Purpose of Review Spurred by the successful application of structural vaccinology to other challenging bacterial and viral pathogens, we review the possibility of exploiting 3D struc- ture computational-based recombinant antigen engineering strategies for the development of a protective melioidosis vaccine.Recent Findings Structure-based epitope design approaches in the melioidosis field are preliminary and applied essentially by one research network. By combining Burkholderia pseudomallei antigen 3D structures and in silico epitope dis- covery methods, a panel of synthetic epitope peptides were designed and tested for their B and T cell stimulatory activi- ties. Several peptides were found to be serodiagnostic for B. pseudomallei infection and two elicited bactericidal antibodies. Summary A significant amount of B. pseudomallei antigen structures, epitopes, and immunological data is available. Future challenges will be to test all available B.pseudomallei epitopes, focusing on combing multiple B/Tcell epitopes onto a single scaffold to generate components, stimulating both arms of the immune system

Structural Vaccinology for Melioidosis Vaccine Design and Immunodiagnostics

A Gori;G Colombo;
2017

Abstract

Purpose of Review Spurred by the successful application of structural vaccinology to other challenging bacterial and viral pathogens, we review the possibility of exploiting 3D struc- ture computational-based recombinant antigen engineering strategies for the development of a protective melioidosis vaccine.Recent Findings Structure-based epitope design approaches in the melioidosis field are preliminary and applied essentially by one research network. By combining Burkholderia pseudomallei antigen 3D structures and in silico epitope dis- covery methods, a panel of synthetic epitope peptides were designed and tested for their B and T cell stimulatory activi- ties. Several peptides were found to be serodiagnostic for B. pseudomallei infection and two elicited bactericidal antibodies. Summary A significant amount of B. pseudomallei antigen structures, epitopes, and immunological data is available. Future challenges will be to test all available B.pseudomallei epitopes, focusing on combing multiple B/Tcell epitopes onto a single scaffold to generate components, stimulating both arms of the immune system
2017
Istituto di Chimica del Riconoscimento Molecolare - ICRM - Sede Milano
Melioidosis . Vaccines . Epitope design . Structural vaccinology . B . pseudomallei . Antigens
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/340407
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