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Journal of Clinical Microbiology, February 2006, p. 417-422, Vol. 44, No. 2
0095-1137/06/$08.00+0     doi:10.1128/JCM.44.2.417-422.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Comparison of Serum Hepatitis C Virus (HCV) RNA and Core Antigen Levels in Patients Coinfected with Human Immunodeficiency Virus and HCV and Treated with Interferon plus Ribavirin

A. Pivert,¹ C. Payan,¹ P. Morand,² S. Fafi-Kremer,² J. Deshayes,³ F. Carrat,³ S. Pol,⁴ P. Cacoub,⁵ C. Perronne,⁶ and F. Lunel^1*

Laboratoire de Bactériologie-Virologie-Hygiène Hospitalière, CHU Angers, France,¹ Laboratoire de Virologie, CHU Grenoble, France,² Inserm U707, Faculté de Médecine St Antoine, Paris, France,³ Service d’Hépatologie, Hôpital Necker-Enfants Malades, Paris, France,⁴ Service de Médecine Interne, Hôpital Pitié-Salpétrière, Paris, France,⁵ Service des Maladies Infectieuses et Tropicales, Hopital Raymond Poincaré, Paris, France⁶

Received 29 August 2005/ Returned for modification 7 October 2005/ Accepted 13 November 2005

Trak-C (Ortho-Clinical Diagnostics) is an enzyme-linked immunosorbent assay-based method capable of quantifying hepatitis C virus (HCV) core antigen (CA) in serum and could be an alternative to molecular detection and quantification of HCV RNA. We have evaluated the Trak-C assay in comparison with an HCV RNA quantitative assay (Versant HCV v3.0; Bayer Diagnostics) in the follow-up of 348 treated, human immunodeficiency virus (HIV)/HCV-coinfected patients included in the ANRS HC02 RIBAVIC trial. ANRS HC02 RIBAVIC is a therapeutic, multicenter, randomized protocol comparing the efficacy of alpha interferon 2b (IFN-2b) (3 million units three times a week)-ribavirin (800 mg/day) to that of pegylated IFN-2b (1.5 µg/kg of body weight/week)-ribavirin (800 mg/day) during 48 weeks of treatment of HIV/HCV-coinfected patients naïve to HCV treatment. Patients were assessed for virological analysis at day 0 and weeks 4, 12, 24, 48, and 72. Correlation of HCV RNA and HCV CA at the initiation of treatment was excellent (r = 0.92). HCV RNA and CA kinetics were similar during follow-up of HCV treatment from day 0 to week 72 whatever the group of response and genotype. The positive and negative predictive values of response to the treatment at week 4 were 59 and 94%, respectively, for HCV RNA load reduction of >2 log and 54 and 94%, respectively, for HCV CA below the threshold value (4.18 log₁₀ pg/ml · 10⁴). Trak-C, a new assay able to quantify CA in HIV/HCV-coinfected patients, correlates well with quantitative HCV RNA assays and is cheaper and easier to perform than molecular technology. HCV CA could be a valuable alternative test for therapeutic follow-up of coinfected patients treated with IFN plus ribavirin in developing countries.

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* Corresponding author. Mailing address: Laboratoire de Bactériologie-Virologie-Hygiène Hospitalière, CHU Angers, 4 rue Larrey, 49933 ANGERS Cedex, France. Phone: 0033-02-41-35-33-19. Fax: 0033-02-41-35-41-64. E-mail: frlunel-fabiani{at}chu-angers.fr.

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Journal of Clinical Microbiology, February 2006, p. 417-422, Vol. 44, No. 2
0095-1137/06/$08.00+0     doi:10.1128/JCM.44.2.417-422.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.