Hybridoma · 2008 · 17 citations · 26 references
Life SciencesCell BiologyImmunologyCellular ImmunologyClinical ImmunologyMonoclonal AntibodiesBotulinum Toxin TherapyBotulinum Toxin TreatmentHybridoma TechnologyMonoclonal Antibody TechnologyMonoclonal Antibody TherapyTherapeutic Monoclonal AntibodiesAntibodiesAntibody Affinity MaturationBotulinum NeurotoxinBotulinum ToxinsHybridoma Cell Line DevelopmentMonoclonal Antibody AffinityMonoclonal Antibody TherapeuticsMyeloma Cell Lines
Monoclonal antibodies have demonstrated significant potential as therapeutics for botulinum neurotoxin exposures. We previously described a hybridoma method for cloning native human antibodies that uses a murine myeloma cell line that ectopically expresses the human telomerase catalytic subunit gene (hTERT) and the murine interleukin-6 gene (mIL-6). Here we describe a heterohybridoma cell line that ectopically expresses mIL-6 and hTERT and has improved stability of hTERT expression. We fused this cell line to human peripheral blood B cells from a subject who had received the botulinum toxoid vaccine, cloning a high-affinity antibody (13A) specific for serotype A botulinum neurotoxin (BoNT/A). The 13A antibody is an affinity-matured, post-germinal center IgG(1) lambda antibody that has partial neutralization activity in vivo. 13A binds an epitope on BoNT/A that overlaps the binding epitope of an IgG antibody previously shown to fully neutralize a lethal dose of BoNT/A in vivo. The 13A antibody may be useful for diagnostic testing or for incorporation into an oligoclonal therapeutic to counteract BoNT/A exposure.
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Telomerase Catalytic Subunit Homologs from Fission Yeast and Human
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IMGT(R), the international ImMunoGeneTics information system(R)
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Life Sciences, Genetics, Immunology +14
SV2 Is the Protein Receptor for Botulinum Neurotoxin A
Min Dong, Felix L. Yeh, William H. Tepp et al. · Science · 2006 · 771 citations