Open AccessLymphocyte activation and subset redistribution in the peripheral blood in acute malaria illness: distinct γδ + T cell patterns in Plasmodium falciparum and P. vivax infections
Author(s) -
WORKU S.,
BJO¨RKMAN A.,
TROYEBLOMBERG M.,
JEMANEH L.,
FA¨RNERT A.,
CHRISTENSSON B.
Publication year - 1997
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.1997.d01-981.x
Subject(s) - malaria , immunology , plasmodium vivax , plasmodium falciparum , cd8 , biology , lymphocyte , flow cytometry , t cell , virology , immune system , medicine
Lymphocyte subset distributions and activation in the peripheral blood were studied in 39 patients with acute malaria and 16 healthy controls from Addis Ababa and Nazareth, Ethiopia. As confirmed by polymerase chain reaction (PCR), 15 patients were infected with Plasmodium falciparum ( Pf ), 17 with P. vivax ( Pv ) and seven were double‐infected (Di) with both Pf and Pv . Three‐colour flow cytometry was used for phenotyping. Total leucocyte and lymphocyte counts were lower in malaria patients than in controls. The T cell count was reduced in Pf patients, while in the Pv and Di patients there was a reduction in the natural killer (NK) cell count. The CD4/CD8 ratio remained unchanged. γδ + T cells were significantly elevated in Pf and Di patients, but not in Pv patients. The increase in γδ + T cells was mostly due to an increase in Vδ1 + cells. Analyses of cellular activation indicated by the expressions of CD25 and HLA‐DR revealed significantly higher numbers of activated CD3 + cells, including γδ + T cells, in all patient groups compared with controls. Our results thus indicate that in acute malaria illness there is a complex pattern of change in lymphocyte subset distribution and activation, including γδ + T cells. These patterns in Pf infection seem to be distinct from those in Pv infection.