| Literature DB >> 29632146 |
Morgan Grau1, Séverine Valsesia1, Julien Mafille1, Sophia Djebali1, Martine Tomkowiak1, Anne-Laure Mathieu1, Daphné Laubreton1, Simon de Bernard2, Pierre-Emmanuel Jouve2, Erwan Ventre1, Laurent Buffat2, Thierry Walzer1, Yann Leverrier1, Jacqueline Marvel3.
Abstract
The pool of memory-phenotype CD8 T cells is composed of Ag-induced (AI) and cytokine-induced innate (IN) cells. IN cells have been described as having properties similar to those of AI memory cells. However, we found that pathogen-induced AI memory cells can be distinguished in mice from naturally generated IN memory cells by surface expression of NKG2D. Using this marker, we described the increased functionalities of AI and IN memory CD8 T cells compared with naive cells, as shown by comprehensive analysis of cytokine secretion and gene expression. However, AI differed from IN memory CD8 T cells by their capacity to migrate to the lung parenchyma upon inflammation or infection, a process dependent on their expression of ITGA1/CD49a and ITGA4/CD49d integrins.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29632146 DOI: 10.4049/jimmunol.1701698
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422