Korean J Lab Med.  2006 Dec;26(6):418-423. 10.3343/kjlm.2006.26.6.418.

Usefulness of Anti-HCV ELISA Test and HCV Reverse Transcriptase-PCR for the Diagnosis of Hepatits C Viral Infection

Affiliations
  • 1Department of Laboratory Medicine, College of Medicine, Kyunghee University, Seoul, Korea. leehejo@khmc.or.kr

Abstract

BACKGROUND: The diagnosis of hepatitis C virus (HCV) infection is screened by anti-HCV enzymelinked immunosorbant assay (ELISA) and confirmed by recombinant immunoblotting assay (RIBA) or HCV RT-PCR. We attempted to evaluate the results between anti-HCV ELISA and a qualitative HCV RT-PCR.
METHODS
Four hundred and twenty patients who were tested with anti-HCV ELISA and HCV RTPCR, simultaneously, from January 2002 to June 2005 were enrolled in this study. Anti-HCV ELISA was performed by AxSYM HCV version 3.0 (Abbott Laboratories, USA). HCV RT-PCR was performed using in-house RT-nested PCR methods from January 2002 to October 2004 and HCV Genotype Amplification Kit (LiPA) (Bayer Healthcare, USA) from November 2004 to June 2005.
RESULTS
Of the 420 patients tested, 321 were positive for anti-HCV ELISA, and 204 were positive for RT-PCR. The positive predictability of anti-HCV ELISA was 63.6%. Among anti-HCV positive patients, RT-PCR was positive in 7.3% of the patients with sample/cut-off (S/CO)<6, compared with 82.8% of the patients with S/CO> or =6. Among the 117 patients with positive anti-HCV, but with negative HCV RT-PCR, 64 had liver diseases such as chronic hepatitis C, chronic hepatitis B, or hepatocellular carcinoma. Twelve patients showed positive HCV RT-PCR, but negative anti-HCV results; of these 9 had hepatic dysfunction.
CONCLUSIONS
In the patients who were positive for anti-HCV ELISA with a low S/CO, HCV RT-PCR positivity was shown in a low proportion. Therefore, in such cases, the results should be confirmed by RIBA or HCV RT-PCR. The liver function test showed increased levels of hepatic enzymes in patients with positive HCV RT-PCR, but negative anti-HCV. Such findings correlate to an early phase of chronic hepatitis C, suggesting the necessity of continuous follow up.

Keyword

Hepatitis C; Anti-HCV ELISA; HCV RT-PCR

MeSH Terms

Carcinoma, Hepatocellular
Delivery of Health Care
Diagnosis*
Enzyme-Linked Immunosorbent Assay*
Follow-Up Studies
Genotype
Hepacivirus
Hepatitis B, Chronic
Hepatitis C
Hepatitis C, Chronic
Humans
Immunoblotting
Liver Diseases
Liver Function Tests
Polymerase Chain Reaction

Reference

References

1. Kim YK, Kim BH, Jin ES, Nam KD, Jang JY, Kim NH, et al. Positive predictability and predictive factors of the third generation Anti-Hepatitis C virus (HCV) ELISA test for HCV infection. Korean J Gastroenterol. 2005; 45:181–8.
2. Hsu HH, Gonzalez M, Foung SK, Feinstone SM, Greenberg HB. Antibodies to hepatitis C virus in low-risk blood donors: implications for counseling positive donors. Gastroenterology. 1991; 101:1724–7.
Article
3. Sugitani M, Inchauspe G, Shindo M, Prince AM. Sensitivity of serological assays to identify blood donors with hepatitis C viremia. Lancet. 1992; 339:1018–9.
4. Garson JA, Tedder RS, Briggs M, Tuke P, Glazebrook JA, Trute A, et al. Detection of hepatitis C viral sequences in blood donations by “nested” polymerase chain reaction and prediction of infectivity. Lancet. 1990; 335:1419–22.
Article
5. Busch MP, Wilber JC, Johnson P, Tobler L, Evans CS. Impact of specimen handling and storage on detection of hepatitis C virus RNA. Transfusion. 1992; 32:420–5.
Article
6. Wang JT, Wang TH, Sheu JC, Lin SM, Lin JT, Chen DS. Effects of anticoagulants and storage of blood samples on efficacy of the polymerase chain reaction assay for hepatitis C virus. J Clin Microbiol. 1992; 30:750–3.
Article
7. Bukh J, Purcell RH, Miller RH. Importance of primer selection for the detection of hepatitis C virus RNA with the polymerase chain reaction assay. Proc Natl Acad Sci USA. 1992; 89:187–91.
Article
8. Cristiano K, Di Bisceglie AM, Hoofnagle JH, Feinstone SM. Hepatitis C viral RNA in serum of patients with chronic non-A, non-B hepatitis: detection by the polymerase chain reaction using multiple primer sets. Hepatology. 1991; 14:51–5.
Article
9. Polywka S, Schroter M, Feucht HH, Zollner B, Laufs R. Relevance of reactivity in commercially available hepatitis C virus antibody assays. J Clin Microbiol. 2001; 39:1665–8.
Article
10. Sung HS, Oh HB, Lee EH. Genotypes of hepatitis C virus amplified from sera non-reactive to Anti-HCV enzyme immunoassay. Korean J Clin Pathol. 2001; 21:141–6.
11. Kee SJ, Shin JH, Suh SP, Ryang DW. Discrepancy between serological markers of enzyme immunoassay and results of polymerase chain reaction for hepatitis B and C viruses in patients with chronic liver diseases. Korean J Clin Pathol. 1996; 16:965–78.
12. Raimondo G, Brunetto MR, Pontisso P, Smedile A, Maina AM, Saitta C, et al. Longitudinal evaluation reveals a complex spectrum of virological profiles in hepatitis B virus/hepatitis C virus-coinfected patients. Hepatology. 2006; 43:100–7.
Article
13. Shih CM, Lo SJ, Miyamura T, Chen SY, Lee YH. Suppression of hepatitis B virus expression and replication by hepatitis C virus core protein in HuH-7 cells. J Virol. 1993; 67:5823–32.
Article
14. Shih CM, Chen CM, Chen SY, Lee YH. Modulation of the trans-suppression activity of hepatitis C virus core protein by phosphorylation. J Virol. 1995; 69:1160–71.
Article
15. Schuttler CG, Fiedler N, Schmidt K, Repp R, Gerlich WH, Schaefer S. Suppression of hepatitis B virus enhancer 1 and 2 by hepatitis C virus core protein. J Hepatol. 2002; 37:855–62.
16. Chen SY, Kao CF, Chen CM, Shih CM, Hsu MJ, Chao CH, et al. Mechanisms for inhibition of hepatitis B virus gene expression and replication by hepatitis C virus core protein. J Biol Chem. 2003; 278:591–607.
Article
17. Arase Y, Ikeda K, Chayama K, Murashima N, Tsubota A, Suzuki Y, et al. Fluctuation patterns of HCV-RNA serum level in patients with chronic hepatitis C. J Gastroenterol. 2000; 35:221–5.
Article
18. Halfon P, Bourliere M, Halimi G, Khiri H, Bertezene P, Portal I, et al. Assessment of spontaneous fluctuations of viral load in untreated patients with chronic hepatitis C by two standardized quantitation methods: branched DNA and Amplicor Monitor. J Clin Microbiol. 1998; 36:2073–5.
Article
19. Pontisso P, Bellati G, Brunetto M, Chemello L, Colloredo G, Di Stefano R, et al. Hepatitis C virus RNA profiles in chronically infected individuals: do they relate to disease activity? Hepatology. 1999; 29:585–9.
Article
Full Text Links
  • KJLM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr