Extensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads

Background: Lymphocytes proliferate considerably following appropriate stimulation in vitro. Autologous T cells are obtained from whole blood or tissue sites in relatively limited amounts. We need a method to expand these cells efficiently, study their functions and manipulate them to create appropr...

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Autores principales: Mirzakhani M., Shahbazi M., Darvish S., Mohammadnia-Afrouzi Mousa
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Lenguaje:EN
Publicado: Sciendo 2018
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Acceso en línea:https://doaj.org/article/f5bfca0cea5240cba62d1f265bdac7e7
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spelling oai:doaj.org-article:f5bfca0cea5240cba62d1f265bdac7e72021-12-02T17:31:31ZExtensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads0324-175010.2478/amb-2018-0004https://doaj.org/article/f5bfca0cea5240cba62d1f265bdac7e72018-03-01T00:00:00Zhttps://doi.org/10.2478/amb-2018-0004https://doaj.org/toc/0324-1750Background: Lymphocytes proliferate considerably following appropriate stimulation in vitro. Autologous T cells are obtained from whole blood or tissue sites in relatively limited amounts. We need a method to expand these cells efficiently, study their functions and manipulate them to create appropriate cells for transferring to the patient with infection and cancer. Objectives: The aim of this study is to determine proliferation ability of two different stimulators on CD4+ lymphocytes. Methods: Lymphocytes were isolated from blood samples of healthy donors after removing adherent cells (monocytes).The efficacy of MACSiBead™ coated with anti-CD2, anti-CD3, anti-CD28 (anti-CD2/CD3/CD28) was compared with Phytohaemagglutinin A (PHA) on CD4+ lymphocytes proliferation using carboxyfluorescein diacetate succinimidyl ester (CFSE) in cell culture media. The percentage of proliferating cells was analyzed using flow cytometry. Results: Both stimulators induced extensive proliferation of CD4+ lymphocytes but proliferation ability of PHA was higher compared to stimulation by anti-CD2/CD3/CD28 MACSiBead™. The proliferation rate of cells stimulated by PHA was 93.8% ± 3.37% whereas it was 85.2% ± 4.7% in cells stimulated by anti-CD2/CD3/CD28 MACSiBead™. Conclusions: Our results show that MACSiBead™ along with PHA can be used to obtain a large number of expanded CD4+ lymphocytes.Mirzakhani M.Shahbazi M.Darvish S.Mohammadnia-Afrouzi MousaSciendoarticleаnti-cd2/cd3/cd28 macsibead™phaproliferationMedicineRENActa Medica Bulgarica, Vol 45, Iss 1, Pp 22-25 (2018)
institution DOAJ
collection DOAJ
language EN
topic аnti-cd2/cd3/cd28 macsibead™
pha
proliferation
Medicine
R
spellingShingle аnti-cd2/cd3/cd28 macsibead™
pha
proliferation
Medicine
R
Mirzakhani M.
Shahbazi M.
Darvish S.
Mohammadnia-Afrouzi Mousa
Extensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads
description Background: Lymphocytes proliferate considerably following appropriate stimulation in vitro. Autologous T cells are obtained from whole blood or tissue sites in relatively limited amounts. We need a method to expand these cells efficiently, study their functions and manipulate them to create appropriate cells for transferring to the patient with infection and cancer. Objectives: The aim of this study is to determine proliferation ability of two different stimulators on CD4+ lymphocytes. Methods: Lymphocytes were isolated from blood samples of healthy donors after removing adherent cells (monocytes).The efficacy of MACSiBead™ coated with anti-CD2, anti-CD3, anti-CD28 (anti-CD2/CD3/CD28) was compared with Phytohaemagglutinin A (PHA) on CD4+ lymphocytes proliferation using carboxyfluorescein diacetate succinimidyl ester (CFSE) in cell culture media. The percentage of proliferating cells was analyzed using flow cytometry. Results: Both stimulators induced extensive proliferation of CD4+ lymphocytes but proliferation ability of PHA was higher compared to stimulation by anti-CD2/CD3/CD28 MACSiBead™. The proliferation rate of cells stimulated by PHA was 93.8% ± 3.37% whereas it was 85.2% ± 4.7% in cells stimulated by anti-CD2/CD3/CD28 MACSiBead™. Conclusions: Our results show that MACSiBead™ along with PHA can be used to obtain a large number of expanded CD4+ lymphocytes.
format article
author Mirzakhani M.
Shahbazi M.
Darvish S.
Mohammadnia-Afrouzi Mousa
author_facet Mirzakhani M.
Shahbazi M.
Darvish S.
Mohammadnia-Afrouzi Mousa
author_sort Mirzakhani M.
title Extensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads
title_short Extensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads
title_full Extensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads
title_fullStr Extensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads
title_full_unstemmed Extensive Proliferation of Cd4+ Lymphocyte by Both Phytohaemagglutinin A and Anti-Cd2/Cd3/ Cd28 Macsibeads
title_sort extensive proliferation of cd4+ lymphocyte by both phytohaemagglutinin a and anti-cd2/cd3/ cd28 macsibeads
publisher Sciendo
publishDate 2018
url https://doaj.org/article/f5bfca0cea5240cba62d1f265bdac7e7
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AT darvishs extensiveproliferationofcd4lymphocytebybothphytohaemagglutininaandanticd2cd3cd28macsibeads
AT mohammadniaafrouzimousa extensiveproliferationofcd4lymphocytebybothphytohaemagglutininaandanticd2cd3cd28macsibeads
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