GENERATION OF SUPPRESSOR CELLS IN THE AUTOLOGOUS MIXED LYMPHOCYTE-REACTION
- 1 January 1981
- journal article
- research article
- Vol. 46 (1) , 185-195
Abstract
When challenged with HLA-A, B and DR incompatible cells, [human] T cells which have been primed in an autologous mixed lymphocyte response (AMLR) show an accelerated (day 2) component of their proliferative response, and the expected primary-style response at day 5. This early response of AMLR-primed cells to allogeneic stimulation, like the response to rechallenge with autologous cells, is abolished by treatment of the primary culture with BUdR [bromodeoxyuridine] and light. Priming in the AMLR probably is not solely to MHC[major histocompatibility complex]-private specificities; an antigenic element common to autologous and allogeneic cells probably is recognized. The AMLR also generates cells with suppressor activities. AMLR-primed cells suppress the proliferative responses of fresh T cells from the same donor to autologous or allogeneic stimulation. Limiting numbers of suppressor cells are more effective suppressors of the autologous, than of the allogeneic, response. Suppressor activity is reduced but not abolished by treatment with mitomycin C. AMLR-primed cells also suppress pokeweed mitogen-induced antibody production by fresh peripheral blood lymphocytes. In some experiments, specific antigen-induced antibody production is also suppressed.This publication has 22 references indexed in Scilit:
- Specificity and Suppressor Function of Human T Cells Responsive to Autologous Non-T CellsThe Journal of Immunology, 1979
- Activation of Suppressor T Cells in Human Autologous Mixed Lymphocyte CultureThe Journal of Immunology, 1979
- Specificity and function of a human autologous reactive T cell.The Journal of Experimental Medicine, 1979
- NATURE OF THE STIMULATORY CELL IN HUMAN ALLOGENEIC AND AUTOLOGOUS MLC REACTIONS - ROLE OF ISOLATED IGM-BEARING B-CELLS1979
- Failure of autologous mixed lymphocyte reactions between T and non-T cells in patients with systemic lupus erythematosus.Proceedings of the National Academy of Sciences, 1978
- Studies of immune functions of patients with systemic lupus erythematosus. i. dysfunction of suppressor t‐cell activity related to impaired generation of, rather than response to, suppressor cellsArthritis & Rheumatism, 1978
- Control of Human B Lymphocyte Responsiveness: Enhanced Suppressor T Cell Activity after in vitro IncubationThe Journal of Immunology, 1978
- Lymphocyte transformation induced by autologous cells. V. generation of immunologic memory and specificity during the autologous mixed lymphocyte reactionThe Journal of Experimental Medicine, 1977
- Lymphocyte transformation induced by autologous cells. IV. Human T-lymphocyte proliferation induced by autologous or allogeneic non-T lymphocytes.The Journal of Experimental Medicine, 1976
- Autologous stimulation of human lymphocyte subpopulation.The Journal of Experimental Medicine, 1975