Literature DB >> 8104714

Expression of sialyl Lewis(x) antigen on human T cells.

S Ohta1, N Hanai, S Habu, T Nishimura.   

Abstract

Sialyl Lewis(x) (sLe(x)) antigen, which has been introduced as tumor-associated cell surface carbohydrates, was demonstrated to be expressed on a subpopulation of human CD4+ and CD8+ T cells. It was also demonstrated that the majority of gamma delta T cells as well as natural killer cells expressed a high level of sLe(x) antigen. The sLe(x) expression on T cells were up-regulated by activation with various T cell stimulants. The sLe(x)+ CD4+ T cells were enriched in CD4+CD45RO+ memory type of T cells but not in CD4+CD45RA+ T cells. Moreover, sLe(x)+ CD4+ T cells were demonstrated to show higher proliferative responses to T cell stimulants such as CD4+CD45RO+ T cells. These results initially clarified the expression of sLe(x) carbohydrate on human T cells and indicated the important role of sLe(x)-expressing T cells in immune responses.

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Year:  1993        PMID: 8104714     DOI: 10.1006/cimm.1993.1258

Source DB:  PubMed          Journal:  Cell Immunol        ISSN: 0008-8749            Impact factor:   4.868


  2 in total

1.  Characterization of E-selectin-binding epitopes expressed by skin-homing T cells.

Authors:  R Priest; M I Bird; R Malhotra
Journal:  Immunology       Date:  1998-08       Impact factor: 7.397

2.  sLex is not responsible for the interaction of sLex-positive memory T lymphocytes with E-selectin.

Authors:  F T Rotteveel; A M van Doornmalen; M van Duin
Journal:  Immunology       Date:  1995-09       Impact factor: 7.397

  2 in total

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