CD7 Is a Differentiation Marker That Identifies Multiple CD8 T Cell Effector Subsets

The adaptive immune response of human CD8 T cells to invading pathogens involves the differentiation of naive cells into memory and effector cells. However, the lineage relationship between memory and effector cells and the differentiation of CD8 T cells into distinct subsets of effector cell subpop...

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Published inThe Journal of immunology (1950) Vol. 170; no. 5; pp. 2349 - 2355
Main Authors Aandahl, Einar M, Sandberg, Johan K, Beckerman, Karen P, Tasken, Kjetil, Moretto, Walter J, Nixon, Douglas F
Format Journal Article
LanguageEnglish
Published United States Am Assoc Immnol 01.03.2003
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Summary:The adaptive immune response of human CD8 T cells to invading pathogens involves the differentiation of naive cells into memory and effector cells. However, the lineage relationship between memory and effector cells and the differentiation of CD8 T cells into distinct subsets of effector cell subpopulations are subjects of considerable debate. CD7 identifies three populations of CD8 T cells: CD7 high (CD7(high)), low (CD7(low)), and negative (CD7(neg)) that translate into subsets with distinct functional properties. The CD7(high) subset contains naive and memory cells and the CD7(low) and CD7(neg) subsets contain effector cells. The effector cells can functionally be divided into cytokine-secreting effector CD8 T cells and lytic effector CD8 T cells. These data provide a model of human CD8 T cell differentiation in which specialized distinct subpopulations can be identified by expression of CD7.
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ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.170.5.2349