Activated CD8 T cells redistribute to antigen-free lymph nodes and exhibit effector and memory characteristics.
Activated CD8 T cells redistribute to antigen-free lymph nodes and exhibit effector and memory characteristics.
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DOI:
10.4049/jimmunol.181.3.1814
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发表时间:
2008-08-01
期刊:
影响因子:
--
通讯作者:
Engelhard VH
中科院分区:
文献类型:
--
作者:
Brinkman CC;Sheasley-O'Neill SL;Ferguson AR;Engelhard VH
“This is an author-produced version of a manuscript accepted for publication in The Journal of Immunology (The JI). The American Association of Immunologists, Inc. (AAI), publisher of The JI, holds the copyright to this manuscript. This version of the manuscript has not yet been copyedited or subjected to editorial proofreading by The JI; hence, it may differ from the final version published in The JI (online and in print). AAI (The JI) is not liable for errors or omissions in this author-produced version of the manuscript or in any version derived from it by the U.S. National Institutes of Health or any other third party. The final, citable version of record can be found at www.jimmunol.org.” Exogenous dendritic cells display restricted trafficking when injected in vivo and stimulate CD8 T cell responses that are localized to a small number of lymphoid compartments. By examining these responses in the presence and absence of FTY720, a drug that causes sequestration of T cells in lymph nodes, we demonstrate that a significant fraction of divided CD8 T cells redistribute into antigen-free lymph nodes within 3 days of activation. Despite variation in the level of expression of CD62L, redistribution of these cells is CD62L-dependent. Redistributed CD8 T cells exhibit characteristics of differentiated effectors. However, when re-isolated from antigen-free lymph nodes 3 days after activation and transferred into naïve mice, they persist for at least 3 weeks and expand upon antigen challenge. Thus, CD8 T cells that redistribute to antigen-free lymph nodes 3 days after immunization contain memory precursors. We suggest that this redistribution process represents an important mechanism for establishment of lymph node resident central memory, and that redistribution to antigen-free nodes is an additional characteristic to be added to those that distinguish memory precursors from terminal effectors.
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