Abstract
Measles remains an important cause of pediatric morbidity and mortality in developing countries, especially among infants who are too young to receive the current licensed live attenuated measles vaccine. We developed two Sindbis virus DNA vaccines encoding the measles virus hemagglutinin (pMSIN-H) and fusion proteins (pMSINH-FdU) and examined their immunogenicities and protective efficacies when administered alone or followed by the live measles virus vaccine in cotton rats. Neutralizing antibodies, mucosal and systemic antibody-secreting cells, memory B cells, and gamma interferon-secreting T cells developed after priming and increased after boosting. pMSIN-H priming conferred 100% protection against pulmonary measles, whereas pMSINH-FdU protected only in conjunction with the live measles virus vaccine boost.
MeSH Terms
Animals
Antibodies, Viral/blood,immunology
Antibody-Producing Cells/immunology
Cytokines/immunology
Hemagglutinins, Viral/genetics,immunology
Humans
Immunity, Mucosal
Immunization, Secondary
Immunologic Memory
Interferon-gamma/metabolism
Lung/immunology,virology
Measles/prevention & control
Measles Vaccine/genetics,immunology
Measles virus/genetics,immunology
Neutralization Tests
Rats
Sigmodontinae
Sindbis Virus/genetics
Vaccines, DNA/genetics,immunology
Viral Fusion Proteins/genetics,immunology
Chemicals
Antibodies, Viral
Cytokines
Hemagglutinins, Viral
Measles Vaccine
Vaccines, DNA
Viral Fusion Proteins
hemagglutinin protein G, measles virus
Interferon-gamma
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Pasetti Marcela F
Center for Vaccine Development, University of Maryland School of Medicine, 685 West Baltimore St., Room 480, Baltimore, Maryland 21201, USA. mpasetti@medicine.umaryland.edu
Ramirez Karina
Resendiz-Albor Aldo
Ulmer Jeffrey
Barry Eileen M
Levine Myron M
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