Literature DB >> 6154084

Expression of both I-A and I-E/C subregion antigens on accessory cells required for in vitro generation of cytotoxic T lymphocytes against alloantigens or TNBS-modified syngeneic cells.

C B Pettinelli, G B Ahmann, G M Shearer.   

Abstract

We have previously reported that radioresistant, Thy 1-negative accessory cells (SAC) are required for the in vitro generation of cytotoxic T-effector cells to allogeneic or trinitrophenyl-modified syngeneic cells. These SAC were found to provide accessory functions irrespective of whether they were syngeneic, semi-syngeneic, or allogeneic to the responding cells. To further characterize the accessory cells active in CML, the expression of Ia antigens on this functional population was assessed by pretreated SAC with anti-Ia reagents and complement and by testing the accessory cell function of these treated populations. The results of these studies demonstrated that the relevant accessory cells for allogeneic and TNP-self CTL express Ia determinants encoded by genes mapping in the I-A and I-E/C subregions. For the TNP-self CTL the accessory function of both SAC syngeneic or allogeneic to the responding and stimulating cells was specifically abrogated by treatment with anti-Ia reagents and complement.

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Year:  1980        PMID: 6154084

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


  6 in total

1.  I. Characterization of cytotoxic effector cells generated from regional lymph nodes after immunization in the footpad.

Authors:  A A Czitrom; N R Gascoigne
Journal:  Immunology       Date:  1983-09       Impact factor: 7.397

2.  Enhancement of rat ACT-1 tumor clonogenicity by xenogeneic mouse macrophages.

Authors:  K W Beagley; L S Horne; R F Noronha; C M Goodall; C M Moore
Journal:  In Vitro       Date:  1984-08

3.  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

4.  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

5.  Major histocompatibility complex restriction of soluble helper molecules in T cell responses to altered self.

Authors:  J M Plate
Journal:  J Exp Med       Date:  1981-05-01       Impact factor: 14.307

6.  Capacity of purified Lyt-2+ T cells to mount primary proliferative and cytotoxic responses to Ia- tumour cells.

Authors:  J Sprent; M Schaefer
Journal:  Nature       Date:  1986 Aug 7-13       Impact factor: 49.962

  6 in total

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