Literature DB >> 115959

Patterns of virus-immune T-cell responsiveness. Comparison of (H-2k X H-2b) leads to H-2b radiation chimeras and negatively selected H-2b lymphocytes.

P C Doherty, J R Bennink.   

Abstract

Negatively selected H-2K(b)D(b) TDL can be induced to respond strongly to vaccinia virus presented in the context of both H-2K(k) and H-2D(b) when stimulated in irradiated H-2K(k)D(b) recipients. Addition of excess (H- 2K(k)D(b) x H-2K(b)D(b))F1 TDL, which are low responders to H-2D(b)-vaccinia virus, does not obviously suppress the reactivity pattern of the H-2K(b)D(b) T cells. However, lymphocytes from chimeras made by reconstituting H- 2K(b)D(b) mice with (H-2K(k)D(k) x H-2K(b)D(b))F(l) bone marrow cells make little, if any, cytotoxic T-cell response to vaccinia virus when sensitized in H-2K(k)D(b) recipients. We have thus documented one instance where the responder phenotype of T ceils from an F(l) {arrow} parent chimera is not equivalent to that associated with the H-2 type of the parental thymus. Lymphocytes from both the chimera and the H-2K(b)D(b) parent (after negative selection) are tolerant to the H-2K(k) and I-A(k) alloantigens encountered in the recipient, but the chimera T cells are also defective in their response to a neoantigen (vaccinia virus) presented in the context of H-2K(k) which the parental T cells invariably recognize. It is thus possible that at least part of the phenomenology associated with the F(l) {arrow} parent radiation chimeras reflects deletion of repertoire in the context of H-2 antigens present during thymocyte ontogeny on other than radiation-resistant thymic epithelium.

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Year:  1979        PMID: 115959      PMCID: PMC2185709          DOI: 10.1084/jem.150.5.1187

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  18 in total

1.  Different rules govern help for cytotoxic T cells and B cells.

Authors:  J R Bennink; P C Doherty
Journal:  Nature       Date:  1978 Dec 21-28       Impact factor: 49.962

2.  Positive and negative allogeneic effects mediated by MLR-primed lymphocytes: quantitation by limiting dilution analysis.

Authors:  R B Corley; B Kindred; I Lefkovits
Journal:  J Immunol       Date:  1978-09       Impact factor: 5.422

3.  Search for suppression of T cells specific for the second nonhost H-2 haplotype in F1 leads to P irradiation bone marrow chimeras.

Authors:  R M Zinkernagel; A Althage
Journal:  J Immunol       Date:  1979-05       Impact factor: 5.422

4.  Reciprocal stimulation of negatively selected high-responder and low-responder T cells in virus-infected recipients.

Authors:  J R Bennink; P C Doherty
Journal:  Proc Natl Acad Sci U S A       Date:  1979-07       Impact factor: 11.205

5.  Primary anti-viral cytotoxic T-cell responses in semiallogeneic chimeras are not absolutely restricted to host H-2 type.

Authors:  R V Blanden; M E Andrew
Journal:  J Exp Med       Date:  1979-02-01       Impact factor: 14.307

6.  Ir-genes in H-2 regulate generation of anti-viral cytotoxic T cells. Mapping to K or D and dominance of unresponsiveness.

Authors:  R M Zinkernagel; A Althage; S Cooper; G Kreeb; P A Klein; B Sefton; L Flaherty; J Stimpfling; D Shreffler; J Klein
Journal:  J Exp Med       Date:  1978-08-01       Impact factor: 14.307

7.  Genetic control of cytolytic t-lymphocyte responses. II. The role of the host genotype in parental leads to F1 radiation chimeras in the control of the specificity of cytolytic T-lymphocyte responses to trinitrophenyl-modified syngeneic cells.

Authors:  P Billings; S J Burakoff; M E Dorf; B Benacerraf
Journal:  J Exp Med       Date:  1978-08-01       Impact factor: 14.307

8.  Cellular and genetic control of antibody responses. V. Helper T-cell recognition of H-2 determinants on accessory cells but not B cells.

Authors:  A Singer; K S Hathcock; R J Hodes
Journal:  J Exp Med       Date:  1979-05-01       Impact factor: 14.307

9.  Cytotoxic T-cell responses in mice infected with influenza and vaccinia viruses vary in magnitude with H-2 genotype.

Authors:  P C Doherty; W E Biddison; J R Bennink; B B Knowles
Journal:  J Exp Med       Date:  1978-08-01       Impact factor: 14.307

10.  In irradiation chimeras, K or D regions of the chimeric host, not of the donor lymphocytes, determine immune responsiveness of antiviral cytotoxic T cells.

Authors:  R M Zinkernagel; A Althage; S Cooper; G Callahan; J Klein
Journal:  J Exp Med       Date:  1978-09-01       Impact factor: 14.307

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  4 in total

1.  Clones of cytotoxic T lymphocytes reactive to haptenated allogeneic cells: precursor frequency and characteristics as determined by a split-culture approach.

Authors:  M F Good; G J Nossal
Journal:  Proc Natl Acad Sci U S A       Date:  1983-03       Impact factor: 11.205

2.  H-2 restriction as a consequence of intentional priming: T cells of fully allogeneic chimeric mice as well as of normal mice respond to foreign antigens in the context of H-2 determinants not encountered on thymic epithelial cells.

Authors:  H Stockinger; K Pfizenmaier; C Hardt; H Rodt; M Röllinghoff; H Wagner
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

3.  Self recognition in allogeneic radiation bone marrow chimeras. A radiation-resistant host element dictates the self specificity and immune response gene phenotype of T-helper cells.

Authors:  A Singer; K S Hathcock; R J Hodes
Journal:  J Exp Med       Date:  1981-05-01       Impact factor: 14.307

4.  Induction of neonatal tolerance to H-2k in B6 mice does not allow the emergence of T cells specific for H-2k plus vaccinia virus.

Authors:  D H Schwartz; P C Doherty
Journal:  J Exp Med       Date:  1982-09-01       Impact factor: 14.307

  4 in total

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