A Novel Immunization Method to Induce Cytotoxic T-Lymphocyte Responses (CTL) Against Plasmid-Encoded Herpes Simplex Virus Type-1 Glycoprotein D

P. E. Cruz, P. L. Khalil, T. D. Dryden, H. C. Chiou, P. S. Fink, Steven J. Berberich, Nancy J. Bigley

Research output: Contribution to journalArticlepeer-review

Abstract

DNA molecules complexed with an asialoglycoprotein–polycation conjugate, consisting of asialoorosomucoid (ASOR) coupled to poly-l-lysine, can enter hepatocytes which bear receptors for ASOR. We used this receptor-mediated DNA delivery system to deliver plasmid DNA encoding glycoprotein D (gD) of herpes simplex virus type 1 to ASOR-positive cells. Maximum expression of gD protein was seen at 3 days after injection of this preparation in approximately 13% of cells from BALB/c mice [hepatocytes from mice injected intravenously (i.v.) or peritoneal exudate cells from mice injected intraperitoneally (i.p.)]. In comparison with mice injected with either the plasmid vector alone or the gD-containing plasmid uncomplexed to ASOR, mice immunized with gD-containing plasmid complexed with ASOR–poly-l-lysine induced marked antigen-specific CTL responses. BALB/c mice immunized with gD–DNA developed a T-cell-mediated CTL response against target cells expressing gD and MHC class II glycoproteins, but not against cells expressing only gD and MHC class I molecules. In C3H mice, gD–DNA induced a T-cell-mediated CTL response against target cells expressing gD and class I MHC molecules. Serum anti-gD antibody in low titers were produced in both strains of mice. DNA complexed with ASOR–poly-l-lysine induced CTL responses in mice.

Original languageAmerican English
JournalVaccine
Volume17
DOIs
StatePublished - Mar 5 1999
Externally publishedYes

Keywords

  • CTL
  • cytotoxic T-lymphocyte responses
  • glycoprotein D
  • immunization
  • plasmid-encoded herpes simplex virus type-1

Disciplines

  • Medical Cell Biology
  • Medical Neurobiology
  • Medical Physiology
  • Medical Sciences
  • Medicine and Health Sciences
  • Neurosciences
  • Physiological Processes

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