Delivery of Foreign Substances to Cells Mediated by Fusion-Active Reconstituted Influenza Virus Envelopes (Virosomes)

References

• Bangham A. D., Standish M. M., Watkins J. C. Diffusion of univalent ions across the lamellae of swollen phospholipids. J. Mol. Biol. 1965; 13: 238
   PubMed Web of Science ®Google Scholar
• Gregoriadis G. Liposome Technology, 2nd Edition. CRC Press, Inc., Boca Raton (FL) 1993
   Google Scholar
• Sato T., Sunamoto J. Recent aspects in the use of liposomes in biotechnology and medicine. Prog. Lipid Res. 1992; 31: 345
   PubMed Web of Science ®Google Scholar
• Mellman I., Fuchs R., Helenius A. Acidification of the endocytic and exocytic pathways. Ann. Rev. Biochem. 1986; 55: 663
   PubMed Web of Science ®Google Scholar
• Connor J., Yatvin M. B., Huang L. pH-sensitive liposomes: acid-induced fusion. Proc. Natl. Acad. Sci. USA 1984; 81: 1715
   PubMed Web of Science ®Google Scholar
• Wang C., Huang L. pH-sensitive immunoliposomes mediate target-cell-specific delivery and controlled expression of a foreign gene in mouse. Proc. Natl. Acad. Sci. USA 1987; 84: 7851
   PubMed Web of Science ®Google Scholar
• Chu C., Dijkstra J., Lai M., Hong K., Szoka F. C. Efficiency of cytoplasmic delivery by pH-sensitive liposomes to cells in culture. Pharmaceut. Res. 1990; 7: 824
   PubMed Web of Science ®Google Scholar
• Collins D. S., Findlay K., Harding C. V. Processing of exogenous liposome-encapsulated antigens in vivo generates class I MHC-restricted T cell responses. J. Immunol. 1992; 148: 3336
   PubMed Web of Science ®Google Scholar
• Nair S., Zhou F., Reddy R., Huang L., Rouse B. T. Soluble proteins delivered to dendritic cells via pH-sensitive liposomes induce primary cytotoxic T Lymphocyte responses in vitro. J. Exp. Med. 1992; 175: 609
   PubMed Web of Science ®Google Scholar
• Legendre J., Szoka F. C., Jr. Delivery of plasmid DNA into mammalian cell lines using pH-sensitive liposomes: comparison with cationic liposomes. Pharmaceut. Res. 1992; 9: 1235
   PubMed Web of Science ®Google Scholar
• Tari A. M., Zhou F., Huang L. Two types of pH-sensitive immunoliposomes. “Liposome Technology, 2nd Edition. Vol. III Interactions of Liposomes with the Biological Milieu”, G. Gregoriadis. CRC Press, Inc., Boca Raton (FL) 1993; 289
   Google Scholar
• Feigner P. L., Gadek T. R., Holm M., Roman R., Chan H. W., Wenz M., Northrop J. P., Ringold G. M., Danielsen M. Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure. Proc. Natl. Acad. Sci. USA 1987; 84: 7413
   PubMed Web of Science ®Google Scholar
• Nair S., Zhou X., Huang L., Rouse B. T. Class I restricted CTL recognition of a soluble protein delivered by liposomes containing lipophilic polylysines. J. Immunol. Meth. 1992; 152: 237
   PubMed Web of Science ®Google Scholar
• Zhou X., Klibanov A. L., Huang L. Lipophilic polylysines mediate efficient DNA transfection in mammalian cells. Biochim. Biophys. Acta 1991; 1065: 8
   PubMed Web of Science ®Google Scholar
• Hyde S. C., Gill D. R., Higgins C. F., Trezise A. E. O., MacVinish L. J., Cuthbert A. W., Ratcliff R., Evans M. J., Colledge W. H. Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy. Nature 1993; 362: 250
   PubMed Web of Science ®Google Scholar
• Marsh M., Helenius A. Virus entry into animal cells. Adv. Virus Res. 1989; 36: 107
   PubMed Web of Science ®Google Scholar
• White J. M. Viral and cellular membrane fusion proteins. Annu. Rev. Physiol. 1990; 52: 675
   PubMed Web of Science ®Google Scholar
• Stegmann T., Morselt H. W. M., Booy F. P., van Breemen J. F. L., Scherphof G., Wilschut J. Functional reconstitution of influenza virus envelopes. EMBO J. 1987; 6: 2651
   PubMed Web of Science ®Google Scholar
• Gordon D. M. Use of novel adjuvants and delivery systems to improve the humoral and cellular immune response to malaria vaccine candidate antigens. Vaccine 1993; 11: 591
   PubMed Web of Science ®Google Scholar
• McClure M. O., Marsh M., Weiss R. Human immunodeficiency virus infection of CD4-bearing cells occurs by a pH-independent mechanism. EMBO J. 1988; 7: 513
   PubMed Web of Science ®Google Scholar
• Stein B. S., Gowda S. D., Lifson J. D., Penhallow R. C., Bensch K. G., Engleman E. G. pH-independent HIV entry into CD4-positive T cells via virus envelope fusion to the plasma membrane. Cell 1987; 49: 659
   PubMed Web of Science ®Google Scholar
• Webster R. G., Bean W. J., Gorman O. T., Chambers T. M., Kawaoka Y. Evolution and ecology of influenza A viruses. Microbiol. Rev. 1992; 56: 152
   PubMedGoogle Scholar
• White J., Helenius A., Gething M. Hemagglutinin of influenza virus expressed from a cloned gene promotes membrane fusion. Nature 1982; 300: 658
   PubMed Web of Science ®Google Scholar
• Stegmann T., Morselt H. W. M., Scholma J., Wilschut J. Fusion of influenza virus in an intracellular acidic compartment measured by fluorescence dequenching. Biochim. Biophys. Acta 1987; 904: 165
   PubMed Web of Science ®Google Scholar
• Stegmann T., Doms R. W., Helenius A. Protein-mediated membrane fusion. Annu. Rev. Biophys. Biophys. Chem. 1989; 18: 187
   PubMedGoogle Scholar
• Wilson I. A., Skehel J. J., Wiley D. C. Structure of the haemagglutinin membrane glycoprotein of influenza virus at 3 Å resolution. Nature 1981; 289: 366
   PubMed Web of Science ®Google Scholar
• Wharton S. A. The role of influenza virus haemagglutinin in membrane fusion. Microbiol. Sciences 1987; 4: 119
   PubMedGoogle Scholar
• Wiley D. C., Skehel J. J. The structure and function of the hemagglutinin membrane glycoprotein of influenza virus. Ann. Rev. Biochem. 1987; 56: 365
   PubMed Web of Science ®Google Scholar
• Doms R. W., White J., Boulay F., Helenius A. Influenza virus hemagglutinin and membrane fusion. “Membrane Fusion.”, J. Wilschut, D. Hoekstra. Marcel Dekker, Inc., New York (NY) 1990; 313
   Google Scholar
• Stegmann T., Delfino J. M., Richards F. M., Helenius A. The HA2 subunit of influenza hemagglutinin inserts into the target membrane prior to fusion. J. Biol. Chem. 1991; 266: 18404
   PubMed Web of Science ®Google Scholar
• Brunner J., Tsurudome M. Fusion-protein membrane interactions as studied by hydrophobic photolabeling. “Viral Fusion Mechanisms.”, J. Bentz. CRC Press, Inc., Boca Raton (FL) 1993; 67
   Google Scholar
• Bentz J. Viral fusion mechanisms. CRC Press, Inc., Boca Raton (FL) 1993
   Google Scholar
• Guy H. R., Durell S. R., Schoch C., Blumenthal R. Analyzing the fusion process of influenza hemagglutinin by mutagenesis and molecular modeling. Biophys. J. 1992; 62: 95
   PubMed Web of Science ®Google Scholar
• Carr C. M., Kim P. S. A spring-loaded mechanism for the conformational change of influenza hemagglutinin. Cell 1993; 73: 823
   PubMed Web of Science ®Google Scholar
• Silvius J. R. Solubilization and functional reconstitution of biomembrane components. Annu. Rev. Biophys. Biomol. Struc. 1992; 21: 323
   PubMedGoogle Scholar
• Walter A., Eidelman O., Ollivon M., Blumenthal R. Functional reconstitution of viral envelopes. “Membrane Fusion.”, J. Wilschut, D. Hoekstra. Marcel Dekker, Inc., New York (NY) 1991; 395
   Google Scholar
• Wilschut J., Bron R. The influenza virus hemagglutinin: membrane fusion activity in intact virions and reconstituted virosomes. “Viral Fusion Mechanisms.”, J. Bentz. CRC Press, Inc., Boca Raton (FL) 1993; 133
   Google Scholar
• Bron R., Ortiz A., Dijkstra J., Stegmann T., Wilschut J. Preparation, properties and applications of reconstituted influenza virus envelopes (virosomes). Meth. Enzymol. 1993; 220: 313
   PubMed Web of Science ®Google Scholar
• Levy D., Gulik A., Seigneuret M., Rigaud J. Phospholipid vesicle solubilization and reconstitution by detergents. Symmetrical analysis of the two processes using octaethyleneglycol mono-n-dodecyl ether. Biochemistry 1990; 29: 9480
   Google Scholar
• Bron R., Kendal A. P., Klenk H. D., Wilschut J. Role of the M2 protein in influenza virus membrane fusion: effects of amantadine and monensin on fusion kinetics. Virology 1993; 195: 804
   PubMed Web of Science ®Google Scholar
• Wilschut J., Bron R., Dijkstra J., Ortiz A., van Ginkel L. C., DeGrado W. F., Rafalski M., Lear J. D. Membrane fusion activity of influenza virus and reconstituted viral envelopes (virosomes). “Progress in Membrane Biotechnology.”, J. C. Gómez-Fernández, D. Chapman, L. Packer. Birkhauser Verlag, Basel (Switserland) 1991; 317
   Google Scholar
• Hoekstra D., de Boer T., Klappe K., Wilschut J. Fluorescence method for measuring the kinetics of fusion between biological membranes. Biochemistry 1984; 23: 5675
   PubMed Web of Science ®Google Scholar
• Wunderli-Allenspach H., Ott S. Kinetics of fusion and lipid transfer between virus receptor containing liposomes and influenza viruses as measured with the octadecylrhodamine B chloride assay. Biochemistry 1990; 29: 1990
   PubMed Web of Science ®Google Scholar
• Galla H. J., Hartmann W. Excimer-forming lipids in membrane research. Chem. Phys. Lipids 1980; 27: 199
   PubMed Web of Science ®Google Scholar
• Wahlberg J. M., Bron R., Wilschut J., Garoff H. Membrane fusion of Semliki Forest virus involves homotrimers of the fusion protein. J. Virol. 1992; 66: 7309
   PubMed Web of Science ®Google Scholar
• Bron R., Wahlberg J. M., Garoff H., Wilschut J. Membrane fusion of Semliki Forest virus in a model system: correlation between fusion kinetics and structural changes in the envelope glycoprotein. EMBO J. 1993; 12: 693
   PubMed Web of Science ®Google Scholar
• Pal R., Barenholz Y., Wagner R. R. Pyrene phospholipid as a biological fluorescent probe for studying fusion of virus membrane with liposomes. Biochemistry 1988; 27: 30
   PubMed Web of Science ®Google Scholar
• Wunderli-Allenspach H., Gunthert M., Ott S. Inactivation of PR8 influenza virus through the octadecylrhodamine B chloride membrane marker. Biochemistry 1993; 32: 900
   PubMed Web of Science ®Google Scholar
• Stegmann T., Schoen P., Bron R., Wey J., Bartoldus I., Ortiz A., Nieva J., Wilschut J. Evaluation of viral membrane fusion assays. Comparison of the octadecylrhodamine dequenching assay with the pyrene excimer assay. Biochemistry 1993, (in press)
   PubMed Web of Science ®Google Scholar
• Bron R., Wilschut J. Cytoplasmic delivery of polypeptide toxins by reconstituted influenza virus envelopes (virosomes). 1993, Submitted
   Google Scholar
• Gould-Fogerite S., Mannino R. J. Rotary dialysis: its application to the preparation of large liposomes and large proteoliposomes (protein-lipid vesicles) with high encapsulation efficiency and efficient reconstitution of membrane proteins. Anal. Biochem. 1985; 148: 15
   PubMed Web of Science ®Google Scholar
• Gould-Fogerite S., Mannino R. J. Targeted fusogenic proteoliposomes: functional reconstitution of membrane proteins through proteincochleate intermediates. “Liposome Technology, 2nd Edition, Vol. III Interactions of Liposomes with the Biological Milieu”, G. Gregoriadis. CRC Press, Inc., Boca Raton (FL) 1992; 261
   Google Scholar
• Helenius A., Mellman I., Wall D., Hubbard A. Endosomes. TIBS 1983; 8: 245
   Web of Science ®Google Scholar
• Dijkstra J., de Haan A., Bron R., Wilschut J., Ryan J. Activation of murine lymphocytes by lipopolysaccharide incorporated in fusogenic, reconstituted influenza virus envelopes (virosomes). 1993, Submitted
   Google Scholar
• Stirpe F., Olsnes S., Pihl A. Gelonin, a new inhibitor of protein synthesis, nontoxic to intact cells. Isolation, characterization, and preparation of cytotoxic complexes with concanavalin A. J. Biol. Chem. 1980; 255: 6947
   PubMed Web of Science ®Google Scholar
• Gould-Fogerite S., Mazurkiewicz J. E., Raska K., Jr., Voelkerding K., Lehman J. M., Mannino R. J. Chimerasome-mediated gene transfer in vitro and in vivo. Gene 1989; 84: 429
   PubMed Web of Science ®Google Scholar
• Lapidot M., Loyter A. Fusion-mediated microinjection of liposome-enclosed DNA into cultured cells with the aid of influenza virus glycoproteins. Exp. Cell Res. 1990; 189: 241
   PubMed Web of Science ®Google Scholar
• Kato K., Nakanishi M., Kaneda Y., Uchida T., Okada Y. Expression of hepatitis B virus surface antigen in adult rat liver. J. Biol. Chem. 1991; 266: 3361
   PubMed Web of Science ®Google Scholar
• Kato K., Kaneda Y., Sakurai M., Nakanishi M., Okada Y. Direct injection of hepatitis B virus DNA into liver induced hepatitis in adult rats. J. Biol. Chem. 1991; 266: 22071
   PubMed Web of Science ®Google Scholar
• Miller M. D., Gould-Fogerite S., Shen L., Woods R. M., Koenig S., Mannino R. J., Letvin N. L. Vaccination of rhesus monkeys with synthetic peptide in a fusogenic proteoliposome elicits simian immunodeficiency virus-specific CD8+ cytotoxic T lymphocytes. J. Exp. Med. 1992; 176: 1739
   PubMed Web of Science ®Google Scholar
• Wiley D. C., Wilson I. A., Skehel J. J. Structural identification of the antibody-binding sites of Hong Kong influenza haemagglutinin and their involvement in antigenic variation. Nature 1981; 289: 373
   PubMed Web of Science ®Google Scholar