| Literature DB >> 23890071 |
Brian S Sheridan1, Pablo A Romagnoli, Quynh-Mai Pham, Han-Hsuan Fu, Francis Alonzo, Wolf-Dieter Schubert, Nancy E Freitag, Leo Lefrançois.
Abstract
The study of T cell memory and the target of vaccine design have focused on memory subsumed by T cells bearing the αβ T cell receptor. Alternatively, γδ T cells are thought to provide rapid immunity, particularly at mucosal borders. Here, we have shown that a distinct subset of mucosal γδ T cells mounts an immune response to oral Listeria monocytogenes (Lm) infection and leads to the development of multifunctional memory T cells capable of simultaneously producing interferon-γ and interleukin-17A in the murine intestinal mucosa. Challenge infection with oral Lm, but not oral Salmonella or intravenous Lm, induced rapid expansion of memory γδ T cells, suggesting contextual specificity to the priming pathogen. Importantly, memory γδ T cells were able to provide enhanced protection against infection. These findings illustrate that γδ T cells play a role with hallmarks of adaptive immunity in the intestinal mucosa.Entities:
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Year: 2013 PMID: 23890071 PMCID: PMC3749916 DOI: 10.1016/j.immuni.2013.06.015
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745