-
Something wrong with this record ?
Assessment of lymphocyte proliferation for diagnostic purpose: Comparison of CFSE staining, Ki-67 expression and (3)H-thymidine incorporation
J. Lašťovička, M. Rataj, J. Bartůňková,
Language English Country United States
Document type Comparative Study, Journal Article
- MeSH
- Lymphocyte Activation MeSH
- Ki-67 Antigen metabolism MeSH
- Fluoresceins MeSH
- Immunoassay methods MeSH
- Immunocompromised Host * MeSH
- Cohort Studies MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Lymphocytes immunology MeSH
- Monitoring, Immunologic MeSH
- Cell Proliferation MeSH
- Flow Cytometry MeSH
- Reproducibility of Results MeSH
- Sensitivity and Specificity MeSH
- Succinimides MeSH
- Thymidine MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Comparative Study 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 (3)H-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 (3)H-thymidine incorporation was 0.546 and correlation between CFSE staining and (3)H-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 (3)H-thymidine assay does not bring any advantages and cannot compare to the competition presented by modern flow cytometric methods available today.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17013570
- 003
- CZ-PrNML
- 005
- 20170428114516.0
- 007
- ta
- 008
- 170413s2016 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.humimm.2016.08.012 $2 doi
- 035 __
- $a (PubMed)27562802
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Lašťovička, Jan $u Department of Immunology, 2nd Medical School and University Hospital Motol, Prague, Czech Republic. Electronic address: jan.lastovicka@lfmotol.cuni.cz.
- 245 10
- $a Assessment of lymphocyte proliferation for diagnostic purpose: Comparison of CFSE staining, Ki-67 expression and (3)H-thymidine incorporation / $c J. Lašťovička, M. Rataj, J. Bartůňková,
- 520 9_
- $a 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 (3)H-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 (3)H-thymidine incorporation was 0.546 and correlation between CFSE staining and (3)H-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 (3)H-thymidine assay does not bring any advantages and cannot compare to the competition presented by modern flow cytometric methods available today.
- 650 _2
- $a proliferace buněk $7 D049109
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a kohortové studie $7 D015331
- 650 _2
- $a průtoková cytometrie $7 D005434
- 650 _2
- $a fluoresceiny $7 D005452
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a imunoanalýza $x metody $7 D007118
- 650 12
- $a imunokompromitovaný pacient $7 D016867
- 650 _2
- $a antigen Ki-67 $x metabolismus $7 D019394
- 650 _2
- $a aktivace lymfocytů $7 D008213
- 650 _2
- $a lymfocyty $x imunologie $7 D008214
- 650 _2
- $a monitorování imunologické $7 D015166
- 650 _2
- $a reprodukovatelnost výsledků $7 D015203
- 650 _2
- $a senzitivita a specificita $7 D012680
- 650 _2
- $a sukcinimidy $7 D013388
- 650 _2
- $a thymidin $7 D013936
- 655 _2
- $a srovnávací studie $7 D003160
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Rataj, Michal $u Department of Immunology, 2nd Medical School and University Hospital Motol, Prague, Czech Republic.
- 700 1_
- $a Bartůňková, Jiřina $u Department of Immunology, 2nd Medical School and University Hospital Motol, Prague, Czech Republic.
- 773 0_
- $w MED00002076 $t Human immunology $x 1879-1166 $g Roč. 77, č. 12 (2016), s. 1215-1222
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/27562802 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20170413 $b ABA008
- 991 __
- $a 20170428114838 $b ABA008
- 999 __
- $a ok $b bmc $g 1200035 $s 974348
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 77 $c 12 $d 1215-1222 $e 20160822 $i 1879-1166 $m Human immunology $n Hum Immunol $x MED00002076
- LZP __
- $a Pubmed-20170413