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Reff Mitchell E

Researcher at Biogen Idec

Publications -  49
Citations -  5840

Reff Mitchell E is an academic researcher from Biogen Idec. The author has contributed to research in topics: Antibody & Antigen. The author has an hindex of 22, co-authored 49 publications receiving 5751 citations. Previous affiliations of Reff Mitchell E include GlaxoSmithKline.

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Journal ArticleDOI

Depletion of B cells in vivo by a chimeric mouse human monoclonal antibody to CD20

TL;DR: In vitro studies showed the ability of C2B8 to bind human C1q, mediate complement-dependent cell lysis of human B-lymphoid cell lines, and lyse human target cells through antibody-dependent cellular cytotoxicity and the possibility of using an "immunologically active" chimeric anti-CD20 antibody as an alternative approach in the treatment of B-cell lymphoma.
Patent

Therapeutic application of chimeric and radiolabeled antibodies to human b lymphocyte restricted differentiation antigen for treatment of b cell lymphoma

TL;DR: In this paper, therapeutic treatment protocols designed for the treatment of B cell lymphoma were presented, which are based upon therapeutic strategies which include the use of administration of immunologically active mouse/human chimeric anti-CD20 antibodies, radiolabeled anti -CD20 antibody, and cooperative strategies comprising the using of chimeric antibody and radio-labeled antibody.
Journal ArticleDOI

Expression of GnTIII in a recombinant anti-CD20 CHO production cell line: Expression of antibodies with altered glycoforms leads to an increase in ADCC through higher affinity for FCγRIII

TL;DR: The gene encoding the rat glycosylation enzyme beta1-4-N-acetylglucosaminyltransferase III (GnTIII) was cloned and coexpressed in a recombinant production Chinese hamster ovary cell line expressing a chimeric mouse/human anti-CD20 IgG1 antibody.
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Elimination of Fc Receptor-Dependent Effector Functions of a Modified IgG4 Monoclonal Antibody to Human CD4

TL;DR: Clenoliximab retains the key immunomodulatory attributes of keliximAB without the liability of strong Fcγ receptor binding, and in initial clinical trials, these properties have translated to a reduced incidence of CD4+ T cell depletion.
Journal ArticleDOI

"Primatization" of recombinant antibodies for immunotherapy of human diseases: a macaque/human chimeric antibody against human CD4.

TL;DR: It is shown that cynomolgus macaques are phylogenetically distant enough to respond against conserved human antigens, and a human/monkey chimeric anti-CD4 antibody with an apparent affinity of 3.2 × 10−11 M and exhibits potent immunosuppressive properties in vitro.