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疟疾的天然体液免疫

Naturally Acquired Humoral Immunity Against Malaria.

机构信息

Department of Microbiology, Immunology and Molecular Genetics, Long School of Medicine, The University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.

出版信息

Front Immunol. 2020 Oct 29;11:594653. doi: 10.3389/fimmu.2020.594653. eCollection 2020.

DOI:10.3389/fimmu.2020.594653
PMID:33193447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7658415/
Abstract

Malaria remains a significant contributor to the global burden of disease, with around 40% of the world's population at risk of infections. The development of an effective vaccine against the malaria parasite would mark a breakthrough in the fight to eradicate the disease. Over time, natural infection elicits a robust immune response against the blood stage of the parasite, providing protection against malaria. In recent years, we have gained valuable insight into the mechanisms by which IgG acts to prevent pathology and inhibit parasite replication, as well as the potential role of immunoglobulin M (IgM) in these processes. Here, we discuss recent advances in our understanding of the mechanisms, acquisition, and maintenance of naturally acquired immunity, and the relevance of these discoveries for the development of a potential vaccine against the blood stage of .

摘要

疟疾仍然是全球疾病负担的一个重要因素,全球约有 40%的人口面临感染的风险。开发出一种针对疟原虫的有效疫苗将标志着消灭这种疾病的斗争取得突破。随着时间的推移,自然感染会引发针对寄生虫血阶段的强大免疫反应,从而提供对疟疾的保护。近年来,我们深入了解了 IgG 预防发病机制和抑制寄生虫复制的作用机制,以及 IgM 在这些过程中的潜在作用。在这里,我们讨论了对自然获得性免疫的机制、获得和维持的理解的最新进展,以及这些发现对开发针对疟原虫血阶段的潜在疫苗的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9479/7658415/0ec200677eb8/fimmu-11-594653-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9479/7658415/9ae1d3238bb5/fimmu-11-594653-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9479/7658415/6ba057dac2bc/fimmu-11-594653-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9479/7658415/0ec200677eb8/fimmu-11-594653-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9479/7658415/9ae1d3238bb5/fimmu-11-594653-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9479/7658415/6ba057dac2bc/fimmu-11-594653-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9479/7658415/0ec200677eb8/fimmu-11-594653-g003.jpg

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Expression of inhibitory receptors by B cells in chronic human infectious diseases restricts responses to membrane-associated antigens.慢性人类传染病中 B 细胞抑制性受体的表达限制了对膜相关抗原的反应。
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Proteome-wide analysis of a malaria vaccine study reveals personalized humoral immune profiles in Tanzanian adults.
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