Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Erika D Reynoso"'
Autor:
Kutlu G Elpek, Angelique Bellemare-Pelletier, Deepali Malhotra, Erika D Reynoso, Veronika Lukacs-Kornek, Rosemarie H DeKruyff, Shannon J Turley
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23921 (2011)
Lymphoid organ-resident DC subsets are thought to play unique roles in determining the fate of T cell responses. Recent studies focusing on a single lymphoid organ identified molecular pathways that are differentially operative in each DC subset and
Externí odkaz:
https://doaj.org/article/6af31aaa801e490a8667050ce6b0a73f
Autor:
Erika D. Reynoso, Shannon J. Turley
Publikováno v:
Journal of Leukocyte Biology. 86:795-801
This review highlights the role of nonhematopoietic cells in the induction and maintenance of peripheral CD8+ T cell tolerance. Bone marrow-derived APCs are considered the predominant cell type involved in the induction and maintenance of T cell tole
Autor:
Zoltán Jakus, Michael Kuligowski, Jonathan L. Chang, Matthew C. Woodruff, Paul R. Hess, Young-A. Kim, Michael C. Carroll, Shannon J. Turley, Vijay K. Kuchroo, Jillian L. Astarita, Takashi Morita, Santiago F. Gonzalez, Anneli Peters, Lindsay A. Sceats, Angelique Bellemare-Pelletier, Kai W. Wucherpfennig, Erika D. Reynoso, Mark L. Kahn, Veronika Lukacs-Kornek, Bettina Franz, Daniel B. Graham, Anne L. Fletcher, Sophie E. Acton, Kutlu G. Elpek, Wojciech Swat, Deepali Malhotra
Publikováno v:
Immunity
Summary To initiate adaptive immunity, dendritic cells (DCs) move from parenchymal tissues to lymphoid organs by migrating along stromal scaffolds that display the glycoprotein podoplanin (PDPN). PDPN is expressed by lymphatic endothelial and fibrobl
Autor:
Shannon J. Turley, Veronika Lukacs-Kornek, Erika D. Reynoso, Mark S Curry, Sophie Pinner, Anne L. Fletcher, Angelique Bellemare-Pelletier, Richard L. Boyd, Ai-ris Y. Collier
Publikováno v:
The Journal of Experimental Medicine
Lymph node stromal cells (LNSCs) can induce potent, antigen-specific T cell tolerance under steady-state conditions. Although expression of various peripheral tissue–restricted antigens (PTAs) and presentation to naive CD8+ T cells has been demonst
Publikováno v:
Advances in experimental medicine and biology. 633
In this review we have highlighted the role of LNSCs in the regulation of CD8+ T cell immune responses in peripheral lymph nodes, thereby adding another layer of protection, in addition to the role of resting DCs, against autoimmunity. LNSCs have rec
Autor:
Shannon J. Turley, Erika D. Reynoso, Roderick T. Bronson, Kutlu G. Elpek, Loise M. Francisco, Arlene H. Sharpe, Gordon J. Freeman, Angelique Bellemare-Pelletier
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 182(4)
The B7 family member programmed death-1 ligand (PD-L1) has been shown to play an inhibitory role in the regulation of T cell responses in several organs. However, the role of PD-L1 in regulating tolerance to self-Ags of the small intestine has not be
Publikováno v:
Crossroads between Innate and Adaptive Immunity II ISBN: 9780387793108
In this review we have highlighted the role of LNSCs in the regulation of CD8+ T cell immune responses in peripheral lymph nodes, thereby adding another layer of protection, in addition to the role of resting DCs, against autoimmunity. LNSCs have rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb08a20867721686967f6cbeb1d7a9c7
https://doi.org/10.1007/978-0-387-79311-5_10
https://doi.org/10.1007/978-0-387-79311-5_10
Autor:
Veronika Lukacs-Kornek, Shannon J. Turley, Deepali Malhotra, Angelique Bellemare-Pelletier, Kutlu G. Elpek, Rosemarie H. DeKruyff, Erika D. Reynoso
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 8, p e23921 (2011)
PLoS ONE, Vol 6, Iss 8, p e23921 (2011)
Lymphoid organ-resident DC subsets are thought to play unique roles in determining the fate of T cell responses. Recent studies focusing on a single lymphoid organ identified molecular pathways that are differentially operative in each DC subset and
Publikováno v:
The FASEB Journal. 22:474-474
Publikováno v:
Clinical Immunology. 127:S105