A novel role of CD30/CD30 ligand signaling in the generation of long-lived memory CD8+ T cells

被引:40
作者
Nishimura, H
Yajima, T
Muta, H
Podack, ER
Tani, K
Yoshikai, Y [1 ]
机构
[1] Kyushu Univ, Med Inst Bioregulat, Ctr Prevent Infect Dis, Div Host Def, Fukuoka 8128582, Japan
[2] Kyushu Univ, Med Inst Bioregulat, Div Mol Genet, Fukuoka 8128582, Japan
[3] Univ Miami, Dept Immunol & Microbiol, Miami, FL 33101 USA
关键词
D O I
10.4049/jimmunol.175.7.4627
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory CD8(+) T cells can be divided into two subsets, central memory (T,m) and effector memory (T,m) CD8(+) T cells. We found that CD30, a member of the TNFR-associated factor (TRAF)-linked TNFR superfamily, signaling is involved in differentiation of long-lived CD8(+) T-CM cells following Listeria monocytogenes infection. Although CD8+ T,m cells transiently accumulated in the nonlymphoid tissues of CD30 ligand (CD153(-/-)) mice after infection, long-lived memory CD8(+) T-CM cells were poorly generated in these mice. CCR7 mRNA expression was down-regulated in CD8(+) T cells of the spleen of CD153(-/-) mice in vivo and the expression was up-regulated in CD8(+) T,m cells by anti-CD30 mAb cross-linking in vitro. These results suggest that CD30/CD30 ligand signaling plays an important role in the generation of long-lived memory CD8(+) T cells at least partly by triggering homing receptors for T-CM cells.
引用
收藏
页码:4627 / 4634
页数:8
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