Literature DB >> 6979580

Role of syngeneic Ia+ accessory cells in the generation of allospecific CTL responses.

O Weinberger, R N Germain, T Springer, S J Burakoff.   

Abstract

Under conditions in which antigen dose is suboptimal, the recognition of Ia determinants is a necessary component of the generation of allospecific CTL responses. With monoclonal anti-Ia antibodies used as blocking reagents, it is demonstrated that the recognition of alloantigens may proceed via two pathways. Alloantigens can be recognized in the context of syngeneic Ia determinants in a similar fashion to conventional antigens. If, however, the Ia+ cells are removed from the responder population, the generation of such responses involves the recognition of allogeneic Ia determinants directly. A non-T, non-B, adherent accessory cell was identified as the critical syngeneic Ia+ cell required for CTL responses in these cultures.

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Year:  1982        PMID: 6979580

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  9 in total

1.  Dendritic cells derived from bone marrow cells fail to acquire and present major histocompatibility complex antigens from other dendritic cells.

Authors:  Penelope A Bedford; Fiona Burke; Andrew J Stagg; Stella C Knight
Journal:  Immunology       Date:  2008-02-07       Impact factor: 7.397

2.  The failure of female cells to present in vitro the male H-Y antigen for secondary cytotoxic T-cell responses.

Authors:  G Biasi; F Dazzi; B Loveland; R Rivarollo; G Asherson
Journal:  Immunogenetics       Date:  1985       Impact factor: 2.846

3.  Regulatory mechanisms in cell-mediated immune responses. Role of I-J and I-C determinants in the activation of H-2I and H-2K/D alloantigen-specific suppressor T cells.

Authors:  S Rich
Journal:  J Exp Med       Date:  1983-09-01       Impact factor: 14.307

4.  Early development of the T cell repertoire. In vivo treatment of neonatal mice with anti-Ia antibodies interferes with differentiation of I-restricted T cells but not K/D-restricted T cells.

Authors:  A M Kruisbeek; M J Fultz; S O Sharrow; A Singer; J J Mond
Journal:  J Exp Med       Date:  1983-06-01       Impact factor: 14.307

5.  Both L3T4+ and Lyt-2+ helper T cells initiate cytotoxic T lymphocyte responses against allogenic major histocompatibility antigens but not against trinitrophenyl-modified self.

Authors:  T Mizuochi; H Golding; A S Rosenberg; L H Glimcher; T R Malek; A Singer
Journal:  J Exp Med       Date:  1985-08-01       Impact factor: 14.307

6.  Rejection of skin allografts by indirect allorecognition of donor class I major histocompatibility complex peptides.

Authors:  J Fangmann; R Dalchau; J W Fabre
Journal:  J Exp Med       Date:  1992-06-01       Impact factor: 14.307

7.  Ia expression by vascular endothelium is inducible by activated T cells and by human gamma interferon.

Authors:  J S Pober; M A Gimbrone; R S Cotran; C S Reiss; S J Burakoff; W Fiers; K A Ault
Journal:  J Exp Med       Date:  1983-04-01       Impact factor: 14.307

8.  Indirect recognition by helper cells can induce donor-specific cytotoxic T lymphocytes in vivo.

Authors:  R S Lee; M J Grusby; L H Glimcher; H J Winn; H Auchincloss
Journal:  J Exp Med       Date:  1994-03-01       Impact factor: 14.307

9.  Characterization of two distinct primary T cell populations that secrete interleukin 2 upon recognition of class I or class II major histocompatibility antigens.

Authors:  T Mizuochi; S Ono; T R Malek; A Singer
Journal:  J Exp Med       Date:  1986-03-01       Impact factor: 14.307

  9 in total

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