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B 细胞在抗原有限的情况下需要 DOCK8 来引发和整合 T 细胞的帮助。

B cells require DOCK8 to elicit and integrate T cell help when antigen is limiting.

机构信息

MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.

出版信息

Sci Immunol. 2024 Aug 9;9(98):eadd4874. doi: 10.1126/sciimmunol.add4874.

Abstract

Dedicator of cytokinesis 8 (DOCK8) immunodeficiency syndrome is characterized by a failure of the germinal center response, a process involving the proliferation and positive selection of antigen-specific B cells. Here, we describe how DOCK8-deficient B cells are blocked at a light-zone checkpoint in the germinal centers of immunized mice, where they are unable to respond to T cell-dependent survival and selection signals and consequently differentiate into plasma cells or memory B cells. Although DOCK8-deficient B cells can acquire and present antigen to initiate activation of cognate T cells, integrin up-regulation, B cell-T cell conjugate formation, and costimulation are insufficient for sustained B cell and T cell activation when antigen availability is limited. Our findings provide an explanation for the failure of the humoral response in DOCK8 immunodeficiency syndrome and insight into how the level of available antigen modulates B cell-T cell cross-talk to fine-tune humoral immune responses and immunological memory.

摘要

细胞分裂蛋白 8(DOCK8)免疫缺陷综合征的特征是生发中心反应失败,这是一个涉及抗原特异性 B 细胞增殖和阳性选择的过程。在这里,我们描述了 DOCK8 缺陷 B 细胞如何在免疫小鼠的生发中心的亮区检查点被阻断,在那里它们无法响应 T 细胞依赖性存活和选择信号,因此无法分化为浆细胞或记忆 B 细胞。尽管 DOCK8 缺陷 B 细胞可以获取和呈递抗原以启动同源 T 细胞的激活,但整合素上调、B 细胞-T 细胞共轭形成和共刺激对于在抗原可用性有限时维持 B 细胞和 T 细胞的激活是不够的。我们的研究结果为 DOCK8 免疫缺陷综合征中体液反应失败提供了一个解释,并深入了解了可用抗原的水平如何调节 B 细胞-T 细胞相互作用,以微调体液免疫反应和免疫记忆。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ae1/7616390/8f6886d1e944/EMS198076-f001.jpg

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