Cell-mediated cytotoxicity against targets bearing Sendai virus glycoproteins in the absence of viral infection

Author:

Abidi T F,Flanagan T D

Abstract

The glycoproteins HN and F and the lipids were solubilized from Sendai virus envelopes by using the nonionic detergent beta-D-octylglucoside. When beta-D-octylglucoside was removed by dialysis, the glycoproteins and lipids reassociated to form vesicles. These vesicles displayed hemagglutinating, neuraminidase, and hemolysin activities comparable to those expressed by the intact virus. The vesicles were used as carriers to transfer the glycoproteins to the surface of P815 cells. The recipient cells were tested for the acquisition of the glycoproteins by demonstration of surface neuraminidase, hemadsorption activity, and antigens. The modified cells were used as targets for natural cell-mediated lysis and were found to be sensitive.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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1. Liposomes and ISCOMS as vaccine formulations;Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes;1995-07

2. Cell-mediated immunity induced in mice after vaccination with a protease activation mutant, TR-2, of Sendai virus;Journal of Virology;1988-07

3. Natural cell-mediated cytotoxicity to cells infected with infectious bovine rhinotracheitis virus;Veterinary Immunology and Immunopathology;1987-01

4. The interaction of Sendai virus glycoprotein-bearing recombinant vesicles with cell surfaces;Biochimica et Biophysica Acta (BBA) - Biomembranes;1986-01

5. SENDAI VIRUS;Viral and Mycoplasmal of Laboratory Rodents;1986

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