IP Library Patent Application 17579281
Patent Application
App. No. 17/579,281

METHODS FOR PRODUCING PREPARATIONS OF RECOMBINANT AAV VIRIONS SUBSTANTIALLY FREE OF EMPTY CAPSIDS

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Patent No.
US None
App. No.
17/579,281
Abstract

Methods for separating AAV empty capsids from mixtures of AAV vector particles and AAV empty capsids are described. The methods use column chromatography techniques and provide for commercially viable levels of recombinant AAV virions.

Claims (69)

1 : A method for purifying AAV vector particles from an AAV preparation comprising AAV vector particles and AAV empty capsids, to provide an AAV product substantially free of AAV empty capsids, said method comprising:

(a) providing a host cell comprising AAV vector particles;

(b) lysing said host cell to obtain a crude cell lysate comprising AAV vector particles and AAV empty capsids;

(c) applying said crude cell lysate to a first cation exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(d) eluting said AAV vector particles and said AAV empty capsids under non-separating conditions to provide an AAV preparation comprising AAV vector particles and AAV empty capsids;

(e) applying the AAV preparation from (d) to a second cation exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(f) adding a low salt buffer to the column from (e) under conditions whereby AAV vector particles are eluted and AAV empty capsids remain bound to the column; and

(g) collecting eluted fractions from (f) that comprise AAV vector particles to provide an AAV product substantially free of AAV empty capsids.

2 : The method of claim 1 , wherein said first cation exchange column comprises a carboxymethylated or sulfonated matrix.

3 : The method of claim 2 , wherein said matrix comprises the functional ligand R—SO 3 —.

4 : The method of claim 1 , wherein said second cation exchange column comprises a carboxymethylated or sulfonated matrix.

5 : The method of claim 4 , wherein said matrix comprises the functional ligand R—SO 3 —.

6 : The method of claim 1 , wherein AAV vector particles are present in said AAV product in an amount of: (a) at least 75%, (b) at least 85%, or (c) at least 90%.

7 - 8 . (canceled)

9 : The method of claim 1 , wherein said AAV vector particles are derived from AAV-2 or AAV5.

10 . (canceled)

11 : The method of claim 1 , further comprising:

(h) applying the fractions from step (g) to an anion exchange chromatography column under conditions whereby said AAV vector particles and AAV empty capsids, if present, bind the column;

(i) adding a low salt buffer to the column from (h) under conditions whereby AAV empty capsids are eluted and AAV vector particles remain bound to the column;

(j) adding a high salt buffer to the column from (i) under conditions whereby AAV vector particles are eluted;

(k) collecting fractions from (j) that comprise AAV vector particles to provide an AAV product substantially free of AAV empty capsids.

12 : A method for purifying AAV vector particles from an AAV preparation comprising AAV vector particles and AAV empty capsids, to provide an AAV product substantially free of AAV empty capsids, said method comprising:

(a) providing a host cell comprising AAV vector particles;

(b) lysing said host cell to obtain a crude cell lysate comprising AAV vector particles and AAV empty capsids;

(c) clarifying said crude cell lysate to provide a clarified cell lysate;

(d) applying said clarified cell lysate to a first cation exchange chromatography column comprising a matrix with the functional ligand R—SO 3 —, under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(e) eluting said AAV vector particles and said AAV empty capsids under non-separating conditions to provide an AAV preparation comprising AAV vector particles and AAV empty capsids;

(f) applying the AAV preparation from (e) to a second cation exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(g) adding a low salt buffer to the column from (f) under conditions whereby AAV vector particles are eluted and AAV empty capsids remain bound to the column;

(h) collecting eluted fractions from (g) that comprise AAV vector particles;

(i) applying the fractions from step (h) to an anion exchange chromatography column under conditions whereby said AAV vector particles and AAV empty capsids, if present, bind the column;

j) adding a low salt buffer to the column from (i) under conditions whereby AAV empty capsids are eluted and AAV vector particles remain bound to the column;

(k) adding a high salt buffer to the column from (j) under conditions whereby AAV vector particles are eluted; and

(l) collecting eluted fractions from (k) that comprise AAV vector particles to provide an AAV product substantially free of AAV empty capsids.

13 : The method of claim 12 , wherein AAV vector particles are present in said AAV product in an amount of: (a) at least 75%, (b) at least 85%, or (c) at least 90%.

14 - 15 . (canceled)

16 : The method of claim 12 , wherein said AAV vector particles are derived from AAV-2 or AAV5.

17 . (canceled)

18 : A method for purifying AAV vector particles from an AAV preparation comprising AAV vector particles and AAV empty capsids, to provide an AAV product substantially free of AAV empty capsids, said method comprising:

(a) providing a host cell comprising AAV vector particles;

(b) lysing said host cell to obtain a crude cell lysate comprising AAV vector particles and AAV empty capsids;

(c) applying said crude cell lysate to a cation exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(d) eluting said AAV vector particles and said AAV empty capsids under non-separating conditions to provide an AAV preparation comprising AAV vector particles and AAV empty capsids;

(e) applying the AAV preparation from (d) to an anion exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(f) adding a low salt buffer to the column from (e) under conditions whereby AAV empty capsids are eluted and AAV vector particles remain bound to the column;

(g) adding a high salt buffer to the column from (f) under conditions whereby AAV vector particles are eluted;

(h) collecting eluted fractions from (g) that comprise AAV vector particles to provide an AAV product substantially free of AAV empty capsids.

19 : The method of claim 18 , further comprising:

(i) applying the AAV preparation from (h) to a second anion exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids, if present, bind the column;

(j) adding a low salt buffer to the column from (i) under conditions whereby AAV empty capsids are eluted and AAV vector particles remain bound to the column;

(k) adding a high salt buffer to the column from (j) under conditions whereby AAV vector particles are eluted;

(l) collecting eluted fractions from (k) that comprise AAV vector particles to provide an AAV product substantially free of AAV empty capsids.

20 : The method of claim 18 , further comprising:

(i) applying the AAV preparation from (h) to a second cation exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(j) adding a low salt buffer to the column from (i) under conditions whereby AAV vector particles are eluted and AAV empty capsids remain bound to the column; and

(k) collecting eluted fractions from (j) that comprise AAV vector particles to provide an AAV product substantially free of AAV empty capsids.

21 : The method of claim 18 , wherein AAV vector particles are present in said AAV product in an amount of: (a) a least 75%, (b) at least 85%, or (c) at least 90%.

22 - 23 . (canceled)

24 : The method of claim 18 , wherein said AAV vector particles are derived from AAV-2 or AAV5.

25 . (canceled)

26 : A method for purifying AAV vector particles from an AAV preparation comprising AAV vector particles and AAV empty capsids, to provide an AAV product substantially free of AAV empty capsids, said method comprising:

(a) applying an AAV preparation comprising AAV vector particles and AAV empty capsids to a cation exchange chromatography column under conditions whereby said AAV vector particles and said AAV empty capsids bind the column;

(b) adding a salt buffer to the column from (a) under conditions whereby AAV vector particles are eluted and AAV empty capsids remain bound to the column; and

(c) collecting eluted fractions from (b) that comprises AAV vector particles to provide an AAV product substantially free of AAV empty capsids.

27 : The method of claim 26 , further comprising:

(d) applying the fractions from step (c) to an anion exchange chromatography column under conditions whereby said AAV vector particles and AAV emptied capsids, if present, bind the column;

(e) adding a salt buffer to the column from (d) under conditions whereby AAV empty capsids are eluted and AAV vector particles remain bound to the column;

(f) adding a buffer with a greater salt concentration relative to the buffer added in (e) to the column from (e) under conditions whereby AAV vector particles are eluted;

(g) collecting fractions from (f) that comprise AAV vector particles to provide and AAV product substantially free of AAV empty capsids.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2022
From: QU, GUANG; WRIGHT, JOHN FRASER
To: AVIGEN, INC.
Reel/Frame 059260/0493 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2022
From: AVIGEN, INC.
To: GENZYME CORPORATION
Reel/Frame 059260/0501 →