Aging leads to disturbed homeostasis of memory phenotype CD8+ cells

Journal of Experimental Medicine

Volumn 195, Issue 3, 2002, Pages 283-293

  Zhang, Xiaohong ^a   Fujii, Hideki ^a   Kishimoto, Hidehiro ^a   LeRoy, Eric ^a   Surh, Charles D ^a   Sprent, Jonathan ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

Aging; CD8+ cells; IFN I; IL 15; T cell turnover

Indexed keywords

CD8 ANTIGEN; HERMES ANTIGEN; INTERFERON; INTERFERON ANTIBODY; INTERLEUKIN 15; PROTEIN BCL 2;

ADOPTIVE TRANSFER; AGING; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL PROLIFERATION; CONTROLLED STUDY; CYTOKINE PRODUCTION; GENE EXPRESSION; MEMORY CELL; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL;

ADOPTIVE TRANSFER; AGING; ANIMALS; ANTIGENS, CD44; APOPTOSIS; BCL-X PROTEIN; CD4-POSITIVE T-LYMPHOCYTES; CD8-POSITIVE T-LYMPHOCYTES; GENE EXPRESSION; GENES, BCL-2; HOMEOSTASIS; IMMUNOLOGIC MEMORY; INTERFERON-BETA; INTERLEUKIN-15; LYMPHOCYTE ACTIVATION; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MICE, TRANSGENIC; PHENOTYPE; PROTO-ONCOGENE PROTEINS C-BCL-2; RNA, MESSENGER;

EID: 0037017378     PISSN: 00221007     EISSN: None     Source Type: Journal    
DOI: 10.1084/jem.20011267     Document Type: Article

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