CD4 T cells from malaria-nonexposed individuals respond to the CD36-Binding Domain of Plasmodium falciparum erythrocyte membrane protein-1 via an MHC class II-TCR-independent pathway

J Immunol. 2006 May 1;176(9):5504-12. doi: 10.4049/jimmunol.176.9.5504.

Abstract

We have studied the human CD4 T cell response to a functionally conserved domain of Plasmodium falciparum erythrocyte membrane protein-1, cysteine interdomain region-1alpha (CIDR-1alpha). Responses to CIDR-1alpha were striking in that both exposed and nonexposed donors responded. The IFN-gamma response to CIDR-1alpha in the nonexposed donors was partially independent of TCR engagement of MHC class II and peptide. Contrastingly, CD4 T cell and IFN-gamma responses in malaria-exposed donors were MHC class II restricted, suggesting that the CD4 T cell response to CIDR-1alpha in malaria semi-immune adults also has a TCR-mediated component, which may represent a memory response. Dendritic cells isolated from human peripheral blood were activated by CIDR-1alpha to produce IL-12, IL-10, and IL-18. IL-12 was detectable only between 6 and 12 h of culture, whereas the IL-10 continued to increase throughout the 24-h time course. These data strengthen previous observations that P. falciparum interacts directly with human dendritic cells, and suggests that the interaction between CIDR-1alpha and the host cell may be responsible for regulation of the CD4 T cell and cytokine responses to P. falciparum-infected erythrocytes reported previously.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Antigens, CD / metabolism
  • Antigens, Differentiation, T-Lymphocyte / metabolism
  • CD36 Antigens / metabolism*
  • CD4-Positive T-Lymphocytes / metabolism*
  • Cell Division
  • Cells, Cultured
  • Cysteine / metabolism
  • Dendritic Cells / metabolism
  • Histocompatibility Antigens Class II / metabolism
  • Humans
  • Interferon-gamma / biosynthesis
  • Killer Cells, Natural / metabolism
  • Lectins, C-Type
  • Malaria / metabolism
  • Malaria / parasitology
  • Plasmodium falciparum / metabolism*
  • Protein Binding
  • Protozoan Proteins / metabolism*
  • Receptors, Antigen, T-Cell / metabolism

Substances

  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CD36 Antigens
  • CD69 antigen
  • Histocompatibility Antigens Class II
  • Lectins, C-Type
  • Protozoan Proteins
  • Receptors, Antigen, T-Cell
  • erythrocyte membrane protein 1, Plasmodium falciparum
  • Interferon-gamma
  • Cysteine