Methods to produce a human plasma-derived IgG preparation enriched in brain disease-related natural IgGs
View Patent ↗The present invention provides, among other aspects, methods for the manufacture of plasma-derived immunoglobulin G compositions highly enriched for anti-brain disease related protein antibodies (e.g., anti-Aβ, anti-RAGE, and anti-α-synuclein antibodies). Advantageously, the methods provided do not affect the manufacturing processes or capabilities for producing plasma-derived IgG therapeutics. Plasma-derived IgG compositions that are highly enriched for anti-brain disease related protein antibodies (e.g., anti-Aβ, anti-RAGE, and anti-α-synuclein antibodies), as also provided here. Methods for the treatment of brain diseases and disorders by administration of plasma-derived IgG compositions highly enriched for anti-brain disease related protein antibodies (e.g., anti-Aβ, anti-RAGE, and anti-α-synuclein antibodies), are also provided.
1. A method for preparing an immunoglobulin preparation enriched in brain disease-related immunoglobulins, the method comprising the steps:
(A) binding a plasma-derived immunoglobulin composition comprising IgG immunoglobulins to a first cation exchange material, wherein a first percentage of the IgG immunoglobulins in the plasma-derived immunoglobulin composition are specific to a brain disease-related protein;
(B) eluting at least 90% of the bound IgG immunoglobulins from the first cation exchange material, in a first cation exchange elution step, using a first cation exchange elution buffer having a pH of 4.0 to 10.0 and a conductivity of 3.0 mS/cm to 16.0 mS/cm, thereby forming a first cation exchange eluate; and
(C) eluting IgG immunoglobulins remaining bound to the first cation exchange material, in a second cation exchange elution step, using a second cation exchange elution buffer having a pH of 4.0 to 10.0 and a conductivity of 100±80 mS/cm, thereby forming a second cation exchange eluate comprising IgG immunoglobulins, wherein a second percentage of the IgG immunoglobulins in the second cation exchange eluate are specific to the brain disease-related protein, wherein the second percentage is greater than the first percentage, and
wherein the brain disease-related protein is selected from the group consisting of amyloid beta (Aβ), alpha-synuclein (SNCA), major prion protein (PrP), huntingtin (HD), prolactin (PRL), beta 2 microglobulin (β2M), cystatin C (CST3), advanced glycosylation end product-specific receptor (RAGE), microtubule-associated protein tau (tau), and ubiquitin (UBB; UBC).
2. The method of claim 1 , wherein at least 95% of the bound immunoglobulins are eluted from the first cation exchange material in step (B).
3. The method of claim 1 , wherein the immunoglobulin specific to a brain disease-related protein is selected from the group consisting of major prion protein (PrP), huntingtin (HD), prolactin (PRL), beta 2 microglobulin (β2M), microtubule-associated protein tau (tau), ubiquitin (UBB; UBC), and cystatin C (CST3).
4. The method of claim 1 , wherein the plasma-derived immunoglobulin composition bound to the first cation exchange material in step (A) has a higher titer of an anti-amyloid beta (anti-Aβ) immunoglobulin, an anti-RAGE immunoglobulin, an anti-α-synuclein immunoglobulin, or another immunoglobulin specific to a brain disease-related protein, as compared to the titer of a plasma-derived immunoglobulin composition prepared from a plasma pool containing plasma from 1,000 random donors.
5. The method of claim 1 , wherein the immunoglobulin specific to a brain disease-related protein is an anti-amyloid beta (anti-Aβ) immunoglobulin.
6. The method of claim 1 , wherein the immunoglobulin specific to a brain disease-related protein is an anti-RAGE immunoglobulin.
7. The method of claim 1 , wherein the immunoglobulin specific to a brain disease-related protein is an anti-α-synuclein immunoglobulin.
8. The method of claim 1 , wherein the first cation exchange material is a weak cation exchange material.
9. The method of claim 1 , wherein the first cation exchange material is a carboxymethyl cation exchange resin.
10. The method of claim 1 , wherein the first cation exchange elution buffer has a pH of 7.0 to 9.5.
11. The method of claim 1 , wherein the first cation exchange elution buffer has a pH of 8.0 to 9.0.
12. The method of claim 1 , wherein the first cation exchange elution buffer has a conductivity of 4.0 mS/cm to 15.0 mS/cm.
13. The method of claim 1 , wherein the first cation exchange elution buffer has a conductivity of 5.0 mS/cm to 8.0 mS/cm.
14. The method of claim 1 , wherein the first cation exchange elution buffer has a pH of 8.5±0.2 and a conductivity of 5.0±1 mS/cm.
15. The method of claim 1 , wherein the second cation exchange elution buffer has a pH of 7.0 to 9.5.
16. The method of claim 1 , wherein the second cation exchange elution buffer has a pH of 8.0 to 9.0.
17. The method of claim 1 , wherein the second cation exchange elution buffer has a conductivity of 80 mS/cm to 150 mS/cm.
18. The method of claim 1 , wherein the second cation exchange elution buffer has a conductivity of 80 mS/cm to 120 mS/cm.
19. The method of claim 1 , wherein the plasma-derived immunoglobulin composition bound to the first cation exchange material in step (A) is prepared by a method that includes an alcohol precipitation step.
20. The method of claim 19 , wherein the alcohol precipitation step includes formation of precipitate selected from the group consisting of a Fraction I precipitate, a Cohn Fraction II precipitate, a Cohn Fraction II+III precipitate, a Cohn Fraction I+II+III precipitate, a precipitate G, a Kistler-Nitschmann precipitate A, and a Kistler-Nitschmann gamma-globulin precipitate.
21. The method of claim 1 , wherein the plasma-derived immunoglobulin composition bound to the first cation exchange material in step (A) is a suspended precipitate G.
22. The method of claim 1 , wherein the plasma-derived immunoglobulin composition bound to the first cation exchange material in step (A) is a plasma fraction that has been enriched by at least one prior chromatographic step.
23. The method of claim 22 , wherein the at least one prior chromatographic step is an anion exchange chromatographic step.
24. The method of claim 1 , further comprising enrichment of immunoglobulin G in the second cation exchange eluate.
25. The method of claim 24 , wherein the enrichment of immunoglobulin G in the second cation exchange eluate includes cation exchange chromatography.
26. The method of claim 25 , wherein the enrichment of immunoglobulin G in the second cation exchange eluate includes steps:
(G) binding immunoglobulin G from the second cation exchange eluate to a second cation exchange material under solution conditions comprising a pH of 4.0 to 10.0 and a conductivity of 1 to 15 mS/cm;
(H) eluting bound immunoglobulin G from the cation exchange material, in a third cation exchange elution step, using a third cation exchange elution buffer having a pH of 4.0 to 10.0 and a conductivity of 15.0 mS/cm to 300 mS/cm; and
(I) recovering a third cation exchange eluate, the third cation exchange eluate enriched in the immunoglobulin specific to a brain disease-related protein.
27. The method of claim 26 , wherein the second cation exchange material is a weak cation exchange resin.
28. The method of claim 26 , wherein the second cation exchange material is a carboxymethyl cation exchange resin.
29. The method of claim 24 , wherein the enrichment of immunoglobulin G in the second cation exchange eluate includes steps:
(J) applying immunoglobulin G to an anion exchange column, in an anion exchange flow through step, under solution conditions comprising a pH of 5.0 to 8.0 and a conductivity of 0.5 mS/cm to 5.0 mS/cm; and
(K) recovering a flow-through fraction from anion exchange flow-through step (J), the flow-through fraction enriched in the immunoglobulin specific to a brain disease-related protein.
30. The method of claim 29 , wherein the solution conditions used in step (J) include a pH of 6.2 to 6.6.
31. The method of claim 1 , further comprising a step:
(L) reducing the viral load of the composition by nanofiltration.
32. A method for preparing an immunoglobulin preparation enriched in brain disease-related immunoglobulins, the method comprising admixing a first immunoglobulin composition prepared by a method according to claim 1 with a second immunoglobulin preparation that is not enriched in brain disease-related immunoglobulin.
33. A method for preparing an immunoglobulin preparation enriched in brain disease-related immunoglobulins, the method comprising the steps:
(A) binding a plasma-derived immunoglobulin composition comprising IgG immunoglobulins to a first cation exchange material, wherein a first percentage of the IgG immunoglobulins in the plasma-derived immunoglobulin composition are specific to a brain disease-related protein;
(B) eluting at least 90% of the bound IgG immunoglobulins from the first cation exchange material, in a first cation exchange elution step, using a first cation exchange elution buffer having a pH of 4.0 to 10.0 and a conductivity of 3.0 mS/cm to 16.0 mS/cm, thereby forming a first cation exchange eluate; and
(C) eluting IgG immunoglobulins remaining bound to the cation exchange material, in a second cation exchange elution step, using a second cation exchange elution buffer having a pH of 4.0 to 10.0 and a conductivity of 80.0 mS/cm to 120.0 mS/cm, thereby forming a second cation exchange eluate comprising IgG immunoglobulins, wherein a second percentage of the IgG immunoglobulins in the second cation exchange eluate are specific to the brain disease-related protein, wherein the second percentage is greater than the first percentage, and
wherein the brain disease-related protein is selected from the group consisting of amyloid beta (Aβ), alpha-synuclein (SNCA), major prion protein (PrP), huntingtin (HD), prolactin (PRL), beta 2 microglobulin (β2M), cystatin C (CST3), advanced glycosylation end product-specific receptor (RAGE), microtubule-associated protein tau (tau), and ubiquitin (UBB; UBC).