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A pandemic-enabled comparison of discovery platforms demonstrates a naïve antibody library can match the best immune-sourced antibodies.
Ferrara, Fortunato; Erasmus, M Frank; D'Angelo, Sara; Leal-Lopes, Camila; Teixeira, André A; Choudhary, Alok; Honnen, William; Calianese, David; Huang, Deli; Peng, Linghan; Voss, James E; Nemazee, David; Burton, Dennis R; Pinter, Abraham; Bradbury, Andrew R M.
  • Ferrara F; Specifica Inc, Santa Fe, NM, 87505, USA.
  • Erasmus MF; Specifica Inc, Santa Fe, NM, 87505, USA.
  • D'Angelo S; Specifica Inc, Santa Fe, NM, 87505, USA.
  • Leal-Lopes C; Bioscience Division, New Mexico Consortium, Los Alamos, NM, 87544, USA.
  • Teixeira AA; Bioscience Division, New Mexico Consortium, Los Alamos, NM, 87544, USA.
  • Choudhary A; Public Health Research Institute, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ, 07103, USA.
  • Honnen W; Public Health Research Institute, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ, 07103, USA.
  • Calianese D; Public Health Research Institute, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ, 07103, USA.
  • Huang D; Life Sciences Institute, Zhejiang University, Hangzhou, China.
  • Peng L; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, 92037, USA.
  • Voss JE; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, 92037, USA.
  • Nemazee D; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, 92037, USA.
  • Burton DR; Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, 92037, USA.
  • Pinter A; Ragon Institute of MGH, MIT and Harvard, Cambridge, MA, 02139, USA.
  • Bradbury ARM; Public Health Research Institute, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ, 07103, USA.
Nat Commun ; 13(1): 462, 2022 01 24.
Article in English | MEDLINE | ID: covidwho-1650125
ABSTRACT
As a result of the SARS-CoV-2 pandemic numerous scientific groups have generated antibodies against a single target the CoV-2 spike antigen. This has provided an unprecedented opportunity to compare the efficacy of different methods and the specificities and qualities of the antibodies generated by those methods. Generally, the most potent neutralizing antibodies have been generated from convalescent patients and immunized animals, with non-immune phage libraries usually yielding significantly less potent antibodies. Here, we show that it is possible to generate ultra-potent (IC50 < 2 ng/ml) human neutralizing antibodies directly from a unique semisynthetic naïve antibody library format with affinities, developability properties and neutralization activities comparable to the best from hyperimmune sources. This demonstrates that appropriately designed and constructed naïve antibody libraries can effectively compete with immunization to directly provide therapeutic antibodies against a viral pathogen, without the need for immune sources or downstream optimization.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Experimental Studies / Observational study / Randomized controlled trials Limits: Animals / Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-021-27799-z

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antibodies, Neutralizing / Spike Glycoprotein, Coronavirus / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Experimental Studies / Observational study / Randomized controlled trials Limits: Animals / Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-021-27799-z