Successful DNA immunization against measles: Neutralizing antibody against either the hemagglutinin or fusion glycoprotein protects rhesus macaques without evidence of atypical measles

Measles remains a principal cause of worldwide mortality, in part because young infants cannot be immunized effectively. Development of new vaccines has been hindered by previous experience with a formalin-inactivated vaccine that predisposed to a severe form of disease (atypical measles). Here we h...

Full description

Saved in:
Bibliographic Details
Published inNature medicine Vol. 6; no. 7; pp. 776 - 781
Main Authors Griffin, Diane E, Polack, Fernando P, Lee, Sok H, Permar, Sallie, Manyara, Elizabeth, Nousari, Hossein G, Jeng, Yaikah, Mustafa, Farah, Valsamakis, Alexandra, Adams, Robert J, Robinson, Harriet L
Format Journal Article
LanguageEnglish
Published United States Nature Publishing Group 01.07.2000
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Measles remains a principal cause of worldwide mortality, in part because young infants cannot be immunized effectively. Development of new vaccines has been hindered by previous experience with a formalin-inactivated vaccine that predisposed to a severe form of disease (atypical measles). Here we have developed and tested potential DNA vaccines for immunogenicity, efficacy and safety in a rhesus macaque model of measles. DNA protected from challenge with wild-type measles virus. Protection correlated with levels of neutralizing antibody and not with cytotoxic T lymphocyte activity. There was no evidence in any group, including those receiving hemagglutinin-encoding DNA alone, of 'priming' for atypical measles.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:1078-8956
1546-170X
DOI:10.1038/77506