The role of macrophage inflammatory protein-1 alpha/CCL3 in regulation of T cell-mediated immunity to Cryptococcus neoformans infection

J Immunol. 2000 Dec 1;165(11):6429-36. doi: 10.4049/jimmunol.165.11.6429.

Abstract

Macrophage inflammatory protein-1alpha (MIP-1alpha/CCL3) is a CC chemokine required for optimal recruitment of leukocytes in response to cryptococcal Ags. MIP-1alpha is expressed in the lungs by day 6 post Cryptococcus neoformans infection and could play a role in the development of cell-mediated immunity. To address this possibility, wild-type (MIP-1alpha(+/+)) mice and MIP-1alpha knockout (MIP-1alpha(-/-)) mice were infected intratracheally with a highly virulent strain of C. neoformans (145A). MIP-1alpha message was detected in the lungs on days 3, 7, and 14 in MIP-1alpha(+/+) mice, but it was undetectable in MIP-1alpha(-/-) mice. On day 16, MIP-1alpha(-/-) mice had a 7-fold increase in C. neoformans burden in the lungs, but no decrease in pulmonary leukocyte recruitment. MIP-1alpha(+/+) and MIP-1alpha(-/-) mice had similar numbers of recruited lymphocytes and monocytes/macrophages. Notably, MIP-1alpha(-/-) mice had a significantly greater number of eosinophils. MIP-1alpha(-/-) mice had extremely high levels of serum IgE. This switch of immune response to a T(2) phenotype was associated with enhanced IL-4 and IL-13 expression in the lungs of MIP-1alpha(-/-) mice compared with MIP-1alpha (+/+) mice. Progression of pulmonary cryptococcosis in the presence of nonprotective T(2) immunity resulted in profound lung damage in MIP-1alpha(-/-) mice (eosinophilic crystal deposition, destruction of lung parenchyma, and pulmonary hemorrhage). Twelve-week survival was dramatically decreased in MIP-1alpha(-/-) mice. These studies, together with our previous studies, demonstrate that MIP-1alpha plays a role in both the afferent (T(1)/T(2) development) and efferent (T(1)-mediated leukocyte recruitment) phases of cell-mediated immunity to C. neoformans.

Publication types

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

MeSH terms

  • Animals
  • Cell Movement / immunology
  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokines, CC / biosynthesis
  • Chemokines, CC / genetics
  • Chemokines, CC / immunology
  • Chemokines, CC / physiology*
  • Cryptococcosis / genetics
  • Cryptococcosis / immunology*
  • Cryptococcosis / microbiology
  • Cryptococcosis / pathology
  • Cryptococcus neoformans / growth & development
  • Cryptococcus neoformans / immunology
  • Gene Deletion
  • Immune Sera / administration & dosage
  • Immune Sera / pharmacology
  • Immunity, Cellular
  • Immunoglobulin E / blood
  • Injections, Intraperitoneal
  • Interferon-gamma / biosynthesis
  • Interleukin-12 / biosynthesis
  • Interleukin-13 / biosynthesis
  • Interleukin-4 / biosynthesis
  • Leukocytes / immunology
  • Lung / immunology
  • Lung / microbiology
  • Lung / pathology
  • Lung Diseases, Fungal / genetics
  • Lung Diseases, Fungal / immunology
  • Lung Diseases, Fungal / microbiology
  • Lung Diseases, Fungal / pathology
  • Macrophage Inflammatory Proteins / biosynthesis
  • Macrophage Inflammatory Proteins / genetics
  • Macrophage Inflammatory Proteins / immunology
  • Macrophage Inflammatory Proteins / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phenotype
  • Pulmonary Eosinophilia / genetics
  • Pulmonary Eosinophilia / immunology
  • Survival Analysis
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokines, CC
  • Immune Sera
  • Interleukin-13
  • Macrophage Inflammatory Proteins
  • Interleukin-12
  • Interleukin-4
  • Immunoglobulin E
  • Interferon-gamma