A human monoclonal antibody combination rescues nonhuman primates from advanced disease caused by the major lineages of Lassa virus

Author:

Cross Robert W.12ORCID,Heinrich Megan L.3,Fenton Karla A.12ORCID,Borisevich Viktoriya12,Agans Krystle N.12ORCID,Prasad Abhishek N.12ORCID,Woolsey Courtney12ORCID,Deer Daniel J.12,Dobias Natalie S.12ORCID,Rowland Megan M.3,Lathigra Raju3,Borrega Rodrigo3ORCID,Geisbert Joan B.12,Garry Robert F.34ORCID,Branco Luis M.3,Geisbert Thomas W.12ORCID

Affiliation:

1. Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555

2. Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555

3. Zalgen Labs, Limited Liability Company, Frederick, MD 21703

4. Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, LA 70112

Abstract

There are no approved treatments for Lassa fever (LF), which is responsible for thousands of deaths each year in West Africa. A major challenge in developing effective medical countermeasures against LF is the high diversity of circulating Lassa virus (LASV) strains with four recognized lineages and four proposed lineages. The recent resurgence of LASV in Nigeria caused by genetically distinct strains underscores this concern. Two LASV lineages (II and III) are dominant in Nigeria. Here, we show that combinations of two or three pan-lineage neutralizing human monoclonal antibodies (8.9F, 12.1F, 37.D) known as Arevirumab-2 or Arevirumab-3 can protect up to 100% of cynomolgus macaques against challenge with both lineage II and III LASV isolates when treatment is initiated at advanced stages of disease on day 8 after LASV exposure. This work demonstrates that it may be possible to develop postexposure interventions that can broadly protect against most strains of LASV.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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