CD4(+) and CD8(+) T cells kill intracellular Mycobacterium tuberculosis by a perforin and Fas/Fas ligand-independent mechanism

J Immunol. 2001 Sep 1;167(5):2734-42. doi: 10.4049/jimmunol.167.5.2734.

Abstract

Cytotoxic effector phenotype and function of MHC-restricted Mycobacterium tuberculosis (MTB)-reactive CD4(+) and CD8(+) T lymphocytes were analyzed from healthy tuberculin skin test-positive persons. After stimulation in vitro with MTB, both CD4(+) and CD8(+) T cells up-regulated mRNA expression for granzyme A and B, granulysin, perforin, and CD95L (Fas ligand). mRNA levels for these molecules were greater for resting CD8(+) than CD4(+) T cells. After MTB stimulation, mRNA levels were similar for both T cell subsets. Increased perforin and granulysin protein expression was confirmed in both in CD4(+) and CD8(+) T cells by flow cytometry. Both T cell subsets lysed MTB-infected monocytes. Biochemical inhibition of the granule exocytosis pathway in CD4(+) and CD8(+) T cells decreased cytolytic function by >90% in both T cell subsets. Ab blockade of the CD95-CD95L interaction decreased cytolytic function for both T cell populations by 25%. CD4(+) and CD8(+) T cells inhibited growth of intracellular MTB in autologous monocytes by 74% and 84%, respectively. However, inhibition of perforin activity, the CD95-CD95L interaction, or both CTL mechanisms did not affect CD4(+) and CD8(+) T cell mediated restriction of MTB growth. Thus, perforin and CD95-CD95L were not involved in CD4(+) and CD8(+) T cell mediated restriction of MTB growth.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, Differentiation, T-Lymphocyte / genetics
  • Antigens, Differentiation, T-Lymphocyte / metabolism
  • Blood Bactericidal Activity / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / microbiology*
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / microbiology*
  • Cytotoxicity, Immunologic
  • Fas Ligand Protein
  • Granzymes
  • Humans
  • In Vitro Techniques
  • Major Histocompatibility Complex
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology
  • Mycobacterium tuberculosis / growth & development
  • Mycobacterium tuberculosis / immunology*
  • Perforin
  • Pore Forming Cytotoxic Proteins
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Up-Regulation
  • fas Receptor / genetics
  • fas Receptor / immunology

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • FASLG protein, human
  • Fas Ligand Protein
  • GNLY protein, human
  • Membrane Glycoproteins
  • Pore Forming Cytotoxic Proteins
  • RNA, Messenger
  • fas Receptor
  • Perforin
  • GZMB protein, human
  • Granzymes
  • Serine Endopeptidases
  • GZMA protein, human