Transforming growth factor beta-induced failure of resistance to infection with blood-stage Plasmodium chabaudi in mice

Infect Immun. 1999 May;67(5):2306-11. doi: 10.1128/IAI.67.5.2306-2311.1999.

Abstract

The role of transforming growth factor beta (TGF-beta) in infection with Plasmodium chabaudi was investigated with resistant and susceptible mouse models. C57BL/10 mice produced gamma interferon (IFN-gamma) and nitric oxide (NO) shortly after infection and cleared the parasite spontaneously. In contrast, BALB/c mice showed a transient enhancement of TGF-beta production, followed by a relative lack of IFN-gamma and NO production, and succumbed to the infection. However, there was no correlation between levels of serum TGF-beta and splenic TGF-beta mRNA in both mouse strains before and after infection. Administration of recombinant TGF-beta (rTGF-beta) rendered resistant mice susceptible because of suppression of subsequent production of IFN-gamma and NO. Administration of anti-TGF-beta antibody to the infected BALB/c mice resulted in remarkable increases in serum IFN-gamma and NO, and the mice resisted the infection. Splenic CD4(+) T and CD11b+ cells of C57BL/10 mice were significantly activated after infection, but this was completely abrogated by administration of rTGF-beta. These results suggested that, in the P. chabaudi-susceptible but not resistant mice, production of TGF-beta was promoted, and subsequent failure of IFN-gamma- and NO-dependent resistance to the parasite was induced. This study is the first to indicate that TGF-beta production was the key event in failure of resistance to mouse malaria.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Base Sequence
  • CD4-Positive T-Lymphocytes / immunology
  • DNA Primers / genetics
  • Female
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / genetics
  • Kinetics
  • Lymphocyte Activation
  • Macrophage-1 Antigen / metabolism
  • Malaria / genetics
  • Malaria / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Nitric Oxide / biosynthesis
  • Nitric Oxide Synthase / genetics
  • Nitric Oxide Synthase Type II
  • Plasmodium chabaudi / immunology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Recombinant Proteins / pharmacology
  • Spleen / immunology
  • Transforming Growth Factor beta / blood*
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / pharmacology*

Substances

  • Antibodies, Monoclonal
  • DNA Primers
  • Macrophage-1 Antigen
  • RNA, Messenger
  • Recombinant Proteins
  • Transforming Growth Factor beta
  • Nitric Oxide
  • Interferon-gamma
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse