Resistance to Paracoccidioides brasiliensis infection is linked to a preferential Th1 immune response, whereas susceptibility is associated with absence of IFN-gamma production

J Interferon Cytokine Res. 2000 Jan;20(1):89-97. doi: 10.1089/107999000312766.

Abstract

The secretion of interferon-gamma (IFN-gamma), interleukin-2 (IL-2), IL-4, IL-5, and IL-10 by antigen-stimulated lymph node cells, eosinophil maturation, and the antibody isotypes produced were examined during intraperitoneal infection of susceptible (B10.A) and resistant (A/Sn) mice with Paracoccidioides brasiliensis. Lymph node cells from resistant mice produced early and sustained levels of IFN-gamma and IL-2, whereas susceptible animals secreted low to undetectable amounts of these type 1 cytokines. Both mouse strains presented late and transient production of IL-4, whereas IL-10 was produced constantly throughout the course of disease. Resistant animals produced increasing levels of IL-5 in the chronic phase of the infection (from the eighth week on), whereas susceptible mice showed two peaks of IL-5 production, at the first and twelfth weeks after infection. Only the susceptible strain presented medullary and splenic eosinophilia concomitant with the raised IL-5 production. In resistant mice, the levels of IgG2a antibodies were significantly higher than those observed in susceptible mice, which preferentially secreted IgG2b and IgA isotypes. Taken together, these results demonstrate that a sustained production of IFN-gamma and IL-2 and a predominant secretion of IgG2a antibodies are associated with resistance to P. brasiliensis. In contrast, the production of low levels of IFN-gamma, early secretion of high levels of IL-5 and IL-10, eosinophilia, and a preferential secretion of IgG2b and IgA isotypes characterize the progressive disease in susceptible animals.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Fungal / biosynthesis
  • B-Lymphocytes / immunology
  • Bone Marrow / pathology
  • Eosinophilia / etiology
  • Eosinophilia / immunology
  • Female
  • Genetic Predisposition to Disease
  • Immunity, Cellular
  • Immunity, Innate
  • Immunoglobulin A / biosynthesis
  • Immunoglobulin G / biosynthesis
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / deficiency*
  • Interferon-gamma / genetics
  • Interleukin-2 / biosynthesis
  • Interleukin-2 / genetics
  • Interleukin-5 / biosynthesis
  • Interleukin-5 / genetics
  • Interleukins / biosynthesis*
  • Interleukins / genetics
  • Interleukins / metabolism
  • Lymph Nodes / immunology
  • Lymphocyte Activation
  • Macrophage Activation
  • Mice
  • Mice, Inbred A
  • Paracoccidioides*
  • Paracoccidioidomycosis / genetics
  • Paracoccidioidomycosis / immunology*
  • Paracoccidioidomycosis / pathology
  • Peritoneal Cavity / cytology
  • Spleen / pathology
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism
  • Th2 Cells / immunology

Substances

  • Antibodies, Fungal
  • Immunoglobulin A
  • Immunoglobulin G
  • Interleukin-2
  • Interleukin-5
  • Interleukins
  • Interferon-gamma