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Rapid generation of a human monoclonal antibody to combat Middle East respiratory syndrome

Identifieur interne : 001048 ( Main/Exploration ); précédent : 001047; suivant : 001049

Rapid generation of a human monoclonal antibody to combat Middle East respiratory syndrome

Auteurs : Davide Corti [Suisse] ; Nadia Passini [Suisse] ; Antonio Lanzavecchia [Suisse] ; Maria Zambon [Royaume-Uni]

Source :

RBID : PMC:7102728

Descripteurs français

English descriptors

Abstract

Summary

The last century has witnessed the emergence of several previously unknown viruses as life-threatening human pathogens. Several examples include HIV, Ebola, Lujo, and, most recently, the Middle East respiratory syndrome (MERS) and Ebola. In this study, we describe a method for the swift generation of a human-derived monoclonal antibody, known as LCA60, as a treatment for MERS infections. LCA60 antibody was generated using the Cellclone Technology from the immortalized B cells of a human donor recovering from MERS. Only four months were required from the initial screening of B cells to the development of a stable CHO cell line suitable for the production of clinical grade antibody, thereby delineating a rapid pathway for the development of antiviral therapies against emerging viruses. Currently, the LCA60 antibody is being considered for clinical development, which includes prophylaxis in individuals at risk and a treatment for severe MERS-CoV infections.


Url:
DOI: 10.1016/j.jiph.2016.04.003
PubMed: 27102927
PubMed Central: 7102728


Affiliations:


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Le document en format XML

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<p>The last century has witnessed the emergence of several previously unknown viruses as life-threatening human pathogens. Several examples include HIV, Ebola, Lujo, and, most recently, the Middle East respiratory syndrome (MERS) and Ebola. In this study, we describe a method for the swift generation of a human-derived monoclonal antibody, known as LCA60, as a treatment for MERS infections. LCA60 antibody was generated using the Cellclone Technology from the immortalized B cells of a human donor recovering from MERS. Only four months were required from the initial screening of B cells to the development of a stable CHO cell line suitable for the production of clinical grade antibody, thereby delineating a rapid pathway for the development of antiviral therapies against emerging viruses. Currently, the LCA60 antibody is being considered for clinical development, which includes prophylaxis in individuals at risk and a treatment for severe MERS-CoV infections.</p>
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