Immunoglobulin G (IgG) concentrate depleted of anti-A and anti-B antibodies and of polyreactive IgGs
View Patent ↗The present invention relates to an immunoglobulin G concentrate for therapeutic use, in which the respective contents of anti-A and anti-B antibodies are in accordance with a negative result in the in vitro indirect Coombs test. This IgG concentrate also has a polyreactive IgG content of between 0.01% and 0.1%, in particular between 0.07% and 0.1%, relative to the total content of IgG.
1. A therapeutic concentrate of polyclonal immunoglobulins G (IgG), wherein the respective contents of anti-A and anti-B antibodies conforms to a negative result for the Coombs in vitro indirect test, in particular a content of anti-A antibodies of no more than 23 ng/mg IgG, and a content of anti-B antibodies of no more than 20 ng/mg IgG, and wherein the residual content of polyreactive IgGs of between 0.01% and 0.1% relative to the total IgG content.
2. The therapeutic concentrate according to claim 1 , further containing stabilizers intended to allow the storage of said concentrate.
3. The therapeutic concentrate according to claim 2 , wherein the stabilizers are a mixture of a sugar alcohol, of glycine and of a non-ionic detergent.
4. The therapeutic concentrate according to claim 1 that can be injected via intravenous route.
5. Method to obtain an IgG concentrate according to claim 1 , comprising the steps of:
a) preparing an IgG concentrate from plasma by ethanol fractionation and/or chromatographic separation, associating a viral inactivation step,
b) immunoaffinity chromatography by percolation of said IgG concentrate on a mixture of media whose matrices are grafted with oligosaccharide groups having antigenic similarity with blood groups A and B, and
c) filtration to remove viruses and/or particles of size greater than 20 nm step (d) collecting and concentrating the IgG.
6. Method according to claim 5 , wherein step a) of the method of the invention comprises pre-purification by precipitation of lipid contaminants from said blood plasma or from an IgG-enriched fraction of said blood plasma, single chromatography on an anion exchange resin conducted at alkaline pH and selective elution of the IgGs in one step using a suitable buffer of pH between 4 and 7.
7. Method according to claim 5 or 6 , wherein the oligosaccharide groups having antigenic similarity with blood groups A and B are trisaccharides corresponding to epitopes of blood groups A and B.
8. Method according to claim 7 , wherein the trisaccharides corresponding to the epitope of blood group A have the structure N-acetyl-galactosamine (GalNAc)—Galactose (Gal)—Fucose (Fuc), and those corresponding to the epitope of blood group B have the structure Galactose-Galactose-Fucose.
9. Method according to claims 5 to 8 , wherein the viral inactivation step is conducted with a solvent-detergent.
10. Method according to claims 5 to 9 , comprising the steps of concentration by ultrafiltration, and sterilizing filtration.
11. Method according to claims 5 - 9 and 10 , wherein filtration to remove viruses is conducted by nanofiltration.
12. Method according to claims 5 - 9 and 10 which, after step c) comprises a step to add stabilizers for the storage of said IgG concentrate.