[go: up one dir, main page]
More Web Proxy on the site http://driver.im/ Skip to main content
NCBI home page
Infection and Immunity logoLink to Infection and Immunity
. 1990 Nov;58(11):3465–3468. doi: 10.1128/iai.58.11.3465-3468.1990

Regulation of magnitude of antibody response to bacterial polysaccharide antigens by thymus-derived lymphocytes.

P J Baker 1
PMCID: PMC313684  PMID: 2228218

Full text

PDF
3465

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baker P. J., Amsbaugh D. F., Stashak P. W., Caldes G., Prescott B. Direct evidence for the involvement of T suppressor cells in the expression of low-dose paralysis to type III pneumococcal polysaccharide. J Immunol. 1982 Mar;128(3):1059–1062. [PubMed] [Google Scholar]
  2. Baker P. J., Barth R. F., Stashak P. W., Amsbaugh D. F. Enhancement of the antibody response to type 3 pneumococcal polysaccharide in mice treated with antilymphocyte serum. J Immunol. 1970 May;104(5):1313–1315. [PubMed] [Google Scholar]
  3. Baker P. J., Fauntleroy M. B., Prescott B. Examination of the differential characteristics of amplifier and contrasuppressor T cells. Immunobiology. 1988 Sep;177(4-5):438–448. doi: 10.1016/S0171-2985(88)80010-X. [DOI] [PubMed] [Google Scholar]
  4. Baker P. J., Fauntleroy M. B., Stashak P. W., Hiernaux J. R., Cantrell J. L., Rudbach J. A. Adjuvant effects of trehalose dimycolate on the antibody response to type III pneumococcal polysaccharide. Infect Immun. 1989 Mar;57(3):912–917. doi: 10.1128/iai.57.3.912-917.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Baker P. J., Fauntleroy M. B., Stashak P. W., McCoy K. L., Chused T. M. Increased amplifier T cell activity in autoimmune NZB mice and its possible significance in the expression of autoimmune disease. Immunobiology. 1986 Jul;171(4-5):400–411. doi: 10.1016/S0171-2985(86)80072-9. [DOI] [PubMed] [Google Scholar]
  6. Baker P. J., Haslov K. R., Fauntleroy M. B., Stashak P. W., Myers K., Ulrich J. T. Enrichment of suppressor T cells by means of binding to monophosphoryl lipid A. Infect Immun. 1990 Mar;58(3):726–731. doi: 10.1128/iai.58.3.726-731.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Baker P. J., Hiernaux J. R., Fauntleroy M. B., Prescott B., Cantrell J. L., Rudbach J. A. Inactivation of suppressor T-cell activity by nontoxic monophosphoryl lipid A. Infect Immun. 1988 May;56(5):1076–1083. doi: 10.1128/iai.56.5.1076-1083.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Baker P. J., Hiernaux J. R., Fauntleroy M. B., Stashak P. W., Prescott B., Cantrell J. L., Rudbach J. A. Ability of monophosphoryl lipid A to augment the antibody response of young mice. Infect Immun. 1988 Dec;56(12):3064–3066. doi: 10.1128/iai.56.12.3064-3066.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Baker P. J. Homeostatic control of antibody responses: a model based on the recognition of cell-associated antibody by regulatory T cells. Transplant Rev. 1975;26:3–20. doi: 10.1111/j.1600-065x.1975.tb00172.x. [DOI] [PubMed] [Google Scholar]
  10. Baker P. J., Reed N. D., Stashak P. W., Amsbaugh D. F., Prescott B. Regulation of the antibody response to type 3 pneumococcal polysaccharide. I. Nature of regulatory cells. J Exp Med. 1973 Jun 1;137(6):1431–1441. doi: 10.1084/jem.137.6.1431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Baker P. J., Stashak P. W., Amsbaugh D. F., Prescott B., Barth R. F. Evidence for the existence of two functionally distinct types of cells which regulate the antibody response to type 3 pneumococcal polysaccharide. J Immunol. 1970 Dec;105(6):1581–1583. [PubMed] [Google Scholar]
  12. Baker P. J., Stashak P. W., Amsbaugh D. F., Prescott B. Characterization of the antibody response to type 3 pneumococcal polysaccharide at the cellular level. I. Dose-response studies and the effect of prior immunization on the magnitude of the antibody response. Immunology. 1971 Apr;20(4):469–480. [PMC free article] [PubMed] [Google Scholar]
  13. Baker P. J., Taylor C. E., Stashak P. W., Fauntleroy M. B., Hasløv K., Qureshi N., Takayama K. Inactivation of suppressor T cell activity by the nontoxic lipopolysaccharide of Rhodopseudomonas sphaeroides. Infect Immun. 1990 Sep;58(9):2862–2868. doi: 10.1128/iai.58.9.2862-2868.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Baker P. J., Taylor C., Fauntleroy M. B., Stashak P. W., Prescott B. The role of antigen in the activation of regulatory T cells by immune B cells. Cell Immunol. 1985 Dec;96(2):376–385. doi: 10.1016/0008-8749(85)90368-5. [DOI] [PubMed] [Google Scholar]
  15. Elkins K. L., Stashak P. W., Baker P. J. Mechanisms of specific immunological unresponsiveness to bacterial lipopolysaccharides. Infect Immun. 1987 Dec;55(12):3093–3102. doi: 10.1128/iai.55.12.3093-3102.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Elkins K. L., Stashak P. W., Baker P. J. Metabolic activity is necessary for activation of T suppressor cells by B cells. J Immunol. 1990 Apr 15;144(8):2859–2864. [PubMed] [Google Scholar]
  17. Elkins K. L., Stashak P. W., Baker P. J. Prior exposure to subimmunogenic amounts of some bacterial lipopolysaccharides induces specific immunological unresponsiveness. Infect Immun. 1987 Dec;55(12):3085–3092. doi: 10.1128/iai.55.12.3085-3092.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Elkins K. L., Stashak P. W., Baker P. J. Transferred B cells from autoimmune NZB/N mice fail to activate T suppressor cells. Cell Immunol. 1987 Nov;110(1):14–27. doi: 10.1016/0008-8749(87)90097-9. [DOI] [PubMed] [Google Scholar]
  19. HUMPHREY J. H., PARROTT D. M., EAST J. STUDIES ON GLOBULIN AND ANTIBODY PRODUCTION IN MICE THYMECTOMIZED AT BIRTH. Immunology. 1964 Jul;7:419–439. [PMC free article] [PubMed] [Google Scholar]
  20. Jones J. M., Amsbaugh D. F., Stashak P. W., Prescott B., Baker P. J., Alling D. W. Kinetics of the antibody response to type III pneumococcal polysaccharide. I. Evidence that suppressor cells function by inhibiting the recruitment and proliferation of antibody-producing cells. J Immunol. 1976 Mar;116(3):647–656. [PubMed] [Google Scholar]
  21. Markham R. B., Reed N. D., Stashak P. W., Prescott B., Amsbaugh D. F., Baker P. J. Effect of concanavalin A on lymphocyte interactions involved in the antibody response to type III pneumococcal polysaccharide. II. Ability of suppressor T cells to act on both B cells and amplified T cells to limit the magnitude of the antibody response. J Immunol. 1977 Sep;119(3):1163–1168. [PubMed] [Google Scholar]
  22. Markham R. B., Stashak P. W., Prescott B., Amsbaugh D. F., Baker P. J. Effect of concanavalin A on lymphocyte interactions involved in the antibody response to type III pneumococcal polysaccharide I. Comparison of the suppression induced by con A and low dose paralysis. J Immunol. 1977 Mar;118(3):952–956. [PubMed] [Google Scholar]
  23. Markham R. B., Stashak P. W., Prescott B., Amsbaugh D. F., Baker P. J. Sensitivity of amplifier T cells involved in the antibody response to type III pneumococcal polysaccharide to anti-lymphocyte serum. J Immunol. 1977 Sep;119(3):1159–1162. [PubMed] [Google Scholar]
  24. McCoy K. L., Baker P. J., Stashak P. W., Chused T. M. Two defects in old New Zealand Black mice are involved in the loss of low-dose paralysis to type III pneumococcal polysaccharide. J Immunol. 1985 Oct;135(4):2438–2442. [PubMed] [Google Scholar]
  25. Morse H. C., 3rd, Prescott B., Cross S. S., Stashak P. W., Baker P. J. Regulation of the antibody response to type III pneumococcal polysaccharide. V. Ontogeny of factors influencing the magnitude of the plaque-forming cell response. J Immunol. 1976 Feb;116(2):279–287. [PubMed] [Google Scholar]
  26. Muller E., Apicella M. A. T-cell modulation of the murine antibody response to Neisseria meningitidis group A capsular polysaccharide. Infect Immun. 1988 Jan;56(1):259–266. doi: 10.1128/iai.56.1.259-266.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. North R. J., Bursuker I. Generation and decay of the immune response to a progressive fibrosarcoma. I. Ly-1+2- suppressor T cells down-regulate the generation of Ly-1-2+ effector T cells. J Exp Med. 1984 May 1;159(5):1295–1311. doi: 10.1084/jem.159.5.1295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Powderly W. G., Pier G. B., Markham R. B. In vitro T cell-mediated killing of Pseudomonas aeruginosa. IV. Nonresponsiveness in polysaccharide-immunized BALB/c mice is attributable to vinblastine-sensitive suppressor T cells. J Immunol. 1986 Sep 15;137(6):2025–2030. [PubMed] [Google Scholar]
  29. Taylor C. E., Amsbaugh D. F., Stashak P. W., Caldes G., Prescott B., Baker P. J. Cell surface antigens and other characteristics of T cells regulating the antibody response to type III pneumococcal polysaccharide. J Immunol. 1983 Jan;130(1):19–23. [PubMed] [Google Scholar]
  30. Taylor C. E., Bright R. T-cell modulation of the antibody response to bacterial polysaccharide antigens. Infect Immun. 1989 Jan;57(1):180–185. doi: 10.1128/iai.57.1.180-185.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Taylor C. E., Stashak P. W., Caldes G., Prescott B., Chused T. E., Brooks A., Baker P. J. Activation of antigen-specific suppressor T cells by B cells from mice immunized with type III pneumococcal polysaccharide. J Exp Med. 1983 Sep 1;158(3):703–717. doi: 10.1084/jem.158.3.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Taylor C. E., Stashak P. W., Chiang J., Leiserson W. M., Caldes G., Prescott B., Baker P. J. Characteristics of amplifier T cells involved in the antibody response to the capsular polysaccharide of type III Streptococcus pneumoniae. J Immunol. 1984 Jun;132(6):3103–3108. [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES