Complementary therapies for inflammation
Article Abstract:
A study generates mice in which the native C5a receptor is replaced by its human counterpart and uses these animals to produce high-affinity monoclonal antibodies (mAbs) capable of preventing and reversing inflammation in a mouse model of rheumatoid arthritis. Antibodies against human C5aR generated using the knock-in strategy had IC50 values at least half those of the best in mAbs raised by a more conventional strategy involving use of C5aR-transferred cells as the immunogen.
Publication Name: Nature Biotechnology
Subject: Business
ISSN: 1087-0156
Year: 2006
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Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria
Article Abstract:
Humanized monoclonal antibody directed against complement component C5, eculizumab, is developed and shown to block proinflammatory and cytolytic effects of terminal complement activation. Approval of eculizumab as a first-in-class complement inhibitor for treating hemolytic disease paroxysmal nocturnal hemoglobinuria (PNH) validated the concept of complement inhibition as an effective therapy.
Publication Name: Nature Biotechnology
Subject: Business
ISSN: 1087-0156
Year: 2007
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Arming antibodies: Prospects and challenges for immunoconjugates
Article Abstract:
Immunoconjugates, monoclonal antibodies (mAbs) coupled to highly toxic agents, including radioisotopes and toxic drugs, are becoming a significant component of anticancer treatments. It is described that by combining the exquisite targeting specificity of mAbs with the enhanced tumor-killing power of toxic side effects than most conventional chemotherapeutic drugs.
Publication Name: Nature Biotechnology
Subject: Business
ISSN: 1087-0156
Year: 2005
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