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早期生活抗生素驱动的失调导致小鼠疫苗免疫反应失调。

Early-Life Antibiotic-Driven Dysbiosis Leads to Dysregulated Vaccine Immune Responses in Mice.

机构信息

Infection & Immunity Theme, South Australian Health and Medical Research Institute, North Terrace, Adelaide, SA 5000, Australia.

Infection & Immunity Theme, South Australian Health and Medical Research Institute, North Terrace, Adelaide, SA 5000, Australia; Department of Immunology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana Chuo-ku, Chiba 260-8670, Japan.

出版信息

Cell Host Microbe. 2018 May 9;23(5):653-660.e5. doi: 10.1016/j.chom.2018.04.009.

Abstract

Antibody-mediated responses play a critical role in vaccine-mediated immunity. However, for reasons that are poorly understood, these responses are highly variable between individuals. Using a mouse model, we report that antibiotic-driven intestinal dysbiosis, specifically in early life, leads to significantly impaired antibody responses to five different adjuvanted and live vaccines. Restoration of the commensal microbiota following antibiotic exposure rescues these impaired responses. In contrast, antibiotic-treated adult mice do not exhibit impaired antibody responses to vaccination. Interestingly, in contrast to impaired antibody responses, immunized mice exposed to early-life antibiotics display significantly enhanced T cell cytokine recall responses upon ex vivo restimulation with the vaccine antigen. Our results demonstrate that, in mice, antibiotic-driven dysregulation of the gut microbiota in early life can modulate immune responses to vaccines that are routinely administered to infants worldwide.

摘要

抗体介导的反应在疫苗介导的免疫中起着至关重要的作用。然而,由于原因尚不清楚,这些反应在个体之间存在很大的差异。我们使用小鼠模型报告称,抗生素驱动的肠道菌群失调,特别是在生命早期,会导致对五种不同佐剂和活疫苗的抗体反应显著受损。抗生素暴露后恢复共生微生物群可挽救这些受损的反应。相比之下,接受抗生素治疗的成年小鼠对疫苗接种不会产生受损的抗体反应。有趣的是,与抗体反应受损相反,暴露于生命早期抗生素的免疫小鼠在用疫苗抗原进行体外再刺激时显示出明显增强的 T 细胞细胞因子回忆反应。我们的结果表明,在小鼠中,生命早期抗生素驱动的肠道微生物群失调可以调节全球常规接种婴儿的疫苗的免疫反应。

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