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Published in: Virology Journal 1/2011

Open Access 01-12-2011 | Research

Response to combination therapy of HCV 3a infected Pakistani patients and the role of NS5A protein

Authors: Ijaz Ali, Sanaullah Khan, Sobia Attaullah, Shahid Niaz Khan, Jabbar Khan, Sami Siraj, Aqib Iqbal, Zahoor A Swati, Muhammad Idrees

Published in: Virology Journal | Issue 1/2011

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Abstract

Background

Hepatitis C virus (HCV) genotype 3a is known to show comparatively better response to combination therapy than genotype 1 and 4. Mutations within NS5A gene of HCV have earlier been implicated with response to interferon (IFN) therapies in chronic HCV patients among various populations. As response to therapy are available in different populations because of the ethnic and viral factors and there was no study available on the phenomenon of resistivity to IFN.

Results

Chronic HCV 3a infected Pakistani patients were kept on IFN-α and ribavirin therapy for six months. NS5A gene of HCV was amplified and sequenced in the case of all the patients prior to therapy and the sequences were analysed for mutations. Out of the total 27 patients, 20 (74.07%) were observed with sustained virological response (SVR), 4 (14.81%) patients were non responder (NR) while 3 (11.11%) patients exhibited in end of treatment response (ETR). Three (3/20) (15%) SVR patients and two (2/3) ETR patients had mutations (ranging from I-V amino acids) within the NS5A ISDR regions. While the rest of the SVR patients (85%) and the NR had no mutations at ISDR region when compared with HCV K3a ISDR.

Conclusions

Mutations within the NS5A gene of HCV 3a genotype may not influence the outcome of combination therapy in Pakistani populations.
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Metadata
Title
Response to combination therapy of HCV 3a infected Pakistani patients and the role of NS5A protein
Authors
Ijaz Ali
Sanaullah Khan
Sobia Attaullah
Shahid Niaz Khan
Jabbar Khan
Sami Siraj
Aqib Iqbal
Zahoor A Swati
Muhammad Idrees
Publication date
01-12-2011
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2011
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/1743-422X-8-258

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