Transmission rates of hepatitis C virus by different batches of a contaminated anti-D immunoglobulin preparation

被引:0
作者
Lawlor, E
Power, J
Garson, JA
Yap, PL
Davidson, F
Columb, G
Smith, D
Pomeroy, L
O'Riordan, J
Simmonds, P
Tedder, RS
机构
[1] Blood Transfus Serv Board, Dublin 4, Ireland
[2] Trinity Coll Dublin, Dublin, Ireland
[3] UCL, Sch Med, Dept Virol, London W1N 8AA, England
[4] Edinburgh & SE Scotland Blood Transfus Serv, Edinburgh, Midlothian, Scotland
[5] Univ Edinburgh, Dept Med Microbiol, Edinburgh, Midlothian, Scotland
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R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: The aim of this study was to determine the hepatitis C virus (HCV) infection rate of recipients of different batches of anti-D immunoglobulin associated with an outbreak of HCV infection which occurred in 1977 and its relationship to the polymerase chain reaction (PCR) status of the implicated batches. This study was undertaken to determine the predictive value of HCV genome detection and quantification for subsequent infection in recipients of an HCV-contaminated anti-D immunoglobulin product for intravenous use. Materials and Methods: Sera from recipients of anti-D were tested by HCV enzyme immunoassay and if found positive were subsequently tested by recombinant immunoblot assay and HCV PCR in a national HCV anti-D screening programme set up in 1994. The HCV status of 1,342 known recipients of infectious or potentially infectious batches has been compared to the amount of HCV RNA in the anti-D batch they received so as to determine the value of PCR in the prediction of infectivity in immunoglobulin preparations. Results: It has been demonstrated that HCV-infected plasma derived from batches of anti-D showing levels of viral genome in excess of 10(4) genomes per millilitre led to infection of up to 60% of recipients. In contrast, batches with unde- tectable levels of HCV genome very rarely transmitted infection. Conclusions: The presence of HCV RNA in intravenous immunoglobulin preparations which have not undergone a specific viral inactivation step is a predictor of HCV infection in recipients.
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页码:138 / 143
页数:6
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共 21 条
[1]   TO C OR NOT TO C - THESE ARE THE QUESTIONS [J].
ALTER, HJ .
BLOOD, 1995, 85 (07) :1681-1695
[2]   ANALYSIS OF A NEW HEPATITIS-C VIRUS TYPE AND ITS PHYLOGENETIC RELATIONSHIP TO EXISTING VARIANTS [J].
CHAN, SW ;
MCOMISH, F ;
HOLMES, EC ;
DOW, B ;
PEUTHERER, JF ;
FOLLETT, E ;
YAP, PL ;
SIMMONDS, P .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :1131-1141
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]  
CRASKE J, 1978, LANCET, V2, P1051
[5]  
CUNNINGHAM C J, 1980, Biochemical Society Transactions, V8, P178
[6]   LONG-TERM PERSISTENCE OF HEPATITIS-C VIRUS-ANTIBODIES IN A SINGLE SOURCE OUTBREAK [J].
DITTMANN, S ;
ROGGENDORF, M ;
DURKOP, J ;
WIESE, M ;
LORBEER, B ;
DEINHARDT, F .
JOURNAL OF HEPATOLOGY, 1991, 13 (03) :323-327
[7]  
*EXP GROUP BLOOD T, 1995, REP EXP GROUP BLOOD
[8]   DETECTION BY PCR OF HEPATITIS-C VIRUS IN FACTOR-VIII CONCENTRATES [J].
GARSON, JA ;
PRESTON, FE ;
MAKRIS, M ;
TUKE, P ;
RING, C ;
MACHIN, SJ ;
TEDDER, RS .
LANCET, 1990, 335 (8703) :1473-1473
[9]   A COMPARISON OF POLYMERASE CHAIN-REACTION AND AN INFECTIVITY ASSAY FOR HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 TITRATION DURING VIRUS INACTIVATION OF BLOOD COMPONENTS [J].
HART, H ;
MCOMISH, F ;
HART, WG ;
SIMMONDS, P ;
YAP, PL .
TRANSFUSION, 1993, 33 (10) :838-841
[10]   Analysis of human plasma products: polymerase chain reaction does not discriminate between live and inactivated viruses [J].
Hilfenhaus, J ;
Groner, A ;
Nowak, T ;
Weimer, T .
TRANSFUSION, 1997, 37 (09) :935-940