| Literature DB >> 31812277 |
Toshiro Hirai1, Sarah K Whitley1, Daniel H Kaplan2.
Abstract
CD8+ memory T cells provide anamnestic host defense against intracellular pathogens and cancer immunosurveillance but are also pathogenic in some autoimmune diseases. In mouse skin, there are two unique subsets of CD8+ memory T cells, resident memory cells that reside long-term in steady state skin and recirculating memory cells that are transient. They have distinct mechanisms of recruitment, development, and maintenance in response to skin-derived signals. In this review, we will focus on these mechanisms and the functional relationship of these two types of CD8+ memory cells with host defense and disease.Entities:
Mesh:
Year: 2019 PMID: 31812277 PMCID: PMC7573784 DOI: 10.1016/j.jid.2019.09.014
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551