Abstract
The adoptive transfer system was initially used to document the requirement for co-operation between hapten-primed and carrier-primed lymphocytes in generating secondary IgA antibody responses. Studies employing anti-theta antiserum and complement to deplete T cells showed that carrier-specific theta-bearing cells are required for IgA responses. Furthermore, non-specific T-cell help could be provided by transfer of normal allogeneic spleen cells into irradiated recipients. When limiting numbers of 'educated' thymus cells were added to a constant number of spleen cells, depleted of T cells, IgM responses were not affected while both IgG and IgA antibody responses were shown to be dependent on the numbers of thymus cells injected. These results provide direct evidence for the participation of theta-bearing T lymphocytes in IgA anti-TNP antibody responses and suggest that IgA lymphocyte precursors may be inherently more sensitive than IgM B cells to the regulatory effects of helper T lymphocytes.
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Selected References
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- Blaese R. M., Weiden P. L., Koski I., Dooley N. Infectious agammaglobulinemia: transmission of immunodeficiency with grafts of agammaglobulinemic cells. J Exp Med. 1974 Oct 1;140(4):1097–1101. doi: 10.1084/jem.140.4.1097. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chiorazzi N., Fox D. A., Katz D. H. Hapten-specific IgE antibody responses in mice. VI. Selective enhancement of IgE antibody production by low doses of X-irradiation and by cyclophosphamide. J Immunol. 1976 Nov;117(5 Pt 1):1629–1637. [PubMed] [Google Scholar]
- Clough J. D., Mims L. H., Strober W. Deficient IgA antibody responses to arsanilic acid bovine serum albumin (BSA) in neonatally thymectomized rabbits. J Immunol. 1971 Jun;106(6):1624–1629. [PubMed] [Google Scholar]
- Ebersole J. L., Taubman M. A., Smith D. J. Thymic control of secretory antibody responses in the rat. J Immunol. 1979 Jul;123(1):19–24. [PubMed] [Google Scholar]
- Elson C. O., Heck J. A., Strober W. T-cell regulation of murine IgA synthesis. J Exp Med. 1979 Mar 1;149(3):632–643. doi: 10.1084/jem.149.3.632. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Golub E. S. Brain-associated stem cell antigen: an antigen shared by brain and hemopoietic stem cells. J Exp Med. 1972 Aug 1;136(2):369–374. doi: 10.1084/jem.136.2.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamaoka T., Katz D. H., Benacerraf B. Hapten-specific IgE antibody responses in mice. II. Cooperative interactions between adoptively transferred T and B lymphocytes in the development of IgE response. J Exp Med. 1973 Sep 1;138(3):538–556. doi: 10.1084/jem.138.3.538. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jerne N. K., Nordin A. A. Plaque Formation in Agar by Single Antibody-Producing Cells. Science. 1963 Apr 26;140(3565):405–405. doi: 10.1126/science.140.3565.405. [DOI] [PubMed] [Google Scholar]
- Katz D. H., Bargatze R. F., Bogowitz C. A., Katz L. R. Regulation of IgE antibody production by serum molecules. IV. Complete Freund's adjuvant induces both enhancing and suppressive activities detectable in the serum of low and high responder mice. J Immunol. 1979 Jun;122(6):2184–2190. [PubMed] [Google Scholar]
- Katz D. H., Bargatze R. F., Bogowitz C. A., Katz L. R. Regulation of IgE antibody production by serum molecules. VII. The IgE-selective damping activity of suppressive factor of allergy (SFA) is exerted across both strain and species restriction barriers. J Immunol. 1980 Feb;124(2):819–824. [PubMed] [Google Scholar]
- Katz D. H., Benacerraf B. The regulatory influence of activated T cells on B cell responses to antigen. Adv Immunol. 1972;15:1–94. doi: 10.1016/s0065-2776(08)60683-5. [DOI] [PubMed] [Google Scholar]
- Katz D. H., Hamaoka T., Newburger P. E., Benacerraf B. Hapten-specific IgE antibody responses in mice. IV. Evidence for distinctive sensitivities of IgE and IgG B lymphocytes to the regulatory influence of T cells. J Immunol. 1974 Sep;113(3):974–983. [PubMed] [Google Scholar]
- Kishimoto T., Hirai Y., Suemura M., Yamamura Y. Regulation of antibody response in different immunoglobulin classes. I. Selective suppression of anti-DNP IgE antibody response by preadministration of DNP-coupled mycobacterium. J Immunol. 1976 Aug;117(2):396–404. [PubMed] [Google Scholar]
- Kishimoto T., Ishizaka K. Regulation of antibody response in vitro. VI. Carrier-specific helper cells for IgG and IgE antibody response. J Immunol. 1973 Sep;111(3):720–732. [PubMed] [Google Scholar]
- Lally E. T., Zitron I. M., Fiorini R. C., Montgomery P. C. Cellular aspects of the murine anti-hapten IgA response. Adv Exp Med Biol. 1978;107:143–150. doi: 10.1007/978-1-4684-3369-2_17. [DOI] [PubMed] [Google Scholar]
- Luzzati A. L., Jacobson E. B. Serum immunoglobulin levels in nude mice. Eur J Immunol. 1972 Oct;2(5):473–474. doi: 10.1002/eji.1830020518. [DOI] [PubMed] [Google Scholar]
- McFarlin D. E., Strober W., Waldmann T. A. Ataxia-telangiectasia. Medicine (Baltimore) 1972 Jul;51(4):281–314. doi: 10.1097/00005792-197207000-00002. [DOI] [PubMed] [Google Scholar]
- Miller J. F., Mitchell G. F. Thymus and antigen-reactive cells. Transplant Rev. 1969;1:3–42. doi: 10.1111/j.1600-065x.1969.tb00135.x. [DOI] [PubMed] [Google Scholar]
- Mishell R. I., Dutton R. W. Immunization of dissociated spleen cell cultures from normal mice. J Exp Med. 1967 Sep 1;126(3):423–442. doi: 10.1084/jem.126.3.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Osborne D. P., Jr, Katz D. H. The allogeneic effect in inbred mice. 3. Unique antigenic structural requirements in the expression of the phenomenon on unprimed cell populations in vivo. J Exp Med. 1973 Apr 1;137(4):991–1008. doi: 10.1084/jem.137.4.991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perey D. Y., Biennenstock J. Effects of bursectomy and thymectomy on ontogeny of fowl IgA, IgG, and IgM. J Immunol. 1973 Aug;111(2):633–637. [PubMed] [Google Scholar]
- Pritchard H., Riddaway J., Micklem H. S. Immune responses in congenitally thymus-less mice. II. Quantitative studies of serum immunoglobulins, the antibody response to sheep erythrocytes, and the effect of thymus allografting. Clin Exp Immunol. 1973 Jan;13(1):125–138. [PMC free article] [PubMed] [Google Scholar]
- Raff M. C. Two distinct populations of peripheral lymphocytes in mice distinguishable by immunofluorescence. Immunology. 1970 Oct;19(4):637–650. [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]
- Stobo J. D., Tomasi T. B. A Low Molecular Weight Immunoglobulin Antigenically Related to 19 S IgM. J Clin Invest. 1967 Aug;46(8):1329–1337. doi: 10.1172/JCI105625. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Suemura M., Kishimoto T., Hirai Y., Yamamura Y. Regulation of antibody response in different immunoglobulin classes. III. In vitro demonstration of "IgE class-specific" suppressor functions of DNP-mycobacterium-primed T cells and the soluble factor released from these cells. J Immunol. 1977 Jul;119(1):149–155. [PubMed] [Google Scholar]
- Tada T., Okumura K. Regulation of homocytotropic antibody formation in the rat. V, Cell cooperation in the anti-hapten homocytotropic antibody response. J Immunol. 1971 Oct;107(4):1137–1145. [PubMed] [Google Scholar]
- Tung A. S., Chiorazzi N., Katz D. H. Regulation of IgE antibody production by serum molecules. I. Serum from complete Freund's adjuvant-immune donors suppresses irradiation-enhanced IgE production in low responder mouse strains. J Immunol. 1978 Jun;120(6):2050–2059. [PubMed] [Google Scholar]
- Waldmann T. A., Broder S., Krakauer R., Durm M., Meade B., Goldman C. Defect in IgA secretion and in IgA specific suppressor cells in patients with selective IgA deficiency. Trans Assoc Am Physicians. 1976;89:215–224. [PubMed] [Google Scholar]
- van Muiswinkel W. B., van Soest P. L. Thymus dependence of the IgA response to sheep erythrocytes. Immunology. 1975 Feb;28(2):287–291. [PMC free article] [PubMed] [Google Scholar]
