Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approach

<p>Abstract</p> <p>Background</p> <p>Common oral diseases and dental caries can be prevented effectively by passive immunization. In humans, passive immunotherapy may require the use of humanized or human antibodies to prevent adverse immune responses against murine epi...

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Main Authors: Barth Stefan, Ma Julian KC, Spiegel Holger, Huhn Michael, Kupper Michael B, Fischer Rainer, Finnern Ricarda
Format: Article
Language:English
Published: BMC 2005-01-01
Series:BMC Biotechnology
Online Access:http://www.biomedcentral.com/1472-6750/5/4
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spelling doaj-12c7d8eefa294a83bcc2c22063512bed2020-11-25T01:38:55ZengBMCBMC Biotechnology1472-67502005-01-0151410.1186/1472-6750-5-4Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approachBarth StefanMa Julian KCSpiegel HolgerHuhn MichaelKupper Michael BFischer RainerFinnern Ricarda<p>Abstract</p> <p>Background</p> <p>Common oral diseases and dental caries can be prevented effectively by passive immunization. In humans, passive immunotherapy may require the use of humanized or human antibodies to prevent adverse immune responses against murine epitopes. Therefore we generated human single chain and diabody antibody derivatives based on the binding characteristics of the murine monoclonal antibody Guy's 13. The murine form of this antibody has been used successfully to prevent <it>Streptococcus mutans </it>colonization and the development of dental caries in non-human primates, and to prevent bacterial colonization in human clinical trials.</p> <p>Results</p> <p>The antibody derivatives were generated using a chain-shuffling approach based on human antibody variable gene phage-display libraries. Like the parent antibody, these derivatives bound specifically to SAI/II, the surface adhesin of the oral pathogen <it>S. mutans</it>.</p> <p>Conclusions</p> <p>Humanization of murine antibodies can be easily achieved using phage display libraries. The human antibody fragments bind the antigen as well as the causative agent of dental caries. In addition the human diabody derivative is capable of aggregating <it>S. mutans in vitro</it>, making it a useful candidate passive immunotherapeutic agent for oral diseases.</p> http://www.biomedcentral.com/1472-6750/5/4
collection DOAJ
language English
format Article
sources DOAJ
author Barth Stefan
Ma Julian KC
Spiegel Holger
Huhn Michael
Kupper Michael B
Fischer Rainer
Finnern Ricarda
spellingShingle Barth Stefan
Ma Julian KC
Spiegel Holger
Huhn Michael
Kupper Michael B
Fischer Rainer
Finnern Ricarda
Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approach
BMC Biotechnology
author_facet Barth Stefan
Ma Julian KC
Spiegel Holger
Huhn Michael
Kupper Michael B
Fischer Rainer
Finnern Ricarda
author_sort Barth Stefan
title Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approach
title_short Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approach
title_full Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approach
title_fullStr Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approach
title_full_unstemmed Generation of human antibody fragments against <it>Streptococcus mutans </it>using a phage display chain shuffling approach
title_sort generation of human antibody fragments against <it>streptococcus mutans </it>using a phage display chain shuffling approach
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2005-01-01
description <p>Abstract</p> <p>Background</p> <p>Common oral diseases and dental caries can be prevented effectively by passive immunization. In humans, passive immunotherapy may require the use of humanized or human antibodies to prevent adverse immune responses against murine epitopes. Therefore we generated human single chain and diabody antibody derivatives based on the binding characteristics of the murine monoclonal antibody Guy's 13. The murine form of this antibody has been used successfully to prevent <it>Streptococcus mutans </it>colonization and the development of dental caries in non-human primates, and to prevent bacterial colonization in human clinical trials.</p> <p>Results</p> <p>The antibody derivatives were generated using a chain-shuffling approach based on human antibody variable gene phage-display libraries. Like the parent antibody, these derivatives bound specifically to SAI/II, the surface adhesin of the oral pathogen <it>S. mutans</it>.</p> <p>Conclusions</p> <p>Humanization of murine antibodies can be easily achieved using phage display libraries. The human antibody fragments bind the antigen as well as the causative agent of dental caries. In addition the human diabody derivative is capable of aggregating <it>S. mutans in vitro</it>, making it a useful candidate passive immunotherapeutic agent for oral diseases.</p>
url http://www.biomedcentral.com/1472-6750/5/4
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