Skip to main content
Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1990 May;80(2):206–212. doi: 10.1111/j.1365-2249.1990.tb05235.x

T cell reactivity to the purified mycobacterial antigens p65 and p70 in leprosy patients and their household contacts.

E Adams 1, R J Garsia 1, L Hellqvist 1, P Holt 1, A Basten 1
PMCID: PMC1535293  PMID: 2192825

Abstract

T cell reactivity to the 70 and 65 kD (p70 and p65) protein antigens derived from Mycobacterium bovis BCG strain was studied by measuring the proliferative responses of peripheral blood mononuclear cells from members of an isolated Aboriginal community resident in the Torres Straits islands. In the nine index leprosy cases the pattern of responsiveness to the purified antigens paralleled that to whole sonicates from M. leprae and BCG. In the 40 contacts of the index cases, a high correlation was observed between the responses to p70 and p65 as well as to the crude sonicates. Significant T cell responses to the purified antigens, as well as the crude sonicates, were obtained with cells from the majority of contacts. Limiting dilution analysis of precursor frequencies in the contacts confirmed the immunogenicity of the purified antigens and excluded both a mitogenic component and the presence of suppressor cells in those moderate or low responders whose blood contained sufficient precursors to be tested. p70 appeared to be more potent in stimulating a proliferative response than p65 at equivalent protein concentrations. No correlation between responder status to either antigen and disease type was detected in families. These findings provide confirmation of the importance of p70 and p65 as major T cell immunogens in man and indicate that they are both potential candidates for inclusion in a bivalent vaccine for leprosy and tuberculosis.

Full text

PDF
208

Selected References

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

  1. Baumgart K., Britton W., Basten A., Bagshawe A. Use of phenolic glycolipid 1 for serodiagnosis of leprosy in a high prevalence village in Papua New Guinea. Trans R Soc Trop Med Hyg. 1987;81(6):1030–1032. doi: 10.1016/0035-9203(87)90388-9. [DOI] [PubMed] [Google Scholar]
  2. Brett S. J., Kingston A. E., Colston M. J. Limiting dilution analysis of the human T cell response to mycobacterial antigens from BCG vaccinated individuals and leprosy patients. Clin Exp Immunol. 1987 Jun;68(3):510–520. [PMC free article] [PubMed] [Google Scholar]
  3. Britton W. J., Hellqvist L., Basten A., Inglis A. S. Immunoreactivity of a 70 kD protein purified from Mycobacterium bovis Bacillus Calmette-Guerin by monoclonal antibody affinity chromatography. J Exp Med. 1986 Sep 1;164(3):695–708. doi: 10.1084/jem.164.3.695. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Britton W. J., Hellqvist L., Basten A., Raison R. L. Mycobacterium leprae antigens involved in human immune responses. I. Identification of four antigens by monoclonal antibodies. J Immunol. 1985 Dec;135(6):4171–4177. [PubMed] [Google Scholar]
  5. Britton W. J., Hellqvist L., Garsia R. J., Basten A. Dominant cell wall proteins of Mycobacterium leprae recognized by monoclonal antibodies. Clin Exp Immunol. 1987 Jan;67(1):31–42. [PMC free article] [PubMed] [Google Scholar]
  6. Cho S. N., Chatterjee D., Brennan P. J. A simplified serological test for leprosy based on a 3,6-di-O-methylglucose-containing synthetic antigen. Am J Trop Med Hyg. 1986 Jan;35(1):167–172. doi: 10.4269/ajtmh.1986.35.167. [DOI] [PubMed] [Google Scholar]
  7. Ivanyi J., Sharp K., Jackett P., Bothamley G. Immunological study of the defined constituents of mycobacteria. Springer Semin Immunopathol. 1988;10(4):279–300. doi: 10.1007/BF02053841. [DOI] [PubMed] [Google Scholar]
  8. Mogensen C. E. The glomerular permeability determined by dextran clearance using Sephadex gel filtration. Scand J Clin Lab Invest. 1968;21(1):77–82. doi: 10.3109/00365516809076979. [DOI] [PubMed] [Google Scholar]
  9. Myrvang B., Godal T., Ridley D. S., Fröland S. S., Song Y. K. Immune responsiveness to Mycobacterium leprae and other mycobacterial antigens throughout the clinical and histopathological spectrum of leprosy. Clin Exp Immunol. 1973 Aug;14(4):541–553. [PMC free article] [PubMed] [Google Scholar]
  10. Opelz G., Terasaki P. I. Lymphocyte antigenicity loss with retention of responsiveness. Science. 1974 Apr 26;184(4135):464–466. doi: 10.1126/science.184.4135.464. [DOI] [PubMed] [Google Scholar]
  11. Saxon A., Feldhaus J., Robins R. A. Single step separation of human T and B cells using AET treated srbc rosettes. J Immunol Methods. 1976;12(3-4):285–288. doi: 10.1016/0022-1759(76)90050-8. [DOI] [PubMed] [Google Scholar]
  12. Smart Y. C., Cox J., Roberts T. K., Brinsmead M. W., Burton R. C. Differential effect of cigarette smoking on recirculating T lymphocyte subsets in pregnant women. J Immunol. 1986 Jul 1;137(1):1–3. [PubMed] [Google Scholar]

Articles from Clinical and Experimental Immunology are provided here courtesy of British Society for Immunology

RESOURCES