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Published online on March 3, 2008, 10.1073/pnas.0708841104
PNAS | March 11, 2008 | vol. 105 | no. 10 | 3727-3732


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BIOLOGICAL SCIENCES / APPLIED BIOLOGICAL SCIENCES
Cost-effective production of a vaginal protein microbicide to prevent HIV transmission

Koreen Ramessar*, Thomas Rademacher{dagger}, Markus Sack{dagger}, Johannes Stadlmann{ddagger}, Dimitris Platis§, Gabriela Stiegler, Nikos Labrou§, Fritz Altmann{ddagger}, Julian Ma||, Eva Stöger{dagger}, Teresa Capell*, and Paul Christou*,**,{dagger}{dagger}

*Departament de Producció Vegetal i Ciència Forestal, Universitat de Lleida, Avenida Alcalde Rovira Roure, 191, Lleida, 25198, Spain; {dagger}Institute for Molecular Biotechnology, Biology VII, RWTH Aachen, Worringerweg 1, 52074 Aachen, Germany; {ddagger}Department of Chemistry, Glycobiology Division, University of Natural Resources and Applied Life Sciences, Muthgasse 18, 1190 Vienna, Austria; §Department of Agricultural Biotechnology, Agricultural University of Athens, Iera Odos 75, 118 55 Athens, Greece; Polymun Scientific, Nussdorfer Laende 11, 1190 Vienna, Austria; ||Saint George's University of London, Cranmer Terrace, London SW17 0RE, United Kingdom; and **Institucio Catalana de Recerca i Estudis Avancats, 08010 Barcelona, Spain

Communicated by M. S. Swaminathan, Taramani Institutional Area, Madras, India, September 22, 2007 (received for review July 24, 2007)

A series of small-molecule microbicides has been developed for vaginal delivery to prevent heterosexual HIV transmission, but results from human clinical trials have been disappointing. Protein-based microbicides, such as HIV-specific monoclonal antibodies, have been considered as an alternative approach. Despite their promising safety profile and efficacy, the major drawback of such molecules is the economy of large-scale production in mammalian cells, the current system of choice. Here, we show that an alternative biomanufacturing platform is now available for one of the most promising anti-HIV antibodies (2G12). Our data show that the HIV-neutralization capability of the antibody is equal to or superior to that of the same antibody produced in CHO cells. We conclude that this protein production system may provide a means to achieve microbicide ingredient manufacture at costs that would allow product introduction and manufacture in the developing world.


Author contributions: J.M., E.S., and P.C. designed research; K.R., T.R., M.S., J.S., D.P., G.S., and T.C. performed research; K.R., M.S., J.S., D.P., N.L., F.A., J.M., E.S., T.C., and P.C. analyzed data; and K.R. and P.C. wrote the paper.

The author declares no conflict of interest.

This article contains supporting information online at www.pnas.org/cgi/content/full/0708841104/DC1.

{dagger}{dagger}To whom correspondence should be addressed. E-mail: christou{at}pvcf.udl.cat

© 2008 by The National Academy of Sciences of the USA


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