TY - JOUR
T1 - Multimeric single-domain antibody complexes protect against bunyavirus infections
AU - Wichgers Schreur, Paul J.
AU - van de Water, Sandra
AU - Harmsen, Michiel
AU - Bermúdez-Méndez, Erick
AU - Drabek, Dubravka
AU - Grosveld, Frank
AU - Wernike, Kerstin
AU - Beer, Martin
AU - Aebischer, Andrea
AU - Daramola, Olalekan
AU - Conde, Sara Rodriguez
AU - Brennan, Karen
AU - Kozub, Dorota
AU - Kristiansen, Maiken Søndergaard
AU - Mistry, Kieran K.
AU - Deng, Ziyan
AU - Hellert, Jan
AU - Guardado-Calvo, Pablo
AU - Rey, Félix A.
AU - van Keulen, Lucien
AU - Kortekaas, Jeroen
PY - 2020/4
Y1 - 2020/4
N2 - The World Health Organization has included three bunyaviruses posing an increasing threat to human health on the Blueprint list of viruses likely to cause major epidemics and for which no, or insufficient countermeasures exist. Here, we describe a broadly applicable strategy, based on llama-derived single-domain antibodies (VHHs), for the development of bunyavirus biotherapeutics. The method was validated using the zoonotic Rift Valley fever virus (RVFV) and Schmallenberg virus (SBV), an emerging pathogen of ruminants, as model pathogens. VHH building blocks were assembled into highly potent neutralizing complexes using bacterial superglue technology. The multimeric complexes were shown to reduce and prevent virus-induced morbidity and mortality in mice upon prophylactic administration. Bispecific molecules engineered to present two different VHHs fused to an Fc domain were further shown to be effective upon therapeutic administration. The presented VHH-based technology holds great promise for the development of bunyavirus antiviral therapies.
AB - The World Health Organization has included three bunyaviruses posing an increasing threat to human health on the Blueprint list of viruses likely to cause major epidemics and for which no, or insufficient countermeasures exist. Here, we describe a broadly applicable strategy, based on llama-derived single-domain antibodies (VHHs), for the development of bunyavirus biotherapeutics. The method was validated using the zoonotic Rift Valley fever virus (RVFV) and Schmallenberg virus (SBV), an emerging pathogen of ruminants, as model pathogens. VHH building blocks were assembled into highly potent neutralizing complexes using bacterial superglue technology. The multimeric complexes were shown to reduce and prevent virus-induced morbidity and mortality in mice upon prophylactic administration. Bispecific molecules engineered to present two different VHHs fused to an Fc domain were further shown to be effective upon therapeutic administration. The presented VHH-based technology holds great promise for the development of bunyavirus antiviral therapies.
U2 - 10.7554/eLife.52716
DO - 10.7554/eLife.52716
M3 - Article
C2 - 32314955
AN - SCOPUS:85083812029
SN - 2050-084X
VL - 9
JO - eLife
JF - eLife
M1 - e52716
ER -