Affiliation:
1. Department of Medicine, Dartmouth-Hitchcock Medical Center, Hanover, New Hampshire 03755
Abstract
Currently, human interferon (IF) assays are generally performed by plaque reduction or visual cytopathic effect methods. Both are time-consuming, subjective in interpretation, and, in the case of the latter, relatively insensitive. An adaption of the dye uptake method for human IF titration which uses foreskin-derived fibroblasts and vesicular stomatitis virus is described. This assay is reproducible and sensitive (1 unit = 3 international units). By direct comparison, however, it is somewhat less sensitive than the plaque reduction assay (1 unit = 1.1 international units). This assay is especially recommended for use in needed clinical investigations of human IF because of its technical simplicity, allowing efficient handling of large numbers of specimens.
Publisher
American Society for Microbiology
Subject
General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine
Reference22 articles.
1. Rapid sensitive assay for interferons based on the inhibition of MM virus nucleic acid synthesis;Allen P. T.;Appl. Microbiol.,1970
2. Rack permitting efficient handling of tissue cultures;Baron S.;Appl. Microbiol.,1966
3. Enhanced interferon production from chick embryo cells aged in vitro;Carver D. H.;Virology,1967
4. Chany C. 1970. Discussion p. 102. In F. T. Perkins and R. H. Regamey (ed.) International symposium on interferon and interferon inducers. S. Karger New York.
5. Finter N. B. 1968. Interferon assays: sensitivity and other aspects p. 203-212. In G. Rita (ed.) The interferons. Academic Press Inc. New York.
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