## Abstract An enzyme‐linked immunosorbent assay (ELISA) was developed for the detection of cytomegalovirus (CMV) in urine using monoclonal antibodies directed against CMV as a capture for viral antigen. The assay was capable of detecting virus at 10^2.3^TCID~50~/ml as determined by titration of st
Detection of cytomegalovirus by ELISA in urine samples is inhibited by β2 microglobulin
✍ Scribed by Jane A. McKeating; Dr. Jane E. Grundy; Zachariah Varghese; Paul D. Griffiths
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 406 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
During development of an enzyme immunoassay for the detection of cytomegalovirus (CMV) we previously discovered that virus found naturally in urine specimens could not be captured onto the solid phase by CMV-specific monoclonal antibodies, whereas these same antibodies could capture CMV from cell culture supernatants. We now report that urine from normal CMV-seronegative individuals contains a substance of molecular weight 11-12,000 daltons that inhibits the ELISA detection of cell culture-grown CMV. The addition of a known urinary protein of this molecular weight, 02 microglobulin (&m; 11,700 daltons), inhibited the detection of cell culture-grown CMV in the ELISA over the concentration range found in clinical urine samples. In contrast, another low molecular weight urinary protein, lysozyme, had no inhibitory effect. &m caused inhibition only when added to the virus preparation and not to the antibody-capture stage. We conclude that &m in urine prevents the detection of CMV by ELISA by binding to the virus and masking its antigenic determinants and we calculate that of the order of lo5 molecules of &m bind to each particle of cell culture-grown CMV. We postulate that CMV in fresh urine specimens is similarly coated with &m, accounting for the failure to detect it by ELISA.
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