Literature DB >> 8186193

Differential proliferative responses in subsets of human CD28+ cells delineated by BB27 mAb.

C Gouttefangeas1, S Jacquot, E Meffre, M Schmid, L Boumsell, A Bensussan.   

Abstract

We report the identification of a novel 140 kDa disulfide-linked dimer expressed by a subset of peripheral blood T lymphocytes. This molecule, which is recognized by mAb BB27, is also detected on cells of the myelomonocytic lineage. In the T cell lineage, its expression is positively modulated after lymphocyte activation. A series of double-labeling experiments revealed that BB27 mAb identifies new CD4 and CD8 cell subsets different from those defined by CD45RA, CD45RO, CD26, CD29, CD31, and CD38. Finally, BB27 mAb also subdivides the CD28 subset. Of the utmost interest is the finding that a proliferative response to CD28 mAb and phorbol myristate acetate stimulation is exclusively obtained in the CD28+BB27+ cell subset, whereas the CD28+BB27- subset fails to proliferate.

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Year:  1994        PMID: 8186193     DOI: 10.1093/intimm/6.3.423

Source DB:  PubMed          Journal:  Int Immunol        ISSN: 0953-8178            Impact factor:   4.823


  2 in total

1.  Interactions between peripheral blood CD8 T lymphocytes and intestinal epithelial cells (iEC).

Authors:  F A Arosa; C Irwin; L Mayer; M de Sousa; D N Posnett
Journal:  Clin Exp Immunol       Date:  1998-05       Impact factor: 4.330

2.  CD101 genetic variants modify regulatory and conventional T cell phenotypes and functions.

Authors:  Laura E Richert-Spuhler; Corinne M Mar; Paurvi Shinde; Feinan Wu; Ting Hong; Evan Greene; Sharon Hou; Katherine Thomas; Raphael Gottardo; Nelly Mugo; Guy de Bruyn; Connie Celum; Jared M Baeten; Jairam R Lingappa; Jennifer M Lund
Journal:  Cell Rep Med       Date:  2021-06-15
  2 in total

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