Cargando…
Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells
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 stimul...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023135/ https://www.ncbi.nlm.nih.gov/pubmed/21173103 http://dx.doi.org/10.1084/jem.20100354 |
_version_ | 1782196649446080512 |
---|---|
author | McCloskey, Megan L. Curotto de Lafaille, Maria A. Carroll, Michael C. Erlebacher, Adrian |
author_facet | McCloskey, Megan L. Curotto de Lafaille, Maria A. Carroll, Michael C. Erlebacher, Adrian |
author_sort | McCloskey, Megan L. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-3023135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30231352011-07-17 Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells McCloskey, Megan L. Curotto de Lafaille, Maria A. Carroll, Michael C. Erlebacher, Adrian J Exp Med Article 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. The Rockefeller University Press 2011-01-17 /pmc/articles/PMC3023135/ /pubmed/21173103 http://dx.doi.org/10.1084/jem.20100354 Text en © 2011 McCloskey et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article McCloskey, Megan L. Curotto de Lafaille, Maria A. Carroll, Michael C. Erlebacher, Adrian Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells |
title | Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells |
title_full | Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells |
title_fullStr | Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells |
title_full_unstemmed | Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells |
title_short | Acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells |
title_sort | acquisition and presentation of follicular dendritic cell–bound antigen by lymph node–resident dendritic cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023135/ https://www.ncbi.nlm.nih.gov/pubmed/21173103 http://dx.doi.org/10.1084/jem.20100354 |
work_keys_str_mv | AT mccloskeymeganl acquisitionandpresentationoffolliculardendriticcellboundantigenbylymphnoderesidentdendriticcells AT curottodelafaillemariaa acquisitionandpresentationoffolliculardendriticcellboundantigenbylymphnoderesidentdendriticcells AT carrollmichaelc acquisitionandpresentationoffolliculardendriticcellboundantigenbylymphnoderesidentdendriticcells AT erlebacheradrian acquisitionandpresentationoffolliculardendriticcellboundantigenbylymphnoderesidentdendriticcells |