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结核分枝杆菌感染中抗体功能的最新研究进展及其在结核疫苗开发中的相关性。

Updates on antibody functions in Mycobacterium tuberculosis infection and their relevance for developing a vaccine against tuberculosis.

机构信息

Department of Medicine, Albert Einstein College of Medicine, 1300 Morris Park Ave, Bronx, NY 10461, United States; Department of Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Ave, Bronx, NY 10461, United States.

Department of Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Ave, Bronx, NY 10461, United States; Center for Cooperative Research bioGUNE (CICbioGUNE), Bizkaia Technology Park, 48160 Derio, Bizkaia, Spain.

出版信息

Curr Opin Immunol. 2018 Aug;53:30-37. doi: 10.1016/j.coi.2018.04.004. Epub 2018 Apr 12.

DOI:10.1016/j.coi.2018.04.004
PMID:29656063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6141321/
Abstract

A more effective vaccine to control tuberculosis (TB), a major global public health problem, is urgently needed. Current vaccine candidates focus predominantly on eliciting cell-mediated immunity but other arms of the immune system also contribute to protection against TB. We review here recent studies that enhance our current knowledge of antibody-mediated functions against Mycobacterium tuberculosis. These findings, which contribute to the increasing evidence that antibodies have a protective role against TB, include demonstrations that firstly distinct human antibody Fc glycosylation patterns, found in latent M. tuberculosis infection but not in active TB, influence the efficacy of the host to control M. tuberculosis infection, secondly antibody isotype influences human antibody functions, and thirdly that antibodies targeting M. tuberculosis surface antigens are protective. We discuss these findings in the context of TB vaccine development and highlight the need for further research on antibody-mediated immunity in M. tuberculosis infection.

摘要

为了控制作为全球主要公共卫生问题之一的结核病(TB),我们急需更有效的疫苗。当前的疫苗候选物主要集中在诱导细胞介导的免疫上,但免疫系统的其他部分也有助于预防 TB。在这里,我们回顾了最近的研究,这些研究增强了我们对抗体介导的抗结核分枝杆菌功能的现有认识。这些发现有助于增加抗体在预防 TB 方面具有保护作用的证据,包括证明首先在潜伏性结核分枝杆菌感染中发现但在活动性 TB 中未发现的人类抗体 Fc 糖基化模式会影响宿主控制结核分枝杆菌感染的效果,其次是抗体同种型会影响人类抗体的功能,第三是针对结核分枝杆菌表面抗原的抗体具有保护作用。我们在结核分枝杆菌感染的疫苗开发背景下讨论了这些发现,并强调需要进一步研究抗体介导的免疫。

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