CC chemokine receptor 1 enhances susceptibility to Leishmania major during early phase of infection

Immunol Cell Biol. 2003 Apr;81(2):114-20. doi: 10.1046/j.0818-9641.2002.01132.x.

Abstract

CC chemokine receptor 1 (CCR1) is expressed on the surfaces of monocytes, lymphocytes, neutrophils and eosinophils. CC chemokine receptor 1 not only regulates leucocyte chemotaxis, but also plays a role in the regulation of Th1/Th2 cytokine responses. To determine the role of CCR1 in regulation of immune response during Leishmania major infection, we analysed the course of cutaneous L. major infection in CCR1-deficient C57BL/6 mice (CCR1-/-) and compared with similarly infected wild-type mice (CCR1+/+). Following L. major infection, CCR1-/- mice developed significantly smaller lesions containing fewer parasites than CCR1+/+ mice. Furthermore, the severity of the inflammation as assessed by the degree of leucocyte infiltration at the site of infection was similar in CCR1+/+ and CCR1-/- mice. Although both groups developed significant antibody responses following L. major infection, CCR1-/- mice produced significantly lower IgE. On day 20 postinfection, LmAg-stimulated lymph node cells from L. major-infected CCR1+/+ and CCR1-/- mice produced comparable levels of IL-12 and IFN-gamma, but those from CCR1-/- mice produced significantly less IL-4 and IL-10. By day 70, lymph node cells from both CCR1+/+ and CCR1-/- mice produced significant amounts of IL-12 and IFN-gamma but low IL-4. At both time points, the draining lymph nodes from CCR1+/+ and CCR1-/- mice contained similar number of leucocytes. These results demonstrate that CCR1 plays a role in pathogenesis of cutaneous L. major infection. Moreover, they also indicate that CCR1 exacerbates L. major infection in C57BL/6 mice by up-regulating Th2-like response rather than inhibiting Th1 development or/and influencing leucocyte chemotaxis.

Publication types

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

MeSH terms

  • Animals
  • Antibody Formation
  • Cytokines / biosynthesis
  • Disease Susceptibility / immunology*
  • Genetic Predisposition to Disease
  • Immunity, Cellular
  • Immunoglobulin G / blood
  • Leishmania major / immunology
  • Leishmaniasis, Cutaneous / immunology*
  • Leishmaniasis, Cutaneous / pathology
  • Lymph Nodes / cytology
  • Lymph Nodes / parasitology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Receptors, CCR1
  • Receptors, Chemokine / genetics
  • Receptors, Chemokine / immunology*
  • Th2 Cells / immunology
  • Time Factors

Substances

  • Ccr1 protein, mouse
  • Cytokines
  • Immunoglobulin G
  • Receptors, CCR1
  • Receptors, Chemokine