| Literature DB >> 24832455 |
Aránzazu Cruz-Adalia1, Guillermo Ramirez-Santiago1, Carmen Calabia-Linares2, Mónica Torres-Torresano1, Lidia Feo2, Marta Galán-Díez3, Elena Fernández-Ruiz4, Eva Pereiro5, Peter Guttmann6, Michele Chiappi7, Gerd Schneider6, José López Carrascosa8, Francisco Javier Chichón7, Gloria Martínez Del Hoyo9, Francisco Sánchez-Madrid4, Esteban Veiga10.
Abstract
Dendritic cells (DCs) phagocytose, process, and present bacterial antigens to T lymphocytes to trigger adaptive immunity. In vivo, bacteria can also be found inside T lymphocytes. However, T cells are refractory to direct bacterial infection, leaving the mechanisms by which bacteria invade T cells unclear. We show that T cells take up bacteria from infected DCs by the process of transinfection, which requires direct contact between the two cells and is enhanced by antigen recognition. Prior to transfer, bacteria localize to the immunological synapse, an intimate DC/T cell contact structure that activates T cells. Strikingly, T cells efficiently eliminate the transinfecting bacteria within the first hours after infection. Transinfected T cells produced high levels of proinflammatory cytokines and were able to protect mice from bacterial challenge following adoptive transfer. Thus, T lymphocytes can capture and kill bacteria in a manner reminiscent of innate immunity.Entities:
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Year: 2014 PMID: 24832455 DOI: 10.1016/j.chom.2014.04.006
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023