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Article: RANTES gene single nucleotide polymorphisms and expression in patients with chronic hepatitis B virus infection
Title | RANTES gene single nucleotide polymorphisms and expression in patients with chronic hepatitis B virus infection |
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Authors | |
Keywords | Hepatitis B virus Infection Polymorphism RANTES gene |
Issue Date | 2005 |
Publisher | Zhonghua Yixuehui. The Journal's web site is located at http://www.cmj.org/ |
Citation | Chinese Medical Journal, 2005, v. 118 n. 11, p. 909-914 How to Cite? |
Abstract | Background: Regulated on activation, normal T-cell expressed and secreted (RANTES) plays a critical role in T-lymphocyte activation and proliferation. The process is involved in both acute and chronic phases of inflammation. The present study was to ascertain the possible correlations between chronic hepatitis B virus (HBV) infection and the RANTES gene polymorphisms and their expression. Methods: The study included 130 HBV negative healthy donors and 152 patients with chronic hepatitis B (CHB) virus infection. The polymerase chain reaction (PCR) and restriction fragment length polymorphisms (RFLPs) were used to detect RANTES gene single nucleotide polymorphisms (SNPs). RANTES levels in the platelet depleted plasma were detected by enzyme linked immunosorbent assay (ELISA). Results: RANTES alleles -403G, -28C and In1. 1T were the predominant alleles in the subjects studied. No significant correlation was found between CHB infection and the RANTES alleles, while a significant correlation was found between CHB infection and increased RANTES expression in platelet depleted plasma (P <0.05). Conclusions: SNPs in RANTES gene do not affect chronic HBV infection or the outcome of interferon-α treatment in patients positive for HBV "e" antigen (HBeAg + ). However, patients with CHB infection express the higher levels of plasma RANTES, which is thus associated with CHB infection. |
Persistent Identifier | http://hdl.handle.net/10722/157410 |
ISSN | 2023 Impact Factor: 7.5 2023 SCImago Journal Rankings: 0.997 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Duan, ZP | en_US |
dc.contributor.author | Zhao, XY | en_US |
dc.contributor.author | Huang, DZ | en_US |
dc.contributor.author | He, LX | en_US |
dc.contributor.author | Chen, Y | en_US |
dc.contributor.author | Zhao, CH | en_US |
dc.contributor.author | Zheng, B | en_US |
dc.date.accessioned | 2012-08-08T08:49:43Z | - |
dc.date.available | 2012-08-08T08:49:43Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | Chinese Medical Journal, 2005, v. 118 n. 11, p. 909-914 | en_US |
dc.identifier.issn | 0366-6999 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/157410 | - |
dc.description.abstract | Background: Regulated on activation, normal T-cell expressed and secreted (RANTES) plays a critical role in T-lymphocyte activation and proliferation. The process is involved in both acute and chronic phases of inflammation. The present study was to ascertain the possible correlations between chronic hepatitis B virus (HBV) infection and the RANTES gene polymorphisms and their expression. Methods: The study included 130 HBV negative healthy donors and 152 patients with chronic hepatitis B (CHB) virus infection. The polymerase chain reaction (PCR) and restriction fragment length polymorphisms (RFLPs) were used to detect RANTES gene single nucleotide polymorphisms (SNPs). RANTES levels in the platelet depleted plasma were detected by enzyme linked immunosorbent assay (ELISA). Results: RANTES alleles -403G, -28C and In1. 1T were the predominant alleles in the subjects studied. No significant correlation was found between CHB infection and the RANTES alleles, while a significant correlation was found between CHB infection and increased RANTES expression in platelet depleted plasma (P <0.05). Conclusions: SNPs in RANTES gene do not affect chronic HBV infection or the outcome of interferon-α treatment in patients positive for HBV "e" antigen (HBeAg + ). However, patients with CHB infection express the higher levels of plasma RANTES, which is thus associated with CHB infection. | en_US |
dc.language | eng | en_US |
dc.publisher | Zhonghua Yixuehui. The Journal's web site is located at http://www.cmj.org/ | en_US |
dc.relation.ispartof | Chinese Medical Journal | en_US |
dc.subject | Hepatitis B virus | - |
dc.subject | Infection | - |
dc.subject | Polymorphism | - |
dc.subject | RANTES gene | - |
dc.subject.mesh | Alleles | en_US |
dc.subject.mesh | Chemokine Ccl5 - Genetics | en_US |
dc.subject.mesh | Genotype | en_US |
dc.subject.mesh | Hepatitis B, Chronic - Drug Therapy - Genetics | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Interferon-Alpha - Therapeutic Use | en_US |
dc.subject.mesh | Polymorphism, Single Nucleotide | en_US |
dc.title | RANTES gene single nucleotide polymorphisms and expression in patients with chronic hepatitis B virus infection | en_US |
dc.type | Article | en_US |
dc.identifier.email | Zheng, B: bzheng@hkucc.hku.hk | en_US |
dc.identifier.authority | Zheng, BJ=rp00353 | en_US |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.pmid | 15978191 | - |
dc.identifier.scopus | eid_2-s2.0-20944442464 | en_US |
dc.identifier.hkuros | 99119 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-20944442464&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 118 | en_US |
dc.identifier.issue | 11 | en_US |
dc.identifier.spage | 909 | en_US |
dc.identifier.epage | 914 | en_US |
dc.identifier.isi | WOS:000229823000005 | - |
dc.publisher.place | China | en_US |
dc.identifier.scopusauthorid | Duan, ZP=7101936556 | en_US |
dc.identifier.scopusauthorid | Zhao, XY=7407577215 | en_US |
dc.identifier.scopusauthorid | Huang, DZ=7403891319 | en_US |
dc.identifier.scopusauthorid | He, LX=7403374259 | en_US |
dc.identifier.scopusauthorid | Chen, Y=25927793500 | en_US |
dc.identifier.scopusauthorid | Zhao, CH=7403563984 | en_US |
dc.identifier.scopusauthorid | Zheng, BJ=7201780588 | en_US |
dc.customcontrol.immutable | sml 130529 | - |
dc.identifier.issnl | 0366-6999 | - |