dc.contributor.author |
Messele,Tsehaynesh |
|
dc.contributor.author |
RoosT. L, Marijke |
|
dc.contributor.author |
Hamann,Dörte |
|
dc.contributor.author |
Koot,Maarten |
|
dc.date.accessioned |
2022-11-24T10:44:20Z |
|
dc.date.available |
2022-11-24T10:44:20Z |
|
dc.date.issued |
2000 |
|
dc.identifier.citation |
Tsehaynesh Messele,Marijke T. L. Roos,Dörte Hamann,Maarten Koot.Nonradioactive Techniques for Measurement of In Vitro T-Cell Proliferation: Alternatives to the [3H]Thymidine Incorporation Assay.Clinical and Diagnostic Laboratory Immunology 7(4):687-92, August 2000 |
|
dc.identifier.uri |
http://172.21.6.100:8080/xmlui/handle/123456789/326 |
|
dc.description.abstract |
T-cell proliferation is an important in vitro parameter of in vivo immune function and has been used as a prognostic marker of human immunodeficiency virus type 1 (HIV-1) disease progression. The proliferative capacity of T cells in response to various stimuli is commonly determined by a radioactive assay based on incorporation of [(3)H]thymidine ([(3)H]TdR) into newly generated DNA. In order to assess techniques for application in laboratories where radioactive facilities are not present, two alternative methods were tested and compared to the [(3)H]TdR assay as a "gold standard." As an alternative, T-cell proliferation was measured by flow cytometric assessment of CD38 expression on T cells and by an enzyme-linked immunosorbent assay (ELISA) based on bromo-2'-deoxyuridine (BrdU) incorporation. Peripheral blood mononuclear cells (PBMCs), either in whole blood or Ficoll-Isopaque separated, from a total of 26 HIV-1-positive and 18 HIV-1-negative Dutch individuals were stimulated with CD3 monoclonal antibody (MAb) alone, a combination of CD3 and CD28 MAbs, or phytohemagglutinin. BrdU incorporation after 3 days of stimulation with a combination of CD3 and CD28 MAbs correlated excellently with the [(3)H]TdR incorporation in both study groups (HIV-1 positives, r = 0.96; HIV-1 negatives, r = 0.83). A significant correlation of absolute numbers of T cells expressing CD38 with [(3)H]TdR incorporation, both in HIV-1-positive (r = 0.96) and HIV-1-negative (r = 0.84) individuals, was also observed under these conditions. The results of this study indicate that determination of both the number of CD38-positive T cells and BrdU incorporation can be used as alternative techniques to measure the in vitro T-cell proliferative capacity. The measurement of CD38 expression on T cells provides the additional possibility to further characterize the proliferating T-cell subsets for expression of other surface markers |
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dc.format.extent |
687-692 |
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dc.subject |
Non radioactive |
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dc.subject |
Measurement |
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dc.subject |
Vitro T-Cell |
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dc.subject |
Proliferation |
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dc.subject |
Thymidine |
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dc.title |
Nonradioactive Techniques for Measurement of In Vitro T-Cell Proliferation: Alternatives to the [3H]Thymidine Incorporation Assay |
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dc.type |
Journal article |
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ep.identifier.status |
Open Access |
|
ep.identifier.status |
Open Access |
|
ep.identifier.doi |
http://DOI:10.1128/CDLI.7.4.687-692.2000 |
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ep.journal |
Clinical and Diagnostic Laboratory Immunology |
|
ep.issue |
4 |
|
ep.volume |
7 |
|