Regulatory T-Cells During Pregnancy Relate to Women's Own Childhood History of Microbial Exposure

IF 1.6 4区 医学 Q1 ANTHROPOLOGY American Journal of Human Biology Pub Date : 2025-02-28 DOI:10.1002/ajhb.70013
Molly M. Fox, Adiba Hassan, Kyle S. Wiley, Dayoon Kwon, Delaney A. Knorr
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Abstract

Objectives

Previous studies found that children with siblings, farm residence, and other proxies of greater microbial contacts had lower rates of hyper-responsive immune disorders. Yet, scientific debate persists regarding whether the human immune system is educated in early life primarily as a function of pathogenic or benign microbial exposures, or both. Furthermore, pregnancy relies on women's intrinsic immunosuppressive function, yet it remained unknown how immunoregulation in pregnant women relates to early-life microbial exposures. Here, we conduct a preliminary examination of whether childhood microbial exposures prime women's pregnancy-related immunoregulatory capacity.

Methods

We administered retrospective questionnaires to estimate 55 pregnant women's early-life exposure to pathogenic (e.g., illness) and benign (e.g., pets; rural residence) microbes. Tolerogenic regulatory T-cells (Tregs) and Treg subtypes were measured by flow cytometry from peripheral blood.

Results

Results show that proxies for both pathogenic and benign exposures were positively associated with Treg concentrations.

Conclusions

These findings offer insights that may help elucidate the relative contributions of early-life pathogenic (“hygiene hypothesis”) and benign (“old friends hypothesis”) microbial exposures toward the expansion of the Treg compartment. Human evolutionary history is characterized by changing microbial exposures as human residency patterns, living environments, and subsistence strategies changed. In this context, our findings suggest the possibility of less gestational pathology in human evolutionary past conditions typified by richer diversity of microbial exposure.

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研究目的 以前的研究发现,有兄弟姐妹、住在农场和其他与微生物接触较多的替代物的儿童患高反应性免疫疾病的比例较低。然而,关于人类免疫系统在生命早期的教育主要是作为病原体或良性微生物接触的功能,还是两者兼而有之,科学界一直存在争论。此外,妊娠依赖于女性固有的免疫抑制功能,但孕妇的免疫调节与生命早期的微生物暴露之间的关系仍然未知。在此,我们对儿童期微生物暴露是否会影响女性与妊娠相关的免疫调节能力进行了初步研究。 方法 我们对 55 名孕妇进行了回顾性问卷调查,以估计她们早年接触致病微生物(如疾病)和良性微生物(如宠物、农村居住地)的情况。通过外周血流式细胞术测量了耐受性调节性 T 细胞(Tregs)和 Treg 亚型。 结果 结果显示,致病性和良性暴露的代用指标与 Treg 的浓度呈正相关。 结论 这些发现提供了一些见解,可能有助于阐明生命早期致病("卫生假说")和良性("老朋友假说")微生物暴露对 Treg 区系扩展的相对贡献。人类进化史的特点是,随着人类居住模式、生活环境和生存策略的改变,所接触的微生物也在不断变化。在这种情况下,我们的研究结果表明,在人类进化的过去,微生物暴露的多样性更丰富,妊娠期病症可能更少。
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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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