HIGH SPECIFICITY OF TRYPANOSOMA-CRUZI EPIMASTIGOTE RIBONUCLEOPROTEIN AS ANTIGEN IN SERODIAGNOSIS OF CHAGAS-DISEASE

Citation
Me. Solana et al., HIGH SPECIFICITY OF TRYPANOSOMA-CRUZI EPIMASTIGOTE RIBONUCLEOPROTEIN AS ANTIGEN IN SERODIAGNOSIS OF CHAGAS-DISEASE, Journal of clinical microbiology, 33(6), 1995, pp. 1456-1460
Citations number
31
Categorie Soggetti
Microbiology
ISSN journal
00951137
Volume
33
Issue
6
Year of publication
1995
Pages
1456 - 1460
Database
ISI
SICI code
0095-1137(1995)33:6<1456:HSOTER>2.0.ZU;2-1
Abstract
We assessed the performance of an enzyme-linked immunosorbent assay (E LISA) with the Trypanosoma cruzi epimastigote ribosomal fraction (Tula huen and Y strains) in order to improve the diagnostic specificity of the test, A total of 100 serum samples from patients with chronic Chag as' disease from Brazil and Argentina were studied, Sera from 116 pati ents, without Chagas) disease, including 10 with active mucocutaneous leishmaniasis and 20 with visceral leishmaniasis, were used as control s, Immunoglobulin G (IgG) antibodies against the ribosomal fraction (r ibonucleoproteins [RNPs]) in the ELISA were found in 97% of samples fr om patients with Chagas' disease, A total of 99% of the sera from pati ents without the disease were negative, including sera from patients w ith mucocutaneous and visceral leishmaniases, The distribution of IgG isotypes in randomly chosen serum samples was determined by ELISA; IgG 1 and IgG3 were predominant (100% exhibited IgG1 and 85% exhibited IgG 3, and 50% also presented the IgG2 isotype, The distribution of the Ig G subclasses was confirmed by the Western blot (immunoblot) technique, When total IgG was assayed by Western blot assay, no correlation was found between the pattern of serum reactivity and the clinical feature s of the patients with Chagas' disease, Therefore, no typical profile of polypeptide recognition could be associated with any clinical form of Chagas' disease (cardiomyopathy or megaviscera), Our results showed that sera from patients with Chagas' disease react with ribosomal ant igens and display a typical profile of IgG isotypes (IgG1 plus IgG3), The RNP ELISA seems to have improved specificity compared with those o f routine techniques such as the indirect immunofluorescence assay and hemagglutination because it better discriminates between patients wit h Chagas' disease and patients without the disease, Since sera from pa tients with leishmaniasis failed to show cross-reactivity with this an tigen, the ELISA seems useful for detecting Chagas' disease as well as confirming the nature of sera, when it is doubtful whether the patien t has Chagas' disease, by the isotype distribution of IgG.