Treatment of B-cell associated diseases such as malignancies and autoimmune diseases using a cold anti-CD20 antibody/radiolabeled anti-CD22 antibody combination

Abstract

Treatment of B-cell associated diseases including autoimmune and B-cell malignancies such as leukemias, lymphomas, using the combination of an anti-CD20 antibody, preferably RITUXAN® and a radiolabeled anti-CD22 antibody, preferably an 90Y labeled humanized anti-CD22 antibody, is described. These therapeutic regimens provide for enhanced depletion of B cells, and therefore reduce the risk in B cell malignancy treatment of relapse associated with RITUXAN® and, moreover, provide for prolonged immunosuppression of B-cell immune responses, especially in the context of autoimmune diseases and transplant.

Description

CROSS REFERENCE TO RELATED APPLICATION [0001] This application claims priority from U.S. Provisional Ser. No. 60 / 212,668, filed Jun. 20, 2000, and which is incorporated herein in its entirety by reference.FIELD OF THE INVENTION [0002] The present invention is concerned with a combination immunotherapy / -radiotherapy involving the administration of a cold anti-CD20 antibody, preferably RITUXAN®, or another anti-CD20 antibody having substantially the same B-cell depleting activity as RITUXAN®, and a radiolabeled anti-CD22 antibody, preferably an yttrium labeled humanized anti-CD22 antibody. In the case of tumor therapy, the initial administration of the cold anti-CD23 antibody helps remove B cells from the circulation, thereby improving the targeting and efficacy of the radiolabeled anti-CD22 antibody. [0003] Also, the subject treatment provides for enhanced immunosuppression vis-à-vis cold CD20 and radiolabeled anti-CD22 therapy alone. This combination therapeutic regimen is useful in...

AI Technical Summary

Benefits of technology

[0025] Preferably, this combination will affect synergistic results vis-à-vis the use of the cold anti-CD20 or radiolabeled anti-CD22 antibody or fragment alone. In a particularly preferred embodiment, this combination will provide for enhanced killing or depletion of tumorigenic B cells because the cold anti-CD20 antibody initially clears most CD20 expressing cells and the radiolabeled anti-CD22 antibody clears substantially all remaining tumorigenic B cells. Optionally, the combination therapy may further include the use of a radiolabeled anti-CD20 antibody, e.g. radiolabeled 2B8 (Zevalin®).

[0026] In another preferred embodiment, this combination will prevent or inhibit relapse in patients with B cell malignancies, e.g. non-Hodgkin's lymphoma, vis-à-vis current Rituxan®-based therapeutic regimens.

Problems solved by technology

A potential problem with using monoclonal antibodies as therapeutics is that non-human monoclonal antibodies (e.g., murine monoclonal antibodies) typically lack human effector functionality, e.g., they are unable to, inter alia, mediate complement dependent lysis or lyse human target cells through antibody-dependent cellular toxicity or Fc-receptor mediated phagocytosis.

Furthermore, non-human monoclonal antibodies can be recognized by the human host as a foreign protein; therefore, repeated injections of such foreign antibodies can lead to the induction of immune responses leading to harmful hypersensitivity reactions.

However, it has not previously been utilized in combination with other therapeutic antibodies.

Therefore, based on the foregoing, while RITUXAN® and other therapies have been reported for treatment of B-cell lymphomas, often such treatments are subject to relapse.