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Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood
The development of point-of-care, cost-effective, and easy-to-use assays for the accurate counting of CD4(+) T cells remains an important focus for HIV-1 disease management. The CD4(+) T cell count provides an indication regarding the overall success of HIV-1 treatments. The CD4(+) T count informati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773767/ https://www.ncbi.nlm.nih.gov/pubmed/35049640 http://dx.doi.org/10.3390/bios12010012 |
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author | Fennell, Robert D. Sher, Mazhar Asghar, Waseem |
author_facet | Fennell, Robert D. Sher, Mazhar Asghar, Waseem |
author_sort | Fennell, Robert D. |
collection | PubMed |
description | The development of point-of-care, cost-effective, and easy-to-use assays for the accurate counting of CD4(+) T cells remains an important focus for HIV-1 disease management. The CD4(+) T cell count provides an indication regarding the overall success of HIV-1 treatments. The CD4(+) T count information is equally important for both resource-constrained regions and areas with extensive resources. Hospitals and other allied facilities may be overwhelmed by epidemics or other disasters. An assay for a physician’s office or other home-based setting is becoming increasingly popular. We have developed a technology for the rapid quantification of CD4(+) T cells. A double antibody selection process, utilizing anti-CD4 and anti-CD3 antibodies, is tested and provides a high specificity. The assay utilizes a microfluidic chip coated with the anti-CD3 antibody, having an improved antibody avidity. As a result of enhanced binding, a higher flow rate can be applied that enables an improved channel washing to reduce non-specific bindings. A wide-field optical imaging system is also developed that provides the rapid quantification of cells. The designed optical setup is portable and low-cost. An ImageJ-based program is developed for the automatic counting of CD4(+) T cells. We have successfully isolated and counted CD4(+) T cells with high specificity and efficiency greater than 90%. |
format | Online Article Text |
id | pubmed-8773767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87737672022-01-21 Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood Fennell, Robert D. Sher, Mazhar Asghar, Waseem Biosensors (Basel) Article The development of point-of-care, cost-effective, and easy-to-use assays for the accurate counting of CD4(+) T cells remains an important focus for HIV-1 disease management. The CD4(+) T cell count provides an indication regarding the overall success of HIV-1 treatments. The CD4(+) T count information is equally important for both resource-constrained regions and areas with extensive resources. Hospitals and other allied facilities may be overwhelmed by epidemics or other disasters. An assay for a physician’s office or other home-based setting is becoming increasingly popular. We have developed a technology for the rapid quantification of CD4(+) T cells. A double antibody selection process, utilizing anti-CD4 and anti-CD3 antibodies, is tested and provides a high specificity. The assay utilizes a microfluidic chip coated with the anti-CD3 antibody, having an improved antibody avidity. As a result of enhanced binding, a higher flow rate can be applied that enables an improved channel washing to reduce non-specific bindings. A wide-field optical imaging system is also developed that provides the rapid quantification of cells. The designed optical setup is portable and low-cost. An ImageJ-based program is developed for the automatic counting of CD4(+) T cells. We have successfully isolated and counted CD4(+) T cells with high specificity and efficiency greater than 90%. MDPI 2021-12-28 /pmc/articles/PMC8773767/ /pubmed/35049640 http://dx.doi.org/10.3390/bios12010012 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fennell, Robert D. Sher, Mazhar Asghar, Waseem Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood |
title | Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood |
title_full | Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood |
title_fullStr | Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood |
title_full_unstemmed | Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood |
title_short | Development of a Microfluidic Device for CD4(+) T Cell Isolation and Automated Enumeration from Whole Blood |
title_sort | development of a microfluidic device for cd4(+) t cell isolation and automated enumeration from whole blood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773767/ https://www.ncbi.nlm.nih.gov/pubmed/35049640 http://dx.doi.org/10.3390/bios12010012 |
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