Literature DB >> 2448237

Antigraft responses to the H-28c antigen by B6 and B6D2F1 mice.

L L Johnson1.   

Abstract

The survival of minor H antigen-bearing skin grafts from donors congenic with C57BL/6 (B6) was compared in B6, B6D2, and AB6 hybrid recipients. In a case singled out for further study, B6 mice were found to reject HW110 skin (H-28c antigen) rapidly, whereas B6D2 mice rejected HW110 skin much more slowly and variably. Both major histocompatibility complex (MHC)-linked and non-MHC genes appeared to affect the survival of HW110 strain skin grafts on B6 and B6D2 recipients. Results of several experiments appear to rule out the sharing of H-28c epitopes between donors and recipients as an explanation for the relatively poor response of B6D2 mice to HW110 skin grafts. Experiments involving bone marrow chimeras produced by the reciprocal exchange of bone marrow between irradiated B6 and B6D2 mice suggest that bone marrow-derived donor cells and non-bone-marrow-derived host cells each contribute to the immune response phenotype with respect to the H-28c antigen. An attempt was made to determine whether B6D2 mice that failed to reject HW110 strain skin grafts possessed suppressor cells specific for the H-28c antigen. Spleen cells from poorly responsive B6D2 mice failed to suppress the rejection of HW110 skin grafts when assayed in immunodeficient mice that were provided with cells from immune B6D2 donors that were highly responsive to HW110 skin grafts.

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Year:  1988        PMID: 2448237     DOI: 10.1007/bf00346581

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  19 in total

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Authors:  R H Schwartz
Journal:  Adv Immunol       Date:  1986       Impact factor: 3.543

2.  Prolonged minor allograft survival in intravenously primed mice--a test of the veto hypothesis.

Authors:  L L Johnson
Journal:  Transplantation       Date:  1987-07       Impact factor: 4.939

3.  Genetic background and expressivity of histocompatibility genes.

Authors:  W K Silvers; R E Billingham
Journal:  Science       Date:  1967-10-06       Impact factor: 47.728

4.  Nonresponsiveness to the male antigen H-Y in H-2 I-A-mutant B6.C-H-2bm12 is not caused by defective antigen presentation.

Authors:  L P de Waal; J de Hoop; M J Stukart; H Gleichmann; R W Melvold; C J Melief
Journal:  J Immunol       Date:  1983-02       Impact factor: 5.422

5.  A protocol for detection of H-Y antigenic variants.

Authors:  L L Johnson
Journal:  Immunogenetics       Date:  1982       Impact factor: 2.846

6.  Immunodominance in the immune response to "multiple" histocompatibility antigens.

Authors:  P J Wettstein; D W Bailey
Journal:  Immunogenetics       Date:  1982       Impact factor: 2.846

7.  Intrathymic T cell differentiation in radiation bone marrow chimeras and its role in T cell emigration to the spleen. An immunohistochemical study.

Authors:  K Hirokawa; T Sado; S Kubo; H Kamisaku; K Hitomi; M Utsuyama
Journal:  J Immunol       Date:  1985-06       Impact factor: 5.422

8.  H-2 effects on cell-cell interactions in the response to single non-H-2 alloantigens. II. H-2D region control of H-7.1-specific stimulator function in mixed lymphocyte culture and susceptibility to lysis by H-7.1-specific cytotoxic cells.

Authors:  P J Wettstein; J A Frelinger
Journal:  J Exp Med       Date:  1977-11-01       Impact factor: 14.307

9.  Cytotoxic T lymphocyte nonresponsiveness to the male antigen H-Y in the H-2Db mutants bm13 and bm14. Complementation of the response in F1 crosses with the I-Ab mutant bm12 nonresponder and failure of B6 or Db mutant mice tolerant of each other to respond to allogeneic male cells.

Authors:  L P De Waal; R W Melvold; C J Melief
Journal:  J Exp Med       Date:  1983-11-01       Impact factor: 14.307

10.  Cytotoxic T-cell responses to H-Y: correlation with the rejection of syngeneic male skin grafts.

Authors:  M Hurme; P R Chandler; C M Hetherington; E Simpson
Journal:  J Exp Med       Date:  1978-03-01       Impact factor: 14.307

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  1 in total

1.  Resistance to Toxoplasma gondii in mice infected as neonates or exposed in utero.

Authors:  L L Johnson
Journal:  Infect Immun       Date:  1994-08       Impact factor: 3.441

  1 in total

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