Cutting Edge: Naive T Cells Masquerading as Memory Cells
Author(s) -
Kaja MuraliKrishna,
Rafi Ahmed
Publication year - 2000
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.165.4.1733
Subject(s) - il 2 receptor , biology , microbiology and biotechnology , cytotoxic t cell , naive t cell , interleukin 21 , cd69 , cd28 , cd40 , cd8 , natural killer t cell , immunology , t cell , memory t cell , homeostasis , zap70 , immune system , t cell receptor , in vitro , genetics
This study shows that naive CD8 T cells can acquire characteristics of memory T cells in the absence of stimulation with specific Ag simply by the process of homeostatic proliferation under lymphopenic conditions. This Ag-independent T cell differentiation pathway did not result in up-regulation of early activation markers (CD69, CD25, CD71), but expression of several memory markers (CD44, CD122, Ly6C) increased progressively with successive divisions. These markers were then stably expressed, and these cells also became more responsive functionally to specific Ag. Thus, all "memory" phenotype T cells in an individual may not be true Ag-experienced cells and may include naive cells masquerading as memory cells. These findings are specially relevant in cases of disease or treatment-induced lymphopenia such as in HIV-infected individuals or transplant recipients. In addition, this study may have implications for autoimmunity because homeostatic proliferation of naive T cells requires interaction with self peptide plus MHC molecules.
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