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前沿:抗原激活的 B 细胞定位于滤泡边缘和随后的生发中心反应需要巨噬细胞。

Cutting edge: Macrophages are required for localization of antigen-activated B cells to the follicular perimeter and the subsequent germinal center response.

机构信息

Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

J Immunol. 2013 May 15;190(10):4923-7. doi: 10.4049/jimmunol.1300350. Epub 2013 Apr 8.

DOI:10.4049/jimmunol.1300350
PMID:23567932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3647009/
Abstract

We demonstrated recently that, after accumulation of Ag-engaged B cells at the T cell zone boundaries in the spleen, these B cells migrate to the perimeter of follicles adjacent to the marginal zone. They undergo rapid proliferation at this site prior to coalescence into germinal centers (GCs). In this article, we report that this phase of migration and expansion of activated Ag-specific B cells, as well as subsequent formation of GCs, does not take place in the absence of splenic macrophages. Our data suggest a previously unappreciated function for macrophages in orchestrating the early phases of T cell-dependent B cell responses and formation of GCs distinct from their potential role in Ag presentation to T cells.

摘要

我们最近证明,在 Ag 结合的 B 细胞在脾脏的 T 细胞区边界处积累之后,这些 B 细胞迁移到邻近边缘区的滤泡的周边。在这个部位,它们在融合形成生发中心(GC)之前迅速增殖。在本文中,我们报告说,这种活化的 Ag 特异性 B 细胞的迁移和扩增阶段,以及随后 GC 的形成,如果没有脾脏巨噬细胞就不会发生。我们的数据表明,巨噬细胞在协调 T 细胞依赖性 B 细胞反应的早期阶段和形成不同于其向 T 细胞呈递 Ag 的潜在作用的 GC 方面具有以前未被认识到的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/3647009/f6b8276f5263/nihms-457010-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/3647009/dd6232021273/nihms-457010-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/3647009/90f15665132a/nihms-457010-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/3647009/f6b8276f5263/nihms-457010-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/3647009/dd6232021273/nihms-457010-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/3647009/90f15665132a/nihms-457010-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/3647009/f6b8276f5263/nihms-457010-f0003.jpg

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本文引用的文献

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S1PR2 links germinal center confinement and growth regulation.S1PR2 将生发中心限制和生长调节联系起来。
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Innate immune functions of macrophage subpopulations in the spleen.
感染会诱导滤泡树突状细胞网络的重组,同时无法产生生发中心。
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PD-1 immunobiology in glomerulonephritis and renal cell carcinoma.PD-1 免疫生物学在肾小球肾炎和肾细胞癌中的作用。
BMC Nephrol. 2021 Mar 6;22(1):80. doi: 10.1186/s12882-021-02257-6.
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Marginal zone SIGN-R1 macrophages are essential for the maturation of germinal center B cells in the spleen.边缘区 SIGN-R1 巨噬细胞对于脾脏生发中心 B 细胞的成熟是必不可少的。
Proc Natl Acad Sci U S A. 2020 Jun 2;117(22):12295-12305. doi: 10.1073/pnas.1921673117. Epub 2020 May 18.
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Multi-omics: Differential expression of IFN-γ results in distinctive mechanistic features linking chronic inflammation, gut dysbiosis, and autoimmune diseases.多组学:IFN-γ 的差异表达导致慢性炎症、肠道菌群失调和自身免疫性疾病之间的独特机制特征相关联。
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TNF-α Contributes to Lymphoid Tissue Disorganization and Germinal Center B Cell Suppression during Intracellular Bacterial Infection.TNF-α 有助于胞内细菌感染期间淋巴组织紊乱和生发中心 B 细胞抑制。
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The continuing story of T-cell independent antibodies.T 细胞非依赖型抗体的持续故事。
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