Methods for preparing a purified maytansinoid conjugate in a solution
This invention describes a method of conjugating a cell binding agent such as an antibody with an effector group (e.g., a cytotoxic agent) or a reporter group (e.g., a radionuclide), whereby the reporter or effector group is first reacted with a bifunctional linker and the mixture is then used without purification for the conjugation reaction with the cell binding agent. The method described in this invention is advantageous for preparation of stably-linked conjugates of cell binding agents, such as antibodies with effector or reporter groups. This conjugation method provides in high yields conjugates of high purity and homogeneity that are without inter-chain cross-linking and inactivated linker residues.
1. A process for preparing a purified conjugate in a solution, wherein the conjugate comprises a maytansinoid comprising a thiol group linked to a cell binding agent, the process comprising the steps of:
(a) contacting a maytansinoid comprising a thiol group with a bifunctional linker reagent to covalently attach the linker to the maytansinoid and thereby prepare an unpurified first mixture comprising the maytansinoid having linkers bound thereto,
(b) conjugating a cell binding agent to the maytansinoid having linkers bound thereto by reacting the unpurified first mixture with the cell binding agent to prepare a second mixture, and
(c) subjecting the second mixture to tangential flow filtration, dialysis, gel filtration, adsorptive chromatography, selective precipitation or a combination thereof to thereby prepare the purified conjugate,
wherein the bifunctional linker reagent is γ-maleimidobutyric acid N-succinimidyl ester (GMBS), and wherein step (b) is carried out in a solution at a pH from about 5 to about 8.7.
2. The process of claim 1 , wherein the pH of the solution in step (b) is from about 6.5 to about 8.5.
3. The process of claim 1 , wherein the second mixture in step (b) is substantially free of undesired cross-linked, hydrolyzed species formed due to intramolecular or inter-molecular reactions.
4. The process of claim 1 , wherein the maytansinoid is DM1.
5. The process of claim 1 , wherein the maytansinoid is DM4.
6. The process of claim 1 , wherein the cell binding agent is an interferon, interleukin 2 (IL-2), interleukin 3 (IL-3), interleukin 4 (IL-4), interleukin 6 (IL-6), insulin, EGF, TGF-a, FGF, G-CSF, VEGF, MCSF, GM-CSF, transferrin, or an antibody.
7. The process of claim 6 , wherein the cell binding agent is an antibody.
8. The process of claim 7 , wherein the antibody is a monoclonal antibody.
9. The process of claim 7 , wherein the antibody is a human or a humanized monoclonal antibody.
10. The process of claim 7 , wherein the antibody is MY9, anti-B4, C242, or an antibody that binds to an antigen selected from EpCAM, CD2, CD3, CD4, CD5, CD6, CD11, CD19, CD20, CD22, CD26, CD30, CD33, CD37, CD38, CD40, CD44, CD56, CD79, CD105, CD138, EphA receptors, EphB receptors, EGFR, EGFRvIII, HER2, HER3, mesothelin, cripto, alphavbeta3, alphavbeta5, and alphavbeta6 integrin.
11. The process of claim 9 , wherein the human or the humanized antibody is huMy9-6, huB4, huC242, huN901, DS6, CNTO 95, B-B4, trastuzumab, pertuzumab, bivatuzumab, sibrotuzumab, rituximab, or a human or humanized antibody that binds to an antigen selected from EphA2 receptor, CD38, and IGF-IR.
12. The process of claim 7 , wherein the antibody is a fragment of an antibody.
13. The process of claim 12 , wherein the fragment of an antibody is a scFv, Fab, Fab′ or F(ab′)2.
14. The process of claim 1 , wherein an excess of maytansinoid relative to the bifunctional linker reagent is used.
15. The process of claim 14 , wherein the process further comprises the step of quenching the excess maytansinoid in the unpurified first mixture with a quenching reagent between steps (a) and (b).
16. The process of claim 15 , wherein the quenching reagent is selected from 4-maleimidobutyric acid, 3-maleimidopropionic acid, N-ethylmaleimide, iodoacetamide, and iodoacetamidopropionic acid.