Abstract
A procedure is described for the in vivo removal of all detectable T lymphocytes from spleen and lymph nodes in mice. A single intraperitoneal injection of monoclonal anti-Thy-1 antibody into mice leads to rapid depletion of functional T cells from peripheral lymphoid organs, but not thymus. The extent of T-cell depletion is dependent on the cytotoxic titre of the anti-Thy-1 antibody used. Antibody with a median cytotoxic titre greater than 10(6) causes the complete removal of cells bearing Thy-1, Lyt-1 and Lyt-2 surface antigens from peripheral lymphoid populations in 3 days. Eight days after treatment Thy-1+, Lyt-1+ and Lyt-2+ cells begin to reappear in these organs. Splenic B cells, assayed by the expression of surface immunoglobulin (sIg) and by mitogenic responsiveness to bacterial lipopolysaccharide (LPS), are not affected by this treatment. The monoclonal anti-Thy-1 antibody does not appear to penetrate thymus tissue and bind to thymocytes. Anti-Thy-1 antibody, but not F(ab')2 is required for in-vivo T-cell depletion. These findings indicate that anti-Thy-1 antibody causes the removal of Thy-1+ cells from peripheral lymphoid tissue, and as the circulating levels of anti-Thy-1 antibody decrease, cells from the thymus repopulate the thymus-dependent areas of the depleted lymphoid organs.
Full text
PDF









Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bach J. F., Dardenne M., Chatenoud L. Immunomodulation of T cells by thymic hormone and monoclonal anti-T cell antibody. Transplant Proc. 1982 Sep;14(3):509–512. [PubMed] [Google Scholar]
- Bethell G. S., Ayers J. S., Hancock W. S., Hearn M. T. A novel method of activation of cross-linked agaroses with 1,1'-carbonyldiimidazole which gives a matrix for affinity chromatography devoid of additional charged groups. J Biol Chem. 1979 Apr 25;254(8):2572–2574. [PubMed] [Google Scholar]
- Cantor H., Boyse E. A. Lymphocytes as models for the study of mammalian cellular differentiation. Immunol Rev. 1977 Jan;33:105–124. doi: 10.1111/j.1600-065x.1977.tb00364.x. [DOI] [PubMed] [Google Scholar]
- Cosimi A. B., Burton R. C., Kung P. C., Colvin R., Goldstein G., Lifter J., Rhodes W., Russell P. S. Evaluation in primate renal allograft recipients of monoclonal antibody to human T-cell subclasses. Transplant Proc. 1981 Mar;13(1 Pt 1):499–503. [PubMed] [Google Scholar]
- Denman A. M., Frenkel E. P. Mode of action of anti-lymphocyte globulin. I. The distribution of rabbit anti-lymphocyte globulin injected into rats and mice. Immunology. 1968 Jan;14(1):107–113. [PMC free article] [PubMed] [Google Scholar]
- Dennert G., Hyman R., Lesley J., Trowbridge I. S. Effects of cytotoxic monoclonal antibody specific for T200 glycoprotein on functional lymphoid cell populations. Cell Immunol. 1980 Aug 1;53(2):350–364. doi: 10.1016/0008-8749(80)90335-4. [DOI] [PubMed] [Google Scholar]
- Ledbetter J. A., Herzenberg L. A. Xenogeneic monoclonal antibodies to mouse lymphoid differentiation antigens. Immunol Rev. 1979;47:63–90. doi: 10.1111/j.1600-065x.1979.tb00289.x. [DOI] [PubMed] [Google Scholar]
- Martin W. J., Miller J. F. Cell to cell interaction in the immune response. IV. Site of action of antilymphocyte globulin. J Exp Med. 1968 Oct 1;128(4):855–874. doi: 10.1084/jem.128.4.855. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McKenzie I. F., Potter T. Murine lymphocyte surface antigens. Adv Immunol. 1979;27:179–338. doi: 10.1016/s0065-2776(08)60263-1. [DOI] [PubMed] [Google Scholar]
- McMaster W. R., Williams A. F. Monoclonal antibodies to Ia antigens from rat thymus: cross reactions with mouse and human and use in purification of rat Ia glycoproteins. Immunol Rev. 1979;47:117–137. doi: 10.1111/j.1600-065x.1979.tb00291.x. [DOI] [PubMed] [Google Scholar]
- Michaelides M., Hogarth P. M., McKenzie I. F. The immunosuppressive effect of monoclonal anti-Lyt-1.1 antibodies in vivo. Eur J Immunol. 1981 Dec;11(12):1005–1012. doi: 10.1002/eji.1830111211. [DOI] [PubMed] [Google Scholar]
- Miller R. A., Maloney D. G., Warnke R., Levy R. Treatment of B-cell lymphoma with monoclonal anti-idiotype antibody. N Engl J Med. 1982 Mar 4;306(9):517–522. doi: 10.1056/NEJM198203043060906. [DOI] [PubMed] [Google Scholar]
- Monaco A. P., Campion J. P., Kapnick S. J. Antilymphocyte globulins. Clinical use of antilymphocyte globulin. Transplant Proc. 1977 Mar;9(1):1007–1018. [PubMed] [Google Scholar]
- Najarian J. S., Ascher N. L. Causes and management of rejection. Transplant Proc. 1979 Mar;11(1):11–16. [PubMed] [Google Scholar]
- Zimmerman B., Tsui F. Immunosuppressive antilymphocyte serum. III. Different subpopulations of T lymphocytes are influenced at different doses of antilymphocyte serum. Transplantation. 1979 Oct;28(4):323–328. doi: 10.1097/00007890-197910000-00012. [DOI] [PubMed] [Google Scholar]
- Zimmerman B., Tsui F. Immunosuppressive antilymphocyte serum. IV. Characterization of a T-cell-specific antibody that shifts T-Lymphocyte subpopulations in vivo. Cell Immunol. 1980 Aug 15;54(1):170–183. doi: 10.1016/0008-8749(80)90199-9. [DOI] [PubMed] [Google Scholar]
- Zimmerman B., Tsui F. Immunosuppressive antithymus and antilymphocyte sera. I. Antisera to detergent-solubilized rat thymus antigens. Transplantation. 1978 Nov;26(5):361–364. [PubMed] [Google Scholar]
