Effector and memory CD8+ T cells can be generated in response to alloantigen independently of CD4+ T cell help

被引:36
作者
Jones, ND [1 ]
Carvalho-Gaspar, M [1 ]
Luo, SQ [1 ]
Brook, MO [1 ]
Martin, L [1 ]
Wood, KJ [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
D O I
10.4049/jimmunol.176.4.2316
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There is now considerable evidence suggesting that CD8(+) T cells are able to generate effector but not functional memory T cells following pathogenic infections in the absence of CD4(+) T cells. We show that following transplantation of allogeneic skin, in the absence of CD4(+) T cells, CD8(+) T cells become activated, proliferate, and expand exclusively in the draining lymph nodes and are able to infiltrate and reject skin allografts. CD44(+)CD8(+) T cells isolated 100 days after transplantation rapidly produce IFN-gamma following restimulation with alloantigen in vitro. In vivo CD44(+)CD8(+) T cells rejected donor-type skin allografts more rapidly than naive CD8(+) T cells demonstrating the ability of these putative memory T cells to mount an effective recall response in vivo. These data form the first direct demonstration that CD8+ T cells are able to generate memory as well as effector cells in response to alloantigen during rejection in the complete absence of CD4(+) T cells. These data have important implications for the design of therapies to combat rejection and serve to reinforce the view that CD8(+) T cell responses to allografts require manipulation in addition to CD4(+) T cell responses to completely prevent the rejection of foreign organ transplants. The Journal of Immunology, 2006, 176: 2316-2323.
引用
收藏
页码:2316 / 2323
页数:8
相关论文
共 37 条
[1]   Cutting edge:: Distinct roles for T help and CD40/CD40 ligand in regulating differentiation of proliferation-competent memory CD8+ T cells [J].
Bachmann, MF ;
Schwarz, K ;
Wolint, P ;
Meijerink, E ;
Martin, S ;
Manolova, V ;
Oxenius, A .
JOURNAL OF IMMUNOLOGY, 2004, 173 (04) :2217-2221
[2]   Peripheral priming of alloreactive T cells by the direct pathway of allorecognition [J].
Baratin, M ;
Bonin, K ;
Daniel, C .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (12) :3305-3314
[3]   Help for cytotoxic-T-cell responses is mediated by CD40 signalling [J].
Bennett, SRM ;
Carbone, FR ;
Karamalis, F ;
Flavell, RA ;
Miller, JFAP ;
Heath, WR .
NATURE, 1998, 393 (6684) :478-480
[4]  
Bourgeois C, 2002, EUR J IMMUNOL, V32, P2199, DOI 10.1002/1521-4141(200208)32:8<2199::AID-IMMU2199>3.0.CO
[5]  
2-L
[6]   A role for CD40 expression on CD8+ T cells in the generation of CD8+ T cell memory [J].
Bourgeois, C ;
Rocha, B ;
Tanchot, C .
SCIENCE, 2002, 297 (5589) :2060-2063
[7]   Chemokine gene expression during allograft rejection: Comparison of two quantitative PCR techniques [J].
Carvalho-Gaspar, M ;
Billing, JS ;
Spriewald, BM ;
Wood, KJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 2005, 301 (1-2) :41-52
[8]   Long-lasting CD8 T cell memory in the absence of CD4 T cells or B cells [J].
DiRosa, F ;
Matzinger, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2153-2163
[9]   Visualization of the in vivo generation of donor antigen-specific effector CD8+T cells during mouse cardiac allograft rejection - In vivo effector CD8+T cell generation during allograft rejection [J].
Gilot, BJ ;
Hara, M ;
Jones, ND ;
van Maurik, A ;
Niimi, M ;
Hadjianastassiou, V ;
Morris, PJ ;
Wood, KJ .
TRANSPLANTATION, 2000, 69 (04) :639-648
[10]   A FAIL-SAFE MECHANISM FOR MAINTAINING SELF-TOLERANCE [J].
GUERDER, S ;
MATZINGER, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (02) :553-564