Am. J. Trop. Med. Hyg., 15(4), 1966, pp. 601-610
Copyright © 1966 by The American Society of Tropical Medicine and Hygiene
Immunological Studies with Group B Arthropod-Borne Viruses
VI. Hemagglutination-Inhibiting Antibody Responses to 17D Yellow Fever Vaccine in Human Subjects with Different Degrees of Complexity of Pre-Vaccination Group B Virus Experience*
John N. Hatgi
,
Charles L. Wisseman, Jr.,
Edward C. Rosenzweig,
Bertram R. Harrington AND
Masami Kitaoka
Department of Microbiology, University of Maryland, School of Medicine, Baltimore, Maryland, and National Institute of Health, Tokyo, Japan
Hemagglutination-inhibiting antibody responses with selected Group B arthropod-borne virus antigens were studied following administration of living attenuated 17D strain yellow fever vaccine to human subjects who had (a) no previous Group B arbovirus experience, (b) only 17D strain vaccine previously, (c) previous inapparent natural Japanese encephalitis virus infection and (d) complex Group B arbovirus experience previously. The results indicate the following:
- 1. Previous homologous or heterologous immunological experience did not suppress the yellow fever HI response to the living vaccine. On the contrary, the response was sometimes enhanced.
- 2. Heterologous HI responses depended upon the nature of the previous Group B arbovirus experience. (a) Subjects with no prevaccination Group B arbovirus experience developed a limited array of low-titered heterologous antibodies. (b) Subjects previously vaccinated with the 17D strain but with no other Group B arbovirus experience exhibited limited intensification and broadening of heterologous HI antibodies. (c) Subjects who had experienced some other Group B virus infection prior to yellow fever vaccination displayed a broad heterologous antibody response producing at times significantly higher HI antibody titers to other viruses.
- 3. Subjects with relatively low, but not with high, yellow fever neutralization indices prior to revaccination tended to show a significant increase in neutralizing antibody level in response to the vaccines.
* This work was carried out under Contract No. DA-49-007-MD-660 with the Medical Research and Development Command, Office of the Surgeon General, Department of the Army under the auspices of the Commission on Immunization of the Armed Forces Epidemiological Board.
Trainee in Virology, Training Grant No. 2E-16, N.I.H. (U.S.P.H.S.). Currently, Chief of the Serology Section, Department of Microbiology.
Copyright © 1966 by the American Society of Tropical Medicine and Hygiene.