Literature DB >> 6153213

Absence of H-2 restriction in primary and secondary mixed-lymphocyte reactions to strong M1s determinants.

K Molnar-Kimber, J Sprent.   

Abstract

Negative and positive selection procedures were used to establish whether the strong proliferative response of T cells to M1sa determinants is H-2 restricted. After negative selection of H-2 determinants in vivo, it was shown that T cells give high primary mixed lymphocyte reactions in vitro to M1sa determinants presented on H-2-incompatible stimulator cells. Other studies demonstrated that (a) negative selection of T cells to M1sa determinants on H-2-incompatible cells removed T cells with specificity for M1sa-bearing H-2-compatible cells, and (b) T cells primed in vitro or in vivo to M1sa determinants on H-2-compatible cells gave high secondary responses to M1sa determinants presented either on H-2-compatible or H-2-incompatible stimulator cells. From these data we conclude that T cells recognize M1sa determinants per se rather than an association of M1sa plus self or allo-H-2 determinants.

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Year:  1980        PMID: 6153213      PMCID: PMC2185787          DOI: 10.1084/jem.151.2.407

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


  20 in total

1.  Cross-reactivity exists between Mlsa and Mlsd lymphocyte-activating determinants as demonstrated by the negative clonal selection of responder cells in a mixed lymphocyte reaction.

Authors:  J J Ryan; A Ahmed; P Kind; K W Sell
Journal:  Transplant Proc       Date:  1979-06       Impact factor: 1.066

2.  T lymphocyte responses to Mls locus antigens involve recognition of H-2 I region gene products.

Authors:  A B Peck; C A Janeway; H Wigzell
Journal:  Nature       Date:  1977-04-28       Impact factor: 49.962

3.  Cytotoxic T cells recognize male antigen and H-2 as distinct entities.

Authors:  H von Boehmer; W Haas; H Pohlit
Journal:  J Exp Med       Date:  1978-04-01       Impact factor: 14.307

4.  T-cell populations specifically depleted of alloreactive potential cannot be induced to lyse H-2-different virus-infected target cells.

Authors:  J R Bennink; P C Doherty
Journal:  J Exp Med       Date:  1978-07-01       Impact factor: 14.307

5.  B-lymphocyte Fc receptor-associated non-H-2 antigens are determined by a single polymorphic locus which is linked to the Mls locus.

Authors:  H B Dickles; A Ahmed; D H Sachs
Journal:  J Exp Med       Date:  1977-12-01       Impact factor: 14.307

6.  The generation of killer cells to trinitrophenyl-modified allogeneic targets by lymphocyte populations negatively selected to strong alloantigens.

Authors:  D B Wilson; K F Lindahl; D H Wilson; J Sprent
Journal:  J Exp Med       Date:  1977-08-01       Impact factor: 14.307

7.  Vaccinia-specific cytotoxic T-cell responses in the context of H-2 antigens not encountered in thymus may reflect aberrant recognition of a virus-H-2 complex.

Authors:  P C Doherty; J C Bennink
Journal:  J Exp Med       Date:  1979-01-01       Impact factor: 14.307

8.  Role of the H-2 complex in induction of T helper cells in vivo. I. Antigen-specific selection of donor T cells to sheep erythrocytes in irradiated mice dependent upon sharing of H-2 determinants between donor and host.

Authors:  J Sprent
Journal:  J Exp Med       Date:  1978-08-01       Impact factor: 14.307

9.  Lethal graft-versus-host disease after bone marrow transplantation across minor histocompatibility barriers in mice. Prevention by removing mature T cells from marrow.

Authors:  R Korngold; J Sprent
Journal:  J Exp Med       Date:  1978-12-01       Impact factor: 14.307

10.  The control of specificity of cytotoxic T lymphocytes by the major histocompatibility complex (AG-B) in rats and identification of a new alloantigen system showing no AG-B restriction.

Authors:  A Marshak; P C Doherty; D B Wilson
Journal:  J Exp Med       Date:  1977-12-01       Impact factor: 14.307

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  14 in total

1.  Multi-gene/allele control of Mlsb of CBA/H.

Authors:  R E Click; A Adelmann
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

2.  Multigene control of Mlsc.

Authors:  R E Click; A Adelmann
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

3.  Immune responses in vitro, XIV. Undetectability of Mlsb- and Mlsc-encoded products on F1 cells possessing Mlsa or Mlsd.

Authors:  R E Click; D Schneider; L A Sitzmann; M M Azar
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

4.  Soluble Mlsa antigens: stimulatory effect in vitro versus suppressive effect in vivo.

Authors:  L Berumen; H Festenstein; O Halle-Pannenko
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

5.  Dissociation of two signals required for activation of resting B cells.

Authors:  M H Julius; H von Boehmer; C L Sidman
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

Review 6.  T cell recognition of antigen in vivo: role of the H-2 complex.

Authors:  J Sprent; R Korngold; K Molnar-Kimber
Journal:  Springer Semin Immunopathol       Date:  1980-08

7.  T lymphocytes responding to Mls-locus antigens are Lyt-1+, 2- and I-A restricted.

Authors:  C A Janeway; E A Lerner; J M Jason; B Jones
Journal:  Immunogenetics       Date:  1980       Impact factor: 2.846

8.  Dominant expression of a distinctive V14+ T-cell antigen receptor alpha chain in mice.

Authors:  H Koseki; H Asano; T Inaba; N Miyashita; K Moriwaki; K F Lindahl; Y Mizutani; K Imai; M Taniguchi
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-01       Impact factor: 11.205

9.  H-2-linked genes determine the level of the primary in vitro anti-Mls response.

Authors:  S Macphail; O Stutman
Journal:  Immunogenetics       Date:  1986       Impact factor: 2.846

10.  Distinct features of dendritic cells and anti-Ig activated B cells as stimulators of the primary mixed leukocyte reaction.

Authors:  J P Metlay; E Puré; R M Steinman
Journal:  J Exp Med       Date:  1989-01-01       Impact factor: 14.307

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