Back

Broadly neutralizing antibodies against emerging delta-coronaviruses

Rexhepaj, M.; Park, Y.-J.; Perruzza, L.; Asarnow, D.; McCallum, M.; Culap, K.; Saliba, C.; Leoni, G.; Balmeli, A.; Yoshiyama, C.; Dickinson, M. S.; Quispe, J.; Brown, J. T.; Tortorici, M. A.; Sprouse, K. R.; Taylor, A. L.; Starr, T. N.; Corti, D.; Begnini, F.; Veesler, D.

2024-04-01 biochemistry
10.1101/2024.03.27.586411 bioRxiv
Show abstract

Porcine deltacoronavirus (PDCoV) spillovers were recently detected in children with acute undifferentiated febrile illness, underscoring recurrent zoonoses of divergent coronaviruses. To date, no vaccines or specific therapeutics are approved for use in humans against PDCoV. To prepare for possible future PDCoV epidemics, we isolated human spike (S)-directed monoclonal antibodies from transgenic mice and found that two of them, designated PD33 and PD41, broadly neutralized a panel of PDCoV variants. Cryo-electron microscopy structures of PD33 and PD41 in complex with the PDCoV receptor-binding domain and S ectodomain trimer provide a blueprint of the epitopes recognized by these mAbs, rationalizing their broad inhibitory activity. We show that both mAbs inhibit PDCoV by competitively interfering with host APN binding to the PDCoV receptor-binding loops, explaining the mechanism of viral neutralization. PD33 and PD41 are candidates for clinical advancement, which could be stockpiled to prepare for possible future PDCoV outbreaks.

Matching journals

The top 5 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.