Characterization of a recombinant adeno-associated virus type 2 Reference Standard Material

M Lock, S McGorray, A Auricchio, E Ayuso… - 2010 - liebertpub.com
M Lock, S McGorray, A Auricchio, E Ayuso, EJ Beecham, V Blouin-Tavel, F Bosch, M Bose…
2010liebertpub.com
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 …
Abstract
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× 10 11 particles/ml; 95% confidence interval [CI], 7.89× 10 11 to 1.05× 10 12 particles/ml), vector genomes ({X}, 3.28× 10 10 vector genomes/ml; 95% CI, 2.70× 10 10 to 4.75× 10 10 vector genomes/ml), transducing units ({X}, 5.09× 10 8 transducing units/ml; 95% CI, 2.00× 10 8 to 9.60× 10 8 transducing units/ml), and infectious units ({X}, 4.37× 10 9 TCID 50 IU/ml; 95% CI, 2.06× 10 9 to 9.26× 10 9 TCID 50 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.
Mary Ann Liebert