WO2007077365A2 - CONCENTRE D’IMMUNOGLOBULINES G (IgG) APPAUVRI EN ANTICORPS ANTI-A ET ANTI-B, ET EN IgG POLYREACTIVES - Google Patents
CONCENTRE D’IMMUNOGLOBULINES G (IgG) APPAUVRI EN ANTICORPS ANTI-A ET ANTI-B, ET EN IgG POLYREACTIVES Download PDFInfo
- Publication number
- WO2007077365A2 WO2007077365A2 PCT/FR2006/002889 FR2006002889W WO2007077365A2 WO 2007077365 A2 WO2007077365 A2 WO 2007077365A2 FR 2006002889 W FR2006002889 W FR 2006002889W WO 2007077365 A2 WO2007077365 A2 WO 2007077365A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- igg
- concentrate
- antibodies
- red blood
- blood cells
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/14—Extraction; Separation; Purification
- C07K1/36—Extraction; Separation; Purification by a combination of two or more processes of different types
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/34—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against blood group antigens
Definitions
- IgG immunoglobulin G
- the present invention relates to an immunoglobulin G (IgG) concentrate depleted of anti-A antibodies.
- IgG immunoglobulin G
- immunoglobulin (Ig) enriched human plasma fractions for the treatment of various congenital infections or deficits has been known since the development of the Cohn ethanol precipitation method (Cohn et al., 1946, J. Am. Chem Soc 68, 459, Uncley et al 1949, J. Am Chem Soc 71, 541). There is, for this purpose, a growing need to produce highly purified, intravenously injectable Ig (IgIV) concentrates from, for example, human plasma.
- IgIV intravenously injectable Ig
- Processes for obtaining immunoglobulins and in particular IgG concentrates may comprise, besides the selective precipitation of the proteins by ethanol, various additional treatments such as precipitation by the
- UPE8P nv. f ⁇ i ⁇ rn ⁇ AT polyethylene glycol the treatment provided by proteolytic enzymes ..., intended to eliminate aggregates of immunoglobulin polymers capable of activating the complement system with associated risks of anaphylactic reactions.
- the presence of dimers in IgGIV has been correlated with falls in blood pressure in vivo (Bleeker WK et al, Blood, 95, 2000, pp. 1856-1861).
- Buchta C. et al, cited above, has considered different approaches to significantly reduce anti-A antibodies, from blood group donors B and O, and anti-B, from A and O blood group donors. in plasma derivatives, such as IgG, to thereby minimize the risk of hemolysis, directly correlated to the levels of these antibodies, during the treatment of patients with these plasma derivatives.
- plasma derivatives such as IgG
- Some approaches are considered unrealistic because of the costs or the complexity of the measures to be taken. It is noted that the anti-A and anti-B antibodies are partially removed during the ethanolic fractionation mentioned above.
- ICT Intracoombs test application.
- the ICT test consists in adding to a suspension of red cells, coated with the anti-A or anti-B antibodies of IgG type contained in the IgG concentrates, a solution of antibodies (antiglobulins) directed against motifs of the Human IgG. These antibodies bind to anti-A or anti-B antibodies attached to red blood cells and thus allow their agglutination by bridging between IgGs.
- the test for anti-A or anti-B antibody is directly inspired by this classic test in haematological serology (Coombs test).
- IVIG must not present agglutination of A or B red blood cells in the 1:64 dilution ICT assay performed with an initial concentration IgG solution of 30 g / l. This is why the IgG samples to be tested should be diluted to obtain a titre, ie the value of the last dilution which no longer causes agglutination.
- Negative ICT test results on IgIV solutions with dilutions lower than the 1:64 dilution, according to the European Pharmacopoeia demonstrate a low level of anti-A and anti-B accepted by it.
- the anti-A and anti-B antibodies are partially removed during the preparation of IgG concentrates by ethanolic fractionation but a residual content which may be higher than the limit of the high standards of the
- the concentrates prepared according to the process developed by the Applicant and described in his patent application WO 02/092632 contain more than those obtained by fractionation with ethanol. Further purification of the IgG concentrates thus obtained against AcaA and AcaB is therefore necessary, since some batches of IgG concentrates may have levels above the threshold allowed by the European Pharmacopoeia for each of them. between them.
- One of the techniques for removing them from IgG concentrates consists in carrying out a purification by affinity chromatography using as support oligosaccharide immunosorbants similar to the antigens A and B of blood groups, such oligosaccharides particularly representing trisaccharides, grafted on a chromatographic matrix.
- the patent application WO 01/27623 describes a process for obtaining a despecified plasma of antibodies of blood groups A and B, that is to say a plasma suitable for any recipient. These specificities are essentially carried by immunoglobulins M (IgM). The despecification is obtained by passing on an experimental affinity support for group A and then on another affinity support, also experimental, for group B. In case of simultaneous presence of anti-A and anti-B (group 0), the successive passage on the two supports is necessary.
- IgM immunoglobulins M
- IgG polyreactivity
- polyclonal antibodies such as IgG are normally combined with a single epitope (antigenic pattern) uniquely. However, this strict specificity of the antibodies may sometimes be broadened to other antigenic motifs and have affinity for secondary epitopes with a weaker binding than for the nominal motif.
- Polyclonal IgG may react more or less strongly with structures such as actin, myosin, trinitrophenyl-modified albumin.
- IVIg intravenous immunoglobulins
- the polyréactive activity of the antibodies present in an IVIG preparation may be due to: the presence of natural antibodies contained in each individual plasma,
- IgG concentrates can therefore be explained by the presence of natural and polyreventive IgG conjugates obtained by the usual purification processes, and represent, depending on the case, 0.5 to 1% of all the polyvalent IgGs.
- Treatment of patients with IgG preparations may require high doses of up to 1-2 g / kg. These dosages lead to treatment in a short time, for example in one day, by amounts 7 to 10 times higher than those of the physiological IgG of the recipient. Therefore, this level of poly-active IgG generated by the manufacturing process in IgG concentrates is likely to cause undesirable side effects, such as fevers, nausea or headache.
- IgG concentrates for therapeutic use in particular for intravenous injection, significantly reduced in anti-A and anti-B antibodies and which are preferably polyréactivity generated by the process of manufacture very reduced compared to the concentrates of IgG currently commercially available, while having an efficacy at least identical in terms of immunotherapy.
- the invention relates to a concentrate of immunoglobulin G for therapeutic use, characterized in that it has respective levels of anti-A and anti-B antibodies consistent with a negative result in the indirect Coombs test in vitro.
- the invention also relates to a process for the manufacture of immunoglobulins G making it possible not to generate these polyréactive antibodies which may be less well tolerated than the natural and anti-idiotypic antibodies.
- the IVIG obtained by the method have a lower polyréactivity than the other IVIG studied.
- the IgGs of these concentrates advantageously represent polyclonal IgG obtained from blood plasma or from a fraction of blood plasma already enriched with IgG.
- IgG concentrates for therapeutic use are at commonly used IgG concentrations, preferably between 50 and 100 g / l. These concentrates are intended for clinical use and may in particular be injected intravenous. For this purpose, they must be virally secure and, where appropriate, contain excipients, such as stabilizers, compatible with this clinical use.
- the Applicant has found that it is possible to provide such IgG concentrates having levels of anti-A and anti-B antibodies significantly lower than those observed in standard IgG concentrates, that is, to those obtained by ethanolic fractionation and / or by the implementation of purification techniques associating chromatographies, as mentioned above, and which have not been the subject of a complementary treatment of elimination of the considered antibodies. Also, their levels are well below the thresholds accepted by the European Pharmacopoeia, which very significantly limits the risk of hemolysis in some recipients in treatment.
- the ICT test can no longer apply, especially under the conditions of the European Pharmacopoeia, since the reactions of Agglutination of red blood cells no longer occur, even with the addition of anti-human IgG antibodies, since the density of anti-A and anti-B antibodies is too low for the establishment of bridges between the red blood cells by anti-A and anti-B antibody bonds fixed on red blood cells and anti-human IgG antibodies.
- the IgG concentrate of the invention comprises an anti-A antibody content of not more than 23 ng / mg IgG, in particular between 19 and 23 ng / mg IgG. and an anti-B antibody content of not more than 20 ng / mg IgG, in particular between 12 and 20 ng / mg IgG.
- the content of residual polytractive IgG is between 0.01% and 0.1%, in particular between 0.07 and 0.1%.
- the content of polyriactive IgG means a molar or mass percentage.
- the IgG concentrates according to the invention are therefore defined by a notable absence of the active principles anti-A and anti-B antibodies which are directed against the epitopes present on red blood cells.
- the IgG concentrates may be in liquid or freeze-dried form in the presence of suitable stabilizers, and stored pending further use.
- stabilizers advantageously represent those developed by the Applicant in his patent application WO 2004/091656 A2, namely a mixture of an alcoholic sugar, preferably mannitol, sorbitol or their isomers, of glycine and a detergent. nonionic, such as Tween "80, Tween" 20, Triton ® X
- the concentrations of the formulation were determined by the Applicant to stabilize the liquid and / or lyophilized forms.
- the final concentrations in the mannitol concentrates are between 30 g / l and 50 g / l, those of the detergent, between 20 and 50 ppm, and those of glycine, between 7 g / l and 10 g / l.
- the concentrations of these compounds represent the final concentrations in the IgG concentrates.
- IgG concentrates for therapeutic use, can in particular be injected intravenously, as indicated above.
- the IgG concentrates according to the invention must be virally secure for example by a conventional solvent-detergent treatment known in the prior art, using for example a mixture Tween "80 / TnBP or Triton ® X 100 / TnBP, and / or undergo filtration steps to possibly eliminate viruses and / or other macromolecules that would not have been removed by virucidal solvent-detergent treatment, such as the prion, agent responsible for transmissible spongiform encephalopathies.
- the invention also relates to a process for obtaining an IgG concentrate as mentioned above, comprising the following steps of: a) preparation of an IgG concentrate by ethanolic fractionation and / or by chromatographic separation, associating a viral inactivation step, b) immunoaffinity chromatography by percolation of said IgG concentrate on a mixture of supports whose matrices are grafted with oligosaccharide groups antigenically similar to blood groups A and B, and c) elimination filtration. viruses and / or particles larger than 20 nm.
- an IgG concentrate according to the invention for therapeutic use, further comprising, preferably, a level of polyregative IgG of less than 0.1% based on the total IgG content.
- such a concentrate comprises a rate of AcaA and unwanted AcaB well below the low limit value of the test described in the European Pharmacopoeia and even giving a negative result by the implementation of the ICT test with such undiluted samples. .
- step a) of the process may in itself be a process for obtaining IgG concentrates, such as those mentioned above. It is an ethanol fractionation developed by Cohn et al or a chromatographic separation, as described for example in EP 0 703 922 and WO 99/64462. Particularly preferred are the methods developed by the Applicant in patent applications WO 94/29334 and WO 02/092632 A1, and most particularly that described in WO 02/092632 A1.
- step a) of method of the invention comprises pre-purification by precipitation of lipid contaminants from a blood plasma or an IgG-enriched blood plasma fraction, a single chromatography on an anion exchange resin carrier carried out at alkaline pH, an Selective elution of IgG in one step by an appropriate buffer at pH of between 4 and 7.
- Step a) of the method comprises a viral inactivation treatment, preferably carried out by solvent-detergent, as described by Horowitz in US Pat. US 4,764,369. It will in particular be judiciously implemented, if necessary, before one or the subsequent chromatrographic step to eliminate in particular the chemical residues of this treatment.
- the IgG fraction thus harvested is already sufficiently concentrated, and can then undergo additional concentration steps by ultrafiltration and sterilizing filtration.
- the chromatographic support consists of a cross-linked natural polymer matrix, of the agarose type, on which grafts or coupling arms are grafted, in turn being grafted, with oligosaccharides advantageously representing trisaccharides corresponding to the epitopes of the blood groups A and B.
- Such a support is very advantageously a gel or resin commercially available under the name GLYCOSORB ABO, obtained from Glycorex Transplantation AS (Sweden).
- the trisaccharide corresponding to the blood group A epitope has the structure below:
- GaINAc N-acetylgalactosamine
- GaI Galactose
- Fucose Fucose
- the trisaccharide corresponding to the blood group B epitope has the following structure:
- the mixture of grafted supports of antigenically similar groups similar to blood group A and blood group B is in a respective proportion of between 25/75 and 75/25 (v / v). It is indeed possible to adjust the proportion of the two supports in the column to the population of donors according to the distribution of blood groups thereof.
- the column will preferably be filled with a 50/50 (v / v) mixture in each specific carrier above. Analytical columns of 15 to 25 cm in length and 0.5 to 1 cm in diameter may be used. In the case of a pilot scale implementation, columns 40 to 60 cm in length and 40 to 60 mm in diameter may be used. In this case, it is possible to load the 600 ml column of immunoaffinity support.
- Such a carrier is stored in 1 M NaOH between two cycles of use. Before use, it is washed with water.
- the immunoaffinity chromatographic column is then charged with IgG concentrate preferably at a rate of from 0.2 to 4 liters, in particular from 1 to 2 liters, per milliliter of support.
- IgG concentrate preferably at a rate of from 0.2 to 4 liters, in particular from 1 to 2 liters, per milliliter of support.
- the specificity of such a support does not require prior conditioning of the IgG fraction, that is to say that any fraction or concentrate of IgG obtained by plasma fractionation techniques of the prior art may be suitable.
- Percolation of the concentrate does not involve the elution mechanism. Therefore, regardless of how the IgG concentrate is obtained, it is drilled through the column, possibly through a pump. This percolation allows the retention of AcaA and AcaB and poly-active IgG.
- the column is then washed with water to recover IgG still present in the dead volume of the column.
- an IgG fraction depleted in AcaA and AcaB is obtained, as well as in polyreventive IgG resulting from the manufacturing process. Indeed, the AcaA and AcaB are retained on their antigenic pattern of the chromatographic support which modifies the conformation.
- the method may comprise, after step b), concentration steps by ultrafiltration and sterilizing filtration.
- the chromatographic column and the support are then washed with an acidic solution, such as glycine-HCl, pH 2, 8, for the desorption of the AcaA and AcaB retained on the support.
- an acidic solution such as glycine-HCl, pH 2, 8, for the desorption of the AcaA and AcaB retained on the support.
- This support is then rinsed with water and treated with a 1M NaOH solution.
- the highly depleted IgG concentrate of polyacrylic AcaA, AcaB and IgG is then subjected to a virus removal filtration resistant to solvent - detergent treatment and / or other size - sensitive particles.
- a virus removal filtration resistant to solvent - detergent treatment and / or other size - sensitive particles greater than 20 nm, such as prions, IgG polymers generated during steps of its manufacture, lipopolysaccharides in micelles, nucleic acids and aggregated proteins.
- Such a treatment advantageously represents nanofiltration, implemented by decreasing porosity filters of 100 to 15 nm, in particular on three filters arranged in series and decreasing retention thresholds of 100, 50 and 20 nm.
- the method may comprise, after step c), an additional step of adding stabilizers in order, firstly, to ensure the stability of the IgG concentrates being stored over time and secondly allow lyophilization avoiding denaturation of IgG in the various phases associated therewith.
- a single, pharmaceutically acceptable stabilizing formulation will be added, serving the purpose of ensuring the stabilization of the two contemplated forms of IgG storage both in liquid and freeze-dried form, and of preserving or even improving the therapeutic efficacy of these IgGs, as described in patent application WO 2004/091656 A2.
- the IgG concentrates are optionally subjected to a subsequent concentration step by ultrafiltration, then sterilizing filtration and can be packaged in flasks and preferably kept at temperatures in the region of 4 ° C.
- the IgG concentrates according to the invention comprise levels of AcaA and
- Such a method of assaying the anti-A and / or anti-B antibodies in the IgG concentrates of the invention comprises the steps of: a) preparing and calibrating a suspension of red blood cells A, B and / or or O Rhesus +, b) prepare monoclonal anti-D antibody solutions in a concentration range of 0 to 200 ng / ml in a biologically acceptable buffer, c) contact said red blood cells with samples of solutions of IgG or with the anti-D monoclonal antibody solutions, and incubate the red blood cell mixtures thus obtained for a predetermined duration, d) add in each mixture of red blood cells a fragment of anti-human IgG antibodies F (ab ') 2) labeled with a fluorochrome and incubating said red blood cells, e) subjecting each mixture of red blood cells obtained in step d) to a flow cytometry, f) determining the content of anti-A and / or anti-B antibodies. in IgG concentrates.
- One embodiment of such a method for determining the anti-A and / or anti-B antibody content may comprise the preparation of a suspension of 1% (v / v) red blood cells of the blood group A. , B and / or 0 in PBS buffer, pH between 7.0 and 7.4, containing from 0.8 to 1.5% by weight bovine serum albumin BSA.
- the red blood cells of the suspension are counted in a usual flow cytometry device, the implementation of which is known to those skilled in the art, then in order to calibrate the suspension at 37 to 43 ⁇ 10 6 red blood cells / ml of suspension.
- Monoclonal anti-D antibody solutions having concentrations ranging from 0 to 200 ng / ml buffer, preferably a PBS buffer, pH 7.0 to 7.4, containing where appropriate, from 0.8 to 1.5% by weight of bovine serum albumin BSA. Each solution thus prepared is assayed by absorptiometry to determine its molar extinction coefficient ( ⁇ ).
- the IgG concentrates of the invention are then adjusted to a concentration in the range of values from 1 to 5 mg / ml, preferably to 1 mg / ml, by means of a PBS buffer, of pH between 7.0 and 7.4, containing from 0.8 to 1.5% by weight bovine serum albumin BSA.
- a volume of 50 to 100 ⁇ l of the red blood cell suspension of each blood group is placed in each well of a microplate, for example 96 wells, then 50 to 100 ⁇ l of IgG solutions in this suspension of red blood cells. or from 50 to 100 ⁇ l of anti-D antibody solutions in this suspension of red blood cells.
- the whole is incubated for periods of between 1 h 30 and 2 h 30, in particular 2 h, at temperatures usually between 30 and 40 ° C., preferably 37 ° C.
- the different red blood cell mixtures thus obtained are then preferably washed with the PBS buffer containing the preceding BSA and is centrifuged, and then each mixture of red blood cells, contained in a well of microplates, is added with 50 to 100 ⁇ l of human anti-IgG goat F (ab ') 2 antibodies labeled with a fluorochrome, such as for example phycoerythrin, present in PBS buffer and BSA defined above.
- a fluorochrome such as for example phycoerythrin
- the different mixtures of red blood cells thus obtained are then washed and subjected to flow cytometry implemented with any suitable apparatus available in the trade comprising a device for detecting fluorescence of the compounds analyzed.
- MFI mean fluorescence intensity
- a method for assaying AcaA and AcaB of the above IgG concentrates is carried out by flow cytometry adapted to the context of the invention, the principle of which is based on the use of human group A or B red blood cells. , according to the specific determination of the titre of the AcaA and the desired AcaB, implementing the detection of a fluorescence signal proportional to the content of these antibodies.
- Such a method of dosing comprises the steps of: a) preparing and calibrating a blood group A or B blood cell suspension, b) contacting said red blood cells with diluted samples of IgG solutions, and incubating the mixture as well as obtained for a predetermined time, c) incubating said red blood cells in the presence of a fluorochrome-labeled anti-IgG antibody, and d) subjecting the red blood cell suspension obtained in step c) to flow cytometry.
- Red blood cells suspension are counted in a usual flow cytometry device, which implementation is known to those skilled in the art, and so calibrate the suspension at 37 to 43.10 e red blood cells / ml of suspension.
- a volume of 50 to 100 ⁇ l of the suspension is placed in each well of a 96-well microplate, then 50 to 100 ⁇ l of different solutions of diluted IgG two in two from a solution of 30 g / ml. 1 until an IgG solution at 0.234 g / l is obtained.
- the whole is incubated for periods between 1:30 and 2:30, in particular 2 hours, at temperatures usually between 30 and 40 0 C, preferably 37 0 C.
- red blood cells are then washed with the PBS buffer containing the preceding BSA and is centrifuged and then 50 to 100 ⁇ l of goat anti-human IgG F (ab ') 2 antibody, labeled with a fluorochrome, are added to each well. that for example phycoerythrin.
- step c) Incubation of the whole (step c)) is carried out for about 20-30 min in the dark.
- the suspension thus obtained is then washed and subjected to flow cytometry implemented with any suitable commercially available apparatus comprising a device for detecting fluorescence of the compounds analyzed.
- Another method of determining the content of anti-A and anti-B antibodies that may be advantageously used consists of in vitro complement lysis, known to those skilled in the art, but which has been specifically developed for the needs of the invention.
- Such an assay method comprises the steps of: a) radiolabeling a suspension of papainous red blood cells selected from blood groups A, B, AB and O, previously counted, by a suitable radioactive marker, b) contacting the radiolabeled RBCs with samples of IgG concentrates to a predetermined volume, c) adding a volume identical to that of step b) of normal blood serum AB, d) incubating the resulting mixture with step c) for a predetermined time, and e) measuring the radioactivity of the incubated solution thus obtained.
- a suspension of 1% papainous red blood cells is prepared
- radiolabeled red cells are then placed in contact with samples of IgG concentrates at a concentration of preferably between 1 and 3 mg / ml, in particular 1.2 mg / ml for 4 -6.10 6 radiolabeled red cells, in a volume of for example 100 ⁇ l.
- a volume identical to the previous one, for example 100 ⁇ l, of normal serum AB blood group is then added to the previous mixture to provide the various factors of the complement pathway.
- reaction mixture thus obtained is then incubated, preferably for periods of between 3 and 5 h, in particular 4 h, at temperatures usually between 30 and 40 ° C., preferably 37 ° C.
- the reaction mixture is then preferably centrifuged, and the radioactivity of the incubated solution is measured by appropriate commercially available devices.
- the measured radioactivity of the solution is proportional to the hemolysis rate of the treated red blood cells and, consequently, to the anti-A and anti-B antibodies.
- hemolysis rates of red blood cells of blood groups A, B and AB obtained by considering an IgG concentrate of the invention, (B3) and a IgG concentrate of the prior art (Cl ) with the lowest hemolysis levels among commercially available concentrates are shown in Table 2 below.
- a sample of IgG concentrate at 40 g / l (B2) is obtained by implementing the method described in WO 02/092632.
- a chromatographic column 50 cm long and 44 mm in diameter is filled with a 50/50 (v / v) mixture of GLYCOSORB ABO e support grafted with trisaccharides corresponding to the epitopes of blood group A and blood group B, then is subjected to a preliminary washing step with 1200 ml of water.
- IgG B2 concentrate is injected at a rate of 0.2 l / ml of support via a pump. Once this volume has been drilled through the column, it is washed with a minimum volume of water for injection (IPP) to recover the IgG present in the column. the dead volume of the column.
- IPP water for injection
- IgG B3 concentrate at about 40 g / l depleted in AcaA, AcaB and in polyreventive IgG is recovered which is subjected to ultrafiltration so that the concentrate is at 60 g / l and a nanofiltration of virus removal on three filters arranged in series and decreasing retention thresholds of 100, 50 and 20 nm.
- Dissolution of the stabilizing excipients consisting of a mixture of glycine at 7 g / l, mannitol at 30 g / l and 20 ppm Tween- ⁇ O in the IgG concentrate at 60 g / l is followed by an adjustment. the concentration of IgG at 50 g / l using PPI water, then the concentrate is sterilely filtered and distributed into flasks.
- a preparation of monoclonal anti-D (called R297) is assayed in Optical Density (OD) at 280 nm against its PBS buffer, pH 7.4.
- a range of from 0 to 200 ng / ml of anti-D monoclonal antibody is achieved at 12 points (200; 150; 100; 75; 50; 25; 12.5; 6.25; 3.13; 1.56; 0.78 and 0 ng / ml).
- a micro round bottom plate In a micro round bottom plate, are deposited in the wells: -50 ⁇ l of the Rhesus +, Rhesus + or Rhesus + red cell suspension at 40 ⁇ 10 6 red blood cells / ml, -50 ⁇ l of the anti-D range or 50 ⁇ l of the samples (IVIG) to be assayed.
- the samples to be assayed are deposited in triplicate.
- the plates are then incubated for 2 hours at 37 ° C. with stirring.
- the plates are centrifuged for 1 minute at 770 g.
- the supernatant is removed by inversion and then 200 ⁇ l of PBS + 1% BSA is added to each well.
- the operation is renewed 3 times.
- Suspensions of red blood cells are read by flow cytometer (Beckman Coulter FC500) according to a suitable program.
- the reading is performed on 50,000 events and the instrument automatically calculates the average fluorescence intensity (IMF) of each range point or sample.
- IMF average fluorescence intensity
- the affinity step is really contributive for the removal of anti-A and anti-B antibodies.
- the product IgNG2 is the product containing the least amount of anti-A and anti-B antibodies.
- a suspension of 1% (v / v) red blood cells of blood group A is prepared in PBS buffer, pH 7.4, containing 1% by weight bovine serum albumin BSA. 50 ⁇ l of the suspension of red blood cells are taken and introduced into a tube for a Beckmann-Coulter Epies XL flow cytometer, as well as 50 ⁇ l of an internal marker solution measuring the flow. The suspension is calibrated at 40.10 e red cells / ml.
- IgG solutions are prepared by successive dilution of a factor 2 of the IgG (v / v) concentrate (B3) obtained in Example 1, the most concentrated batch being at 30 g / l. more diluted to 0.234 g / l. A volume of 50 ⁇ l of the suspension is then placed in each well of a 96-well microplate and then 50 ⁇ l of the various diluted IgG solutions. The whole is incubated for 2h at a temperature of 37 0 C, with stirring.
- the incubation of the whole is carried out for 30 minutes in the dark.
- the procedure is the same with red blood cells B.
- a suspension of 1% (v / v) papainous red blood cells of the blood group A, B, AB or O is prepared which is then counted in a Malassez cell to obtain 10 e red blood cells.
- 100 ⁇ Ci of 51 Cr (1 volume per 1 volume of red blood cells) is added. The whole is incubated for 1 hour and the radiolabeled red cells are then washed 5 times.
- radiolabelled red blood cells are then contacted with samples of concentrates IgG (B2) obtained in Example 1 at a concentration of 1.2 mg / ml to 5.10 s radiolabeled red cells in a volume of 100 .mu.l.
- a volume identical to the previous one of 100 ⁇ l of normal blood serum AB is then added to the previous mixture to provide the various complement factors.
- the reaction mixture thus obtained is then incubated for 4 hours at a temperature of 37 ° C.
- the reaction mixture is then centrifuged for 1 minute at 2000 rpm, and the radioactivity of the supernatant solution incubated is measured according to appropriate devices available commercially.
- the measured radioactivity of the solution is proportional to the hemolysis rate of the treated red blood cells and, consequently, to the anti-A and anti-B antibody content.
- Identical procedures were performed with red blood cells B, AB and O, all being rhesus +, and with a serum sample of the 0+ group. This procedure is implemented with three different lots of IgG (B2).
- the method is applied to three batches of commercial samples of IgG concentrates, labeled C2 to C4, and a C5 serum sample of group 0+, included as a negative control.
- the measured radioactivity of the solution is proportional to the hemolysis rate of the red blood cells treated and, consequently, to the amount of anti-A and anti-B antibodies fixed on the red blood cells.
- the results obtained show that the IgG B3 concentrate which has been subjected to affinity chromatography according to the invention contains the smallest amount of AcaA and AcaB since the hemolysis rate of the red blood cells from the different blood groups is the weakest. Haemolysis with 0+ phenotype red cells, included as a negative control, was not observed.
- Table 5 shows the enrichment factors of the poly-active IgG samples B2, B3 and C4 of Example 3, the IgG content was arbitrarily set at 1, for reference.
- the IgG B3 concentrate of the invention contains from 5 to 8 times less polyrefective IgG than the concentrate of the prior art C4.
- IgG (B3) depleted of AcaA, AcaB, and polyriactive IgG, with IgG (B1) concentrates.
- the study focused on mice deficient in Fc ⁇ RI and Fc ⁇ RIII receptors treated in order to evaluate the immunomodulatory activity of the IgG concentrates according to the invention. These animals serve as a model for thrombocytopenic purpura.
- an IgG concentrate (B1) obtained by ethanolic fractionation according to Cohn was used as a control.
- Teeling J. L et al (Blood, 15/08/2001, vol 98, number 4, pp.1095-1099). Platelets, collapsed by injection of monoclonal antiplatelet IgG 9.10 8 / ml at the level of 2.10 8 / ml, amount to 7.10 8 / ml in animals treated with IgG concentrates B1 and B3 at a therapeutic dose of 1 g / kg.
- the immunomodulatory activity of the IgG B3 concentrate according to the invention was not modified by the implementation of the immunoaffinity chromatography.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biophysics (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Analytical Chemistry (AREA)
- Epidemiology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
Abstract
Description
Claims
Priority Applications (15)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK06847150.7T DK1968634T3 (da) | 2005-12-26 | 2006-12-26 | Fremgangsmåde til fremstilling af et immunglobulin G (IgG)-koncentrat med formindsket indhold af anti-A- og anti-B-stoffer |
BRPI0620600-0A BRPI0620600B1 (pt) | 2005-12-26 | 2006-12-26 | Método para obter um concentrado terapêutico de imunoglobulinas g |
CA2634997A CA2634997C (fr) | 2005-12-26 | 2006-12-26 | Concentre d'immunoglobulines g (igg) appauvri en anticorps anti-a et anti-b, et en igg polyreactives |
ES06847150.7T ES2517540T3 (es) | 2005-12-26 | 2006-12-26 | Procedimiento de preparación de concentrado de inmunoglobulinas G (IgG) empobrecido en anticuerpos anti-A y anti-B |
KR1020087018476A KR101250095B1 (ko) | 2005-12-26 | 2006-12-26 | 항-A 및 항-B 항체 그리고 다중반응성 IgGs가 결핍된면역글로블린 G(IgG) 농축물 |
AU2006334278A AU2006334278B2 (en) | 2005-12-26 | 2006-12-26 | Immunoglobulin G (IgG) concentrate depleted of anti-A and anti-B antibodies and of polyreactive IgGs |
PL11162751T PL2345425T3 (pl) | 2005-12-26 | 2006-12-26 | Koncentrat immunoglobulin G (IgG) zubożony w przeciwciała anty-A i anty-B oraz w polireaktywne IgG |
EP11162751.9A EP2345425B1 (fr) | 2005-12-26 | 2006-12-26 | CONCENTRÉ D'IMMUNOGLOBULINES G (IgG) APPAUVRI EN ANTICORPS ANTI-A ET ANTI-B, ET EN IgG POLYRÉACTIVES |
PL06847150T PL1968634T3 (pl) | 2005-12-26 | 2006-12-26 | Sposób wytwarzania koncentratu immunoglobulin g (igg) zubożonego pod względem przeciwciał anty-a i anty-b |
JP2008548014A JP5726403B2 (ja) | 2005-12-26 | 2006-12-26 | 抗Aおよび抗B抗体、ならびに多反応性IgGが減少した免疫グロブリンG(IgG)濃縮物 |
CN2006800494486A CN101346153B (zh) | 2005-12-26 | 2006-12-26 | 除去抗A、抗B抗体以及多反应性免疫球蛋白IgG的免疫球蛋白G(IgG)浓缩物 |
US12/159,199 US8153382B2 (en) | 2005-12-26 | 2006-12-26 | Immunoglobulin G (IgG) concentrate depleted of anti-A and anti-B antibodies and of polyreactive IgGs |
EP06847150.7A EP1968634B1 (fr) | 2005-12-26 | 2006-12-26 | PROCÉDÉ DE PRÉPARATION DE CONCENTRE D' IMMUNOGLOBULINES G (IgG) APPAUVRI EN ANTICORPS ANTI-A ET ANTI-B |
IL192289A IL192289A (en) | 2005-12-26 | 2008-06-18 | Immunoglobulin g (igg) concentrate with reduced levels of anti- a and anti-b antibodies |
IL231806A IL231806A (en) | 2005-12-26 | 2014-03-30 | Method for Extracting Immunoglobulin G (IgG) with Reduced Anti-a and Anti-B Antibody. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0513311A FR2895263B1 (fr) | 2005-12-26 | 2005-12-26 | Concentre d'immunoglobines g (lg) appauvri en anticorps anti-a et anti-b, et en igg polyreactives |
FR0513311 | 2005-12-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007077365A2 true WO2007077365A2 (fr) | 2007-07-12 |
WO2007077365A3 WO2007077365A3 (fr) | 2007-08-30 |
Family
ID=36956126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2006/002889 WO2007077365A2 (fr) | 2005-12-26 | 2006-12-26 | CONCENTRE D’IMMUNOGLOBULINES G (IgG) APPAUVRI EN ANTICORPS ANTI-A ET ANTI-B, ET EN IgG POLYREACTIVES |
Country Status (15)
Country | Link |
---|---|
US (1) | US8153382B2 (fr) |
EP (3) | EP2792366A1 (fr) |
JP (3) | JP5726403B2 (fr) |
KR (1) | KR101250095B1 (fr) |
CN (3) | CN101346153B (fr) |
AU (1) | AU2006334278B2 (fr) |
BR (1) | BRPI0620600B1 (fr) |
CA (1) | CA2634997C (fr) |
DK (2) | DK2345425T3 (fr) |
ES (2) | ES2690664T3 (fr) |
FR (1) | FR2895263B1 (fr) |
IL (2) | IL192289A (fr) |
PL (2) | PL1968634T3 (fr) |
TR (1) | TR201814658T4 (fr) |
WO (1) | WO2007077365A2 (fr) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010076496A1 (fr) | 2008-12-17 | 2010-07-08 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Utilisation d'un concentre d'immunoglobulines g (igg) appauvri en anticorps anti-a et anti-b pour le traitement de l'ictere neonatal par incompatibilite foetomaternelle dans le systeme abo |
WO2010076537A1 (fr) | 2008-12-30 | 2010-07-08 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Composition d'immunoglobulines g |
WO2011061454A1 (fr) | 2009-11-20 | 2011-05-26 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Utilisation d'immunoglobulines polyvalentes pour traiter une cirrhose hepatique alcoolique ou metabolique |
WO2011138561A1 (fr) | 2010-05-05 | 2011-11-10 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procédé de mesure de l'activation du complément par des igg |
WO2012017156A1 (fr) | 2010-07-19 | 2012-02-09 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Composition d'immunoglobulines humaines concentrees |
JP2012521776A (ja) * | 2009-03-31 | 2012-09-20 | ロイコケア・アクチェンゲゼルシャフト | 生物機能性組成物の滅菌の手段および方法 |
WO2012143484A1 (fr) | 2011-04-20 | 2012-10-26 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procede de preparation d'un produit plasmatique deplete en un ou plusieurs facteurs thrombogenes |
WO2013007740A1 (fr) | 2011-07-11 | 2013-01-17 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procede de preparation d'un concentre d'immunoglobulines polyvalentes |
WO2015136217A1 (fr) | 2014-03-11 | 2015-09-17 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procédé de préparation de protéines plasmatiques humaines |
FR3026950A1 (fr) * | 2014-10-09 | 2016-04-15 | Lab Francais Du Fractionnement | Procede de preparation de plasma universel |
WO2016177871A1 (fr) | 2015-05-07 | 2016-11-10 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Composition enrichie en immunoglobulines polyclonales anti-a et/ou anti-b |
EP3141558B1 (fr) | 2015-09-08 | 2019-05-22 | Merck Patent GmbH | Support de chromatographie d'affinite pour elimination d'anticorps anti-a et/ou anti-b |
WO2019129848A1 (fr) | 2017-12-29 | 2019-07-04 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procédé de purification d'anticorps à partir de lait brut |
US10611826B2 (en) | 2013-07-05 | 2020-04-07 | Laboratoire Français Du Fractionnement Et Des Biotechnologies | Affinity chromatography matrix |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2895263B1 (fr) | 2005-12-26 | 2008-05-30 | Lab Francais Du Fractionnement | Concentre d'immunoglobines g (lg) appauvri en anticorps anti-a et anti-b, et en igg polyreactives |
FR2949195B1 (fr) | 2009-08-24 | 2011-10-14 | Lfb Biomedicaments | Poche de stockage de solution therapeutique |
US20130273571A1 (en) * | 2010-05-05 | 2013-10-17 | Arryx, Inc. | Method of functionalizing human red blood cells with antibody |
FR2961107B1 (fr) * | 2010-06-15 | 2012-07-27 | Lab Francais Du Fractionnement | Composition d'immunoglobulines humaines stabilisee |
US10156574B2 (en) | 2013-04-29 | 2018-12-18 | Adimab, Llc | Polyspecificity reagents, methods for their preparation and use |
FR3035799B1 (fr) * | 2015-05-06 | 2017-05-05 | Elicityl | Support pour la purification de liquides biologiques |
FR3035794B1 (fr) * | 2015-05-06 | 2017-05-05 | Elicityl | Procede pour la purification du sang total ou d'un produit issu du sang |
US10697982B2 (en) | 2015-09-08 | 2020-06-30 | Merck Patent Gmbh | Methods of evaluating quality of a chromatography media which binds anti-A or anti-B antibodies |
US10697983B2 (en) | 2015-09-08 | 2020-06-30 | Merck Patent Gmbh | Methods of evaluating quality of media suitable for removing anti-A or anti-B antibodies |
US20180305401A1 (en) * | 2015-10-21 | 2018-10-25 | Cambryn Biologics, Llc | Processes for purifying proteins from plasma |
CN108101981B (zh) * | 2018-01-15 | 2019-06-04 | 四川远大蜀阳药业有限责任公司 | 一种静注免疫球蛋白的生产工艺 |
CN109239335A (zh) * | 2018-09-11 | 2019-01-18 | 广州万孚生物技术股份有限公司 | 联检试纸条及其制备方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001058510A1 (fr) | 2000-02-08 | 2001-08-16 | Glycorex Transplantation Ab | Support oligosaccharide destine notamment a retirer des anticorps du sang |
WO2002092632A1 (fr) | 2001-05-11 | 2002-11-21 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procede de preparation de concentres d'immunoglobulines humaines a usage therapeutique |
WO2004091656A2 (fr) | 2003-04-09 | 2004-10-28 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies. Groupement D'interet Public | Formulation stabilisante pour compositions d'immunoglobulines G sous forme liquide et sous forme lyophilisEe |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR513311A (fr) | 1916-05-04 | 1921-02-12 | Raphael Von Ostrejko | Procédé et installation pour la préparation de charbon décolorant |
US4664913A (en) | 1982-05-24 | 1987-05-12 | Xoma Corporation | Method for treating plasma for transfusion |
DK166763C (da) | 1983-03-16 | 1993-07-12 | Immuno Ag | Immunoglobulin-g-holdig fraktion |
US4764369A (en) | 1983-07-14 | 1988-08-16 | New York Blood Center Inc. | Undenatured virus-free biologically active protein derivatives |
US4946788A (en) * | 1985-06-11 | 1990-08-07 | Ciba-Geigy Corporation | Purified immunoglobulin-related factor, novel monoclonal antibodies, hybridoma cell lines, processes and applications |
JPS622162A (ja) * | 1985-06-28 | 1987-01-08 | Mutsuo Kitahama | 抗bモノクロ−ナル抗体およびその製造法 |
JPH0662436B2 (ja) | 1986-05-19 | 1994-08-17 | 株式会社ミドリ十字 | 静注用免疫グロブリン製剤の製造方法 |
AT391810B (de) | 1988-02-26 | 1990-12-10 | Immuno Ag | Verwendung von chymotrypsin zum unwirksammachen des praekallikrein-aktivators |
DK0447585T4 (da) | 1990-03-22 | 2003-09-01 | Biotest Pharma Gmbh | Fremgangsmåde til fremstilling af et intravenøst tolerant immunglobulin-G-præparat |
CA2148219C (fr) * | 1992-10-30 | 1998-12-29 | Charles W. Rittershaus | Mesure de la quantite totale d'une molecule cible dans un echantillon; methode fondee sur ce processus |
FR2706466B1 (fr) | 1993-06-14 | 1995-08-25 | Aetsrn | Concentré d'immunoglobulines G à usage thérapeutique et procédé de production dudit concentré. |
CA2136698A1 (fr) | 1994-11-25 | 1996-05-26 | M. Abdul Mazid | Compositions a base de resine et methodes pour les utiliser |
US5776711A (en) * | 1996-11-12 | 1998-07-07 | The Regents Of The University Of California | Simultaneous human ABO and RH(D) blood typing or antibody screening by flow cytometry |
ID27417A (id) | 1998-06-09 | 2001-04-05 | Statens Seruminstitut | Proses untuk memproduksi immunoglobulin untuk pemberian melalui intravena dan produk-produk immunoglobulin lainnya |
CA2375112C (fr) * | 1999-06-03 | 2011-04-26 | Advanced Extravascular Systems | Elimination en une etape de molecules indesirables dans le sang circulant |
FR2794461B1 (fr) | 1999-06-07 | 2004-01-23 | Lab Francais Du Fractionnement | Procede de preparation de nouvelles fractions d'ig humaines possedant une activite immunomodulatrice |
MXPA02003517A (es) | 1999-10-08 | 2004-09-10 | Vi Technologies Inc | Composiciones sanguineas desprovistas de isoaglutinina y metodo para elaborarlas. |
JP4493882B2 (ja) * | 2001-06-19 | 2010-06-30 | 株式会社カネカ | 抗原およびこの抗原を識別するモノクローナル抗体 |
US20040101909A1 (en) | 2002-08-20 | 2004-05-27 | Hema-Quebec, 2535 Boul. Laurier, Ste-Foy, Quebec, Canada G1V 4M3 | Purification of polyreactive autoantibodies and uses thereof |
FR2895263B1 (fr) | 2005-12-26 | 2008-05-30 | Lab Francais Du Fractionnement | Concentre d'immunoglobines g (lg) appauvri en anticorps anti-a et anti-b, et en igg polyreactives |
-
2005
- 2005-12-26 FR FR0513311A patent/FR2895263B1/fr active Active
-
2006
- 2006-12-26 DK DK11162751.9T patent/DK2345425T3/en active
- 2006-12-26 CA CA2634997A patent/CA2634997C/fr active Active
- 2006-12-26 ES ES11162751.9T patent/ES2690664T3/es active Active
- 2006-12-26 AU AU2006334278A patent/AU2006334278B2/en active Active
- 2006-12-26 BR BRPI0620600-0A patent/BRPI0620600B1/pt active IP Right Grant
- 2006-12-26 ES ES06847150.7T patent/ES2517540T3/es active Active
- 2006-12-26 US US12/159,199 patent/US8153382B2/en active Active
- 2006-12-26 PL PL06847150T patent/PL1968634T3/pl unknown
- 2006-12-26 CN CN2006800494486A patent/CN101346153B/zh active Active
- 2006-12-26 JP JP2008548014A patent/JP5726403B2/ja active Active
- 2006-12-26 EP EP20140170934 patent/EP2792366A1/fr not_active Withdrawn
- 2006-12-26 CN CN2012104120215A patent/CN102921004A/zh active Pending
- 2006-12-26 KR KR1020087018476A patent/KR101250095B1/ko active IP Right Grant
- 2006-12-26 WO PCT/FR2006/002889 patent/WO2007077365A2/fr active Application Filing
- 2006-12-26 CN CN201310308621.1A patent/CN103394084B/zh active Active
- 2006-12-26 TR TR2018/14658T patent/TR201814658T4/tr unknown
- 2006-12-26 PL PL11162751T patent/PL2345425T3/pl unknown
- 2006-12-26 DK DK06847150.7T patent/DK1968634T3/da active
- 2006-12-26 EP EP11162751.9A patent/EP2345425B1/fr not_active Revoked
- 2006-12-26 EP EP06847150.7A patent/EP1968634B1/fr active Active
-
2008
- 2008-06-18 IL IL192289A patent/IL192289A/en not_active IP Right Cessation
-
2013
- 2013-02-27 JP JP2013036624A patent/JP2013151507A/ja active Pending
-
2014
- 2014-03-30 IL IL231806A patent/IL231806A/en not_active IP Right Cessation
-
2015
- 2015-01-19 JP JP2015007494A patent/JP5944543B2/ja active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001058510A1 (fr) | 2000-02-08 | 2001-08-16 | Glycorex Transplantation Ab | Support oligosaccharide destine notamment a retirer des anticorps du sang |
WO2002092632A1 (fr) | 2001-05-11 | 2002-11-21 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procede de preparation de concentres d'immunoglobulines humaines a usage therapeutique |
WO2004091656A2 (fr) | 2003-04-09 | 2004-10-28 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies. Groupement D'interet Public | Formulation stabilisante pour compositions d'immunoglobulines G sous forme liquide et sous forme lyophilisEe |
Non-Patent Citations (7)
Title |
---|
BLEEKER W.K. ET AL., BLOOD, vol. 95, 2000, pages 1856 - 1861 |
HOUT M S ET AL.: "Specific removal of anti-A and anti-B antibodies by using modified dialysis filters", ASAIO JOURNAL (AMERICAN SOCIETY FOR ARTIFICIAL INTERNAL ORGANS: 1992, vol. 46, no. 6, November 2000 (2000-11-01), pages 702 - 706 |
KNEZEVIC-MARAMICA IRINA ET AL.: "Intravenous immune globulins: an update for clinicians.", TRANSFUSION., vol. 43, no. 10, October 2003 (2003-10-01), pages 1460 - 1480 |
MAZID M A ET AL.: "An improved affinity support and immunoadsorbent with a synthetic blood group oligosaccharide and polymer coating for hemoperfusion", JOURNAL OF APPLIED BIOMATERIALS: AN OFFICIAL JOURNAL OF THE SOCIETY FOR BIOMATERIALS. SPRING, vol. 3, no. 1, April 1992 (1992-04-01) |
NICHOLLS M D ET AL.: "HEMOLYSIS INDUCED BY INTRAVENOUSLY-ADMINISTERED IMMUNOGLOBULIN", MEDICAL JOURNAL OF AUSTRALIA, vol. 150, no. 7, 1989, pages 404 - 406 |
See also references of EP1968634A2 |
STEINBUCH ET AL., REV. FRANÇ. ET. CLIN. ET BIOL., vol. XIV, 1969, pages 1054 |
Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102316899A (zh) * | 2008-12-17 | 2012-01-11 | 法国分裂暨生物科技实验室 | 抗-a和抗-b抗体经耗竭的免疫球蛋白g(igg)浓缩物在用于治疗由母体-胎儿关于abo系统的不相容性所引起的新生儿黄疸中的用途 |
WO2010076496A1 (fr) | 2008-12-17 | 2010-07-08 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Utilisation d'un concentre d'immunoglobulines g (igg) appauvri en anticorps anti-a et anti-b pour le traitement de l'ictere neonatal par incompatibilite foetomaternelle dans le systeme abo |
WO2010076537A1 (fr) | 2008-12-30 | 2010-07-08 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Composition d'immunoglobulines g |
US11564865B2 (en) | 2009-03-31 | 2023-01-31 | Leukocare Ag | Means and methods of sterilization of biofunctional compositions |
JP2012521776A (ja) * | 2009-03-31 | 2012-09-20 | ロイコケア・アクチェンゲゼルシャフト | 生物機能性組成物の滅菌の手段および方法 |
JP2016028593A (ja) * | 2009-03-31 | 2016-03-03 | ロイコケア・アクチェンゲゼルシャフト | 生物機能性組成物の滅菌の手段および方法 |
WO2011061454A1 (fr) | 2009-11-20 | 2011-05-26 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Utilisation d'immunoglobulines polyvalentes pour traiter une cirrhose hepatique alcoolique ou metabolique |
WO2011138561A1 (fr) | 2010-05-05 | 2011-11-10 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procédé de mesure de l'activation du complément par des igg |
US8790881B2 (en) | 2010-05-05 | 2014-07-29 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Method for measuring IgG-mediated complement activation |
WO2012017156A1 (fr) | 2010-07-19 | 2012-02-09 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Composition d'immunoglobulines humaines concentrees |
EP3150225A1 (fr) | 2010-07-19 | 2017-04-05 | Laboratoire Français du Fractionnement et des Biotechnologies | Composition d'immunoglobulines humaines concentrees |
WO2012143484A1 (fr) | 2011-04-20 | 2012-10-26 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procede de preparation d'un produit plasmatique deplete en un ou plusieurs facteurs thrombogenes |
FR2974301A1 (fr) * | 2011-04-20 | 2012-10-26 | Lab Francais Du Fractionnement | Procede de preparation d'un produit plasmatique deplete en un ou plusieurs facteurs thrombogenes |
EP2699248B1 (fr) | 2011-04-20 | 2017-02-08 | Laboratoire Français du Fractionnement et des Biotechnologies | Procédé de préparation d'un produit plasmatique déplété en un ou plusieurs facteurs thrombogenes |
US9718856B2 (en) | 2011-07-11 | 2017-08-01 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Method for preparing a concentrate of polyvalent immunoglobulin |
TWI579301B (zh) * | 2011-07-11 | 2017-04-21 | 法國分裂與生物技術實驗室 | 多價免疫球蛋白之濃縮物之製造方法 |
WO2013007740A1 (fr) | 2011-07-11 | 2013-01-17 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procede de preparation d'un concentre d'immunoglobulines polyvalentes |
FR2977893A1 (fr) * | 2011-07-11 | 2013-01-18 | Lab Francais Du Fractionnement | Procede de preparation d'un concentre d'immunoglobulines polyvalentes |
US10611826B2 (en) | 2013-07-05 | 2020-04-07 | Laboratoire Français Du Fractionnement Et Des Biotechnologies | Affinity chromatography matrix |
WO2015136217A1 (fr) | 2014-03-11 | 2015-09-17 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procédé de préparation de protéines plasmatiques humaines |
FR3026950A1 (fr) * | 2014-10-09 | 2016-04-15 | Lab Francais Du Fractionnement | Procede de preparation de plasma universel |
WO2016055647A3 (fr) * | 2014-10-09 | 2016-06-02 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procede de preparation de plasma universel |
EP3459552A1 (fr) * | 2014-10-09 | 2019-03-27 | Laboratoire Français du Fractionnement et des Biotechnologies | Procédé de preparation de plasma universel |
US10357512B2 (en) | 2014-10-09 | 2019-07-23 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Method for preparing universal plasma |
FR3035971A1 (fr) * | 2015-05-07 | 2016-11-11 | Lab Francais Du Fractionnement | Composition enrichie en immunoglobulines polyclonales anti-a et/ou anti-b |
WO2016177871A1 (fr) | 2015-05-07 | 2016-11-10 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Composition enrichie en immunoglobulines polyclonales anti-a et/ou anti-b |
EP3141558B1 (fr) | 2015-09-08 | 2019-05-22 | Merck Patent GmbH | Support de chromatographie d'affinite pour elimination d'anticorps anti-a et/ou anti-b |
EP3141558B2 (fr) † | 2015-09-08 | 2022-02-16 | Merck Patent GmbH | Support de chromatographie d'affinite pour elimination d'anticorps anti-a et/ou anti-b |
WO2019129848A1 (fr) | 2017-12-29 | 2019-07-04 | Laboratoire Francais Du Fractionnement Et Des Biotechnologies | Procédé de purification d'anticorps à partir de lait brut |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2345425B1 (fr) | CONCENTRÉ D'IMMUNOGLOBULINES G (IgG) APPAUVRI EN ANTICORPS ANTI-A ET ANTI-B, ET EN IgG POLYRÉACTIVES | |
CN106995496B (zh) | 用于去除抗a和/或抗b抗体的新型亲和层析介质 | |
EP2358391B1 (fr) | Utilisation d'un concentre d'immunoglobulines g (igg) appauvri en anticorps anti-a et anti-b pour le traitement de l'ictere neonatal par incompatibilite foetomaternelle dans le systeme abo | |
WO2000074717A1 (fr) | NOUVELLES FRACTIONS D'Ig POSSEDANT UNE ACTIVITE IMMUNOMODULATRICE | |
AU2013200440B2 (en) | Immunoglobulin G (IgG) concentrate depleted of anti-A and anti-B antibodies and of polyreactive IgGs | |
AU2013206196B2 (en) | Immunoglobulin G (IgG) concentrate depleted of anti-A and anti-B antibodies and of polyreactive IgGs | |
WO2016177871A1 (fr) | Composition enrichie en immunoglobulines polyclonales anti-a et/ou anti-b | |
FR2578425A1 (fr) | Preparations d'immunoglobulines presentant des titres eleves en anticorps bloquants anti-allergenes, leur preparation et leurs applications pour le traitement d'allergies |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200680049448.6 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2634997 Country of ref document: CA Ref document number: 2008548014 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 5843/DELNP/2008 Country of ref document: IN Ref document number: 2006847150 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006334278 Country of ref document: AU |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020087018476 Country of ref document: KR |
|
ENP | Entry into the national phase |
Ref document number: 2006334278 Country of ref document: AU Date of ref document: 20061226 Kind code of ref document: A |
|
WWP | Wipo information: published in national office |
Ref document number: 2006334278 Country of ref document: AU |
|
WWP | Wipo information: published in national office |
Ref document number: 2006847150 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12159199 Country of ref document: US |
|
ENP | Entry into the national phase |
Ref document number: PI0620600 Country of ref document: BR Kind code of ref document: A2 Effective date: 20080626 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 231806 Country of ref document: IL |