BACULOVIRUS-EXPRESSED HERPES-SIMPLEX VIRUS TYPE-2 GLYCOPROTEIN-D IS IMMUNOGENIC AND PROTECTIVE AGAINST LETHAL HSV CHALLENGE
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LANDOLFI, V
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
LANDOLFI, V
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ZARLEY, CD
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
ZARLEY, CD
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ABRAMOVITZ, AS
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
ABRAMOVITZ, AS
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FIGUEROA, N
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
FIGUEROA, N
[1
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WU, SL
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
WU, SL
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BLASIAK, M
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
BLASIAK, M
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ISHIZAKA, ST
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
ISHIZAKA, ST
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MISHKIN, EM
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LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USALEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
MISHKIN, EM
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机构:
[1] LEDERLE PRAXIS BIOL, DEPT VIRAL VACCINE RES & DEV, PEARL RIVER, NY 10965 USA
Herpes simplex virus type 2 glycoprotein D (gD2) was cloned and expressed in the baculovirus-Spodoptera frugiperda system. Milligram quantities of glycoprotein were recovered from suspension culture and subjected to purification by ion-exchange and immunoaffinity chromatography. The resultant purified gD existed as a homogeneous 57 500 M(W) monomeric species demonstrating reactivity with anti-gD monoclonal antibodies including those directed at a non-sequential neutralizing epitope of gD. Immunization of Balb/c mice with doses of 0.1-10.0 mug of AlPO4-absorbed gD resulted in elicitation of humoral and cellular responses to both HSV1 and HSV2 as well as to purified gD1 and gD2. Immunized mice receiving an infectious dose of 1 x 10(6) p.f.u. of HSV2 via the footpad route were significantly protected against infection at all doses tested when compared with unimmunized AlPO4 and uninoculated control animals.