Literature DB >> 6967411

Qed-1--a target for unrestricted killing by T cells.

K F Lindahl, B Hausmann.   

Abstract

Two prototype target determinants for unrestricted killing by T cells are defined: Qed-1a, detected on B6.Tlaa targets by C3H/HeJ lymphocytes primed in vivo and restimulated in vitro by B10.BR spleen cells; and Qed-1b, detected on C57BL/6J lymphocytes by B10.BR anti-C3H/HeJ effector cells generated in the same manner. Other mouse strains can be typed for Qed-1 by the ability of their lymphocytes to inhibit one of these lytic reactions. Of 55 inbred strains, 52 expressed either Qed-1a or Qed-1b, which thus behaved as products of alleles of a single locus, Qed-1. The remaining three strains, all H-2r, did not compete against specific lysis of Qed-1a, but inhibited Qed-1b-specific lysis only in part; it is proposed that these strains carry a third allele or haploype, Qed-1c. The Qed-1 locus was mapped distal to Qa-2. Qed-1b was found on both normal and mitogen-activated lymphocytes and did not appear confined to any lymphoid subpopulation. Cytotoxic responses, not restricted by H-2 and specific for antigens controlled by the Tla region, could be induced in several combinations of H-2-identical strains differing at Qed-1. Cells of some strains, like B10.BR, NZB, and SWR, responded directly in culture, even without priming in vivo.

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Year:  1980        PMID: 6967411     DOI: 10.1002/eji.1830100413

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  24 in total

1.  Immunodominance in the T-cell response to multiple non-H-2 histocompatibility antigens. II. Observation of a hierarchy among dominant antigens.

Authors:  P J Wettstein
Journal:  Immunogenetics       Date:  1986       Impact factor: 2.846

2.  Primary cytotoxic T-cell response in vitro against Mls antigens in NZB-mice.

Authors:  U Botzenhardt; J Müller-Quernheim
Journal:  Clin Exp Immunol       Date:  1987-09       Impact factor: 4.330

3.  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

4.  MHC epitopes of KS and Dd restrict the same population of cytolytic T lymphocytes.

Authors:  J D Tyler; C S David
Journal:  Immunogenetics       Date:  1983       Impact factor: 2.846

5.  H-2 haplotypes, genes and antigens: second listing. II. The H-2 complex.

Authors:  J Klein; F Figueroa; C S David
Journal:  Immunogenetics       Date:  1983       Impact factor: 2.846

6.  Leukemia-cell rejection due to T-region encoded antigens.

Authors:  G Biasi; D Collavo; P Zanovello; L Chieco-Bianchi
Journal:  Immunogenetics       Date:  1981-03-01       Impact factor: 2.846

7.  Genetic control of B- and T-lymphocyte abnormalities of NZB mice in crosses with B10.D2 mice.

Authors:  W F Davidson; T M Chused; H C Morse
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

8.  Lymphocyte-mediated cytotoxicity against allogeneic tumour cells. IV. Fine specificity mapping and characterization of concanavalin A-activated cytotoxic effector lymphocytes.

Authors:  J D Waterfield; D F Nixon; M G Mair
Journal:  Immunology       Date:  1981-12       Impact factor: 7.397

9.  Mta, a maternally inherited cell surface antigen of the mouse, is transmitted in the egg.

Authors:  K F Lindahl; K Bürki
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

10.  Rat major histocompatibility RT1.C antigens of restricted tissue distribution consist of two polypeptide chains with molecular weights of about 42 000 and 12 500.

Authors:  D Haustein; W Stock; E Günther
Journal:  Immunogenetics       Date:  1982-03       Impact factor: 2.846

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