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P. L. Summers

Researcher at Walter Reed Army Institute of Research

Publications -  30
Citations -  1519

P. L. Summers is an academic researcher from Walter Reed Army Institute of Research. The author has contributed to research in topics: Virus & Flavivirus. The author has an hindex of 21, co-authored 30 publications receiving 1493 citations.

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Monoclonal Antibodies Against Dengue 2 Virus E-Glycoprotein Protect Mice Against Lethal Dengue Infection,

TL;DR: The protective monoclonal antibodies were directed against viral determinants that fell into at least three spatially separate families of epitopes on E-glycoprotein, the antigenicities of which were preserved after heat/detergent denaturation.
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Monoclonal antibodies for dengue virus prM glycoprotein protect mice against lethal dengue infection

TL;DR: Five murine monoclonal antibodies reactive against the prM glycoproteins of DEN-3 and -4 were used to passively protect mice in vivo against lethal challenge with homologous and heterologous dengue virus serotypes, the first report of prM-specific Mabs that are protective in mice.
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Immunization of mice with dengue structural proteins and nonstructural protein NS1 expressed by baculovirus recombinant induces resistance to dengue virus encephalitis.

TL;DR: A recombinant baculovirus containing a 4.0-kilobase dengue virus cDNA sequence that codes for the three virus structural proteins, capsid (C) protein, premembrane (PreM)protein, and envelope glycoprotein (E) and nonstructural proteins NS1 and NS2a is constructed.
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Flavivirus entry into cultured mosquito cells and human peripheral blood monocytes

TL;DR: The entry modes of Japanese encephalitis (JE) and dengue-2 (DEN-2) viruses into C6/36 mosquito cells and of DEN-2 virus into human peripheral blood monocytes in vitro were studied and implications of the entry mode to an early process of natural, mosquito-transmitted infection are discussed.
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Expression of dengue virus structural proteins and nonstructural protein NS1 by a recombinant vaccinia virus.

TL;DR: A recombinant vaccinia virus containing cloned DNA sequences coding for the three structural proteins and nonstructural proteins NS1 and NS2a of dengue type 4 virus was constructed, and an immune response to the PreM and E glycoproteins was not detected.