International Immunology · 1992 · 108 citations · 0 references
Life SciencesImmunologyInfectious DiseasesAdaptive ImmunityCellular ImmunologyParasite ImmunologyCell-mediated ImmunityLymphocyte ActivationMajor Histocompatibility ComplexT Cell ActivationT Cell BiologyT-cell Responses To ParasitesClassical Mhc MoleculesMalaria ImmunologyMalaria ImmunoregulationMalaria-associated T Cell ResponsesMhc Class Ii MoleculesPlasmodium FalciparumSchizont AntigensStaphylococcal Enterotoxins
A Plasmodium falciparum schizont lysate has been previously described as being a powerful inducer of proliferation for human peripheral T lymphocytes. In this report we study the phenotype of cycling T cells from unexposed donors and examine how the P. falciparum lysate compares with the conventional T cell mitogen phytohemagglutinin (PHA), a known superantigen staphylococcal enterotoxin B (SEB), and a classical antigen pure protein derivative (PPD). We show that for this lymphoproliferative activity interaction with the MHC class II molecule is required and that in the presence of P. falciparum the great majority of the cycling cells at day 6 are gamma delta T cells, all of them bearing V gamma 9 V delta 2. Our results suggest that P. falciparum induces a T cell proliferative response that resembles a response of human peripheral blood gamma delta T cells to superantigen. This observation is in agreement with the elevated level of peripheral gamma delta lymphocytes observed during and after malaria acute infection.