CD4 T Cell Responses to a Variant Antigen of the Malaria ParasitePlasmodium falciparum,Erythrocyte Membrane Protein–1, in Individuals Living in Malaria‐Endemic Areas
Author(s) -
Catherine E. M. Allsopp,
Latifu A. Sanni,
Lieke Reubsaet,
Francis M. Ndungu,
Chris Newbold,
Tabitha Mwangi,
Kevin Marsh,
Jean Langhorne
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/339521
Subject(s) - malaria , plasmodium falciparum , parasite hosting , biology , virology , antigen , erythrocyte membrane , plasmodium (life cycle) , immunology , genetics , membrane , world wide web , computer science
Plasmodium falciparum erythrocyte membrane protein-1 (PfEMP-1) is a variant antigen on the surface of malaria-infected red blood cells. Antibody responses to PfEMP-1 correlate with immunity, and, therefore, PfEMP-1 may be a good candidate for a malaria vaccine. However, the specificity of CD4 T cells required for a protective variant-specific antibody response is not known. We have measured the CD4 T cell response to 3 different regions that are relatively homologous among different PfEMP-1 variants. The response to the cysteine-rich interdomain region was unusual in that the majority of donors, whether malaria exposed or not, had positive CD4 T cell, interleukin-10, and interferon-gamma responses. The CD4 T cell response to the exon 2 and duffy binding-like domain proteins was significantly greater in malaria-exposed donors than in unexposed Europeans, which suggests that these regions contain peptides recognized by T cells, which thus may be useful as components of a vaccine.
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