TY - JOUR
T1 - Neutralizing monoclonal antibodies against the Gn and the Gc of the andes virus glycoprotein spike complex protect from virus challenge in a preclinical hamster model
AU - Duehr, James
AU - McMahon, Meagan
AU - Williamson, Brandi
AU - Amanat, Fatima
AU - Durbin, Alan
AU - Hawman, David W.
AU - Noack, Danny
AU - Uhl, Skyler
AU - Tan, Gene S.
AU - Feldmann, Heinz
AU - Krammer, Florian
N1 - Funding Information:
We thank Shirin Strohmeier and Andres Javier for their astute technical assistance in producing recombinant proteins; Seth Epstein and Randy A. Albrecht for managing the BSL3 facility at the Icahn School of Medicine at Mount Sinai; Raffael Nachbagauer for assistance in BSL3 work and for providing custom mouse ClipArt; the Institutional Biosafety Committee of Mount Sinai for their prompt and vital advisory role in ensuring our experiments were conducted with the upmost rigor; Teddy John Wohlbold for providing preliminary results and the concept of some figures; Kimberly Meade-White and Elaine Haddock of the Laboratory of Virology and members of the Rocky Mountain Veterinary Branch, all under the Division of Intramural Research (DIR), NAID, NIH, for support with infectious work and animal care and handling; Amar Parvate and Erica Saphire at the La Jolla Institute of Immunology for their assistance in troubleshooting our structural models; Alicia Solorzano, Lingling Liu, and Julie Durocher for their swift help coordinating the acquisition and transfer of viral isolates; Gorky Estrella and Jefferey Bethea at the Center for Comparative Medicine at Mount Sinai for maintaining and administrating the animal vivarium at Mount Sinai. The following reagents were obtained from BEI resources: anti-nucleocapsid polyclonal rabbit IgG for ANDV (NR- 9673). James Duehr was partially funded through NIH training fellowship 5T32AI007647-18. Gene S. Tan is supported with startup funding from the J. Craig Venter Institute. This project was financially supported by institutional seed funding to Florian Krammer, and funding was partially provided by the Intramural Research Program, NIAID, NIH. All data supporting our conclusions are contained in the manuscript. We declare no competing interests. J.D., M.M., B.W., F.A., A.D., D.N., S.U., and D.W.H. performed experiments. J.D., G.S.T., H.F., and F.K. designed the experiments and analyzed the data. J.D. and F.K. wrote the manuscript. All authors edited the manuscript
Funding Information:
James Duehr was partially funded through NIH training fellowship 5T32AI007647-18. Gene S. Tan is supported with startup funding from the J. Craig Venter Institute. This project was financially supported by institutional seed funding to Florian Krammer, and funding was partially provided by the Intramural Research Program, NIAID, NIH. All data supporting our conclusions are contained in the manuscript. We declare no competing interests.
Publisher Copyright:
© 2020 Duehr et al.
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Hantaviruses are the etiological agent of hemorrhagic fever with renal syndrome (HFRS) and hantavirus cardiopulmonary syndrome (HCPS). The latter is associated with case fatality rates ranging from 30% to 50%. HCPS cases are rare, with approximately 300 recorded annually in the Americas. Recently, an HCPS outbreak of unprecedented size has been occurring in and around Epuyén, in the southwestern Argentinian state of Chubut. Since November of 2018, at least 29 cases have been laboratory confirmed, and human-to-human transmission is suspected. Despite posing a significant threat to public health, no treatment or vaccine is available for hantaviral disease. Here, we describe an effort to identify, characterize, and develop neutralizing and protective antibodies against the glycoprotein complex (Gn and Gc) of Andes virus (ANDV), the causative agent of the Epuyén outbreak. Using murine hybridoma technology, we generated 19 distinct monoclonal antibodies (MAbs) against ANDV GnGc. When tested for neutralization against a recombinant vesicular stomatitis virus expressing the Andes glycoprotein (GP) (VSV-ANDV), 12 MAbs showed potent neutralization and 8 showed activity in an antibody-dependent cellular cytotoxicity reporter assay. Escape mutant analysis revealed that neutralizing MAbs targeted both the Gn and the Gc. Four MAbs that bound different epitopes were selected for preclinical studies and were found to be 100% protective against lethality in a Syrian hamster model of ANDV infection. These data suggest the existence of a wide array of neutralizing antibody epitopes on hantavirus GnGc with unique properties and mechanisms of action. IMPORTANCE Infections with New World hantaviruses are associated with high case fatality rates, and no specific vaccine or treatment options exist. Furthermore, the biology of the hantaviral GnGc complex, its antigenicity, and its fusion machinery are poorly understood. Protective monoclonal antibodies against GnGc have the potential to be developed into therapeutics against hantaviral disease and are also great tools to elucidate the biology of the glycoprotein complex.
AB - Hantaviruses are the etiological agent of hemorrhagic fever with renal syndrome (HFRS) and hantavirus cardiopulmonary syndrome (HCPS). The latter is associated with case fatality rates ranging from 30% to 50%. HCPS cases are rare, with approximately 300 recorded annually in the Americas. Recently, an HCPS outbreak of unprecedented size has been occurring in and around Epuyén, in the southwestern Argentinian state of Chubut. Since November of 2018, at least 29 cases have been laboratory confirmed, and human-to-human transmission is suspected. Despite posing a significant threat to public health, no treatment or vaccine is available for hantaviral disease. Here, we describe an effort to identify, characterize, and develop neutralizing and protective antibodies against the glycoprotein complex (Gn and Gc) of Andes virus (ANDV), the causative agent of the Epuyén outbreak. Using murine hybridoma technology, we generated 19 distinct monoclonal antibodies (MAbs) against ANDV GnGc. When tested for neutralization against a recombinant vesicular stomatitis virus expressing the Andes glycoprotein (GP) (VSV-ANDV), 12 MAbs showed potent neutralization and 8 showed activity in an antibody-dependent cellular cytotoxicity reporter assay. Escape mutant analysis revealed that neutralizing MAbs targeted both the Gn and the Gc. Four MAbs that bound different epitopes were selected for preclinical studies and were found to be 100% protective against lethality in a Syrian hamster model of ANDV infection. These data suggest the existence of a wide array of neutralizing antibody epitopes on hantavirus GnGc with unique properties and mechanisms of action. IMPORTANCE Infections with New World hantaviruses are associated with high case fatality rates, and no specific vaccine or treatment options exist. Furthermore, the biology of the hantaviral GnGc complex, its antigenicity, and its fusion machinery are poorly understood. Protective monoclonal antibodies against GnGc have the potential to be developed into therapeutics against hantaviral disease and are also great tools to elucidate the biology of the glycoprotein complex.
KW - Andes virus
KW - Hantavirus
KW - MAb
KW - Sin nombre virus
UR - http://www.scopus.com/inward/record.url?scp=85082380978&partnerID=8YFLogxK
U2 - 10.1128/mBio.00028-20
DO - 10.1128/mBio.00028-20
M3 - Article
C2 - 32209676
AN - SCOPUS:85082380978
SN - 2161-2129
VL - 11
JO - mBio
JF - mBio
IS - 2
M1 - e00028-20
ER -