| Literature DB >> 30413351 |
Sarah K Whiteside1, Jeremy P Snook1, Matthew A Williams1, Janis J Weis2.
Abstract
T cell responses are essential for appropriate protection against pathogens. T cell immunity is achieved through the ability to discriminate between foreign and self-molecules, and this relies heavily on stringent T cell receptor (TCR) specificity. Recently, bystander activated T lymphocytes, that are specific for unrelated epitopes during an antigen-specific response, have been implicated in diverse diseases. Numerous infection models have challenged the classic dogma of T cell activation as being solely dependent on TCR and major histocompatibility complex (MHC) interactions, indicating an unappreciated role for pathogen-associated receptors on T cells. We discuss here the specific roles of bystander activated T cells in pathogenesis, shedding light on the ability of these cells to modulate disease severity independently from TCR recognition.Entities:
Keywords: T cell activation; autoimmunity; bystander; cancer; infection; pathogenesis; signaling
Mesh:
Substances:
Year: 2018 PMID: 30413351 PMCID: PMC6269193 DOI: 10.1016/j.it.2018.10.003
Source DB: PubMed Journal: Trends Immunol ISSN: 1471-4906 Impact factor: 16.687