Q1 · MEDICINE
Article
Author: Vapalahti, Olli ; Bradfute, Steven B. ; Ulrich, Rainer G. ; Chandran, Kartik ; Strandin, Tomas ; Polanco, Laura C. ; Guardado-Calvo, Pablo ; Keller, Markus ; Bakken, Russell R. ; Pehau-Arnaudet, Gerard ; Wigren-Byström, Julia ; Sakharkar, Mrunal ; Wec, Anna Z. ; Bornholdt, Zachary A. ; Serris, Alexandra ; Jangra, Rohit K. ; Forsell, Mattias N. E. ; Geoghegan, James C. ; Herbert, Andrew S. ; Walker, Laura M. ; Ahlm, Clas ; Dye, John M. ; Slough, Megan M. ; Mittler, Eva ; O’Brien, Cecilia M. ; Rey, Felix A. ; Zeitlin, Larry ; Abelson, Dafna M. ; Tynell, Janne
The rodent-borne hantavirus Puumala virus (PUUV) and related agents cause hemorrhagic fever with renal syndrome (HFRS) in humans. Other hantaviruses, including Andes virus (ANDV) and Sin Nombre virus, cause a distinct zoonotic disease, hantavirus cardiopulmonary syndrome (HCPS). Although these infections are severe and have substantial case fatality rates, no FDA-approved hantavirus countermeasures are available. Recent work suggests that monoclonal antibodies may have therapeutic utility. We describe here the isolation of human neutralizing antibodies (nAbs) against tetrameric Gn/Gc glycoprotein spikes from PUUV-experienced donors. We define a dominant class of nAbs recognizing the “capping loop” of Gn that masks the hydrophobic fusion loops in Gc. A subset of nAbs in this class, including ADI-42898, bound Gn/Gc complexes but not Gn alone, strongly suggesting that they recognize a quaternary epitope encompassing both Gn and Gc. ADI-42898 blocked the cell entry of seven HCPS- and HFRS-associated hantaviruses, and single doses of this nAb could protect Syrian hamsters and bank voles challenged with the highly virulent HCPS-causing ANDV and HFRS-causing PUUV, respectively. ADI-42898 is a promising candidate for clinical development as a countermeasure for both HCPS and HFRS, and its mode of Gn/Gc recognition informs the development of broadly protective hantavirus vaccines.