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dc.contributor.authorLock, Martin
dc.contributor.authorMcGorray, Susan
dc.contributor.authorAuricchio, Alberto
dc.contributor.authorAyuso, Eduard
dc.contributor.authorBeecham, E. Jeffrey
dc.contributor.authorBlouin-Tavel, Veronique
dc.contributor.authorBosch, Fatima
dc.contributor.authorBose, Mahuya
dc.contributor.authorBryne, Barry J.
dc.contributor.authorCaton, Tina
dc.contributor.authorChiorini, John A.
dc.contributor.authorChtarto, Abdelwahed
dc.contributor.authorClark, K. Reed
dc.contributor.authorConlon, Thomas
dc.contributor.authorDarmon, Christophe
dc.contributor.authorDoria, Monica
dc.contributor.authorDouar, Anne
dc.contributor.authorFlotte, Terence R.
dc.contributor.authorFrancis, Joyce D.
dc.contributor.authorFrancois, Achille
dc.contributor.authorGiacca, Mauro
dc.contributor.authorKorn, Michael T.
dc.contributor.authorKorytov, Irina
dc.contributor.authorLeon, Xavier
dc.contributor.authorLeuchs, Barbara
dc.contributor.authorLux, Gabriele
dc.contributor.authorMelas, Catherine
dc.contributor.authorMizukami, Hiroaki
dc.contributor.authorMoullier, Philippe
dc.contributor.authorMuller, Marcus
dc.contributor.authorOzawa, Keiya
dc.contributor.authorPhilipsberg, Tina
dc.contributor.authorPoulard, Karine
dc.contributor.authorRaupp, Christina
dc.contributor.authorRiviere, Christel
dc.contributor.authorRoosendaal, Sigrid D.
dc.contributor.authorSamulski, Richard Jude
dc.contributor.authorSoltys, Steven M.
dc.contributor.authorSurosky, Richard
dc.contributor.authorTenenbaum, Liliane
dc.contributor.authorThomas, Darby L.
dc.contributor.authorvan Montfort, Bart
dc.contributor.authorVeres, Gabor
dc.contributor.authorWright, J. Fraser
dc.contributor.authorXu, Yili
dc.contributor.authorZelenaia, Olga
dc.contributor.authorZentilin, Lorena
dc.contributor.authorSnyder, Richard O.
dc.date2022-08-11T08:10:14.000
dc.date.accessioned2022-08-23T17:00:39Z
dc.date.available2022-08-23T17:00:39Z
dc.date.issued2010-10-14
dc.date.submitted2012-01-11
dc.identifier.citationHum Gene Ther. 2010 Oct;21(10):1273-85. <a href="http://dx.doi.org/10.1089/hum.2009.223">Link to article on publisher's site</a>
dc.identifier.issn1043-0342 (Linking)
dc.identifier.doi10.1089/hum.2009.223
dc.identifier.pmid20486768
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43839
dc.description.abstractA recombinant adeno-associated virus serotype 2 Reference Standard Material (rAAV2 RSM) has been produced and characterized with the purpose of providing a reference standard for particle titer, vector genome titer, and infectious titer for AAV2 gene transfer vectors. Production and purification of the reference material were carried out by helper virus-free transient transfection and chromatographic purification. The purified bulk material was vialed, confirmed negative for microbial contamination, and then distributed for characterization along with standard assay protocols and assay reagents to 16 laboratories worldwide. Using statistical transformation and modeling of the raw data, mean titers and confidence intervals were determined for capsid particles ({X}, 9.18 x 10(1)(1) particles/ml; 95% confidence interval [CI], 7.89 x 10(1)(1) to 1.05 x 10(1)(2) particles/ml), vector genomes ({X}, 3.28 x 10(1) vector genomes/ml; 95% CI, 2.70 x 10(1) to 4.75 x 10(1) vector genomes/ml), transducing units ({X}, 5.09 x 10 transducing units/ml; 95% CI, 2.00 x 10 to 9.60 x 10 transducing units/ml), and infectious units ({X}, 4.37 x 10 TCID IU/ml; 95% CI, 2.06 x 10 to 9.26 x 10 TCID IU/ml). Further analysis confirmed the identity of the reference material as AAV2 and the purity relative to nonvector proteins as greater than 94%. One obvious trend in the quantitative data was the degree of variation between institutions for each assay despite the relatively tight correlation of assay results within an institution. This relatively poor degree of interlaboratory precision and accuracy was apparent even though attempts were made to standardize the assays by providing detailed protocols and common reagents. This is the first time that such variation between laboratories has been thoroughly documented and the findings emphasize the need in the field for universal reference standards. The rAAV2 RSM has been deposited with the American Type Culture Collection and is available to the scientific community to calibrate laboratory-specific internal titer standards. Anticipated uses of the rAAV2 RSM are discussed.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20486768&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957240/pdf/hum.2009.223.pdf
dc.subjectBiological Assay
dc.subjectDNA, Viral
dc.subject*Dependovirus
dc.subjectElectrophoresis, Polyacrylamide Gel
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subject*Genetic Vectors
dc.subjectGenome, Viral
dc.subjectHelper Viruses
dc.subjectPolymerase Chain Reaction
dc.subjectReference Standards
dc.subjectTransduction, Genetic
dc.subjectVirus Replication
dc.subjectAllergy and Immunology
dc.subjectGenetics and Genomics
dc.subjectPediatrics
dc.titleCharacterization of a recombinant adeno-associated virus type 2 Reference Standard Material
dc.typeJournal Article
dc.source.journaltitleHuman gene therapy
dc.source.volume21
dc.source.issue10
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1051&amp;context=peds_pulmonary&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/peds_pulmonary/52
dc.identifier.contextkey2441414
refterms.dateFOA2022-08-23T17:00:39Z
html.description.abstract<p>A recombinant adeno-associated virus serotype 2 Reference Standard Material (rAAV2 RSM) has been produced and characterized with the purpose of providing a reference standard for particle titer, vector genome titer, and infectious titer for AAV2 gene transfer vectors. Production and purification of the reference material were carried out by helper virus-free transient transfection and chromatographic purification. The purified bulk material was vialed, confirmed negative for microbial contamination, and then distributed for characterization along with standard assay protocols and assay reagents to 16 laboratories worldwide. Using statistical transformation and modeling of the raw data, mean titers and confidence intervals were determined for capsid particles ({X}, 9.18 x 10(1)(1) particles/ml; 95% confidence interval [CI], 7.89 x 10(1)(1) to 1.05 x 10(1)(2) particles/ml), vector genomes ({X}, 3.28 x 10(1) vector genomes/ml; 95% CI, 2.70 x 10(1) to 4.75 x 10(1) vector genomes/ml), transducing units ({X}, 5.09 x 10 transducing units/ml; 95% CI, 2.00 x 10 to 9.60 x 10 transducing units/ml), and infectious units ({X}, 4.37 x 10 TCID IU/ml; 95% CI, 2.06 x 10 to 9.26 x 10 TCID IU/ml). Further analysis confirmed the identity of the reference material as AAV2 and the purity relative to nonvector proteins as greater than 94%. One obvious trend in the quantitative data was the degree of variation between institutions for each assay despite the relatively tight correlation of assay results within an institution. This relatively poor degree of interlaboratory precision and accuracy was apparent even though attempts were made to standardize the assays by providing detailed protocols and common reagents. This is the first time that such variation between laboratories has been thoroughly documented and the findings emphasize the need in the field for universal reference standards. The rAAV2 RSM has been deposited with the American Type Culture Collection and is available to the scientific community to calibrate laboratory-specific internal titer standards. Anticipated uses of the rAAV2 RSM are discussed.</p>
dc.identifier.submissionpathpeds_pulmonary/52
dc.contributor.departmentDepartment of Pediatrics
dc.contributor.departmentGene Therapy Center
dc.source.pages1273-85


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