Cutting Edge: Analysis of Human Vα24+CD8+ NK T Cells Activated by α-Galactosylceramide-Pulsed Monocyte-Derived Dendritic Cells

Tsuyoshi Takahashi(Tokyo Medical University), Shigeru Chiba(Tokyo Medical University), Mie Nieda(Japanese Red Cross Society, Japan), Takeshi Azuma(Tokyo Medical University), Soichiro Ishihara(The University of Tokyo), Yoichi Shibata(Institute for Transfusion Medicine), Takeo Juji(Japanese Red Cross Society, Japan), Hisamaru Hirai(Tokyo Medical University)
The Journal of Immunology
April 1, 2002
Cited by 199Open Access
Full Text

Abstract

Human Valpha24(+) NKT cells constitute a counterpart of mouse Valpha14(+) NKT cells, both of which use an invariant TCR-alpha chain. The human Valpha24(+) NKT cells as well as mouse Valpha14(+) NKT cells are activated by glycolipids in a CD1d-restricted manner and produce many immunomodulatory cytokines, possibly affecting the immune balance. In mice, it has been considered from extensive investigations that Valpha14(+)CD8(+) NKT cells that express invariant TCR do not exist. Here we introduce human Valpha24(+)CD8(+) NKT cells. These cells share important features of Valpha24(+) NKT cells in common, but in contrast to CD4(-)CD8(-) (double-negative) or CD4(+) Valpha24(+) NKT cells, they do not produce IL-4. Our discovery may extend and deepen the research field of Valpha24(+) NKT cells as well as help to understand the mechanism of the immune balance-related diseases.


Related Papers

No related papers found

Powered by citation graph analysis