The quasispecies nature of hepatitis C virus (HCV) in patients with mixed HCV subtype infection was compared with that in patients with single HCV subtype infection. The number of HCV quasispecies was compared between 35 patients with mixed HCV subtype infection and 83 patients with single subtype i
Detection of hepatitis C virus in thyroid tissue from patients with chronic HCV infection
✍ Scribed by Javier Bartolomé; Elena Rodríguez-Iñigo; Pedro Quadros; Sonia Vidal; Isabel Pascual-Miguelañez; José Antonio Rodríguez-Montes; Luis García-Sancho; Vicente Carreño
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 181 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Thyroid dysfunctions are common in chronic hepatitis C virus (HCV) infection. HCV‐RNA has been detected by reverse‐transcription polymerase chain reaction (PCR) in thyroid from HCV infected patients with acquired immunodeficiency syndrome. However, morphological evidence of HCV replication in thyroid cells from immune competent patients has not been provided. In situ hybridization and real‐time‐PCR were used to analyze HCV‐RNA replication in thyroid tissue from 11 patients (3 anti‐HCV, serum HCV‐RNA positive; 8 anti‐HCV negative). Genomic and antigenomic HCV‐RNA was detected in the thyroid of the 3 anti‐HCV positive patients at concentrations of 2.6 × 10^4^, 1.7 × 10^4^, and 8.6 × 10^3^ copies/µg of total RNA (genomic) and 3.2 × 10^2^, 4.3 × 10^3^ and 2.9 × 10^2^ HCV‐RNA copies/µg of total RNA (antigenomic). No HCV‐RNA was detected in the thyroid tissue of the 8 anti‐HCV negative patients. Presence of genomic/antigenomic HCV‐RNA in the 3 anti‐HCV positive cases was confirmed by in situ hybridization. Signals were observed in the cytoplasm of the thyroid cells. In conclusion, the data obtained indicate that HCV may infect cells of the thyroid in immune competent patients with chronic HCV infection. The pathogenic implications of this finding merit further research. J. Med. Virol. 80:1588–1594, 2008. © 2008 Wiley‐Liss, Inc.
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