Assessment of lymphocyte proliferation for diagnostic purpose: Comparison of CFSE staining, Ki-67 expression and 3H-thymidine incorporation
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články
PubMed
27562802
DOI
10.1016/j.humimm.2016.08.012
PII: S0198-8859(16)30436-0
Knihovny.cz E-zdroje
- Klíčová slova
- (3)H-thymidine incorporation, CFSE staining, Flow cytometry, Ki-67 expression, Lymphocyte proliferation, Phytohemagglutinin,
- MeSH
- aktivace lymfocytů MeSH
- antigen Ki-67 metabolismus MeSH
- fluoresceiny MeSH
- imunoanalýza metody MeSH
- imunokompromitovaný pacient * MeSH
- kohortové studie MeSH
- kultivované buňky MeSH
- lidé MeSH
- lymfocyty imunologie MeSH
- monitorování imunologické MeSH
- proliferace buněk MeSH
- průtoková cytometrie MeSH
- reprodukovatelnost výsledků MeSH
- senzitivita a specificita MeSH
- sukcinimidy MeSH
- thymidin MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- srovnávací studie MeSH
- Názvy látek
- 5-(6)-carboxyfluorescein diacetate succinimidyl ester MeSH Prohlížeč
- antigen Ki-67 MeSH
- fluoresceiny MeSH
- sukcinimidy MeSH
- thymidin MeSH
The capability of lymphocytes to respond to antigenic or mitogenic stimulation is an important feature in the diagnosis of various immunodeficiencies and immune disorders. We used large cohorts of both immune compromised patients and healthy controls to measure lymphocyte proliferations by means of three methods: CFSE staining, Ki-67 expression and 3H-thymidine incorporation. The advantages and disadvantages of each method was then evaluated for use in routine clinical diagnostic. The statistical analysis was performed between the outcomes and the correlation between all three methods was computed. CFSE and Ki-67 assay correlated well with the r=0.767, correlation between Ki-67 expression and 3H-thymidine incorporation was 0.546 and correlation between CFSE staining and 3H-thymidine incorporation was 0.337. The differences between these three methods concerning complexity, sensitivity and reliability as well as the financial aspects are discussed hereafter. CFSE and its analogues provide the cheapest and reasonable choice for measuring lymphocyte proliferation, while Ki-67 represents a more expensive, but more sensitive and robust method. The original 3H-thymidine assay does not bring any advantages and cannot compare to the competition presented by modern flow cytometric methods available today.
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