Affinity chromatography matrix
The invention relates to an affinity chromatography matrix, as a gel, comprising polymeric particles on which at least one oligosaccharide corresponding to a blood group A epitope and/or blood group B is grafted, via a spacer, characterized in that the density of oligosaccharides is comprised between 0.2 and 0.7 mg/ml of matrix. The invention also relates to the uses of this matrix for preparing concentrates of immunoglobulins for therapeutic use.
1. An affinity chromatography matrix, in form of a gel, comprising polymeric particles on which at least one oligosaccharide corresponding to a blood group A and/or group B epitope is grafted via a spacer, wherein:
the density of oligosaccharides is from about 0.3 to about 0.4 mg/ml of the matrix and
said spacer has a formula provided by
NH—R1-CO—NH—R2- (I),
wherein R1 is a C 5 alkyl group, R2 is a C 3 alkyl group, and said spacer is bound through its amine function to the particle.
2. The matrix according to claim 1 , comprising (i) polymeric particles on which at least one oligosaccharide corresponding to a blood group A epitope is grafted, and/or (ii) polymeric particles on which at least one oligosaccharide corresponding to a blood group B epitope is grafted.
3. The matrix according to claim 2 , comprising (i) polymeric particles on which at least one oligosaccharide corresponding to a blood group A epitope is grafted, and (ii) polymeric particles on which at least one oligosaccharide corresponding to a blood group B epitope is grafted.
4. The matrix according to claim 1 , comprising polymeric particles on which both at least one oligosaccharide corresponding to a blood group A epitope and at least one oligosaccharide corresponding to a blood group B epitope, are grafted.
5. The matrix according to claim 1 , comprising a mixture of (i) polymeric particles on which at least one oligosaccharide corresponding to a blood group A epitope is grafted, (ii) polymeric particles on which at least one oligosaccharide corresponding to a blood group B epitope is grafted, and (iii) polymeric particles on which both at least one oligosaccharide corresponding to a blood group A epitope, and at least one oligosaccharide corresponding to a blood group B epitope, are grafted.
6. The matrix according to claim 1 , wherein the oligosaccharide corresponding to a blood group A epitope and/or the oligosaccharide corresponding to a blood group B epitope is a trisaccharide.
7. The matrix according to claim 6 , wherein the oligosaccharide corresponding to a blood group A epitope is a trisaccharide N-acetylgalactosamine (GalNAc)-Galactose (Gal)-Fucose.
8. The matrix according to claim 6 , wherein the oligosaccharide corresponding to a blood group B epitope is an oligosaccharide Galactose-Galactose-Fucose.
9. The matrix according to claim 3 , wherein the polymeric particles on which at least one oligosaccharide corresponding to a blood group A epitope is grafted, and the polymeric particles on which at least one oligosaccharide corresponding to a blood group B epitope is grafted, are mixed in a proportion of 25/75 to 75/25 (v/v), preferably about 50/50 (v/v).
10. The matrix according to claim 1 , wherein the polymer is a cross-linked polymer.
11. The matrix according to claim 10 , wherein the polymer is cellulose.
12. A method of using the matrix as defined in claim 1 , in an affinity chromatography binding anti-A and/or anti-B antibodies.
13. The method of using the matrix according to claim 12 , for producing on an industrial scale immunoglobulins G (IgG) for therapeutic use.
14. A process for preparing a concentrate of immunoglobulins G (IgG) for therapeutic use, comprising obtaining an Ig composition from blood plasma, by ethanol fractionation and/or caprylic fractionation and/or chromatographic separation, and subjecting the Ig composition to affinity chromatography using the matrix of claim 1 to remove the anti-A and/or anti-B antibodies from the Ig composition.
15. The matrix according to claim 1 , wherein the density of oligosaccharides is about 0.3 mg/ml of matrix.
16. The matrix according to claim 11 , wherein the particles are porous, cross-linked cellulose beads.
17. An affinity chromatography matrix, in form of a gel, comprising polymeric particles on which at least one oligosaccharide corresponding to a blood group A and/or group B epitope is grafted via a spacer, wherein:
the at least one oligosaccharide is a trisaccharide;
the density of oligosaccharides is from about 0.3 to about 0.4 mg/ml of the matrix;
said spacer has a formula provided by
NH—R1-CO—NH—R2- (I),
wherein R1 is a C 5 alkyl group, R2 is a C 3 alkyl group, and said spacer is bound through its amine function to the particle; and
the particles are porous cross-linked cellulose beads.