CD40L expression permits CD8+ T cells to execute immunologic helper functions

被引:77
作者
Frentsch, Marco [1 ]
Stark, Regina [1 ]
Matzmohr, Nadine [1 ]
Meier, Sarah [1 ]
Durlanik, Sibel [1 ]
Schulz, Axel R. [1 ]
Stervbo, Ulrik [1 ]
Juerchott, Karsten [2 ]
Gebhardt, Friedemann [3 ]
Heine, Guido [4 ]
Reuter, Morgan A. [5 ]
Betts, Michael R. [5 ]
Busch, Dirk [3 ]
Thiel, Andreas [1 ]
机构
[1] Charite, Berlin Brandenburg Ctr Regenerat Therapies, D-13353 Berlin, Germany
[2] Humboldt Univ, Inst Theoret Biol, D-10099 Berlin, Germany
[3] Tech Univ Munich, Inst Med Microbiol, D-80290 Munich, Germany
[4] Charite, Allergie Ctr Charite, D-13353 Berlin, Germany
[5] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
EPSTEIN-BARR-VIRUS; DENDRITIC CELLS; B-CELLS; LIGAND; CD154; LYMPHOCYTES; GENERATION; MOLECULES; RESPONSES; ABSENCE;
D O I
10.1182/blood-2013-02-483586
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
CD8(+) T cells play an essential role in immunity against intracellular pathogens, with cytotoxicity being considered their major effector mechanism. However, we here demonstrate that a major part of central and effector memory CD8(+) T cells expresses CD40L, one key molecule for CD4(+) T-cell-mediated help. CD40L(+) CD8(+) T cells are detectable among human antigen-specific immune responses, including pathogens such as influenza and yellow fever virus. CD40L(+) CD8(+) T cells display potent helper functions in vitro and in vivo, such as activation of antigen-presenting cells, and exhibit a cytokine expression signature similar to CD4(+) T cells and unrelated to cytotoxic CD8(+) T cells. The broad occurrence of CD40L(+) CD8(+) T cells in cellular immunity implicates that helper functions are not only executed by major histocompatibility complex (MHC) class II-restricted CD4(+) helper T cells but are also a common feature of MHC class I-restricted CD8(+) T cell responses. Due to their versatile functional capacities, human CD40L(+) CD8(+) T cells are promising candidate cells for immune therapies, particularly when CD4(+) T-cell help or pathogen-associated molecular pattern signals are limited.
引用
收藏
页码:405 / 412
页数:8
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