Generation and characterization of hybridoma antibodies for immunotherapy of tularemia.

Abstract

Tularemia is caused by the Gram-negative facultative intracellular bacterium Francisella tularensis, which has been classified as a category A select agent-a likely bioweapon. The high virulence of F. tularensis and the threat of engineered antibiotic resistant variants warrant the development of new therapies to combat this disease. We have characterized 14 anti-Francisella hybridoma antibodies derived from mice infected with F. tularensis live vaccine strain (LVS) for potential use as immunotherapy of tularemia. All 14 antibodies cross-reacted with virulent F. tularensis type A clinical isolates, 8 bound to a purified preparation of LVS LPS, and 6 bound to five protein antigens, identified by proteome microarray analysis. An IgG2a antibody, reactive with the LPS preparation, conferred full protection when administered either systemically or intranasally to BALB/c mice post challenge with a lethal dose of intranasal LVS; three other antibodies prolonged survival. These anti-Francisella hybridoma antibodies could be converted to chimeric versions with mouse V regions and human C regions to serve as components of a recombinant polyclonal antibody for clinical testing as immunotherapy of tularemia. The current study is the first to employ proteome microarrays to identify the target antigens of anti-Francisella monoclonal antibodies and the first to demonstrate the systemic and intranasal efficacy of monoclonal antibodies for post-exposure treatment of respiratory tularemia.

• Authors: Zhaohua Lu, Marly I Roche, Julia H Hui, Berkay Unal, Philip L Felgner, Sunita Gulati, Guillermo Madico, Jacqueline Sharon
• Journal: Immunology letters (Immunol Lett) Vol. 112 Issue 2 Pg. 92-103 (Oct 15 2007) ISSN: 0165-2478 [Print] Netherlands
• PMID: 17764754 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Antibodies, Bacterial
• Antibodies, Monoclonal
• Antigens, Bacterial
• Bacterial Vaccines
• Lipopolysaccharides

Topics

• Administration, Intranasal
• Adoptive Transfer
• Animals
• Antibodies, Bacterial (classification, immunology, therapeutic use)
• Antibodies, Monoclonal (classification, immunology, therapeutic use)
• Antigens, Bacterial (immunology)
• Bacterial Vaccines (administration & dosage)
• Cell Line, Tumor
• Cross Reactions
• Disease Models, Animal
• Enzyme-Linked Immunosorbent Assay
• Female
• Francisella tularensis (immunology, pathogenicity)
• Humans
• Hybridomas (immunology, microbiology)
• Immunization (methods)
• Lipopolysaccharides (immunology)
• Mice
• Mice, Inbred BALB C
• Mice, Inbred C57BL
• Protein Array Analysis
• Tularemia (immunology, microbiology, therapy)