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Inactivation of parvovirus B19 during pasteurization of human serum albumin

BACKGROUND : It has been shown that HSA may be contaminated with parvovirus B19 (B19) DNA. However, the presence of B19 DNA does not necessarily indicate infectious virus. HSA is pasteurized at 60°C for 10 hours and it remains unclear whether this procedure inactivates B19. Studies with animal parvo...

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Published in:Transfusion (Philadelphia, Pa.) Pa.), 2002-08, Vol.42 (8), p.1011-1018
Main Authors: Blümel, Johannes, Schmidt, Ivo, Willkommen, Hannelore, Löwer, Johannes
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description BACKGROUND : It has been shown that HSA may be contaminated with parvovirus B19 (B19) DNA. However, the presence of B19 DNA does not necessarily indicate infectious virus. HSA is pasteurized at 60°C for 10 hours and it remains unclear whether this procedure inactivates B19. Studies with animal parvoviruses indicate considerable heat resistance at 60°C. However, due to the lack of a suitable cell culture system, the pasteurization process has not been investigated in the past. STUDY DESIGN AND METHODS : The recently described cell clone KU812Ep6 was used to establish a system for investigation of B19 inactivation during pasteurization. Virus‐infected cells were detected by immunofluorescent staining of viral capsid antigen and by RT‐PCR assay of virus‐specific capsid mRNA. RESULTS : B19 was inactivated after 10 minutes at 60°C for ≥4 log . In contrast, porcine parvovirus was widely resistant at 60°C. Inactivation of B19 was independent of the analyzed albumin products (5, 20, and 25% albumin from three manufacturers) and from the specific virus source used for the inactivation experiments. Degradation of B19 DNA by deoxyribonuclease I treatment after pasteurization indicated that the virus capsid is destroyed during heat treatment. CONCLUSION : Heat resistance of B19 markedly differs from heat resistance of animal parvoviruses. While animal parvoviruses widely withstand pasteurization of albumin, B19 was rapidly inactivated. These results confirm the safety of pasteurized albumin and are in line with its good clinical safety record with respect to B19 infection. However, conclusions regarding the safety of other blood‐derived medicinal products should not be derived from B19 inactivation in albumin, because different processes or different composition of product intermediates may significantly influence B19 stability during heat treatment.
doi_str_mv 10.1046/j.1537-2995.2002.00158.x
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However, the presence of B19 DNA does not necessarily indicate infectious virus. HSA is pasteurized at 60°C for 10 hours and it remains unclear whether this procedure inactivates B19. Studies with animal parvoviruses indicate considerable heat resistance at 60°C. However, due to the lack of a suitable cell culture system, the pasteurization process has not been investigated in the past. STUDY DESIGN AND METHODS : The recently described cell clone KU812Ep6 was used to establish a system for investigation of B19 inactivation during pasteurization. Virus‐infected cells were detected by immunofluorescent staining of viral capsid antigen and by RT‐PCR assay of virus‐specific capsid mRNA. RESULTS : B19 was inactivated after 10 minutes at 60°C for ≥4 log . In contrast, porcine parvovirus was widely resistant at 60°C. Inactivation of B19 was independent of the analyzed albumin products (5, 20, and 25% albumin from three manufacturers) and from the specific virus source used for the inactivation experiments. Degradation of B19 DNA by deoxyribonuclease I treatment after pasteurization indicated that the virus capsid is destroyed during heat treatment. CONCLUSION : Heat resistance of B19 markedly differs from heat resistance of animal parvoviruses. While animal parvoviruses widely withstand pasteurization of albumin, B19 was rapidly inactivated. These results confirm the safety of pasteurized albumin and are in line with its good clinical safety record with respect to B19 infection. 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However, the presence of B19 DNA does not necessarily indicate infectious virus. HSA is pasteurized at 60°C for 10 hours and it remains unclear whether this procedure inactivates B19. Studies with animal parvoviruses indicate considerable heat resistance at 60°C. However, due to the lack of a suitable cell culture system, the pasteurization process has not been investigated in the past. STUDY DESIGN AND METHODS : The recently described cell clone KU812Ep6 was used to establish a system for investigation of B19 inactivation during pasteurization. Virus‐infected cells were detected by immunofluorescent staining of viral capsid antigen and by RT‐PCR assay of virus‐specific capsid mRNA. RESULTS : B19 was inactivated after 10 minutes at 60°C for ≥4 log . In contrast, porcine parvovirus was widely resistant at 60°C. Inactivation of B19 was independent of the analyzed albumin products (5, 20, and 25% albumin from three manufacturers) and from the specific virus source used for the inactivation experiments. Degradation of B19 DNA by deoxyribonuclease I treatment after pasteurization indicated that the virus capsid is destroyed during heat treatment. CONCLUSION : Heat resistance of B19 markedly differs from heat resistance of animal parvoviruses. While animal parvoviruses widely withstand pasteurization of albumin, B19 was rapidly inactivated. These results confirm the safety of pasteurized albumin and are in line with its good clinical safety record with respect to B19 infection. However, conclusions regarding the safety of other blood‐derived medicinal products should not be derived from B19 inactivation in albumin, because different processes or different composition of product intermediates may significantly influence B19 stability during heat treatment.</description><subject>Biological and medical sciences</subject><subject>Hot Temperature</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Parvovirus B19, Human - growth &amp; development</subject><subject>Parvovirus, Porcine - growth &amp; development</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. 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Diet therapy and various other treatments (general aspects)</topic><topic>Serum Albumin</topic><topic>Virology - methods</topic><topic>Virus Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blümel, Johannes</creatorcontrib><creatorcontrib>Schmidt, Ivo</creatorcontrib><creatorcontrib>Willkommen, Hannelore</creatorcontrib><creatorcontrib>Löwer, Johannes</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blümel, Johannes</au><au>Schmidt, Ivo</au><au>Willkommen, Hannelore</au><au>Löwer, Johannes</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inactivation of parvovirus B19 during pasteurization of human serum albumin</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2002-08</date><risdate>2002</risdate><volume>42</volume><issue>8</issue><spage>1011</spage><epage>1018</epage><pages>1011-1018</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><coden>TRANAT</coden><abstract>BACKGROUND : It has been shown that HSA may be contaminated with parvovirus B19 (B19) DNA. 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Inactivation of B19 was independent of the analyzed albumin products (5, 20, and 25% albumin from three manufacturers) and from the specific virus source used for the inactivation experiments. Degradation of B19 DNA by deoxyribonuclease I treatment after pasteurization indicated that the virus capsid is destroyed during heat treatment. CONCLUSION : Heat resistance of B19 markedly differs from heat resistance of animal parvoviruses. While animal parvoviruses widely withstand pasteurization of albumin, B19 was rapidly inactivated. These results confirm the safety of pasteurized albumin and are in line with its good clinical safety record with respect to B19 infection. 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subjects Biological and medical sciences
Hot Temperature
Humans
Kinetics
Medical sciences
Miscellaneous
Parvovirus B19, Human - growth & development
Parvovirus, Porcine - growth & development
Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
Serum Albumin
Virology - methods
Virus Activation
title Inactivation of parvovirus B19 during pasteurization of human serum albumin
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