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Journal of Clinical Microbiology, February 2004, p. 707-712, Vol. 42, No. 2
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.2.707-712.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Use of the Trypanosoma cruzi Recombinant Complement Regulatory Protein To Evaluate Therapeutic Efficacy following Treatment of Chronic Chagasic Patients

Wendell S. F. Meira,1,2* Lúcia M. C. Galvão,1 Eliane D. Gontijo,3 George L. L. Machado-Coelho,4 Karen A. Norris,2 and Egler Chiari1

Departamento de Parasitologia, Instituto de Ciências Biológicas,1 Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte,4 Escola de Farmácia, Universidade Federal de Ouro Preto, Ouro Preto, Minas Gerais, Brazil,3 Department of Immunology, University of Pittsburgh, Pittsburgh, Pennsylvania2

Received 17 June 2003/ Returned for modification 25 August 2003/ Accepted 27 October 2003

One of the greatest concerns in Chagas' disease is the absence of reliable methods for the evaluation of chemotherapy efficacy in treated patients. The tests available to evaluate cure after the specific treatment are the complement-mediated lysis (CoML) and flow cytometry tests, but they are not feasible for routine clinical use. In this study, we evaluated an enzyme-linked immunosorbent assay (ELISA) based on the recombinant Trypanosoma cruzi complement regulatory protein (rCRP) as a method to determine parasite clearance in comparison to the CoML and other methods such as conventional serology, hemoculture, and PCR in serum samples of 31 patients collected before and after the treatment, monitored for an average of 27.7 months after chemotherapy. The results showed that the percentage of patient samples that were positive by rCRP ELISA was reduced from 100 to 70.3, 62.5, 71.4, and 33.4% in the first, second, third, and fourth years after treatment, respectively, while the samples positive by CoML were reduced to 85.2, 81.2, 71.4, and 33.4% during the same period, demonstrating the same significant tendency in the reduction of positive samples. On the other hand, the conventional serology (CS) tests did not present this reduction. The percentage of samples positive by PCR was initially 77.4% and decreased to 55.5, 68.7, 47.7, and 50.0% at the fourth year after treatment, confirming the drastic clearance of circulating parasites after treatment. Our results strongly suggest that the rCRP ELISA was capable of detecting the early therapeutic efficacy in treated patients and confirmed its superiority over the CS tests and parasitologic methods.


* Corresponding author. Present address: University of Pittsburgh, Department of Immunology, Biomedical Science Tower—Room E1004, 200 Lothrop St., Pittsburgh, PA 15213. Phone: (412) 648-8854. Fax: (412) 383-8096. E-mail: wsm2{at}pitt.edu.


Journal of Clinical Microbiology, February 2004, p. 707-712, Vol. 42, No. 2
0095-1137/04/$08.00+0     DOI: 10.1128/JCM.42.2.707-712.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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