| Literature DB >> 23719298 |
Marco Frentsch1, Regina Stark, Nadine Matzmohr, Sarah Meier, Sibel Durlanik, Axel R Schulz, Ulrik Stervbo, Karsten Jürchott, Friedemann Gebhardt, Guido Heine, Morgan A Reuter, Michael R Betts, Dirk Busch, Andreas Thiel.
Abstract
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.Entities:
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Year: 2013 PMID: 23719298 PMCID: PMC4548794 DOI: 10.1182/blood-2013-02-483586
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113