Your browser doesn't support javascript.
loading
Immunogenicity of a killed bivalent (O1 and O139) whole cell oral cholera vaccine, Shanchol, in Haiti.
Charles, Richelle C; Hilaire, Isabelle J; Mayo-Smith, Leslie M; Teng, Jessica E; Jerome, J Gregory; Franke, Molly F; Saha, Amit; Yu, Yanan; Kovác, Paul; Calderwood, Stephen B; Ryan, Edward T; LaRocque, Regina C; Almazor, Charles P; Qadri, Firdausi; Ivers, Louise C; Harris, Jason B.
Afiliação
  • Charles RC; Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Hilaire IJ; Partners In Health, Boston, Massachusetts, United States of America.
  • Mayo-Smith LM; Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
  • Teng JE; Partners In Health, Boston, Massachusetts, United States of America; Division of Global Health Equity, Brigham and Women's Hospital, Boston, Massachusetts, United States of America.
  • Jerome JG; Partners In Health, Boston, Massachusetts, United States of America.
  • Franke MF; Partners In Health, Boston, Massachusetts, United States of America; Department of Global Health and Social Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Saha A; International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Yu Y; Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
  • Kovác P; National Institute of Diabetes and Digestive and Kidney Diseases, Laboratory of Bioorganic Chemistry, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Calderwood SB; Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America; Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachuset
  • Ryan ET; Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America; Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston
  • LaRocque RC; Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Almazor CP; Partners In Health, Boston, Massachusetts, United States of America.
  • Qadri F; International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Ivers LC; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America; Partners In Health, Boston, Massachusetts, United States of America; Division of Global Health Equity, Brigham and Women's Hospital, Boston, Massachusetts, United States of America; Department of Global
  • Harris JB; Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS Negl Trop Dis ; 8(5): e2828, 2014 May.
Article em En | MEDLINE | ID: mdl-24786645
BACKGROUND: Studies of the immunogenicity of the killed bivalent whole cell oral cholera vaccine, Shanchol, have been performed in historically cholera-endemic areas of Asia. There is a need to assess the immunogenicity of the vaccine in Haiti and other populations without historical exposure to Vibrio cholerae. METHODOLOGY/PRINCIPAL FINDINGS: We measured immune responses after administration of Shanchol, in 25 adults, 51 older children (6-17 years), and 47 younger children (1-5 years) in Haiti, where cholera was introduced in 2010. A≥4-fold increase in vibriocidal antibody titer against V. cholerae O1 Ogawa was observed in 91% of adults, 74% of older children, and 73% of younger children after two doses of Shanchol; similar responses were observed against the Inaba serotype. A≥2-fold increase in serum O-antigen specific polysaccharide IgA antibody levels against V. cholerae O1 Ogawa was observed in 59% of adults, 45% of older children, and 61% of younger children; similar responses were observed against the Inaba serotype. We compared immune responses in Haitian individuals with age- and blood group-matched individuals from Bangladesh, a historically cholera-endemic area. The geometric mean vibriocidal titers after the first dose of vaccine were lower in Haitian than in Bangladeshi vaccinees. However, the mean vibriocidal titers did not differ between the two groups after the second dose of the vaccine. CONCLUSIONS/SIGNIFICANCE: A killed bivalent whole cell oral cholera vaccine, Shanchol, is highly immunogenic in Haitian adults and children. A two-dose regimen may be important in Haiti, and other populations lacking previous repeated exposures to V. cholerae.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Cólera / Cólera / Vibrio cholerae O1 / Vibrio cholerae O139 País/Região como assunto: Caribe / Haiti Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Cólera / Cólera / Vibrio cholerae O1 / Vibrio cholerae O139 País/Região como assunto: Caribe / Haiti Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos