Why, Immunologically, Housing-Related Fungi and Endotoxins (and Other Chronic Pro-Inflammatory Stressors) Risk Latent Tuberculosis Reactivation, Severe Asthma, and Translocating and Invasive Infections in Indigenous Communities in Canada

IF 1.7 4区 医学 Q1 ANTHROPOLOGY
Stacie Burke
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Abstract

Type 1/M1/TH1 and type 3/M1/TH17 pro-inflammatory switches are risks for latent Mycobacterium tuberculosis (Mtb) reactivation and ongoing infection transmission. This paper considers the heavy toll of reactivation risk in Indigenous communities in Canada and the chronic, everyday pro-inflammatory stressors connected with type 3/M1/TH17 immune switching, including household fungal and endotoxin exposures that fuel reactivation risk. The paper argues that regular or chronic pro-inflammatory stressors are risks not only for latent Mtb reactivation and ongoing transmission, but also, via compromised type 4/M2/TH22 mucosal barrier protections, severe asthma and translocated, possibly invasive, bacterial, viral, and fungal infections. Individual and community efforts to reduce chronic pro-inflammatory stressors are important, but as the immunological, switch-inducing rationale suggests, unless chronic pro-inflammatory risks associated with housing are mediated, tuberculosis reactivation and other health risks will likely persist.

为什么,免疫学,住房相关真菌和内毒素(和其他慢性促炎应激源)风险潜伏结核再激活,严重哮喘,易位和侵袭性感染在加拿大土著社区。
1/M1/TH1型和3/M1/TH17型促炎开关是潜在结核分枝杆菌(Mtb)再激活和持续感染传播的风险。本文考虑了加拿大土著社区中再激活风险的沉重代价,以及与3/M1/TH17型免疫转换相关的慢性、日常促炎应激源,包括增加再激活风险的家庭真菌和内毒素暴露。本文认为,常规或慢性促炎应激源不仅有潜在Mtb再激活和持续传播的风险,而且还可能通过4型/M2/TH22粘膜屏障保护受损,导致严重哮喘和易位性(可能是侵袭性的)细菌、病毒和真菌感染。个人和社区减少慢性促炎应激源的努力很重要,但正如免疫学、开关诱导原理所表明的那样,除非介导与住房相关的慢性促炎风险,否则结核病再激活和其他健康风险可能会持续存在。
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来源期刊
CiteScore
4.80
自引率
13.80%
发文量
124
审稿时长
4-8 weeks
期刊介绍: The American Journal of Human Biology is the Official Journal of the Human Biology Association. The American Journal of Human Biology is a bimonthly, peer-reviewed, internationally circulated journal that publishes reports of original research, theoretical articles and timely reviews, and brief communications in the interdisciplinary field of human biology. As the official journal of the Human Biology Association, the Journal also publishes abstracts of research presented at its annual scientific meeting and book reviews relevant to the field. The Journal seeks scholarly manuscripts that address all aspects of human biology, health, and disease, particularly those that stress comparative, developmental, ecological, or evolutionary perspectives. The transdisciplinary areas covered in the Journal include, but are not limited to, epidemiology, genetic variation, population biology and demography, physiology, anatomy, nutrition, growth and aging, physical performance, physical activity and fitness, ecology, and evolution, along with their interactions. The Journal publishes basic, applied, and methodologically oriented research from all areas, including measurement, analytical techniques and strategies, and computer applications in human biology. Like many other biologically oriented disciplines, the field of human biology has undergone considerable growth and diversification in recent years, and the expansion of the aims and scope of the Journal is a reflection of this growth and membership diversification. The Journal is committed to prompt review, and priority publication is given to manuscripts with novel or timely findings, and to manuscripts of unusual interest.
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