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Clinical and Diagnostic Laboratory Immunology, January 2001, p. 112-118, Vol. 8, No. 1
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.1.112-118.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Anti-Trypanosoma cruzi Immunoglobulin G1 Can Be a Useful Tool for Diagnosis and Prognosis of Human Chagas' Disease

Flávia Drumond Cordeiro,1 Olindo Assis Martins-Filho,1,* Manoel Otávio Da Costa Rocha,2 Sheila Jorge Adad,3 Rodrigo Corrêa-Oliveira,1 and Alvaro José Romanha1

Centro de Pesquisas René Rachou, FIOCRUZ1 and Hospital das Clínicas, Faculdade de Medicina, Universidade Federal de Minas Gerais,2 Belo Horizonte and Faculdade de Medicina do Triângulo Mineiro, Uberaba,3 Minas Gerais, Brazil

Received 28 April 2000/Returned for modification 25 July 2000/Accepted 20 September 2000

Two functionally distinct antibodies, categorized as conventional serology antibodies (CSA) and lytic antibodies (LA) have been described in Chagas' disease, based on their ability to bind to fixed epimastigotes (EPI) or live trypomastigotes (TRYPO), respectively. In this study, the profile of immunoglobulin G (IgG) subclasses of CSA and LA were analyzed by flow cytometry using serum samples from chronic chagasic patients with the indeterminate (IND), cardiac (CARD), and digestive (DIG) clinical forms of the disease. The results were expressed as percentage of positive fluorescent parasites (PPFP) for each sample. CSA showed a higher PPFP than LA for all samples. At serum dilutions between 1:256 and 1:2,048, IgG1 anti-EPI was able to distinguish chagasic from nonchagasic individuals. Different profiles of IgG subclasses were observed for CSA and LA. IgG1 and IgG2 were the main subclasses in CSA, whereas IgG1 and IgG3 were the predominant ones in LA. The reactivity of IgG2 anti-EPI was greater in IND and CARD than in DIG patients. Furthermore, a low level of IgG1 and IgG3 LA was associated with most of the CARD patients. On the other hand, a high level of IgG1 LA was associated with most of the IND patients. In summary, our findings indicate the potential of IgG1 anti-EPI for serological diagnosis of Chagas' disease, providing further evidence for a protective role of LA, and show that IgG1 anti-live Trypanosoma cruzi TRYPO may be used to predict the risk of cardiac damage in Chagas' disease.


* Corresponding author. Mailing address: Laboratório de Doença de Chagas, Centro de Pesquisas René Rachou, FIOCRUZ, Av. Augusto de Lima, 1715, Belo Horizonte MG 30190-002 Brazil. Phone: 55 (31) 3295-3566, ext. 165. Fax: 55 (31) 3295-3115. E-mail: oamfilho{at}cpqrr.fiocruz.br.


Clinical and Diagnostic Laboratory Immunology, January 2001, p. 112-118, Vol. 8, No. 1
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.1.112-118.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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