Abstract
Tolerance can be induced in adult mice by a single intravenous injection of 0.5 mg dinitrophenylated bovine gamma globulin. The cellular mechanism of the unresponsive state is different depending upon whether the tolerance is induced in normal intact adult mice or in reconstituted, irradiated mice. The tolerant state induced in intact mice is characterized by a high avidity of the residual antibody- forming cells in partially tolerant animals and a prompt reversibility on cell transfer. The overall properties of this unresponsive state are consistent with the hypothesis that it is mediated by the production of small amounts of high affinity antibody in response to the tolerance- inducing injection of antigen. In contrast, the unresponsiveness induced in reconstituted, irradiated mice by the same procedure was characterized by a low avidity of the residual antibody-forming cells in partially tolerant animals and stability on transfer of spleen cells from unresponsive into irradiated recipients. No suppressor cell activity was detected and mixed cell transfer studies were consitent with the view that this unresponsive state represented a B-lymphocyte clonal deletion. The presence or absence of T lymphocytes in the population of cells used for reconstituting the irradiated recipients did not effect the ease of tolernace induction or the cellular mechanism of the tolerant state which was produced. If irradiated mice reconstituted with B and T lymphocytes were rested for 2 wk before tolerance induction then a reversible "high affinity"-type tolerance is obtained such as is typical of normal intact animals. Restorationof a "normal" response to the tolerance-inducing injection of antigen is dependent upon the presence of thymus cells in the population of cells used for reconstitution. It is suggested that the structural integrity of the lymphoid tissue is critical in determining whether B cell will be rendered tolerant after exposure to antigen in vivo.
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Selected References
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- Andersson B. Studies on the regulation of avidity at the level of the single antibody-forming cell. The effect of antigen dose and time after immunization. J Exp Med. 1970 Jul 1;132(1):77–88. doi: 10.1084/jem.132.1.77. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Andersson B., Wigzell H. Studies on antibody avidity at the cellular level. Effects of immunological paralysis and administered antibody. Eur J Immunol. 1971 Nov;1(5):384–390. doi: 10.1002/eji.1830010516. [DOI] [PubMed] [Google Scholar]
- Bell E. B., Shand F. L. Persisting T cells in rats tolerant of human serum albumin. The significance of tolerant and nonimmune T cells which preferentially restrict high affinity antibody synthesis. Eur J Immunol. 1976 Jul;5(7):481–486. doi: 10.1002/eji.1830050710. [DOI] [PubMed] [Google Scholar]
- Birnbaum G., Weksler M. E., Siskind G. W. Demonstration of an antibody-mediated tolerance state and its effect on antibody affinity. J Exp Med. 1975 Feb 1;141(2):411–426. doi: 10.1084/jem.141.2.411. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bystryn J. C., Graf M. W., Uhr J. W. Regulation of antibody formation by serum antibody. II. Removal of specific antibody by means of exchange transfusion. J Exp Med. 1970 Dec 1;132(6):1279–1287. doi: 10.1084/jem.132.6.1279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Davie J. M., Paul W. E., Katz D. H., Benacerraf B. Hapten-specific tolerance. Preferential depression of the high affinity antibody response. J Exp Med. 1972 Sep 1;136(3):426–438. doi: 10.1084/jem.136.3.426. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DeLisi C., Goldstein B. On the mechanism of hemolytic plaque inhibition. Immunochemistry. 1974 Oct;11(10):661–665. doi: 10.1016/0019-2791(74)90223-7. [DOI] [PubMed] [Google Scholar]
- Gershon R. K. T cell control of antibody production. Contemp Top Immunobiol. 1974;3:1–40. doi: 10.1007/978-1-4684-3045-5_1. [DOI] [PubMed] [Google Scholar]
- Goidl E. A., Birnbaum G., Siskind G. W. Determination of antibody avidity at the cellular level by the plaque inhibition technique: effect of valence of the inhibitor. J Immunol Methods. 1975;8(1-2):47–45. doi: 10.1016/0022-1759(75)90080-0. [DOI] [PubMed] [Google Scholar]
- Goidl E. A., Klass J., Siskind G. W. Ontogeny of B-lymphocyte function. II. Ability of endotoxin to increase the heterogeneity of affinity of the immune response of B lymphocytes from fetal mice. J Exp Med. 1976 Jun 1;143(6):1503–1520. doi: 10.1084/jem.143.6.1503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Golub E. S. Brain-associated theta antigen: reactivity of rabbit anti-mouse brain with mouse lymphoid cells. Cell Immunol. 1971 Aug;2(4):353–361. doi: 10.1016/0008-8749(71)90070-0. [DOI] [PubMed] [Google Scholar]
- Hamaoka T., Inada T., Yamashita U., Kitagawa M. Preventive effect of hapten-reactive thymus-derived helper lymphocytes on the tolerance induction in hapten-specific precursors of antibody-forming cells. J Immunol. 1975 Jun;114(6):1771–1778. [PubMed] [Google Scholar]
- Katz D. H., Davie J. M., Paul W. E., Benacerraf B. Carrier function in anti-hapten antibody responses. IV. Experimental conditions for the induction of hapten-specific tolerance or for the stimulation of anti-hapten anamnestic responses by "nonimmunogenic" hapten-polypeptide conjugates. J Exp Med. 1971 Jul 1;134(1):201–223. doi: 10.1084/jem.134.1.201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Muramatsu S., Amagai T., Katura Y. Tolerance induction in TxXBT and TxXB mice. Immunology. 1975 May;28(5):943–957. [PMC free article] [PubMed] [Google Scholar]
- Rittenberg M. B., Pratt K. L. Antitrinitrophenyl (TNP) plaque assay. Primary response of Balb/c mice to soluble and particulate immunogen. Proc Soc Exp Biol Med. 1969 Nov;132(2):575–581. doi: 10.3181/00379727-132-34264. [DOI] [PubMed] [Google Scholar]
- Schrader J. W. Induction of immunological tolerance to a thymus-dependent antigen in the absence of thymus-derived cells. J Exp Med. 1974 May 1;139(5):1303–1316. doi: 10.1084/jem.139.5.1303. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schrader J. W. Mechanism of activation of the bone marrow-derived lymphocyte. 3. A distinction between a macrophage-produced triggering signal and the amplifying effect on triggered B lymphocytes of allogeneic interactions. J Exp Med. 1973 Dec 1;138(6):1466–1480. doi: 10.1084/jem.138.6.1466. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schrader J. W., Nossal G. J. Effector cell blockade. A new mechanism of immune hyporeactivity induced by multivalent antigens. J Exp Med. 1974 Jun 1;139(6):1582–1598. doi: 10.1084/jem.139.6.1582. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schrader J. W. Specific activation of the bone marrow-derived lymphocyte by antigen presented in a non-multivalent form. J Exp Med. 1973 Mar 1;137(3):844–849. doi: 10.1084/jem.137.3.844. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Strayer D. S., Cosenza H., Lee W. M., Rowley D. A., Köhler H. Neonatal tolerance induced by antibody against antigen-specific receptor. Science. 1974 Nov 15;186(4164):640–643. doi: 10.1126/science.186.4164.640. [DOI] [PubMed] [Google Scholar]
- Theis G. A., Siskind G. W. Selection of cell populations in induction of tolerance: affinity of antibody formed in partially tolerant rabbits. J Immunol. 1968 Jan;100(1):138–141. [PubMed] [Google Scholar]
- Weigle W. O., Chiller J. M., Habicht G. S. Effect of immunological unresponsiveness on different cell populations. Transplant Rev. 1972;8:3–25. doi: 10.1111/j.1600-065x.1972.tb01562.x. [DOI] [PubMed] [Google Scholar]
- Werblin T. P., Kim Y. T., Quagliata F., Siskind G. W. Studies on the control of antibody synthesis. 3. Changes in heterogeneity of antibody affinity during the course of the immune response. Immunology. 1973 Mar;24(3):477–492. [PMC free article] [PubMed] [Google Scholar]
- Werblin T. P., Siskind G. W. Effect of tolerance and immunity on antibody affinity. Transplant Rev. 1972;8:104–136. doi: 10.1111/j.1600-065x.1972.tb01566.x. [DOI] [PubMed] [Google Scholar]