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Novel microneutralization assay for HCMV using automated data collection and analysis
In addition to being sensitive and specific, an assay for the assessment of neutralizing antibody activity from clinical trial samples must be amenable to automation for use in high-volume screening. To that effect, we developed a 96-well microplate assay for the measurement of HCMV-neutralizing act...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Elsevier B.V.
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1933494/ https://www.ncbi.nlm.nih.gov/pubmed/17343873 http://dx.doi.org/10.1016/j.jim.2007.02.001 |
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author | Abai, Anna Maria Smith, Larry R. Wloch, Mary K. |
author_facet | Abai, Anna Maria Smith, Larry R. Wloch, Mary K. |
author_sort | Abai, Anna Maria |
collection | PubMed |
description | In addition to being sensitive and specific, an assay for the assessment of neutralizing antibody activity from clinical trial samples must be amenable to automation for use in high-volume screening. To that effect, we developed a 96-well microplate assay for the measurement of HCMV-neutralizing activity in human sera using the HCMV-permissive human cell line HEL-299 and the laboratory strain of HCMV AD169. The degree to which neutralizing antibodies diminish HCMV infection of cells in the assay is determined by quantifying the nuclei of infected cells based on expression of the 72 kDa IE1 viral protein. Nuclear IE1 is visualized using a highly sensitive immunoperoxidase staining and the stained nuclei are counted using an automated ELISPOT analyzer. The use of Half Area 96-well microplates, with wells in which the surface area of the well bottom is half the area of a standard 96-well microplate plate, improves signal detection compared with standard microplates and economizes on the usage of indicator cells, virus, and reagents. The staining process was also streamlined by using a microplate washer and data analysis was simplified and accelerated by employing a software program that automatically plots neutralization curves and determines NT(50) values using 4-PL curve fitting. The optimized assay is not only fast and convenient, but also specific, sensitive, precise and reproducible and thus has the characteristics necessary for use in measuring HCMV-neutralizing activity in the sera of vaccine trial subjects such as the recipients of Vical's HCMV pDNA vaccine candidates. |
format | Text |
id | pubmed-1933494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-19334942007-07-26 Novel microneutralization assay for HCMV using automated data collection and analysis Abai, Anna Maria Smith, Larry R. Wloch, Mary K. J Immunol Methods Article In addition to being sensitive and specific, an assay for the assessment of neutralizing antibody activity from clinical trial samples must be amenable to automation for use in high-volume screening. To that effect, we developed a 96-well microplate assay for the measurement of HCMV-neutralizing activity in human sera using the HCMV-permissive human cell line HEL-299 and the laboratory strain of HCMV AD169. The degree to which neutralizing antibodies diminish HCMV infection of cells in the assay is determined by quantifying the nuclei of infected cells based on expression of the 72 kDa IE1 viral protein. Nuclear IE1 is visualized using a highly sensitive immunoperoxidase staining and the stained nuclei are counted using an automated ELISPOT analyzer. The use of Half Area 96-well microplates, with wells in which the surface area of the well bottom is half the area of a standard 96-well microplate plate, improves signal detection compared with standard microplates and economizes on the usage of indicator cells, virus, and reagents. The staining process was also streamlined by using a microplate washer and data analysis was simplified and accelerated by employing a software program that automatically plots neutralization curves and determines NT(50) values using 4-PL curve fitting. The optimized assay is not only fast and convenient, but also specific, sensitive, precise and reproducible and thus has the characteristics necessary for use in measuring HCMV-neutralizing activity in the sera of vaccine trial subjects such as the recipients of Vical's HCMV pDNA vaccine candidates. Elsevier B.V. 2007-04-30 2007-02-23 /pmc/articles/PMC1933494/ /pubmed/17343873 http://dx.doi.org/10.1016/j.jim.2007.02.001 Text en Copyright © 2007 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Abai, Anna Maria Smith, Larry R. Wloch, Mary K. Novel microneutralization assay for HCMV using automated data collection and analysis |
title | Novel microneutralization assay for HCMV using automated data collection and analysis |
title_full | Novel microneutralization assay for HCMV using automated data collection and analysis |
title_fullStr | Novel microneutralization assay for HCMV using automated data collection and analysis |
title_full_unstemmed | Novel microneutralization assay for HCMV using automated data collection and analysis |
title_short | Novel microneutralization assay for HCMV using automated data collection and analysis |
title_sort | novel microneutralization assay for hcmv using automated data collection and analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1933494/ https://www.ncbi.nlm.nih.gov/pubmed/17343873 http://dx.doi.org/10.1016/j.jim.2007.02.001 |
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