| Literature DB >> 26072286 |
Joseph J C Thome1, Donna L Farber2.
Abstract
Intensified efforts to promote protective T cell-based immunity in vaccines and immunotherapies have created a compelling need to expand our understanding of human T cell function and maintenance beyond its characterization in peripheral blood. Mouse studies of T cell immunity show that, in response to infection, T cells migrate to diverse sites and persist as tissue-resident memory T cells (TRM), which mediate rapid in situ protection on antigen recall. Here we discuss new approaches to probe human T cell immunity, including novel sampling, that indicate a broad distribution and high frequency of human TRM in multiple sites. These newer findings further implicate anatomic compartmentalization as a generalized mechanism for long-term maintenance of human T cells throughout life.Entities:
Keywords: immune homeostasis; immune memory; mucosal immunity; naïve T cells; peripheral blood
Mesh:
Year: 2015 PMID: 26072286 PMCID: PMC4491028 DOI: 10.1016/j.it.2015.05.003
Source DB: PubMed Journal: Trends Immunol ISSN: 1471-4906 Impact factor: 16.687