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Induction of neutralizing antibodies against SARS-CoV-2 variants by a multivalent mRNA-lipid nanoparticle vaccine encoding SARS-CoV-2/SARS-CoV Spike protein receptor-binding domains in mice.
Zhang, Qiong; Tiwari, Shashi; Wen, Jing; Wang, Shaobo; Wang, Lingling; Li, Wanyu; Zhang, Lingzhi; Rawling, Stephen; Cheng, Yong; Jokerst, Jesse; Rana, Tariq M.
Affiliation
  • Zhang Q; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Tiwari S; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Wen J; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Wang S; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Wang L; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Li W; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Zhang L; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Rawling S; Division of Infectious Diseases, Department of Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
  • Cheng Y; Department of NanoEngineering, University of California San Diego, La Jolla, CA, United States of America.
  • Jokerst J; Department of NanoEngineering, University of California San Diego, La Jolla, CA, United States of America.
  • Rana TM; Division of Genetics, Department of Pediatrics, Program in Immunology, Bioinformatics and Systems Biology Program, Institute for Genomic Medicine, UCSD Center for AIDS Research, University of California San Diego, La Jolla, California, United States of America.
PLoS One ; 19(4): e0300524, 2024.
Article de En | MEDLINE | ID: mdl-38635805
ABSTRACT
To address the need for multivalent vaccines against Coronaviridae that can be rapidly developed and manufactured, we compared antibody responses against SARS-CoV, SARS-CoV-2, and several variants of concern in mice immunized with mRNA-lipid nanoparticle vaccines encoding homodimers or heterodimers of SARS-CoV/SARS-CoV-2 receptor-binding domains. All vaccine constructs induced robust anti-RBD antibody responses, and the heterodimeric vaccine elicited an IgG response capable of cross-neutralizing SARS-CoV, SARS-CoV-2 Wuhan-Hu-1, B.1.351 (beta), and B.1.617.2 (delta) variants.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: SARS-CoV-2 / COVID-19 Limites: Animals / Humans Langue: En Journal: PLoS One Sujet du journal: CIENCIA / MEDICINA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: SARS-CoV-2 / COVID-19 Limites: Animals / Humans Langue: En Journal: PLoS One Sujet du journal: CIENCIA / MEDICINA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique