Elimination of Fc receptor binding of human immunoglobulin G in immunofluorescence assays for herpes simplex virus antibodies

Author:

Gallo D

Abstract

The binding of human immunoglobulin G by Fc receptors in herpes simplex virus (HSV)-infected cells can cause false-positive interpretations in the immunofluorescence test for HSV antibody. When the infected cell smears were treated with 10% glacial acetic acid for 5 min and rinsed in phosphate-buffered saline before the immunofluorescence test was performed, the Fc receptors were completely inactivated, resulting in a reliable method for HSV antibody detection.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference5 articles.

1. Evaluation and reporting of enzyme immunoassay determinations of antibody to herpes simplex virus in sera and cerebrospinal fluid;Cremer N. E.;J. Clin. Microbiol.,1982

2. Multiple-antigen slide test for detection of immunoglobulin M antibodies in newborn and infant sera by immunofluorescence;Gallo D.;J. Clin. Microbiol.,1981

3. Anti-complement immunofluorescence test for antibodies to human cytomegalovirus;Kettering J. D.;J. Clin. Microbiol.,1977

4. Riggs J. L. 1979. Immunofluorescent staining p. 141-151. In E. H. Lennette and N. J. Schmidt (ed.) Diagnostic procedures for viral rickettsial and chlamydial infections 5th ed. American Public Health Association Inc. Washington D.C.

5. The IgG receptor induced by herpes simplex virus: studies using radioiodinated IgG;Westmoreland D.;J. Gen. Virol.,1974

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