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Characterization of two affinity matured Anti-Yersinia pestis F1 human antibodies with medical countermeasure potential.
Velappan, Nileena; Biryukov, Sergei S; Rill, Nathaniel O; Klimko, Christopher P; Rosario-Acevedo, Raysa; Shoe, Jennifer L; Hunter, Melissa; Dankmeyer, Jennifer L; Fetterer, David P; Bedinger, Daniel; Phipps, Mary E; Watt, Austin J; Abergel, Rebecca J; Dichosa, Armand; Kozimor, Stosh A; Cote, Christopher K; Lillo, Antonietta M.
Afiliación
  • Velappan N; Biosciences Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.
  • Biryukov SS; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Rill NO; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Klimko CP; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Rosario-Acevedo R; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Shoe JL; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Hunter M; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Dankmeyer JL; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Fetterer DP; Biostatisitics Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Bedinger D; Carterra, Walnut Creek, CA, United States of America.
  • Phipps ME; Los Alamos National Laboratory, Center Alamos for Integrated Nanotechnologies, Los Alamos, NM, United States of America.
  • Watt AJ; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
  • Abergel RJ; Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States of America.
  • Dichosa A; Department of Nuclear Engineering, University of California, Berkeley, CA, United States of America.
  • Kozimor SA; Biosciences Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.
  • Cote CK; Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.
  • Lillo AM; Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States of America.
PLoS One ; 19(7): e0305034, 2024.
Article en En | MEDLINE | ID: mdl-38954719
ABSTRACT
Yersinia pestis, the causative agent of plague and a biological threat agent, presents an urgent need for novel medical countermeasures due to documented cases of naturally acquired antibiotic resistance and potential person-to-person spread during a pneumonic infection. Immunotherapy has been proposed as a way to circumvent current and future antibiotic resistance. Here, we describe the development and characterization of two affinity matured human antibodies (αF1Ig AM2 and αF1Ig AM8) that promote survival of mice after exposure to aerosolized Y. pestis. We share details of the error prone PCR and yeast display technology-based affinity maturation process that we used. The resultant matured antibodies have nanomolar affinity for Y. pestis F1 antigen, are produced in high yield, and are resilient to 37°C stress for up to 6 months. Importantly, in vitro assays using a murine macrophage cell line demonstrated that αF1Ig AM2 and αF1Ig AM8 are opsonic. Even more importantly, in vivo studies using pneumonic plague mouse models showed that 100% of the mice receiving 500 µg of IgGs αF1Ig AM2 and αF1Ig AM8 survived lethal challenge with aerosolized Y. pestis CO92. Combined, these results provide evidence of the quality and robustness of αF1Ig AM2 and αF1Ig AM8 and support their development as potential medical countermeasures against plague.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Peste / Yersinia pestis / Anticuerpos Antibacterianos Límite: Animals / Female / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Peste / Yersinia pestis / Anticuerpos Antibacterianos Límite: Animals / Female / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos