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. 1989 May;57(5):1374–1379. doi: 10.1128/iai.57.5.1374-1379.1989

Vaccination with Mycobacterium bovis BCG affects the distribution of Fc receptor-bearing T lymphocytes in experimental pulmonary tuberculosis.

R A Bartow 1, D N McMurray 1
PMCID: PMC313285  PMID: 2523350

Abstract

Inbred strain 2 guinea pigs were vaccinated with Mycobacterium bovis BCG or were left unvaccinated and challenged 6 weeks later by the respiratory route with virulent Mycobacterium tuberculosis. By using a double rosette assay with isotype-specific antibody-coated ox and uncoated rabbit erythrocytes, the proportions of T lymphocytes bearing Fc receptors for immunoglobulin G (IgG) (T gamma cells) or IgM (T mu cells) were quantified in tissues taken from animals that were killed within 4 weeks postchallenge. Tuberculin reactivity in vivo and in vitro and antimycobacterial resistance were also measured. BCG vaccination protected the guinea pigs and resulted in significantly enhanced proportions of T mu cells in the blood during the first 3 weeks and in the spleen during weeks 2 and 3 postchallenge. Levels of T gamma cells declined in all tissues during the first 3 weeks of infection and were unaffected by prior vaccination with BCG. Increased proportions of T mu cells in the blood were accompanied by dramatic tuberculin skin reactions and purified protein derivative-induced lymphoproliferation in BCG-vaccinated guinea pigs during the first 2 weeks following virulent pulmonary challenge. Peak levels of T mu cells in the spleens of vaccinated animals at 2 weeks coincided with the first appearance of virulent mycobacteria in that organ. BCG vaccination appears to influence immunoregulatory events in pulmonary tuberculosis through effects on the distribution of IgM Fc receptor-bearing (T mu cell) T lymphocytes.

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Selected References

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  1. Chaparas S. D. Immunity in tuberculosis. Bull World Health Organ. 1982;60(4):447–462. [PMC free article] [PubMed] [Google Scholar]
  2. Cohen M. K., Bartow R. A., Mintzer C. L., McMurray D. N. Effects of diet and genetics on Mycobacterium bovis BCG vaccine efficacy in inbred guinea pigs. Infect Immun. 1987 Feb;55(2):314–319. doi: 10.1128/iai.55.2.314-319.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ellner J. J. Suppressor adherent cells in human tuberculosis. J Immunol. 1978 Dec;121(6):2573–2579. [PubMed] [Google Scholar]
  4. Grover A. A., Kim H. K., Wiegeshaus E. H., Smith D. W. Host-parasite relationships in experimental airborne tuberculosis. II. Reproducible infection by means of an inoculum preserved at -70 C. J Bacteriol. 1967 Oct;94(4):832–835. doi: 10.1128/jb.94.4.832-835.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hussein S., Curtis J., Akuffo H., Turk J. L. Dissociation between delayed-type hypersensitivity and resistance to pathogenic mycobacteria demonstrated by T-cell clones. Infect Immun. 1987 Mar;55(3):564–567. doi: 10.1128/iai.55.3.564-567.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hussein S., Curtis J., Griffiths D., Turk J. L. Study of DTH and resistance in Mycobacterium lepraemurium infection using a T-cell line isolated from mice infected with Mycobacterium bovis (BCG). Cell Immunol. 1987 Apr 1;105(2):423–431. doi: 10.1016/0008-8749(87)90089-x. [DOI] [PubMed] [Google Scholar]
  7. Kataoka S., Itoh K., Kurane I., Kumagai K. Detection of guinea pig T mu and T gamma cells by a double rosette assay. J Immunol Methods. 1982;51(1):89–100. doi: 10.1016/0022-1759(82)90385-4. [DOI] [PubMed] [Google Scholar]
  8. Kleinhenz M. E., Ellner J. J. Antigen responsiveness during tuberculosis: regulatory interactions of T cell subpopulations and adherent cells. J Lab Clin Med. 1987 Jul;110(1):31–40. [PubMed] [Google Scholar]
  9. Kleinhenz M. E., Ellner J. J. Divergent T gamma cell functions in antigen-induced blastogenesis: facilitory interactions with Tnon gamma cells and participation in monocyte- and prostaglandin-mediated suppression. J Lab Clin Med. 1983 Nov;102(5):751–761. [PubMed] [Google Scholar]
  10. Mackaness G. B., Lagrange P. H., Ishibashi T. The modifying effect of BCG on the immunological induction of T cells. J Exp Med. 1974 Jun 1;139(6):1540–1552. doi: 10.1084/jem.139.6.1540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Markowicz S., Siwicki J. K., Steffen J. A. TG and TnonG lymphocyte involvement in the proliferative response to PHA. I. Reactivity and regulatory functions of TG and TnonG subsets in the proliferative response of T lymphocytes. Arch Immunol Ther Exp (Warsz) 1987;35(1):11–21. [PubMed] [Google Scholar]
  12. McMurray D. N., Carlomagno M. A., Mintzer C. L., Tetzlaff C. L. Mycobacterium bovis BCG vaccine fails to protect protein-deficient guinea pigs against respiratory challenge with virulent Mycobacterium tuberculosis. Infect Immun. 1985 Nov;50(2):555–559. doi: 10.1128/iai.50.2.555-559.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. McMurray D. N., Mintzer C. L., Tetzlaff C. L., Carlomagno M. A. The influence of dietary protein on the protective effect of BCG in guinea pigs. Tubercle. 1986 Mar;67(1):31–39. doi: 10.1016/0041-3879(86)90029-2. [DOI] [PubMed] [Google Scholar]
  14. Moretta L., Mingari M. C., Moretta A., Cooper M. D. Human T lymphocyte subpopulations: studies of the mechanism by which T cells bearing Fc receptors for IgG suppress T-dependent B cell differentiation induced by pokeweed mitogen. J Immunol. 1979 Mar;122(3):984–990. [PubMed] [Google Scholar]
  15. Moretta L., Mingari M. C., Romanzi C. A. Loss of Fc receptors for IgG from human T lymphocytes exposed to IgG immune complexes. Nature. 1978 Apr 13;272(5654):618–620. doi: 10.1038/272618a0. [DOI] [PubMed] [Google Scholar]
  16. Moretta L., Webb S. R., Grossi C. E., Lydyard P. M., Cooper M. D. Functional analysis of two human T-cell subpopulations: help and suppression of B-cell responses by T cells bearing receptors for IgM or IgG. J Exp Med. 1977 Jul 1;146(1):184–200. doi: 10.1084/jem.146.1.184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pichler W. J., Gendelman F. W., Nelson D. L. Fc receptors on human T lymphocytes. II. Cytotoxic capabilities of human T gamma, T mu, B, and L cells. Cell Immunol. 1979 Feb;42(2):410–417. doi: 10.1016/0008-8749(79)90206-5. [DOI] [PubMed] [Google Scholar]
  18. Shaw S., Pichler W. J., Nelson D. L. Fc receptors on human T-lymphocytes. III. Characterization of subpopulations involved in cell-mediated lympholysis and antibody-dependent cellular cytotoxicity. J Immunol. 1979 Feb;122(2):599–604. [PubMed] [Google Scholar]
  19. Smith D. W., McMurray D. N., Wiegeshaus E. H., Grover A. A., Harding G. E. Host-parasite relationships in experimental airborne tuberculosis. IV. Early events in the course of infection in vaccinated and nonvaccinated guinea pigs. Am Rev Respir Dis. 1970 Dec;102(6):937–949. doi: 10.1164/arrd.1970.102.6.937. [DOI] [PubMed] [Google Scholar]
  20. Smith D., Harding G., Chan J., Edwards M., Hank J., Muller D., Sobhi F. Potency of 10 BCG vaccines as evaluated by their influence on the bacillemic phase of experimental airborne tuberculosis in guinea-pigs. J Biol Stand. 1979 Jul;7(3):179–197. doi: 10.1016/s0092-1157(79)80021-9. [DOI] [PubMed] [Google Scholar]
  21. Stadecker M. J., Bishop G., Wortis H. H. Rosette formation by guinea pig thymocytes and thymus derived lymphocytes with rabbit red blood cells. J Immunol. 1973 Dec;111(6):1834–1837. [PubMed] [Google Scholar]
  22. Tsuyuguchi I., Shiratsuchi H., Teraoka O., Hirano T. Increase in T cells bearing IgG Fc receptors in peripheral blood of patients with tuberculosis by in vitro stimulation with purified protein derivative. Am Rev Respir Dis. 1980 Jun;121(6):951–957. doi: 10.1164/arrd.1980.121.6.951. [DOI] [PubMed] [Google Scholar]
  23. Wadee A. A., Joffe M. I., Lomnitzer R., Rabson A. R. Mononuclear cell function in Mycobacterium tuberculosis infected guinea pigs. Clin Immunol Immunopathol. 1983 Sep;28(3):325–333. doi: 10.1016/0090-1229(83)90099-5. [DOI] [PubMed] [Google Scholar]
  24. Wiegeshaus E. H., McMurray D. N., Grover A. A., Harding G. E., Smith D. W. Host-parasite relationships in experimental airborne tuberculosis. 3. Relevance of microbial enumeration to acquired resistance in guinea pigs. Am Rev Respir Dis. 1970 Sep;102(3):422–429. doi: 10.1164/arrd.1970.102.3.422. [DOI] [PubMed] [Google Scholar]

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