MALARIA DIAGNOSIS - IDENTIFICATION OF AN ANTI-40-KDA POLYPEPTIDE ANTIBODY-RESPONSE ASSOCIATED WITH ACTIVE OR RECENT INFECTION AND STUDY OF THE IGG IGM RATIO OF ANTIBODIES TO BLOOD-STAGE PLASMODIUM-FALCIPARUM ANTIGENS/
Hc. Balthazarguedes et al., MALARIA DIAGNOSIS - IDENTIFICATION OF AN ANTI-40-KDA POLYPEPTIDE ANTIBODY-RESPONSE ASSOCIATED WITH ACTIVE OR RECENT INFECTION AND STUDY OF THE IGG IGM RATIO OF ANTIBODIES TO BLOOD-STAGE PLASMODIUM-FALCIPARUM ANTIGENS/, Parasitology research, 81(4), 1995, pp. 305-309
The need for an alternative methodology to assess disease activity in
the case of malaria led us to evaluate the usefulness of studying the
humoral immune response to establish the diagnosis of past or recent m
alaria. For this purpose, we analyzed sera from 439 individuals living
in endemic areas of the Amazon region (Ariquemes, Rondonia). Individu
als were classified according to the number and the date of past crise
s. The enzyme-linked immunosorbent assay (ELISA) was performed to eval
uate the IgG/IgM ratio so as to discriminate acute or recent malaria f
rom past infections against crude and defined (SPF70) Plasmodium falci
parum asexual blood-stage antigens. We also analyzed the humoral immun
e response against components presented in crude P. falciparum antigen
by the immunoblot technique. Use of the IgG/IgM ratio values did not
allow us to differentiate acute from past infections. However, when we
analyzed the humoral immune response to parasite components, we were
capable of identifying a polypeptide with a molecular weight ranging u
p to 40 kDa, which was recognized by all parasitized polyinfected indi
viduals studied but not by individuals with negative thick blood smear
s. In view of these data, we conclude that the 40-kDa polypeptide may
represent a powerful tool in the diagnosis of acute malaria, mainly fo
r screening blood donors in endemic areas.