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PMID: 6170721 Published · ppublish English Journal Article

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

The Journal of experimental medicine ·Vol. 154 ·No. 5 ·1981-11-01 ·Pages 1652-70

Glimcher LH, Longo DL, Green I, Schwartz RH

Abstract

A system has been described that produces a murine syngeneic mixed lymphocyte response (MLR) comparable in magnitude to an allogeneic MLR. The responder cells in these cultures exhibit the classic immunologic characteristics of both memory and specificity. Studies using radiation-induced bone marrow chimeras of F(1) {arrow} parent type indicated that, similar to many other T cell-mediated immune responses, the response of the T lymphocytes in the syngeneic MLR was major histocompatibility complex-restricted and was determined by the environment in which the T cells matured. Using responder T cells from F(1) {arrow} parent chimeras and stimulator cells from H-2 recombinant strains, it was possible to map the genes involved in the stimulation to the K and/or I regions. In addition, blocking studies with monoclonal anti-Ia antibodies suggested that in the B10.A strain the critical molecules were products of both the I-A(k) and I-E(k) subregions. The issue of whether the syngeneic MLR is directed solely at self I-region antigens or whether the response represents proliferation to an unknown antigen in association with self I-region determinants was also addressed. Secondary syngeneic MLR were successfully performed in normal mouse serum and with stimulator cells prepared in the absence of bovine serum albumin to rule out the possibility that xenogeneic serum antigens were involved in the stimulation. The possibility that the syngeneic MLR might represent a secondary response to environmental antigens was eliminated by using germ- free mice as a source of stimulator cells and by demonstrating that spleen cells from unimmunized, fully allogeneic chimeras (B10.A {arrow} B10) could generate a normal syngeneic MLR even though such chimeras could not be primed to respond to any foreign antigens unless supplemented in vivo with a source of antigen-presenting cells syngeneic to the B10 host. The possibility that the syngeneic MLR was a primary response to a foreign antigen was considered unlikely because by using our culture conditions we could not obtain a primary antigen response or a secondary antigen response after in vitro priming to a variety of potent foreign antigens. Finally, the possibility that the syngeneic MLR represents a response to a variety of minor histocompatibility self antigens in association with self Ia molecules was eliminated by showing that the secondary responses to H-2 compatible, non-H-2 different strain (A/J vs. B10.A and C3H, or BALB/c vs. B10.D2 and DBA/2) were comparable to the secondary responses to syngeneic stimulators. Thus, we conclude that the target antigens in the syngeneic MLR are solely determinants on self Ia molecules, although the functionally equivalent possibility of a single, nonpolymorphic, minor self antigen seen in association with self Ia molecules cannot be excluded.

MeSH Terms
Animals Cattle Cell Differentiation Centrifugation, Density Gradient Epitopes Genetic Code Histocompatibility Antigens Class II Immunologic Memory Lymphocyte Culture Test, Mixed Mice Mice, Inbred A Mice, Inbred BALB C Mice, Inbred C3H Mice, Inbred C57BL Protein Biosynthesis Radiation Chimera Serum Albumin, Bovine/pharmacology Spleen/cytology T-Lymphocytes/immunology
Chemicals
Epitopes Histocompatibility Antigens Class II Serum Albumin, Bovine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Glimcher L H
Longo D L
Green I
Schwartz R H
References (38)
38 references, click to expand
  1. Cytotoxic T cells learn specificity for self H-2 during differentiation in the thymus.
    Nature. 1978 Jan 19;271(5642):251-3 PMID: 304527
  2. Self recognition in allogeneic radiation bone marrow chimeras. A radiation-resistant host element dictates the self specificity and immune response gene phenotype of T-helper cells.
    J Exp Med. 1981 May 1;153(5):1286-301 PMID: 6166716
  3. In a fully H-2 incompatible chimera, T cells of donor origin can respond to minor histocompatibility antigens in association with either donor or host H-2 type.
    J Exp Med. 1978 Jul 1;148(1):84-92 PMID: 78964
  4. 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.
    J Exp Med. 1978 Sep 1;148(3):727-45 PMID: 308984
  5. The somatic generation of immune recognition.
    Eur J Immunol. 1971 Jan;1(1):1-9 PMID: 14978855
  6. Syngeneic mixed lymphocyte reaction between thymocytes and peripheral lymphoid cells in mice: strain specificity and nature of the target cell.
    J Immunol. 1973 Feb;110(2):376-83 PMID: 4265142
  7. Adult murine lymph node cells respond blastogenically to a new differentiation antigen on isologous and autologous B lymphocytes.
    J Immunol. 1975 Mar;114(3):971-5 PMID: 122992
  8. Association of immunity and tolerance to host H-2 determinants in irradiated F1 hybrid mice reconstituted with bone marrow cells from one parental strain.
    J Exp Med. 1975 Aug 1;142(2):321-31 PMID: 124761
  9. Autologous stimulation of human lymphocyte subpopulation.
    J Exp Med. 1975 Nov 1;142(5):1327-33 PMID: 127826
  10. Lymphocyte transformation induced by autologous cells. IV. Human T-lymphocyte proliferation induced by autologous or allogeneic non-T lymphocytes.
    J Exp Med. 1976 May 1;143(5):1042-54 PMID: 131174
  11. Nature of the antigenic complex recognized by T lymphocytes. I. Analysis with an in vitro primary response to soluble protein antigens.
    J Exp Med. 1976 Nov 2;144(5):1263-73 PMID: 62818
  12. Two different VH gene products make up the T-cell receptors.
    Scand J Immunol. 1976;5(9):993-1001 PMID: 63988
  13. Hypothesis: why do so many lymphocytes respond to major histocompatibility antigens?
    Cell Immunol. 1977 Mar 1;29(1):1-5 PMID: 300293
  14. Thymic maturation in vitro by a secretory product from macrophages.
    J Immunol. 1977 May;118(5):1780-7 PMID: 140194
  15. In a radiation chimaera, host H-2 antigens determine immune responsiveness of donor cytotoxic cells.
    Nature. 1977 Sep 29;269(5627):417-8 PMID: 302918
  16. Lymphocyte transformation induced by autologous cells. V. Generation of immunologic memory and specificity during the autologous mixed lymphocyte reaction.
    J Exp Med. 1977 Dec 1;146(6):1833-8 PMID: 144773
  17. Two-gene control of the expression of a murine Ia antigen.
    J Exp Med. 1978 Oct 1;148(4):925-39 PMID: 100572
  18. Syngeneic mixed lymphocyte reaction in mice: strain distribution, kinetics, participating cells, and absence in NZB mice.
    J Immunol. 1978 Nov;121(5):1889-92 PMID: 152331
  19. 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.
    J Exp Med. 1978 Dec 1;148(6):1510-22 PMID: 102728
  20. Role of H-2 gene products in the function of T helper cells from normal and chimeric mice in vivo.
    Immunol Rev. 1978;42:108-37 PMID: 83698
  21. The influence of the major histocompatibility complex on the function of T-helper cells in antibody formation.
    Immunol Rev. 1978;42:202-23 PMID: 83700
  22. Thymus and lymphohemopoietic cells: their role in T cell maturation in selection of T cells' H-2-restriction-specificity and in H-2 linked Ir gene control.
    Immunol Rev. 1978;42:224-70 PMID: 83701
  23. The influence of thymus H-2 antigens on the specificity of maturing killer and helper cells.
    Immunol Rev. 1978;42:3-19 PMID: 83702
  24. Primary anti-viral cytotoxic T-cell responses in semiallogeneic chimeras are not absolutely restricted to host H-2 type.
    J Exp Med. 1979 Feb 1;149(2):535-8 PMID: 216768
  25. 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.
    J Exp Med. 1979 Sep 19;150(3):646-52 PMID: 113479
  26. Cellular and genetic control of antibody responses. VI. Expression of Ir gene function by H-2a accessory cells, but not H-2a T or B cells in responses to TNP-(T,G)-A--L.
    J Immunol. 1979 Dec;123(6):2823-9 PMID: 115922
  27. Studies on the generation and expression of H-2-controlled T helper function in chimeric mice: evidence for two levels of H-2 resitriction.
    Eur J Immunol. 1979 Sep;9(9):730-6 PMID: 315878
  28. Stimulating cell types in the autologous mixed leukocyte reaction in man.
    J Immunol. 1980 Jan;124(1):227-32 PMID: 6444227
  29. The syngeneic mixed leukocyte reaction: the genetic requirements for the recognition of self resemble the requirements for the recognition of antigen in association with self.
    J Immunol. 1980 Apr;124(4):1773-8 PMID: 6154080
  30. Contribution of dendritic cells to stimulation of the murine syngeneic mixed leukocyte reaction.
    J Exp Med. 1980 May 1;151(5):1196-212 PMID: 6445399
  31. Gene complementation. Neither Ir-GLphi gene need be present in the proliferative T cell to generate an immune response to Poly(Glu55Lys36Phe9)n.
    J Exp Med. 1980 Jun 1;151(6):1452-67 PMID: 6770025
  32. T cells and macrophages involved in the autologous mixed lymphocyte reaction are required for the response to conventional antigen.
    J Immunol. 1980 Sep;125(3):1374-9 PMID: 6447724
  33. The autologous mixed lymphocyte reaction in strains of mice with autoimmune disease.
    J Immunol. 1980 Oct;125(4):1832-8 PMID: 6447732
  34. Macrophage heterogeneity in man. A subpopulation of HLA-DR-bearing macrophages required for antigen-induced T cell activation also contains stimulators for autologous-reactive T cells.
    J Exp Med. 1980 Sep 1;152(3):581-93 PMID: 6997424
  35. Features of cells controlling H-2-restricted presentation of antigen to T helper cells in vivo.
    J Immunol. 1980 Nov;125(5):2089-96 PMID: 6968772
  36. Complementation between I region genes is revealed by a hybridoma anti-Ia antibody.
    Transplantation. 1981 Apr;31(4):308-10 PMID: 6939161
  37. Inhibition of antigen-induced proliferation of T cells from radiation-induced bone marrow chimeras by a monoclonal antibody directed against an Ia determinant on the antigen-presenting cell.
    Proc Natl Acad Sci U S A. 1981 Jan;78(1):514-8 PMID: 6165995
  38. A clonal deletion model for Ir gene control of the immune response.
    Scand J Immunol. 1978;7(1):3-10 PMID: 76333
Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1981-11-01
Pages
1652-70
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2186517
Subset
IM
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