Literature DB >> 6165590

Cytotoxic T lymphocytes generated across and I-Ab mutant difference are directed against a molecule bearing Ia antigens.

L P de Waal, C J Melief, R W Melvold.   

Abstract

The recently discovered B6.C-H-2bm12 (bm12) histocompatibility mutant bears a mutation of the I-A subregion of the H-2b haplotype. We have studied cytotoxic T lymphocytes (CTL) generated in secondary mixed lymphocyte culture (MLC) between the bm12 mutant and the strain of origin C57BL/6 (B6). In both directions, strong CTL responses were generated against lipopolysaccharide-stimulated, but not against concanavalin A-stimulated target cells. Studies of the specificity of the bm12 anti-B6 CTL response, using target cells from a panel of H-2 recombinants, showed that the CTL were directed against specificities of the I-Ab subregion. This conclusion was confirmed by the observation that the bm12 anti-B6 CTL could be specifically blocked by anti-Iab, but not by anti-Kb antisera. EL4 tumor cells, which express Kb and Db but not Iab antigens, were not lysed by the CTL. The combined data confirm that bm12 is an I-A subregion mutant and indicate that the I-A subregion antigens, recognized by antibody and those recognized by CTL, are probably present on the same molecules. The CTL effector cells generated in secondary MLC across the I-Ab mutant difference had the surface phenotype Lyt 1- 2+.

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Year:  1981        PMID: 6165590     DOI: 10.1002/eji.1830110317

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


  6 in total

1.  Cytotoxic T-cell response to H-Y antigen by B6.C-H-2bm12 and B10.BR mice.

Authors:  A Juretić; E Juretić; Z A Nagy; J Klein
Journal:  Immunology       Date:  1985-08       Impact factor: 7.397

2.  I-A subregion control of the transfer of delayed type hypersensitivity (DTH).

Authors:  M S Sandrin; I F McKenzie
Journal:  Immunogenetics       Date:  1982       Impact factor: 2.846

3.  The murine bm12 gene conversion provides evidence that T cells recognize predominantly Ia conformation.

Authors:  H Y Tse; S Kanamori; W D Walsh; T H Hansen
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

4.  Allosuppressor and allohelper T cells in acute and chronic graft-vs.-host disease. II. F1 recipients carrying mutations at H-2K and/or I-A.

Authors:  A G Rolink; S T Pals; E Gleichmann
Journal:  J Exp Med       Date:  1983-02-01       Impact factor: 14.307

5.  Gain/loss of poly(Glu50Tyr50)/poly(Glu60Ala30Tyr10) responsiveness in the bm12 mutant strain.

Authors:  H Y Lei; R W Melvold; S D Miller; C Waltenbaugh
Journal:  J Exp Med       Date:  1982-08-01       Impact factor: 14.307

6.  Graft-vs.-host-associated immune suppression is activated by recognition of allogeneic murine I-A antigens.

Authors:  G M Shearer; R B Levy
Journal:  J Exp Med       Date:  1983-03-01       Impact factor: 14.307

  6 in total

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