早期疫苗反应性的变异性。

IF 3.7 4区 医学 Q2 CELL BIOLOGY
Michael E Pichichero
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引用次数: 0

摘要

早期接种疫苗会引发可变的抗体和细胞免疫反应,有时会使完全接种疫苗的儿童无法抵御危及生命的传染病。特定的免疫细胞群和免疫网络可能在早期生命的前100天出现的机会窗口中有一个关键的发展和校准期。在疫苗反应的早期生命决定因素中,本综述将重点关注涉及婴儿微生物群和代谢组发育的可改变因素:抗生素暴露、母乳喂养与配方奶粉喂养以及新生儿剖腹产与阴道分娩。还综述了微生物群如何作为疫苗反应的天然佐剂,以及微生物群衍生的代谢物如何影响疫苗反应。早期疫苗反应性差可能与感染易感性增加有关,因为这两种表型具有相似的免疫失调特征。当干预措施具有最高成功潜力时,应寻求一种早期疫苗接种前的内型,以预测疫苗反应轨迹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variability of vaccine responsiveness in early life

Vaccinations in early life elicit variable antibody and cellular immune responses, sometimes leaving fully vaccinated children unprotected against life-threatening infectious diseases. Specific immune cell populations and immune networks may have a critical period of development and calibration in a window of opportunity occurring during the first 100 days of early life. Among the early life determinants of vaccine responses, this review will focus on modifiable factors involving development of the infant microbiota and metabolome: antibiotic exposure, breast versus formula feeding, and Caesarian section versus vaginal delivery of newborns. How microbiota may serve as natural adjuvants for vaccine responses and how microbiota-derived metabolites influence vaccine responses are also reviewed. Early life poor vaccine responsiveness can be linked to increased infection susceptibility because both phenotypes share similar immunity dysregulation profiles. An early life pre-vaccination endotype, when interventions have the highest potential for success, should be sought that predicts vaccine response trajectories.

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来源期刊
Cellular immunology
Cellular immunology 生物-免疫学
CiteScore
8.20
自引率
2.30%
发文量
102
审稿时长
30 days
期刊介绍: Cellular Immunology publishes original investigations concerned with the immunological activities of cells in experimental or clinical situations. The scope of the journal encompasses the broad area of in vitro and in vivo studies of cellular immune responses. Purely clinical descriptive studies are not considered. Research Areas include: • Antigen receptor sites • Autoimmunity • Delayed-type hypersensitivity or cellular immunity • Immunologic deficiency states and their reconstitution • Immunologic surveillance and tumor immunity • Immunomodulation • Immunotherapy • Lymphokines and cytokines • Nonantibody immunity • Parasite immunology • Resistance to intracellular microbial and viral infection • Thymus and lymphocyte immunobiology • Transplantation immunology • Tumor immunity.
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