Recombinant adeno-associated virus particle purification comprising an affinity purification step

1. A method for obtaining purified recombinant Adeno-Associated Virus (rAAV) particles, comprising the steps of:

a) treating a starting material previously obtained from cells producing rAAV particles with a detergent, said starting material comprising a cell lysate and/or a culture supernatant;

b) performing a depth filtration of said a starting material using a depth filter membrane comprising borosilicate glass microfibers and mixed esters of cellulose, whereby a rAAV-containing clarified composition is provided;

c) submitting the rAAV-containing clarified composition to an immunoaffinity purification step and eluting the rAAV particles at acidic pH, whereby a first rAAV-enriched composition is provided;

d) neutralizing the acidic pH of said first rAAV-enriched composition of step c) to neutral or basic pH;

e) submitting the first rAAV-enriched composition of step d) at least once to:

e1) a step of anion-exchange chromatography on a chromatographic support, wherein elution is performed by using a salt gradient and wherein the rAAV-containing fraction is collected, whereby a second rAAV-enriched composition is provided; or

e2) a step of density gradient centrifugation, wherein the rAAV-containing fraction is collected, whereby a second rAAV-enriched composition is provided;

f) submitting the second rAAV-enriched composition to a step of tangential flow filtration, whereby purified recombinant Adeno-Associated Virus (rAAV) particles are provided,

wherein the method does not comprise an apatite chromatography step or a cation-exchange chromatography step, and

wherein the rAAV particles belong to an AAV serotype selected from the group consisting of AAV4, AAVrh10, AAV2, AAV8, and AAV9.

2. The method according to claim 1 , wherein step c) is performed by using a chromatography support onto which antibodies or fragments thereof directed to said rAAV particles are immobilized.

3. The method according to claim 2 , wherein said antibodies or fragments thereof are monoclonal.

4. The method according to claim 2 , wherein said antibodies or fragments thereof are camelid antibodies or fragments thereof.

5. The method according to claim 1 , wherein at step e1), the chromatographic support is a monolithic chromatographic support.

6. The method according to claim 1 , wherein step f) is performed by using a filter membrane having a molecular weight cut-off value ranging from 20 kDa to 150 kDa.

7. The method according to claim 1 , wherein the rAAV particles belong to the AAV serotype AAV4.

8. The method according to claim 1 , wherein the rAAV particles consist of rAAV4 particles containing DNA comprising an expression cassette encoding human RPE65.

9. The method according to claim 1 , wherein said purified rAAV particles are suitable for use in gene therapy and further comprise a heterologous nucleic acid encoding a gene product.

10. The method according to claim 9 , wherein said heterologous nucleic acid encoding gene product encodes a hormone, a growth receptor, a ligand, a protein, a siRNA, an antisense molecule, a miRNA, or a ribozyme.

11. The method according to claim 1 , wherein the rAAV particles belong to the AAV serotype AAVrh10.

12. The method according to claim 1 , wherein the rAAV particles belong to the AAV serotype AAV2.