Immune mechanisms in the pathogenesis of pulmonary tuberculosis

Rev Infect Dis. 1989 Mar-Apr:11 Suppl 2:S369-78. doi: 10.1093/clinids/11.supplement_2.s369.

Abstract

The pathogenesis of pulmonary tuberculosis and the beneficial and detrimental effects of the host's cell-mediated immune response in this disease are reviewed. Tubercle bacilli are hardly facultative intracellular pathogens that live and multiply in nonactivated macrophages. Before tubercle bacilli can be destroyed by macrophages, these cells must be activated by T lymphocytes and their lymphokines. Such activation is the essence of cell-mediated immunity. Cell-mediated immunity also has a detrimental component, called delayed-type hypersensitivity. This component causes caseous necrosis of host tissues whenever the bacillary antigens reach high levels. Such levels occur intracellularly in macrophages of highly susceptible hosts and extracellularly in liquefied caseous foci of resistant hosts. Vaccines containing antigens that create more cell-mediated immunity and less delayed-type hypersensitivity are greatly needed.

Publication types

  • Review

MeSH terms

  • Bacterial Vaccines
  • Humans
  • Hypersensitivity, Delayed
  • Immunity, Cellular
  • Lymphocyte Activation
  • Lymphokines / immunology
  • Macrophage Activation
  • Macrophages / immunology
  • Macrophages / microbiology
  • Mycobacterium tuberculosis / immunology
  • Tuberculin Test
  • Tuberculosis, Pulmonary / etiology*
  • Tuberculosis, Pulmonary / immunology
  • Tuberculosis, Pulmonary / pathology

Substances

  • Bacterial Vaccines
  • Lymphokines