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淋巴结驻留树突状细胞摄取和呈递滤泡树突状细胞结合抗原。

Acquisition and presentation of follicular dendritic cell-bound antigen by lymph node-resident dendritic cells.

机构信息

Department of Pathology, New York University School of Medicine, New York, NY 10016, USA.

出版信息

J Exp Med. 2011 Jan 17;208(1):135-48. doi: 10.1084/jem.20100354. Epub 2010 Dec 20.

DOI:10.1084/jem.20100354
PMID:21173103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3023135/
Abstract

Follicular dendritic cells (DCs [FDCs]) are prominent stromal cell constituents of B cell follicles with the remarkable ability to retain complement-fixed antigens on their cell surface for extended periods of time. These retained immune complexes have long been known to provide the antigenic stimulus that drives antibody affinity maturation, but their role in cellular immunity has remained unclear. In this study, we show that FDC-retained antigens are continually sampled by lymph node-resident DCs for presentation to CD8 T cells. This novel pathway of antigen acquisition was detectable when FDCs were loaded with purified antigens bound into classical antigen-antibody immune complexes, as well as after pregnancy, when they are loaded physiologically with antigens associated with the complement-fixed microparticles released from the placenta into maternal blood. In both cases, ensuing antigen presentation was profoundly tolerogenic, as it induced T cell deletion even under inflammatory conditions. These results significantly broaden the scope of FDC function and suggest new ways that the complement system and persistent antigen presentation might influence T cell activation and the maintenance of peripheral immune tolerance.

摘要

滤泡树突状细胞 (DCs [FDCs]) 是 B 细胞滤泡中突出的基质细胞成分,具有将补体固定抗原保留在其细胞表面的显著能力,保留的时间很长。这些保留的免疫复合物长期以来一直被认为提供了驱动抗体亲和力成熟的抗原刺激,但它们在细胞免疫中的作用仍然不清楚。在这项研究中,我们表明 FDC 保留的抗原被淋巴结驻留的 DC 持续取样,以呈递给 CD8 T 细胞。当 FDC 加载与经典抗原-抗体免疫复合物结合的纯化抗原时,可以检测到这种新的抗原获取途径,以及在怀孕时,当它们生理性地加载与从胎盘释放到母血中的补体固定微粒相关的抗原时。在这两种情况下,随后的抗原呈递都是明显的耐受原性的,因为它甚至在炎症条件下诱导 T 细胞删除。这些结果大大拓宽了 FDC 功能的范围,并提出了补体系统和持续抗原呈递可能影响 T 细胞激活和外周免疫耐受维持的新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/f7fc56c824a3/JEM_20100354_GS_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/e6f5496b9b0f/JEM_20100354_RGB_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/d4f26ada32e0/JEM_20100354_GS_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/697539ded09e/JEM_20100354_GS_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/434b0610b0f6/JEM_20100354_GS_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/3e966fd6a4ca/JEM_20100354_RGB_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/5d64519621eb/JEM_20100354_GS_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/f7fc56c824a3/JEM_20100354_GS_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/e6f5496b9b0f/JEM_20100354_RGB_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/d4f26ada32e0/JEM_20100354_GS_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/697539ded09e/JEM_20100354_GS_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/434b0610b0f6/JEM_20100354_GS_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/3e966fd6a4ca/JEM_20100354_RGB_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/5d64519621eb/JEM_20100354_GS_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2367/3023135/f7fc56c824a3/JEM_20100354_GS_Fig7.jpg

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