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Human monoclonal IgG isotypes differ in complement activating function at the level of C4 as well as C1q

Humanized antibodies are likely to have a major role in therapy and it is important to define their interaction with physiological effectors. By comparing a matched series of chimeric human mAbs we found that igG1 was most efficient in complement lysis, although IgG3 bound more C1q. To resolve this...

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Bibliografiske detaljer
Format: Artigo
Sprog:Inglês
Udgivet: The Rockefeller University Press 1988
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Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2188986/
https://ncbi.nlm.nih.gov/pubmed/3260935
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