Enhancement of in vivo immune response by tumor necrosis factor

J Immunol. 1987 Dec 1;139(11):3676-9.

Abstract

Interleukin 1 (IL-1) has been shown to regulate several immunologic functions. Since tumor necrosis factor (TNF) shares many biologic properties with IL-1, we have investigated here the role of TNF in the modulation of the immune response. We have thus tested low doses of human recombinant TNF-alpha (hu rTNF-alpha) for its capacity to enhance the in vivo antibody responses evaluated at the cellular level in the hemolytic plaque assay. It was found that hu rTNF-alpha, like human IL-1 beta, is able to enhance the immune response to a T cell-dependent antigen (sheep red blood cells). Interestingly, at variance with human recombinant IL-1 beta, hu rTNF-alpha was not able to enhance the in vivo antibody response to a T cell-independent antigen (type III pneumococcal polysaccharide). These results suggest that low levels of TNF may have a role in the modulation of the immune response in vivo and shed new light on the biologic significance of this mediator.

MeSH terms

  • Animals
  • Antibody Formation / drug effects*
  • Antigens, T-Independent / immunology*
  • Interleukin-1 / pharmacology
  • Male
  • Mice
  • Mice, Inbred C3H / immunology
  • Recombinant Proteins / pharmacology
  • Stimulation, Chemical
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Antigens, T-Independent
  • Interleukin-1
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha