牛奶免疫力的权衡会影响婴儿患传染病的风险。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2022-06-13 eCollection Date: 2022-01-01 DOI:10.1093/emph/eoac020
Katherine Wander, Masako Fujita, Siobhan M Mattison, Margaret Duris, Megan Gauck, Tessa Hopt, Katherine Lacy, Angela Foligno, Rebecca Ulloa, Connor Dodge, Frida Mowo, Ireen Kiwelu, Blandina T Mmbaga
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引用次数: 0

摘要

背景和目的:人类的免疫系统在进化过程中,既要防止感染,又要控制免疫介导的损伤,还要耐受共生微生物。这种保护与伤害之间的权衡几乎肯定会延伸到乳汁的免疫系统:方法:在坦桑尼亚乞力马扎罗山的母乳喂养母婴二人组中,我们通过体外白细胞介素-6的增加来描述乳汁对肠炎沙门氏菌(传染性病原体)和大肠杆菌(良性目标)的促炎性免疫反应。我们通过被动监测来描述婴儿感染传染病的情况。我们使用 Cox 比例危险模型来描述牛奶免疫活性与婴儿传染病之间的关系:结果:在婴儿中,呼吸道感染的风险随着牛奶对肠炎双球菌体外促炎反应的增加而降低(危险比 [HR]:0.68;95% 置信区间 [CI]:0.54,0.86;P:0.001),而胃肠道感染的风险随着牛奶对大肠杆菌体外促炎反应的增加而增加(HR:1.44;95% CI:1.05,1.99;P:0.022)。牛奶对肠炎球菌和大肠杆菌的促炎反应呈正相关(Spearman's rho:0.60;P:0.000):这些研究结果表明了牛奶免疫活动中的权衡问题:适当的促炎活动的益处是以错误的促炎活动的危害为代价的。这种权衡可能会以复杂的方式影响婴儿的健康,这取决于当时的传染病状况。母婴二元组合如何优化牛奶的促炎免疫活动,应该是未来牛奶免疫系统生态进化研究的一个核心问题。
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Tradeoffs in milk immunity affect infant infectious disease risk.

Background and objectives: The human immune system has evolved to balance protection against infection with control of immune-mediated damage and tolerance of commensal microbes. Such tradeoffs between protection and harm almost certainly extend to the immune system of milk.

Methodology: Among breastfeeding mother-infant dyads in Kilimanjaro, Tanzania, we characterized in vitro proinflammatory milk immune responses to Salmonella enterica (an infectious agent) and Escherichia coli (a benign target) as the increase in interleukin-6 after 24 h of incubation with each bacterium. We characterized incident infectious diseases among infants through passive monitoring. We used Cox proportional hazards models to describe associations between milk immune activity and infant infectious disease.

Results: Among infants, risk for respiratory infections declined with increasing milk in vitro proinflammatory response to S. enterica (hazard ratio [HR]: 0.68; 95% confidence interval [CI]: 0.54, 0.86; P: 0.001), while risk for gastrointestinal infections increased with increasing milk in vitro proinflammatory response to E. coli (HR: 1.44; 95% CI: 1.05, 1.99; P: 0.022). Milk proinflammatory responses to S. enterica and E. coli were positively correlated (Spearman's rho: 0.60; P: 0.000).

Conclusions and implications: These findings demonstrate a tradeoff in milk immune activity: the benefits of appropriate proinflammatory activity come at the hazard of misdirected proinflammatory activity. This tradeoff is likely to affect infant health in complex ways, depending on prevailing infectious disease conditions. How mother-infant dyads optimize proinflammatory milk immune activity should be a central question in future ecological-evolutionary studies of the immune system of milk.

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