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A combination of potently neutralizing monoclonal antibodies isolated from an Indian convalescent donor protects against the SARS-CoV-2 Delta variant.
Hingankar, Nitin; Deshpande, Suprit; Das, Payel; Rizvi, Zaigham Abbas; Wibmer, Constantinos Kurt; Mashilo, Poppy; Ansari, Mohammed Yousuf; Burns, Alison; Barman, Shawn; Zhao, Fangzhu; Mukherjee, Sohini; Torres, Jonathan L; Chattopadhyay, Souvick; Mehdi, Farha; Sutar, Jyoti; Rathore, Deepak Kumar; Pargai, Kamal; Singh, Janmejay; Sonar, Sudipta; Jakhar, Kamini; Dandotiya, Jyotsna; Bhattacharyya, Sankar; Mani, Shailendra; Samal, Sweety; Singh, Savita; Kshetrapal, Pallavi; Thiruvengadam, Ramachandran; Batra, Gaurav; Medigeshi, Guruprasad; Ward, Andrew B; Bhatnagar, Shinjini; Awasthi, Amit; Sok, Devin; Bhattacharya, Jayanta.
  • Hingankar N; IAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Deshpande S; IAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Das P; IAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Rizvi ZA; Immuno-biology Lab, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Wibmer CK; Immunology Core, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Mashilo P; National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS), Johannesburg, South Africa.
  • Ansari MY; National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS), Johannesburg, South Africa.
  • Burns A; IAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Barman S; Scripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Zhao F; IAVI Neutralizing Antibody Center and the Collaboration for AIDS Vaccine Discovery (CAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Mukherjee S; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Torres JL; Scripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Chattopadhyay S; IAVI Neutralizing Antibody Center and the Collaboration for AIDS Vaccine Discovery (CAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Mehdi F; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Sutar J; Scripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Rathore DK; IAVI Neutralizing Antibody Center and the Collaboration for AIDS Vaccine Discovery (CAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Pargai K; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Singh J; IAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Sonar S; IAVI, New York, United States of America.
  • Jakhar K; IAVI, New Delhi, India.
  • Dandotiya J; Scripps Consortium for HIV/AIDS Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Bhattacharyya S; IAVI Neutralizing Antibody Center and the Collaboration for AIDS Vaccine Discovery (CAVD), The Scripps Research Institute, La Jolla, California, United States of America.
  • Mani S; Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Samal S; Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Singh S; Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Kshetrapal P; IAVI HIV Vaccine Translational Research Laboratory, IAVI-THSTI partnership program, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Thiruvengadam R; IAVI, New York, United States of America.
  • Batra G; IAVI, New Delhi, India.
  • Medigeshi G; Immunology Core, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Ward AB; Bioassay laboratory, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Bhatnagar S; Bioassay laboratory, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Awasthi A; Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Sok D; Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
  • Bhattacharya J; Immuno-biology Lab, Translational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
PLoS Pathog ; 18(4): e1010465, 2022 04.
Article in English | MEDLINE | ID: covidwho-1817511
ABSTRACT
Although efficacious vaccines have significantly reduced the morbidity and mortality of COVID-19, there remains an unmet medical need for treatment options, which monoclonal antibodies (mAbs) can potentially fill. This unmet need is exacerbated by the emergence and spread of SARS-CoV-2 variants of concern (VOCs) that have shown some resistance to vaccine responses. Here we report the isolation of five neutralizing mAbs from an Indian convalescent donor, out of which two (THSC20.HVTR04 and THSC20.HVTR26) showed potent neutralization of SARS-CoV-2 VOCs at picomolar concentrations, including the Delta variant (B.1.617.2). One of these (THSC20.HVTR26) also retained activity against the Omicron variant. These two mAbs target non-overlapping epitopes on the receptor-binding domain (RBD) of the spike protein and prevent virus attachment to its host receptor, human angiotensin converting enzyme-2 (hACE2). Furthermore, the mAb cocktail demonstrated protection against the Delta variant at low antibody doses when passively administered in the K18 hACE2 transgenic mice model, highlighting their potential as a cocktail for prophylactic and therapeutic applications. Developing the capacity to rapidly discover and develop mAbs effective against highly transmissible pathogens like coronaviruses at a local level, especially in a low- and middle-income country (LMIC) such as India, will enable prompt responses to future pandemics as an important component of global pandemic preparedness.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Animals Language: English Journal: PLoS Pathog Year: 2022 Document Type: Article Affiliation country: Journal.ppat.1010465

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Animals Language: English Journal: PLoS Pathog Year: 2022 Document Type: Article Affiliation country: Journal.ppat.1010465