Literature DB >> 6217271

Cytotoxic T lymphocyte responses in allogeneic radiation bone marrow chimeras. The chimeric host strictly dictates the self-repertoire of Ia-restricted T cells but not H-2K/D-restricted T cells.

S M Bradley, A M Kruisbeek, A Singer.   

Abstract

The present report has used fully H-2 allogeneic radiation bone marrow chimeras to assess the role of host restriction elements in determining the self-specificity of Ia- and H-2K/D-restricted T cells that participate in the generation of trinitrophenyl (TNP)-specific cytotoxic T lymphocytes (CTL). It was demonstrated that there exists a stringent requirement for the recognition of host thymic-type Ia determinants, but there exists only a preference for host thymic-type H-2K/D determinants. Indeed, once the stringent requirement for recognition of host Ia determinants was fulfilled, anti-TNP CTL were generated in response to TNP-modified stimulators that expressed either donor-type or host-type H-2K/D determinants. The CTL that were generated in response to TNP-modified donor-type stimulators were shown to be specific for TNP and restricted to the non-thymic H-2K/D determinants of the chimeric donor. Thus, these results demonstrate in a single immune response that the thymic hypothesis accurately predicts the self-specificity expressed by Ia-restricted T cells, but does not fully account for the self-specificity expressed by H-2K/D-restricted T cells. These results are consistent with the concept that H-2K/D-restricted T cells, but not Ia-restricted T cells, can differentiate into functional competence either intrathymically or extra-thymically. The present results are also informative for understanding the cellular interactions that are required for the generation of antigen-specific CTL responses. The Ia-restricted T cells that are required for the generation of H-2K/D-restricted anti-TNP CTL were shown to be helper T (TH) cells since (a) like TH cells functioning in antibody responses, they were specific for Ia determinants expressed by accessory cells, and (b) their function could be replaced by either TNP-primed, irradiated TH cells or by nonspecific soluble helper factors. It was also shown that the T-T cell interaction between Ia-restricted TH cells and H-2K/D-restricted precursor CTL (pCTL) is not Ia restricted. Rather, the results demonstrate that the generation of anti-TNP CTL responses involve two parallel sets of major histocompatibility complex-restricted cell interactions, an Ia-restricted TH-accessory cell interaction required for TH cell activation, and an H-2K/D-restricted pCTL-stimulator cell interaction required for pCTL stimulation. The interaction between activated TH cells and stimulated pCTL is mediated, at least in part, by nonspecific soluble helper factors.

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Year:  1982        PMID: 6217271      PMCID: PMC2186858          DOI: 10.1084/jem.156.6.1650

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


  25 in total

1.  Cell-mediated cytotoxicity to trinitrophenyl-modified syngeneic lymphocytes.

Authors:  G M Shearer
Journal:  Eur J Immunol       Date:  1974-08       Impact factor: 5.532

2.  Separation of mouse spleen cells by passage through columns of sephadex G-10.

Authors:  I A Ly; R I Mishell
Journal:  J Immunol Methods       Date:  1974-08       Impact factor: 2.303

3.  Cellular and genetic control of antibody responses in vitro. I. Cellular requirements for the generation of genetically controlled primary IgM responses to soluble antigens.

Authors:  R J Hodes; A Singer
Journal:  Eur J Immunol       Date:  1977-12       Impact factor: 5.532

4.  Properties of monoclonal antibodies to mouse Ig allotypes, H-2, and Ia antigens.

Authors:  V T Oi; P P Jones; J W Goding; L A Herzenberg; L A Herzenberg
Journal:  Curr Top Microbiol Immunol       Date:  1978       Impact factor: 4.291

5.  Major histocompatibility complex-linked immune-responsiveness is acquired by lymphocytes of low-responder mice differentiating in thymus of high-responder mice.

Authors:  H von Boehmer; W Haas; N K Jerne
Journal:  Proc Natl Acad Sci U S A       Date:  1978-05       Impact factor: 11.205

6.  Restricted helper function of F1 leads to parent bone marrow chimeras controlled by K-end of H-2 complex.

Authors:  J Sprent
Journal:  J Exp Med       Date:  1978-06-01       Impact factor: 14.307

7.  The lymphoreticular system in triggering virus plus self-specific cytotoxic T cells: evidence for T help.

Authors:  R M Zinkernagel; G N Callahan; A Althage; S Cooper; J W Streilein; J Klein
Journal:  J Exp Med       Date:  1978-03-01       Impact factor: 14.307

8.  H-2 antigens of the thymus determine lymphocyte specificity.

Authors:  P J Fink; M J Bevan
Journal:  J Exp Med       Date:  1978-09-01       Impact factor: 14.307

9.  The role of H-2 linked genes in helper T-cell function. IV. Importance of T-cell genotype and host environment in I-region and Ir gene expression.

Authors:  J W Kappler; P Marrack
Journal:  J Exp Med       Date:  1978-12-01       Impact factor: 14.307

10.  On the thymus in the differentiation of "H-2 self-recognition" by T cells: evidence for dual recognition?

Authors:  R M Zinkernagel; G N Callahan; A Althage; S Cooper; P A Klein; J Klein
Journal:  J Exp Med       Date:  1978-03-01       Impact factor: 14.307

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  19 in total

1.  Purified hematopoietic stem cell grafts induce tolerance to alloantigens and can mediate positive and negative T cell selection.

Authors:  J A Shizuru; I L Weissman; R Kernoff; M Masek; Y C Scheffold
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-15       Impact factor: 11.205

Review 2.  Mixed hematopoietic chimerism and transplantation tolerance.

Authors:  B Nikolic; M Sykes
Journal:  Immunol Res       Date:  1997       Impact factor: 2.829

3.  Cyclosporin A and anti-Ia antibody cause a maturation defect of CD4+8- cells in organ-cultured fetal thymus.

Authors:  Y Takeuchi; S Habu; K Okumura; G Suzuki
Journal:  Immunology       Date:  1989-03       Impact factor: 7.397

4.  On the role of thymic epithelium vs. bone marrow-derived cells in repertoire selection of T cells.

Authors:  R M Zinkernagel; A Althage
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

Review 5.  Induction of MHC-restricted specificity and tolerance in the thymus.

Authors:  D Lo; Y Ron; J Sprent
Journal:  Immunol Res       Date:  1986       Impact factor: 2.829

6.  Bone marrow-derived thymic antigen-presenting cells determine self-recognition of Ia-restricted T lymphocytes.

Authors:  D L Longo; A M Kruisbeek; M L Davis; L A Matis
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

Review 7.  Acquisition of MHC-restriction specificities: role of thymic stromal cells.

Authors:  A M Kruisbeek; D L Longo
Journal:  Surv Immunol Res       Date:  1985

8.  Tolerance of CD8+ T cells developing in parent-->F1 chimeras prepared with supralethal irradiation: step-wise induction of tolerance in the intrathymic and extrathymic environments.

Authors:  H Kosaka; J Sprent
Journal:  J Exp Med       Date:  1993-02-01       Impact factor: 14.307

9.  Class II-positive hematopoietic cells cannot mediate positive selection of CD4+ T lymphocytes in class II-deficient mice.

Authors:  J S Markowitz; H Auchincloss; M J Grusby; L H Glimcher
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-01       Impact factor: 11.205

10.  Evidence for a single-niche model of positive selection.

Authors:  M Merkenschlager; C Benoist; D Mathis
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-22       Impact factor: 11.205

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