention measures, this one is relatively easy to desist from if we decide that the math doesn't work out in favor of it. You turn the lamp off, and people stop getting doses. It is relatively difficult to desist from, say, vaccines. Obviously, you can stop giving them in the future, but it's tough to remove a chemical change from people after they've been exposed to the chemical change.
Structurally, this is only affecting the top layers of your skin cells, most of which are dead. After you stop getting doses, you stop getting doses.
Yeah. You could imagine that maybe there's some crazy edge case where getting a sufficient dose to the upper layers of skin causes some protein structural change. It diffuses down through the lower skin layer. These are things you sort of have to struggle to think of. At a certain point, reasoning under uncertainty and reasoning about risk just gets kind of nuts.
Yeah. Well, this has been a very informative conversation for me. Are there any thoughts that you would like to leave the audience with with respect to Far-UVC or AeroLamp in particular?
8. Making Clean Air Mainstream
There's a lot of interest in clean air recently. There are big foundations that are putting a lot of money into it. Speaking as a capitalist and as a guy who runs a company, it'd be great if people bought a lot of AeroLamps. But I think in the industry and for the world in general, the really important thing is awareness.
Some sort of global awareness program, some sort of marketing and informational campaign, or some sort of thing like that could easily benefit the world more than almost anything else you can do, right? There's just so little knowledge about this as a technology. To begin with, most people have never even heard of UV for disinfection. But even among people who have heard of UV for disinfection, almost no one has heard of 222 nm. The pitch is really easy.
It's a cool science-fiction technology where you're using special wavelengths to decrease the risk of getting sick. Everyone is eager once they know about it, but almost nobody knows about it. And I think that if you're thinking, “How can I make this more widespread? How can I make it more common? How can I enable the world to get better faster?” information is the main bottleneck.
Yeah. And when we're talking about clean air, I think far-UVC is only one part of the solution. Air filtration and ventilation are also part of that. If you're a parent of a kid, you can lean on your kid's school, daycare, workplace, community centers, or social events that you participate in and ask, “How clean is the air in this building? Can we make it cleaner? Can I help?”
Whether that is far-UVC with AeroLamp or with a different company, we're very cheap, so we think that's attractive. But we're also an open-source company, so in principle, anyone can just take the CAD files published on our GitHub and make their own. Clean air needs to be much more of a thing. There are groups, like a lot of these still-COVIDing groups, and they're fighting the good fight, but it's just not enough. It needs to be much more of a social movement, and there needs to be a broad coalition for upgrading our buildings so that they're not making us sick all the time.
Mm-hmm. So, putting your fingers to the wind here, if the end goal is a social movement and widespread deployment of this in many built environments, if there were hypothetically a well-resourced capitalist listening to this and thinking, “Okay, but where do I spend the first $1 million?” would you want it, at this point, spent on a trial deployment and some papers about that? Or would you want it in, I don't know, a social media marketing campaign to get Taylor Swift or someone to adopt this and achieve adoption that way?
I'm saying something that's kind of absurd, but are we more limited by the formal evidence at this point, or are we more limited by just getting more people to know about it?
I think the latter, but you could easily argue the other way around.
Yeah, I would say the former, just because I think that might be a more robust way to get the word out relative to Taylor Swift doing it. I do think that we are maybe early enough that too much attention could have something of an IFSR effect. So we want to scale responsibly.
I'm a fan of trial deployments. I think we've already started seeing effects, with AeroLamps just being around in San Francisco and Berkeley venues. Also here in D.C., increasing numbers of group houses and event spaces are having these. The more that they're around and people are like, “Oh, yeah, that's just a normal piece of infrastructure,” I think that can function on its own.
I think Taylor Swift talking about far-UVC right now could be very good, very bad, or have no effect at all.
Yeah, honestly, if I were going to pick a celebrity, it wouldn't be Taylor Swift. I think it would be Paris Hilton, because if high-end hotel brands get associated with clean air, I think that would be pretty valuable.
Yeah. Oh, boy. We will be paying for the sort of political-economy consequences of the pandemic for a long time, unfortunately. But one of them is that, in some quarters, there is some skepticism regarding anything broadly associated with public health. Phew, there's much one could say about that.
Well, I think the political angle here is—it is tough, but I think there's a completely nonpolitical, capitalist angle that's pretty feasible. If you run a business that employs people who are highly paid, you're internalizing the costs of sickness there yourself, right?
That applies whether it's someone in your office who gets sick or someone's kid gets sick and then they're out taking care of their kid. I was doing some economic analysis on this a couple of years back, and a significant part of the economic cost of colds is actually caregiver absenteeism rather than direct absenteeism, because kids get sick a lot more. They're more vulnerable.
Yeah, and this is something we saw a lot during COVID: a lot of private companies had interventions that were not state-level mandated, right? This is something we've been trying to do: get in contact with people at Google, because Google is big enough and has enough things going on that it has someone who's in charge of the overall health of Google employees, right?
If we can get someone like that on board, they don't need to do any sort of campaign convincing the average person about these interventions. They just need to do the math and say, “Oh, we think this will benefit Google on the bottom line,” right? And that's a very different sort of calculation.
A lot of financial firms during COVID, quite early on, saw the writing on the wall and implemented clean-air interventions in their offices quite quickly. High-quality far-UVC was not broadly available then, but high levels of ventilation and filtration—companies absolutely saw the business case there.
Obviously, now we're in a different situation. Post-pandemic, things are tougher, but I think it's not impossible. At a certain price point, the business case is quite good.
Generally speaking, I'm an optimist, but the thing that I worry about a little bit is that it could turn into a situation where there's something of a heckler's veto, and the one person in an organization who is most opposed to public health measures might decide to fixate on this as something they definitely don't want. Hopefully, that doesn't happen.
What we've seen is that this is a huge problem when trying to formally run a study. If you're trying to run a study on clean-air effectiveness or far-UVC effectiveness, and we'd like to install these in a space for the study, that is extremely vulnerable to the heckler's veto. You just need one person who's not totally comfortable with it, and the IRB will never let you do it.
It's actually quite a bit easier if a building owner decides, “You know what? We want this. We're installing it.” Generally, in offices, we've found that employees are usually much more on board, and it's the building manager who's like, “Eh, do we really want to spend this money?” So we find that it is often substantively driven by employee demands in the office case.
I think normal technology diffusion or deployment is substantially less vulnerable. The nice thing about that is, if somebody has decided to install this technology because they think it's good and they want to benefit from it, there's nothing stopping you from studying the effects of it later on. So we can still get good evidence without rendering ourselves super vulnerable to the heckler's veto.
And just playing out the micro-politics of this sort of thing, the vaccines have a great individual cost. You have to take time out of your day, go out, get jabbed, and it's a very unpleasant experience, which is more unpleasant than it needs to be. It's amazing to me that we haven't made ShotGuard or something similar the standard of care everywhere.
Be that as it may, there's a visceral unpleasantness to vaccines in a way that there isn't to there being a box in the corner. It doesn't emit anything visible, and it will simply stand there for, hopefully, the rest of time. We're hoping that we successfully get this deployed and that it performs to our expectations—or outperforms them—in the amount of actual impact it has on lived experience.
And thanks very much, Misha and Vivian, for being on the program today. We will follow along with interest as this diffuses into society.
Yeah. It's great to be on here.
Yeah. Great to chat.