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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Selected References
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- Bennink J. R., Doherty P. C. T-cell populations specifically depleted of alloreactive potential cannot be induced to lyse H-2-different virus-infected target cells. J Exp Med. 1978 Jul 1;148(1):128–135. doi: 10.1084/jem.148.1.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dickles H. B., Ahmed A., Sachs D. H. B-lymphocyte Fc receptor-associated non-H-2 antigens are determined by a single polymorphic locus which is linked to the Mls locus. J Exp Med. 1977 Dec 1;146(6):1678–1692. doi: 10.1084/jem.146.6.1678. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Doherty P. C., Bennink J. C. 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. J Exp Med. 1979 Jan 1;149(1):150–157. doi: 10.1084/jem.149.1.150. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Festenstein H. Immunogenetic and biological aspects of in vitro lymphocyte allotransformation (MLR) in the mouse. Transplant Rev. 1973;15:62–88. doi: 10.1111/j.1600-065x.1973.tb00111.x. [DOI] [PubMed] [Google Scholar]
- Festenstein H. Pertinent features of M locus determinants including revised nomenclature and strain distribution. Transplantation. 1974 Dec;18(6):555–557. [PubMed] [Google Scholar]
- Festenstein H. The Mls system. Transplant Proc. 1976 Sep;8(3):339–342. [PubMed] [Google Scholar]
- Julius M. H., Simpson E., Herzenberg L. A. A rapid method for the isolation of functional thymus-derived murine lymphocytes. Eur J Immunol. 1973 Oct;3(10):645–649. doi: 10.1002/eji.1830031011. [DOI] [PubMed] [Google Scholar]
- Katz D. H., Benacerraf B. The function and interrelationships of T-cell receptors, Ir genes and other histocompatibility gene products. Transplant Rev. 1975;22:175–195. doi: 10.1111/j.1600-065x.1975.tb01559.x. [DOI] [PubMed] [Google Scholar]
- Korngold R., Sprent J. Lethal graft-versus-host disease after bone marrow transplantation across minor histocompatibility barriers in mice. Prevention by removing mature T cells from marrow. J Exp Med. 1978 Dec 1;148(6):1687–1698. doi: 10.1084/jem.148.6.1687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marshak A., Doherty P. C., Wilson D. B. 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. J Exp Med. 1977 Dec 1;146(6):1773–1790. doi: 10.1084/jem.146.6.1773. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nisbet N. W., Edwards J. The H-2D and H-2K regions of the major histocompatibility system and the M locus of the mouse investigated by parabiosis. Transplant Proc. 1973 Dec;5(4):1411–1416. [PubMed] [Google Scholar]
- Peck A. B., Janeway C. A., Jr, Wigzell H. T lymphocyte responses to Mls locus antigens involve recognition of H-2 I region gene products. Nature. 1977 Apr 28;266(5605):840–842. doi: 10.1038/266840a0. [DOI] [PubMed] [Google Scholar]
- Peck A. B., Wigzell H., Janeway C., Jr, Andersson L. C. Environmental and genetic control of T cell activation in vitro: a study using isolated alloantigen-activated T cell clones. Immunol Rev. 1977;35:146–180. doi: 10.1111/j.1600-065x.1977.tb00239.x. [DOI] [PubMed] [Google Scholar]
- Ryan J. J., Ahmed A., Kind P., Sell K. W. 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. Transplant Proc. 1979 Jun;11(2):1377–1378. [PubMed] [Google Scholar]
- Röllinghoff M., Pfizenmeier K., Trostmann H., Wagner H. T cell proliferation in the mixed lymphocyte culture does not necessarily result in the generation of cytotoxic T effector cells. Eur J Immunol. 1975 Aug;5(8):560–564. doi: 10.1002/eji.1830050811. [DOI] [PubMed] [Google Scholar]
- Sprent J. Circulating T and B lymphocytes of the mouse. I. Migratory properties. Cell Immunol. 1973 Apr;7(1):10–39. doi: 10.1016/0008-8749(73)90180-9. [DOI] [PubMed] [Google Scholar]
- Sprent J. 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. J Exp Med. 1978 Aug 1;148(2):478–489. doi: 10.1084/jem.148.2.478. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sprent J., von Boehmer H. Activation of T lymphocytes to M locus determinants in vivo. I. Quantitation of T cell proliferation and migration into thoracic duct lymph. Eur J Immunol. 1976 May;6(5):352–358. doi: 10.1002/eji.1830060510. [DOI] [PubMed] [Google Scholar]
- Wilson D. B., Lindahl K. F., Wilson D. H., Sprent J. The generation of killer cells to trinitrophenyl-modified allogeneic targets by lymphocyte populations negatively selected to strong alloantigens. J Exp Med. 1977 Aug 1;146(2):361–367. doi: 10.1084/jem.146.2.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- von Boehmer H., Haas W., Pohlit H. Cytotoxic T cells recognize male antigen and H-2 as distinct entities. J Exp Med. 1978 Apr 1;147(4):1291–1295. doi: 10.1084/jem.147.4.1291. [DOI] [PMC free article] [PubMed] [Google Scholar]