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19n01, a broadly neutralizing antibody against omicron BA.1, BA.2, BA.4/5, and other SARS-CoV-2 variants of concern.
García-Vega, Melissa; Melgoza-González, Edgar A; Hernández-Valenzuela, Sofía; Hinojosa-Trujillo, Diana; Reséndiz-Sandoval, Mónica; Llamas-Covarrubias, Mara Anais; Loza-López, Martín; Valenzuela, Olivia; Soto-Gaxiola, Alan; Hernández-Oñate, Miguel A; Mata-Haro, Verónica; Cassaniti, Irene; Sammartino, Josè Camilla; Ferrari, Alessandro; Simonelli, Luca; Pedotti, Mattia; Sun, Rui; Zuo, Fanglei; Baldanti, Fausto; Varani, Luca; Marcotte, Harold; Pan-Hammarström, Qiang; Hernández, Jesús.
  • García-Vega M; Laboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C. Hermosillo, Sonora, Mexico.
  • Melgoza-González EA; Laboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C. Hermosillo, Sonora, Mexico.
  • Hernández-Valenzuela S; Laboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C. Hermosillo, Sonora, Mexico.
  • Hinojosa-Trujillo D; Laboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C. Hermosillo, Sonora, Mexico.
  • Reséndiz-Sandoval M; Laboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C. Hermosillo, Sonora, Mexico.
  • Llamas-Covarrubias MA; Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
  • Loza-López M; Laboratory of Functional Analysis in silico, The University of Tokyo, Shirokanedai, Tokyo, Japan.
  • Valenzuela O; Departamento de Ciencias Químico Biológicas, División de Ciencias de la Salud, Universidad de Sonora, Hermosillo, Sonora, Mexico.
  • Soto-Gaxiola A; Hospital General del Estado de Sonora "Dr. Ernesto Ramos Bours", Secretaria de Salud del Estado de Sonora, Hermosillo, Sonora, Mexico.
  • Hernández-Oñate MA; Laboratorio de Fisiología y Biología Molecular de Plantas, Centro de Investigación en Alimentación y Desarrollo, A.C. Hermosillo, Sonora, Mexico.
  • Mata-Haro V; Laboratorio de Microbiología e Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C. Hermosillo, Sonora, Mexico.
  • Cassaniti I; Microbiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Sammartino JC; Microbiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Ferrari A; Microbiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Simonelli L; Institute for Research in Biomedicine, Università della Svizzera italiana (USI), Bellinzona, Switzerland.
  • Pedotti M; Institute for Research in Biomedicine, Università della Svizzera italiana (USI), Bellinzona, Switzerland.
  • Sun R; Division of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
  • Zuo F; Division of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
  • Baldanti F; Microbiology and Virology Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Varani L; Department of Clinical, Surgical, Diagnostics and Pediatric Sciences, University of Pavia, Pavia, Italy.
  • Marcotte H; Institute for Research in Biomedicine, Università della Svizzera italiana (USI), Bellinzona, Switzerland.
  • Pan-Hammarström Q; Division of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
  • Hernández J; Division of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
iScience ; 26(4): 106562, 2023 Apr 21.
Article in English | MEDLINE | ID: covidwho-2295366
ABSTRACT
This study reports the isolation and characterization of a human monoclonal antibody (mAb) called 19n01. This mAb was isolated by using single-cell RNAseq of B cells from donors infected with the ancestral strain. This mAb possesses a potent and broad capacity to bind and neutralize all previously circulating variants of concern (VOCs), including Omicron sublineages BA.1, BA.2, and BA.4/5. The pseudovirus neutralization assay revealed robust neutralization capacity against the G614 strain, BA.1, BA.2, and BA.4/5, with inhibitory concentration (IC50) values ranging from 0.0035 to 0.0164 µg/mL. The microneutralization assay using the G614 strain and VOCs demonstrated IC50 values of 0.013-0.267 µg/mL. Biophysical and structural analysis showed that 19n01 cross-competes with ACE2 binding to the receptor-binding domain (RBD) and the kinetic parameters confirmed the high affinity against the Omicron sublineages (KD of 61 and 30 nM for BA.2 and BA.4/5, respectively). These results suggest that the 19n01 is a remarkably potent and broadly reactive mAb.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Randomized controlled trials Topics: Variants Language: English Journal: IScience Year: 2023 Document Type: Article Affiliation country: J.isci.2023.106562

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Randomized controlled trials Topics: Variants Language: English Journal: IScience Year: 2023 Document Type: Article Affiliation country: J.isci.2023.106562