Selected article for: "beta cov and CoV replication"

Author: Roodink, Ilse; van Erp, Maartje; Li, Andra; Potter, Sheila; van Duijnhoven, Sander M J; Kuipers, Arthur J; Kazemier, Bert; van Geffen, Ellen; Hemrika, Wieger; Berkeveld, Bob; Sonnemans, Glenn; de Vries, Britte S; Boers, Bianca; Smits, Milou; Meurs, Sanne; de Pooter, Maaike; Thom, Alexandra; Duplantis, Barry N; Romijn, Roland A; Houser, Jeremy; Bath, Jennifer; Abdiche, Yasmina N
Title: Cornering an Ever-Evolving Coronavirus: TATX-03, a fully human synergistic multi-antibody cocktail targeting the SARS-CoV-2 Spike Protein with in vivo efficacy
  • Cord-id: zw82d0us
  • Document date: 2021_7_21
  • ID: zw82d0us
    Snippet: The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has created an ongoing global human health crisis and will likely become endemic, requiring novel sustainable therapeutic strategies. We report on the discovery of a fully human multi-antibody cocktail (TATX-03) targeting diversified non-overlapping epitopes on the SARS-CoV-2 spike protein that suppressed replication-competent viral titers to undetectable levels in the lungs of SARS-CoV-2 challenged hamsters upon both
    Document: The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has created an ongoing global human health crisis and will likely become endemic, requiring novel sustainable therapeutic strategies. We report on the discovery of a fully human multi-antibody cocktail (TATX-03) targeting diversified non-overlapping epitopes on the SARS-CoV-2 spike protein that suppressed replication-competent viral titers to undetectable levels in the lungs of SARS-CoV-2 challenged hamsters upon both prophylactic and therapeutic administration. While monotherapy with two of the individual cocktail components also showed clear in vivo protection, neither recapitulated the efficacy of TATX-03. This synergistic effect was further supported by examining in vivo efficacy of these individual antibodies and corresponding combination therapy at a lower dose. Furthermore, in vitro screenings using VSV-particles pseudo-typed with spike proteins representing the SARS-CoV-2 variants of concern Alpha, Beta, and Delta showed that TATX-03 maintained its neutralization potency. These results merit further development of TATX-03 as a potential therapy for SARS-CoV-2 infection with resistance to mutagenic escape.

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