Literature DB >> 349111

Primary in vitro cell-mediated lympholysis reaction of NZB mice against unmodified targets syngeneic at the major histocompatibility complex.

U Botzenhardt, J Klein, M Ziff.   

Abstract

T-cell cytotoxicity of NZV mice was tested after in vitro sensitization against a group of H-2 identical strains (BALB/c, B10.D2, DBA/2, HW19). A highly significant and unexpected unidirectional cell-mediated lympholysis (CML) reaction by the sensitized NZB effector cells on these targets was found. After sensitization in vitro with stimulator cells of one H-2d strain, NZB effector cells (H-2d) lysed all other H-2d targets and to a lesser degree, some non-H-2d targets (C57BL/10, DBA/1, B10.Q, CBA, B10.S, A.SW). NZB targets were not lysed. Differences in the major histocompatibility region between NZB and other H-2d strains could be excluded as a possible explanation for the observed reaction of NZB (H-2d) against other H-2d strains. These results consequently represent the first description of a primary in vitro CML directed against determinants not coded for in the major histocompatibility complex. The responsible effector cells are demonstrated to be T cells. The CML of NZB against H-2 identiical targets appears best explained by a reaction against minor histocompatibility antigens. This, and the observed cross-reactions, would indicate that the cytotoxic T-cell system in NZB mice is not subjected to restrictions found in all normal mouse strains tested until now under similar conditions. It is suggested that this hyperreactivity is related to the autoimmune responsiveness of the NZB strain.

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Year:  1978        PMID: 349111      PMCID: PMC2184272          DOI: 10.1084/jem.147.5.1435

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


  28 in total

1.  Age and genetic influence on immunity in NZB and autoimmune-resistant mice.

Authors:  G Fernandes; E J Yunis; R A Good
Journal:  Clin Immunol Immunopathol       Date:  1976-11

2.  THE NATURAL HISTORY OF AUTOIMMUNE DISEASE IN NZB MICE. A COMPARISON WITH THE PATTERN OF HUMAN AUTOIMMUNE MANIFESTATIONS.

Authors:  M C HOLMES; F M BURNET
Journal:  Ann Intern Med       Date:  1963-09       Impact factor: 25.391

3.  Renal disease associated with positive lupus erythematosus tests in a cross-bred strain of mice.

Authors:  B J HELYER; J B HOWIE
Journal:  Nature       Date:  1963-01-12       Impact factor: 49.962

4.  Age-associated decline in the in vitro development of cytotoxic lymphocytes in NZB mice.

Authors:  T Hirano; A A Nordin
Journal:  J Immunol       Date:  1976-10       Impact factor: 5.422

5.  Secondary in vitro responses of T lymphocytes to non-H-2 alloantigens self-H-2-restricted responses induced in heterologous serum are not dependent on primary-stimulating non-H-2 alloantigens.

Authors:  A B Peck; L C Andersson; H Wigzell
Journal:  J Exp Med       Date:  1977-04-01       Impact factor: 14.307

6.  In vitro and in vivo cytotoxicity to EL-4 sarcoma in New Zealand mice.

Authors:  M E Gershwin; R J Klingenstein; T M Chused; A D Steinberg
Journal:  J Immunol       Date:  1974-12       Impact factor: 5.422

7.  Comparison of T cell-mediated immune responsiveness of NZB, (NZB x &NZW)F1 hybrid and other murine strains.

Authors:  R M Zinkernagel; F J Dixon
Journal:  Clin Exp Immunol       Date:  1977-07       Impact factor: 4.330

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.  Relative inability to induce tolerance in adult NZB and NZB-NZW F1 mice.

Authors:  P J Staples; N Talal
Journal:  J Exp Med       Date:  1969-01-01       Impact factor: 14.307

10.  The major histocompatibility complex determines susceptibility to cytotoxic T cells directed against minor histocompatibility antigens.

Authors:  M J Bevan
Journal:  J Exp Med       Date:  1975-12-01       Impact factor: 14.307

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  18 in total

1.  Primary cytotoxic T-cell response in vitro against Mls antigens in NZB-mice.

Authors:  U Botzenhardt; J Müller-Quernheim
Journal:  Clin Exp Immunol       Date:  1987-09       Impact factor: 4.330

2.  The pathogenesis of murine systemic lupus erythematosus. Rous--Whipple Award lecture.

Authors:  F J Dixon
Journal:  Am J Pathol       Date:  1979-10       Impact factor: 4.307

3.  Experimental models of lymphoproliferative disease. The mouse as a model for human non-Hodgkin's lymphomas and related leukemias.

Authors:  P K Pattengale; C R Taylor
Journal:  Am J Pathol       Date:  1983-11       Impact factor: 4.307

4.  Equal distribution of T-lymphocyte subpopulations in thymus and spleen cells of NZB and BALB/c mice.

Authors:  J Müller-Quernheim; U Botzenhardt; D von Steldern
Journal:  Rheumatol Int       Date:  1984       Impact factor: 2.631

5.  Genetic control of B- and T-lymphocyte abnormalities of NZB mice in crosses with B10.D2 mice.

Authors:  W F Davidson; T M Chused; H C Morse
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

6.  Chromosome 1 locus required for induction of CTL to H-2-compatible cells in NZB mice.

Authors:  W F Davidson; B J Mathieson; C A Kozak; T M Chused; H C Morse
Journal:  Immunogenetics       Date:  1982-03       Impact factor: 2.846

7.  Genetic and functional analyses of the primary in vitro CTL: response of NZB lymphocytes to H-2-compatible cells.

Authors:  W F Davidson; T M Chused; H C Morse
Journal:  Immunogenetics       Date:  1981-03-01       Impact factor: 2.846

8.  In vivo modulation of thymus-derived lymphocytes with monoclonal antibodies in mice. III. Spontaneous and natural cytotoxic effector cells.

Authors:  A G Herbert; G S Le Gros; S Bidawid; J D Watson
Journal:  Immunology       Date:  1984-02       Impact factor: 7.397

9.  T-cell hyperreactivity of NZB mice against H-2 identical cells. Equal cytotoxic T lymphocyte precursor frequency against H-2 allogeneic and H-2 syngeneic target cells in NZB.

Authors:  J Müller; R Bartlett; U Botzenhardt
Journal:  Rheumatol Int       Date:  1983       Impact factor: 2.631

10.  Cells in bone marrow and in T cell colonies grown from bone marrow can suppress generation of cytotoxic T lymphocytes directed against their self antigens.

Authors:  S Muraoka; R G Miller
Journal:  J Exp Med       Date:  1980-07-01       Impact factor: 14.307

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