Abstract
T-cell clones were derived from autoimmune prone (NZB) and non-autoimmune (C58) strains of mice and tested for their effects in several assays of B-cell responsiveness. Clones from the C58 strain suppressed lipopolysaccharide LPS-stimulated B-cell proliferation, activation and immunoglobulin synthesis. In contrast, an NZB-derived clone enhanced these measures of B-cell response. The effects of the NZB clone were more notable on splenic target populations taken from mice 6 months of age or older. MHC-compatible DBA/2 spleen cells also showed enhancement of B-cell activation, but not of immunoglobulin synthesis by the NZB clone. It has been shown previously that all of the clones suppress T-cell proliferative responses. A potentially important skewing of the immune system toward humoral rather than cellular responses is therefore mediated by this clone derived from an autoimmune strain.
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Selected References
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- Bocchieri M. H., Smith J. B. Detection of autologous mixed lymphocyte reaction responding cells and their precursor frequency in NZB mice. Cell Immunol. 1982 Dec;74(2):345–357. doi: 10.1016/0008-8749(82)90035-1. [DOI] [PubMed] [Google Scholar]
- Brodeur B. R., Merigan T. C. Suppressive effect of interferon on the humoral immune response to sheep red blood cells in mice. J Immunol. 1974 Oct;113(4):1319–1325. [PubMed] [Google Scholar]
- Dauphinée M. J., Talal N. Failure of NZB spleen to respond to prethymic bone marrow suppressor cells. J Immunol. 1979 Mar;122(3):936–941. [PubMed] [Google Scholar]
- David C., Meo T., McCormick J., Shreffler D. Expression of individual Ia specificities on T and B cells. I. Studies with mitogen-induced blast cells. J Exp Med. 1976 Jan 1;143(1):218–224. doi: 10.1084/jem.143.1.218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fieser T. M., Gershwin M. E., Steinberg A. D., Dixon F. J., Theofilopoulos A. N. Abrogation of murine lupus by the xid gene is associated with reduced responsiveness of B cells to T-cell-helper signals. Cell Immunol. 1984 Sep;87(2):708–713. doi: 10.1016/0008-8749(84)90040-6. [DOI] [PubMed] [Google Scholar]
- Gutierrez C., Howard M., Gaspar M. L., Raveche E. S. Differential proliferative responses of B cells from BALB/c and autoimmune NZB mice to B-cell growth factor(s). Clin Immunol Immunopathol. 1986 May;39(2):319–328. doi: 10.1016/0090-1229(86)90095-4. [DOI] [PubMed] [Google Scholar]
- Hashimoto N., Zubler R. H. Colorimetric B cell proliferation assay based on alkaline phosphatase activity. Selective measurement of B cell proliferation in the presence of other cell types. J Immunol Methods. 1986 Jun 10;90(1):97–103. doi: 10.1016/0022-1759(86)90389-3. [DOI] [PubMed] [Google Scholar]
- Hom J. T., Talal N. Decreased syngeneic mixed lymphocyte reaction in autoimmune susceptible mice. Scand J Immunol. 1982 Feb;15(2):195–203. doi: 10.1111/j.1365-3083.1982.tb00638.x. [DOI] [PubMed] [Google Scholar]
- Julius M. H., Heusser C. H. Autoreactive or self restricted? Eur J Immunol. 1986 Jul;16(7):867–870. doi: 10.1002/eji.1830160726. [DOI] [PubMed] [Google Scholar]
- Koch N., Arnold B., Hämmerling G. J., Heuer J., Kölsch E. Structural comparison of I-A antigens produced by a cloned murine T suppressor cell line with B-cell-derived I-A. Immunogenetics. 1983;17(5):497–505. doi: 10.1007/BF00696873. [DOI] [PubMed] [Google Scholar]
- Sakane T., Steinberg A. D., Green I. Failure of autologous mixed lymphocyte reactions between T and non-T cells in patients with systemic lupus erythematosus. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3464–3468. doi: 10.1073/pnas.75.7.3464. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith J. B., Knowlton R. P., Koons L. S. Normal antibody-dependent killer cell function in patients with chronic lymphocytic leukemia. J Natl Cancer Inst. 1977 May;58(5):1497–1499. doi: 10.1093/jnci/58.5.1497. [DOI] [PubMed] [Google Scholar]
- Smith J. B., Pasternak R. D. Syngeneic mixed lymphocyte reaction in mice: strain distribution, kinetics, participating cells, and absence in NZB mice. J Immunol. 1978 Nov;121(5):1889–1892. [PubMed] [Google Scholar]
- Smith J. B., Talal N. Significance of self-recognition and interleukin-2 for immunoregulation, autoimmunity and cancer. Scand J Immunol. 1982 Oct;16(4):269–278. doi: 10.1111/j.1365-3083.1982.tb00723.x. [DOI] [PubMed] [Google Scholar]
- Smith J. B., Wolos J. A., Bocchieri M. H. Mechanisms of help and suppression in the AMLR: studies in normal and NZB mice. Behring Inst Mitt. 1983 May;(72):37–46. [PubMed] [Google Scholar]
- Wolos J. A., Smith J. B. Helper cells in the autologous mixed lymphocyte reaction. I. Generation of cytotoxic T cells recognizing modified self H-2. J Immunol. 1981 Aug;127(2):711–715. [PubMed] [Google Scholar]
- Wolos J. A., Spagnoli B., Smith J. B. Suppression of a polyclonal B-cell response by supernatants from the murine autologous mixed lymphocyte reaction. Cell Immunol. 1985 Nov;96(1):61–70. doi: 10.1016/0008-8749(85)90340-5. [DOI] [PubMed] [Google Scholar]
- Wysocki L. J., Sato V. L. "Panning" for lymphocytes: a method for cell selection. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2844–2848. doi: 10.1073/pnas.75.6.2844. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zauderer M., Campbell H., Johnson D. R., Seman M. Helper functions of antigen-induced specific and autoreactive T cell colonies. J Mol Cell Immunol. 1984;1(2):65–77. [PubMed] [Google Scholar]
