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疟疾感染中的T滤泡辅助细胞及其在抗体诱导中的作用。

T-follicular helper cells in malaria infection and roles in antibody induction.

作者信息

Soon Megan S F, Nalubega Mayimuna, Boyle Michelle J

机构信息

Department of Infectious Diseases, QIMR-Berghofer, 300 Herston Road, Herston, QLD, 4006, Australia.

Infectious Diseases Research Collaboration, Tororo District Hospital, Tororo, Uganda.

出版信息

Oxf Open Immunol. 2021 Apr 10;2(1):iqab008. doi: 10.1093/oxfimm/iqab008. eCollection 2021.

Abstract

Immunity to malaria is mediated by antibodies that block parasite replication to limit parasite burden and prevent disease. Cytophilic antibodies have been consistently shown to be associated with protection, and recent work has improved our understanding of the direct and Fc-mediated mechanisms of protective antibodies. Antibodies also have important roles in vaccine-mediated immunity. Antibody induction is driven by the specialized CD4 T cells, T-follicular helper (Tfh) cells, which function within the germinal centre to drive B-cell activation and antibody induction. In humans, circulating Tfh cells can be identified in peripheral blood and are differentiated into subsets that appear to have pathogen/vaccination-specific roles in antibody induction. Tfh cell responses are essential for protective immunity from infection in murine models of malaria. Our understanding of the activation of Tfh cells during human malaria infection and the importance of different Tfh cell subsets in antibody development is still emerging. This review will discuss our current knowledge of Tfh cell activation and development in malaria, and the potential avenues and pitfalls of targeting Tfh cells to improve malaria vaccines.

摘要

对疟疾的免疫是由抗体介导的,这些抗体可阻断寄生虫复制以限制寄生虫负荷并预防疾病。嗜细胞抗体一直被证明与保护作用相关,最近的研究增进了我们对保护性抗体的直接机制和Fc介导机制的理解。抗体在疫苗介导的免疫中也发挥着重要作用。抗体诱导由专门的CD4 T细胞,即滤泡辅助性T(Tfh)细胞驱动,这些细胞在生发中心发挥作用,驱动B细胞活化和抗体诱导。在人类中,循环Tfh细胞可在外周血中被识别,并分化为不同的亚群,这些亚群似乎在抗体诱导中具有病原体/疫苗特异性作用。在疟疾的小鼠模型中,Tfh细胞反应对于抵抗感染的保护性免疫至关重要。我们对人类疟疾感染期间Tfh细胞的激活以及不同Tfh细胞亚群在抗体产生中的重要性的理解仍在不断发展。本综述将讨论我们目前对疟疾中Tfh细胞激活和发育的认识,以及靶向Tfh细胞以改进疟疾疫苗的潜在途径和陷阱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/921b/9914587/9ce6a149506b/iqab008f1.jpg

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