Francis A. Ennis
Food and Drug Administration
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Publication
Featured researches published by Francis A. Ennis.
The Journal of Pediatrics | 1977
Paul Albrecht; Francis A. Ennis; Edward J. Saltzman; Saul Krugman
A serologic study was made in 34 children immunized against measles at the age of 12 months. Using a sensitive virus neutralization test, it was found that many of the children had pre-existing maternal antibody to measles virus. Children with high pre-existing antibody titers failed to seroconvert. Children with lower pre-existing antibody titers seroconverted, but the resulting antibody titer was significantly lower than in children without pre-existing antibody titer. The results of this study demonstrate a probably mechanism for measles vaccine failure in 12-month-old children and support the recommendation of the Public Health Service Advisory Committee on Immunization Practices to postpone measles vaccination to 15 months of age.
Archives of Virology | 1978
H. Sato; Paul Albrecht; John T. Hicks; B. C. Meyer; Francis A. Ennis
SummaryA sensitive mumps virus plaque neutralization test has been developed based on the potentiation of virus-antibody complexes by heterologous anti-immunoglobulins (AIG). The enhanced neutralization test was approximately 100 times more sensitive than the conventional neutralization test or the hemagglutination-inhibition test. Using AIG against human immunoglobulin G (IgG) or human IgM permitted determination of the relative titers of the two classes of mumps antibody. The test does not require special equipment or expertise and can be readily introduced in virological laboratories.
Journal of Immunological Methods | 1981
Barbara L. Pope; Andrew J. Hapel; W. John Martin; B. Merchant; Francis A. Ennis
Spleen cells from mice immunized with vaccinia or influenza viruses were mixed with spleen cells from mice immunized by dinitrophenyl-keyhole limpet hemocyanin (DNP-KLH) and transferred into irradiated syngeneic recipient mice which were subsequently restimulated with trinitrophyenylates (TNP) or unmodified viruses. One week later, spleens were removed and assayed for indirect anti-DNP plaque-forming cells (PFC). When spleen cells from both influenza and vaccinia primed mice were restimulated with the haptenated form of the virus used for the initial immunization there was an enhanced PFC response compared to that seen with spleen cells from unprimed mice.
Archives of Virology | 1979
H. Sato; Paul Albrecht; Francis A. Ennis
SummaryUnder defined plaquing conditions, three attenuated strains of rubella virus showed different plaque morphology and plaque size when tested in Vero cell cultures. The Cendehill strain of rubella virus formed distinct, ring-shaped plaques, while strains HPV 77 and RA 27/3 produced clear plaques that could be distinguished by their different size. These distinguishing characteristics remained preserved even after the vaccine strains were passaged five consecutive times in Vero cell cultures.
JAMA Pediatrics | 1979
Hiroshi Sato; Paul Albrecht; David W. Reynolds; Sergio Stagno; Francis A. Ennis
The Journal of Infectious Diseases | 1976
John L. Sullivan; Ronald E. Mayner; David W. Barry; Francis A. Ennis
The Journal of Infectious Diseases | 1980
Walter R. Dowdle; J. D. Millar; Lawrence B. Schonberger; Francis A. Ennis; J. R. Lamontagne
The Journal of Infectious Diseases | 1977
Colin McLaren; Martha W. Verbonitz; Sylvester Daniel; George E. Grubbs; Francis A. Ennis
The Journal of Infectious Diseases | 1977
Thomas G. Wise; Peter R. Pavan; Francis A. Ennis
Japanese journal of medical science & biology | 1978
Hiroshi Sato; Paul Albrecht; Akira Shishido; Francis A. Ennis