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Integrated pipeline for the accelerated discovery of antiviral antibody therapeutics.

Authors :
Gilchuk P
Bombardi RG
Erasmus JH
Tan Q
Nargi R
Soto C
Abbink P
Suscovich TJ
Durnell LA
Khandhar A
Archer J
Liang J
Fouch ME
Davidson E
Doranz BJ
Jones T
Larson E
Ertel S
Granger B
Fuerte-Stone J
Roy V
Broge T
Linnekin TC
Linde CH
Gorman MJ
Nkolola J
Alter G
Reed SG
Barouch DH
Diamond MS
Crowe JE Jr
Van Hoeven N
Thackray LB
Carnahan RH
Source :
Nature biomedical engineering [Nat Biomed Eng] 2020 Nov; Vol. 4 (11), pp. 1030-1043. Date of Electronic Publication: 2020 Aug 03.
Publication Year :
2020

Abstract

The emergence and re-emergence of highly virulent viral pathogens with the potential to cause a pandemic creates an urgent need for the accelerated discovery of antiviral therapeutics. Antiviral human monoclonal antibodies (mAbs) are promising candidates for the prevention and treatment of severe viral diseases, but their long development timeframes limit their rapid deployment and use. Here, we report the development of an integrated sequence of technologies, including single-cell mRNA-sequence analysis, bioinformatics, synthetic biology and high-throughput functional analysis, that enables the rapid discovery of highly potent antiviral human mAbs, the activity of which we validated in vivo. In a 78-d study modelling the deployment of a rapid response to an outbreak, we isolated more than 100 human mAbs that are specific to Zika virus, assessed their function, identified that 29 of these mAbs have broadly neutralizing activity, and verified the therapeutic potency of the lead candidates in mice and non-human primate models of infection through the delivery of an antibody-encoding mRNA formulation and of the respective IgG antibody. The pipeline provides a roadmap for rapid antibody-discovery programmes against viral pathogens of global concern.

Details

Language :
English
ISSN :
2157-846X
Volume :
4
Issue :
11
Database :
MEDLINE
Journal :
Nature biomedical engineering
Publication Type :
Academic Journal
Accession number :
32747832
Full Text :
https://doi.org/10.1038/s41551-020-0594-x