Literature DB >> 113479

Genetic control of the immune response to collagen. II. Antibody responses produced in fetal liver restored radiation chimeras and thymus reconstituted F1 hybrid nude mice.

S M Hedrick, J Watson.   

Abstract

The level of antibody produced in response to calf skin collagen in mice is influenced by genes which are closely linked to the I region of the H-2 major histocompatibility complex. This influence is shown to be expressed during lymphoid maturation by testing the antibody responsiveness to collagen in two types of chimeric mice. First, high responder and low responder parental strain mice were lethally irradiated and restored with fetal liver cells from (high X low responder) F1 mice. These F1 leads to parent chimeras exhibited an immune response phenotype characteristic of the irradiated parental strain animals, establishing that H-2 determinants of the host affect antigen responsiveness. Second, (high X low responder) F1 congenitally athymic (nude) mice were restored with fetal thymus transplants from either high or low responder parental strain mice. After a period of maturation these mice were shown to be competent for a T-dependent IgG response to SRBC. The responsiveness to collagen in these mice was characteristic of the parental strain thymus donors, indicating that the expression of H-2 determinants in thymic tissue during lymphoid maturation influences the antibody response phenotype expressed by mice.

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Year:  1979        PMID: 113479      PMCID: PMC2185645          DOI: 10.1084/jem.150.3.646

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


  19 in total

1.  The major histocompatibility complex of the mouse.

Authors:  J Klein
Journal:  Science       Date:  1979-02-09       Impact factor: 47.728

Review 2.  The somatic generation of immune recognition.

Authors:  N K Jerne
Journal:  Eur J Immunol       Date:  1971-01       Impact factor: 5.532

3.  In a radiation chimaera, host H-2 antigens determine immune responsiveness of donor cytotoxic cells.

Authors:  M J Bevan
Journal:  Nature       Date:  1977-09-29       Impact factor: 49.962

Review 4.  Functional specificity of thymus- dependent lymphocytes.

Authors:  W E Paul; B Benacerraf
Journal:  Science       Date:  1977-03-25       Impact factor: 47.728

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.  Adaptive differentiation of murine lymphocytes. I. Both T and B lymphocytes differentiating in F1 transplanted to parental chimeras manifest preferential cooperative activity for partner lymphocytes derived from the same parental type corresponding to the chimeric host.

Authors:  D H Katz; B J Skidmore; L R Katz; C A Bogowitz
Journal:  J Exp Med       Date:  1978-09-01       Impact factor: 14.307

8.  Restricted helper function of F1 hybrid T cells positively selected to heterologous erythrocytes in irradiated parental strain mice. II. Evidence for restrictions affecting helper cell induction and T-B collaboration, both mapping to the K-end of the H-2 complex.

Authors:  J Sprent
Journal:  J Exp Med       Date:  1978-04-01       Impact factor: 14.307

9.  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

10.  Thymic reconstitution of nude F1 mice with one or both parental thymus grafts.

Authors:  R M Zinkernagel; A Althage; G Callahan
Journal:  J Exp Med       Date:  1979-09-19       Impact factor: 14.307

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  12 in total

1.  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 2.  Acquisition of MHC-restriction specificities: role of thymic stromal cells.

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

Review 3.  Function of macrophages as antigen presenting cells.

Authors:  J Schroer; A S Rosenthal
Journal:  Springer Semin Immunopathol       Date:  1980-08

4.  Thymic reconstitution of H-2-linked T-cell responses to thyroglobulin or insulin.

Authors:  R Maron; I R Cohen
Journal:  Immunogenetics       Date:  1983       Impact factor: 2.846

5.  Effect on IgE production of transplanted cultured thymic fragments.

Authors:  M Nishikawa; R Hong
Journal:  Immunology       Date:  1987-01       Impact factor: 7.397

6.  Murine syngeneic mixed lymphocyte response. I. Target antigens are self Ia molecules.

Authors:  L H Glimcher; D L Longo; I Green; R H Schwartz
Journal:  J Exp Med       Date:  1981-11-01       Impact factor: 14.307

7.  Responder T cells depleted of alloreactive cells react to antigen presented on allogeneic macrophages from nonresponder strains.

Authors:  N Ishii; C N Baxevanis; Z A Nagy; J Klein
Journal:  J Exp Med       Date:  1981-09-01       Impact factor: 14.307

8.  Gene complementation. Neither Ir-GLphi gene need be present in the proliferative T cell to generate an immune response to Poly(Glu55Lys36Phe9)n.

Authors:  D L Longo; R H Schwartz
Journal:  J Exp Med       Date:  1980-06-01       Impact factor: 14.307

9.  Self-recognition specificity expressed by T cells from nude mice. Absence of detectable Ia-restricted T cells in nude mice that do exhibit self-K/D-restricted T cell responses.

Authors:  A M Kruisbeek; M L Davis; L A Matis; D L Longo
Journal:  J Exp Med       Date:  1984-09-01       Impact factor: 14.307

10.  Absence of the Lyt-2-,L3T4+ lineage of T cells in mice treated neonatally with anti-I-A correlates with absence of intrathymic I-A-bearing antigen-presenting cell function.

Authors:  A M Kruisbeek; J J Mond; B J Fowlkes; J A Carmen; S Bridges; D L Longo
Journal:  J Exp Med       Date:  1985-05-01       Impact factor: 14.307

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