Abstract
In order to identify the molecule(s) interacting with the I-J determinant on suppressor T cells, we have generated two anti-idiotypic sera: one to monoclonal anti-I-Jd antibody and one to monoclonal anti-I-Jk antibody. These antisera specifically block suppressor T-cell function in a genetically restricted manner and have no effect on helper T-cell activation. Both recognize a marker on primary monocytes and B cells but not on T cells. A myeloma cell line bearing this marker has been identified. Therefore, these antisera may recognize a molecule on cells interacting with suppressor T cells that is involved in mediating suppressor T-cell activity. The relationship between the T-cell I-J determinant and the molecule identified by the anti-idiotype may be similar to the relationship between the receptor on helper T cells and Ia molecules.
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- Bottomly K., Kaye J., Jones B., Jones F., 3rd, Janeway C. A., Jr A cloned, antigen-specific, Ia-restricted Lyt-1+,2- T cell with suppressive activity. J Mol Cell Immunol. 1983;1(1):42–49. [PubMed] [Google Scholar]
- Feldmann M., Kontiainen S. Suppressor cell induction in vitro. II. Cellular requirements of suppressor cell induction. Eur J Immunol. 1976 Apr;6(4):302–305. doi: 10.1002/eji.1830060413. [DOI] [PubMed] [Google Scholar]
- Fleisher T. A., Greene W. C., Uchiyama T., Goldman C. K., Nelson D. L., Blaese R. M., Waldmann T. A. Characterization of a soluble suppressor of human B cell immunoglobulin biosynthesis produced by a continuous human suppressor T cell line. J Exp Med. 1981 Jul 1;154(1):156–167. doi: 10.1084/jem.154.1.156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Flood P. M., Janeway C. A., Jr, Gershon R. K. B cell-deprived mice lack functional expression of certain T suppressor cell subsets. J Mol Cell Immunol. 1984;1(3):167–176. [PubMed] [Google Scholar]
- Greene M. I., Sy M. S., Kripke M., Benacerraf B. Impairment of antigen-presenting cell function by ultraviolet radiation. Proc Natl Acad Sci U S A. 1979 Dec;76(12):6591–6595. doi: 10.1073/pnas.76.12.6591. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hayes C. E., Klyczek K. K., Krum D. P., Whitcomb R. M., Hullett D. A., Cantor H. Chromosome 4 Jt gene controls murine T cell surface I-J expression. Science. 1984 Feb 10;223(4636):559–563. doi: 10.1126/science.6607530. [DOI] [PubMed] [Google Scholar]
- L'age-Stehr J., Teichmann H., Gershon R. K., Cantor H. Stimulation of regulatory T cell circuits by immunoglobulin-dependent structures on activated B cells. Eur J Immunol. 1980 Jan;10(1):21–26. doi: 10.1002/eji.1830100105. [DOI] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lei H. Y., Waltenbaugh C. Regulation of immune responses by I-J gene products. IV. Distinct suppressor factors derived from "nonsuppressor" A strain mice. J Immunol. 1984 Oct;133(4):1723–1729. [PubMed] [Google Scholar]
- Lowy A., Drebin J. A., Monroe J. G., Granstein R. D., Greene M. I. Genetically restricted antigen presentation for immunological tolerance and suppression. Nature. 1984 Mar 22;308(5957):373–375. doi: 10.1038/308373a0. [DOI] [PubMed] [Google Scholar]
- Morrison S. L. Sequentially derived mutants of the constant region of the heavy chain of murine immunoglobulins. J Immunol. 1979 Aug;123(2):793–800. [PubMed] [Google Scholar]
- Murphy D. B., Herzenberg L. A., Okumura K., Herzenberg L. A., McDevitt H. O. A new I subregion (I-J) marked by a locus (Ia-4) controlling surface determinants on suppressor T lymphocytes. J Exp Med. 1976 Sep 1;144(3):699–712. doi: 10.1084/jem.144.3.699. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Okuda K., Minami M., Sherr D. H., Dorf M. E. Hapten-specific T cell responses to 4-hydroxy-3-nitrophenyl acetyl. XI. Pseudogenetic restrictions of hybridoma suppressor factors. J Exp Med. 1981 Aug 1;154(2):468–479. doi: 10.1084/jem.154.2.468. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Preud'Homme J. L., Birshtein B. K., Scharff M. D. Variants of a mouse myeloma cell line that synthesize immunoglobulin heavy chains having an altered serotype. Proc Natl Acad Sci U S A. 1975 Apr;72(4):1427–1430. doi: 10.1073/pnas.72.4.1427. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schwarzbaum S., Halpern R., Diamond B. The generation of macrophage-like cell lines by transfection with SV40 origin defective DNA. J Immunol. 1984 Mar;132(3):1158–1162. [PubMed] [Google Scholar]
- Sege K., Peterson P. A. Use of anti-idiotypic antibodies as cell-surface receptor probes. Proc Natl Acad Sci U S A. 1978 May;75(5):2443–2447. doi: 10.1073/pnas.75.5.2443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steinmetz M., Minard K., Horvath S., McNicholas J., Srelinger J., Wake C., Long E., Mach B., Hood L. A molecular map of the immune response region from the major histocompatibility complex of the mouse. Nature. 1982 Nov 4;300(5887):35–42. doi: 10.1038/300035a0. [DOI] [PubMed] [Google Scholar]
- Usui M., Aoki I., Sunshine G. H., Dorf M. E. A role for macrophages in suppressor cell induction. J Immunol. 1984 Apr;132(4):1728–1734. [PubMed] [Google Scholar]
- Waltenbaugh C. Regulation of immune responses by I-J gene products. I. Production and characterization of anti-I-J monoclonal antibodies. J Exp Med. 1981 Nov 1;154(5):1570–1583. doi: 10.1084/jem.154.5.1570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wassermann N. H., Penn A. S., Freimuth P. I., Treptow N., Wentzel S., Cleveland W. L., Erlanger B. F. Anti-idiotypic route to anti-acetylcholine receptor antibodies and experimental myasthenia gravis. Proc Natl Acad Sci U S A. 1982 Aug;79(15):4810–4814. doi: 10.1073/pnas.79.15.4810. [DOI] [PMC free article] [PubMed] [Google Scholar]