Antibody discovery: sourcing of monoclonal antibody variable domains.

Curr Drug Discov Technol

VP, Biologics Research, Biotechnology COE, Janssen Research & Development, LLC, Pharmaceutical Companies of Johnson & Johnson, SH22-22462, 1400 Welsh & McKean Rds., PO Box 776, Spring House, PA 19477, USA.

Published: March 2014

AI Article Synopsis

  • Historically, therapeutic antibodies have primarily come from mouse IgG, which are often modified to create chimeric or humanized versions.
  • Recently, there has been an increase in using human antibodies sourced from transgenic mice, phage display libraries, and human B lymphocytes.
  • Notably, while 26 of the 36 approved antibodies have mouse origins, there is ongoing exploration of unconventional sources like camelids, sharks, and chickens for new therapeutic antibodies.

Article Abstract

Historically, antibody variable domains for therapeutic antibodies have been sourced primarily from the mouse IgG repertoire, and typically either chimerized or humanized. More recently, human antibodies from transgenic mice producing human IgG, phage display libraries, and directly from human B lymphocytes have been used more broadly as sources of antibody variable domains for therapeutic antibodies. Of the total 36 antibodies approved by major maket regulatory agencies, the variable domain sequences of 26 originate from the mouse. Of these, four are marketed as murine antibodies (of which one is a mouse-rat hybrid IgG antibody), six are mouse-human chimeric antibodies, and 16 are humanized. Ten marketed antibodies have originated from human antibody genes, three isolated from phage libraries of human antibody genes and seven from transgenic mice producing human antibodies. Five antibodies currently in clinical trials have been sourced from camelids, as well as two from non-human primates, one from rat, and one from rabbit. Additional sources of antibody variable domains that may soon find their way into the clinic are potential antibodies from sharks and chickens. Finally, the various methods for retrieval of antibodies from humans, mouse and other sources, including various display technologies and amplification directly from B cells, are described.

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http://dx.doi.org/10.2174/1570163810666131120150043DOI Listing

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