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Cationic lipids direct a viral glycoprotein into the class I major histocompatibility complex antigen-presentation pathway.
Author(s) -
Christopher M. Walker,
M. J. Selby,
Ann L. Erickson,
Didier Cataldo,
J P Valensi,
Gary Van Nest
Publication year - 1992
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.89.17.7915
Subject(s) - ctl* , cytotoxic t cell , virology , antigen , biology , major histocompatibility complex , mhc class i , cd8 , antigen presentation , cationic liposome , immunology , t cell , immune system , transfection , cell culture , biochemistry , genetics , in vitro
Recombinant glycoprotein B (gB) of herpes simplex virus (HSV) was processed and presented by class I major histocompatibility complex (MHC) molecules after delivery into cells by using N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammonium methyl sulfate (DOTAP), a commercially available cationic lipid used for DNA transfection. Cells treated with DOTAP-associated gB were susceptible to lysis by class I MHC-restricted, HSV-specific cytotoxic T lymphocytes (CTL), and the treated cells restimulated memory gB-specific CTL activity in spleen cells from HSV-infected mice. gB-specific CTL responses were detected in mice immunized with recombinant gB and DOTAP but not in those receiving gB emulsified in complete Freund's adjuvant. Thus, cationic lipids may facilitate induction of CD8+ T-cell responses in vaccinations with recombinant antigens, and they may serve as readily available reagents for dissecting class I MHC immunity to viruses and other intracellular pathogens.

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