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Human monoclonal antibodies against chikungunya virus target multiple distinct epitopes in the E1 and E2 glycoproteins.
Quiroz, Jose A; Malonis, Ryan J; Thackray, Larissa B; Cohen, Courtney A; Pallesen, Jesper; Jangra, Rohit K; Brown, Rebecca S; Hofmann, Daniel; Holtsberg, Frederick W; Shulenin, Sergey; Nyakatura, Elisabeth K; Durnell, Lorellin A; Rayannavar, Vinayak; Daily, Johanna P; Ward, Andrew B; Aman, M Javad; Dye, John M; Chandran, Kartik; Diamond, Michael S; Kielian, Margaret; Lai, Jonathan R.
Afiliación
  • Quiroz JA; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Malonis RJ; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Thackray LB; Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, United States of America.
  • Cohen CA; Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, United States of America.
  • Pallesen J; Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Jangra RK; Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Brown RS; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Hofmann D; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Holtsberg FW; Integrated Biotherapeutics Inc., Rockville, Maryland, United States of America.
  • Shulenin S; Integrated Biotherapeutics Inc., Rockville, Maryland, United States of America.
  • Nyakatura EK; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Durnell LA; Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, United States of America.
  • Rayannavar V; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Daily JP; Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Ward AB; Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California, United States of America.
  • Aman MJ; Integrated Biotherapeutics Inc., Rockville, Maryland, United States of America.
  • Dye JM; Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, United States of America.
  • Chandran K; Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, United States of America.
  • Diamond MS; Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, United States of America.
  • Kielian M; Department of Molecular Microbiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, United States of America.
  • Lai JR; Department of Pathology & Immunology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, United States of America.
PLoS Pathog ; 15(11): e1008061, 2019 11.
Article en En | MEDLINE | ID: mdl-31697791
ABSTRACT
Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes persistent arthritis in a subset of human patients. We report the isolation and functional characterization of monoclonal antibodies (mAbs) from two patients infected with CHIKV in the Dominican Republic. Single B cell sorting yielded a panel of 46 human mAbs of diverse germline lineages that targeted epitopes within the E1 or E2 glycoproteins. MAbs that recognized either E1 or E2 proteins exhibited neutralizing activity. Viral escape mutations localized the binding epitopes for two E1 mAbs to sites within domain I or the linker between domains I and III; and for two E2 mAbs between the ß-connector region and the B-domain. Two of the E2-specific mAbs conferred protection in vivo in a stringent lethal challenge mouse model of CHIKV infection, whereas the E1 mAbs did not. These results provide insight into human antibody response to CHIKV and identify candidate mAbs for therapeutic intervention.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Glicoproteínas / Virus Chikungunya / Proteínas del Envoltorio Viral / Fiebre Chikungunya / Anticuerpos Monoclonales / Anticuerpos Antivirales / Epítopos Límite: Adult / Animals / Humans Idioma: En Revista: PLoS Pathog Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Glicoproteínas / Virus Chikungunya / Proteínas del Envoltorio Viral / Fiebre Chikungunya / Anticuerpos Monoclonales / Anticuerpos Antivirales / Epítopos Límite: Adult / Animals / Humans Idioma: En Revista: PLoS Pathog Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos