Es. Umezawa et al., TRYPANOSOMA-CRUZI DEFINED ANTIGENS IN THE SEROLOGICAL EVALUATION OF AN OUTBREAK OF ACUTE CHAGAS-DISEASE IN BRAZIL (CATOLE DO ROCHA, PARAIBA), Memorias do Instituto Oswaldo Cruz, 91(1), 1996, pp. 87-93
Immunoglobulin G and M humoral response to recombinant protein B13 and
glycoconjugate LPPG Trypanosoma cruzi defined antigens was evaluated
by ELISA in 18 patients in the acute phase of Chagas disease, who were
contaminated on the same occasion. LPPG showed 100% positivity detect
ing both IgM and IgG antibodies, while positivity of 55-65% was observ
ed for B13. An epimastigote alkaline extract (EPI) also showed high se
nsitivity for acute IgM (100%) and IgG (90%) antibodies. However LPPG
had better discriminatory reactivity since with EPI two patients showe
d negative IgG and several other sera presented OD values for IgG and
IgM antibodies very close to the cutoff Thus, it is suggested that det
ection of IgM antibodies by LPPG may be used for diagnosis of the acut
e phase of Chagas disease. An intense decline of IgG and IgM antibodie
s to the three antigens was absented in response to anti-T cruzi chemo
therapy in all acute phase patients. After treatment, six (30%) indivi
duals maintained IgG positivity to EPI, LPPG, and B13 with lower react
ivity than that measured at the acute phase. For comparison, serology
of a group of 22 patients in the chronic phase of Chagas disease and a
lso submitted to chemotherapy was determined. Positive IgM antibodies
to EPI, LPPG and B13 were detected in only 5-9% cases. In all chronic-
phase patients IgG antibodies highly reactive to the three antigens we
re present and no significant decrease resulted after benznidazole adm
inistration. These observations reinforce previous reports that treatm
ent in the acute phase may reduce or eliminate the parasite.