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Therapeutic effect of CT-P59 against SARS-CoV-2 South African variant.
Ryu, Dong-Kyun; Song, Rina; Kim, Minsoo; Kim, Young-Il; Kim, Cheolmin; Kim, Jong-In; Kwon, Ki-Sung; Tijsma, Aloys Sl; Nuijten, Patricia M; van Baalen, Carel A; Hermanus, Tandile; Kgagudi, Prudence; Moyo-Gwete, Thandeka; Moore, Penny L; Choi, Young Ki; Lee, Soo-Young.
  • Ryu DK; Biotechnology Research Institute, Celltrion Inc., Incheon, Republic of Korea.
  • Song R; Biotechnology Research Institute, Celltrion Inc., Incheon, Republic of Korea.
  • Kim M; Biotechnology Research Institute, Celltrion Inc., Incheon, Republic of Korea.
  • Kim YI; College of Medicine and Medical Research Institute, Chungbuk National University, Cheongju, Republic of Korea.
  • Kim C; Biotechnology Research Institute, Celltrion Inc., Incheon, Republic of Korea.
  • Kim JI; Biotechnology Research Institute, Celltrion Inc., Incheon, Republic of Korea.
  • Kwon KS; Biotechnology Research Institute, Celltrion Inc., Incheon, Republic of Korea.
  • Tijsma AS; Viroclinics Biosciences, Rotterdam, the Netherlands.
  • Nuijten PM; Viroclinics Biosciences, Rotterdam, the Netherlands.
  • van Baalen CA; Viroclinics Biosciences, Rotterdam, the Netherlands.
  • Hermanus T; National Institute for Communicable Disease, Johannesburg of the National Health Laboratory Services, South Africa.
  • Kgagudi P; National Institute for Communicable Disease, Johannesburg of the National Health Laboratory Services, South Africa.
  • Moyo-Gwete T; National Institute for Communicable Disease, Johannesburg of the National Health Laboratory Services, South Africa.
  • Moore PL; National Institute for Communicable Disease, Johannesburg of the National Health Laboratory Services, South Africa.
  • Choi YK; College of Medicine and Medical Research Institute, Chungbuk National University, Cheongju, Republic of Korea.
  • Lee SY; Biotechnology Research Institute, Celltrion Inc., Incheon, Republic of Korea. Electronic address: sooyoung.lee@celltrion.com.
Biochem Biophys Res Commun ; 566: 135-140, 2021 08 20.
Article in English | MEDLINE | ID: covidwho-1260666
ABSTRACT
The global circulation of newly emerging variants of SARS-CoV-2 is a new threat to public health due to their increased transmissibility and immune evasion. Moreover, currently available vaccines and therapeutic antibodies were shown to be less effective against new variants, in particular, the South African (SA) variant, termed 501Y.V2 or B.1.351. To assess the efficacy of the CT-P59 monoclonal antibody against the SA variant, we sought to perform as in vitro binding and neutralization assays, and in vivo animal studies. CT-P59 neutralized B.1.1.7 variant to a similar extent as to wild type virus. CT-P59 showed reduced binding affinity against a RBD (receptor binding domain) triple mutant containing mutations defining B.1.351 (K417N/E484K/N501Y) also showed reduced potency against the SA variant in live virus and pseudovirus neutralization assay systems. However, in vivo ferret challenge studies demonstrated that a therapeutic dosage of CT-P59 was able to decrease B.1.351 viral load in the upper and lower respiratory tracts, comparable to that observed for the wild type virus. Overall, although CT-P59 showed reduced in vitro neutralizing activity against the SA variant, sufficient antiviral effect in B.1.351-infected animals was confirmed with a clinical dosage of CT-P59, suggesting that CT-P59 has therapeutic potential for COVID-19 patients infected with SA variant.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin G / Antibodies, Neutralizing / Antibodies, Monoclonal, Humanized / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Animals / Female / Humans Country/Region as subject: Africa Language: English Journal: Biochem Biophys Res Commun Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin G / Antibodies, Neutralizing / Antibodies, Monoclonal, Humanized / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Animals / Female / Humans Country/Region as subject: Africa Language: English Journal: Biochem Biophys Res Commun Year: 2021 Document Type: Article