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Infection and Immunity, April 1999, p. 1688-1693, Vol. 67, No. 4
Department of Molecular Microbiology and
Immunology, School of Hygiene and Public Health, Johns Hopkins
University, Baltimore, Maryland 21205
Received 15 October 1998/Returned for modification 16 December
1998/Accepted 14 January 1999
Immunological intervention, in addition to vector control and
malaria chemotherapy, will be needed to stop the resurgence of malaria,
a disease with a devastating impact on the health of 300 to 500 million
people annually. We have pursued a vaccination strategy, based on DNA
immunization in mice with genes encoding two antigens present on the
sexual stages of Plasmodium falciparum, Pfs25 and Pfg27, to
induce biologically important antibodies that can block development of
the parasite in the Anopheles mosquito and thus
transmission of the disease. DNA encoding Pfs25 when administered by
the intramuscular route, either alone or with DNA encoding Pfg27, had
the most potent transmission-blocking effects, resulting in up to a
97% decrease in oocyst numbers in mosquito midguts and a 75% decrease
in rate of infection. Immunization with DNA encoding a Pfg27-Pfs25
fusion protein was less effective and DNA encoding Pfg27 elicited
antibodies in sera that had only modest effects on the infectivity of
the parasite. These results show for the first time that DNA
vaccination can result in potent transmission-blocking antibodies in
mice and suggest that the Pfs25 gene should be included as part of a
multicomponent DNA vaccine.
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Immunization of Mice with DNA-Based Pfs25 Elicits
Potent Malaria Transmission-Blocking Antibodies
*
Corresponding author. Mailing address: Department of
Molecular Microbiology and Immunology, School of Hygiene and Public
Health, Johns Hopkins University, 615 N. Wolfe St., Baltimore, MD
21205. Phone: (410) 955-7177. Fax: (410) 955-0105. E-mail:
nkumar{at}jhsph.edu.
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