Analytical and clinical characterization of an optimized dual monoclonal sandwich ELISA for the quantification of thymidine kinase 1 (TK1) protein in human blood samples.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 27 09 2021
accepted: 16 09 2022
entrez: 6 10 2022
pubmed: 7 10 2022
medline: 12 10 2022
Statut: epublish

Résumé

Thymidine Kinase 1 (TK1) plays an important role in DNA precursor synthesis and serum TK1 activity has been used as a biomarker for prognosis and therapy monitoring of different malignancies. AroCell has developed a dual monoclonal antibody ELISA for determination of TK1 protein in clinical samples. The purpose of the study is to validate the ELISA analytically in relation to the gold standard, [3H]-deoxythymidine (dThd) phosphorylation assay for TK1 activity using sera from patients with different malignancies. The colorimetric TK 210 ELISA was validated analytically by assessment of precision, linearity, interfering substances, and stability. For the clinical validation, serum samples from patients with hematological malignancies (n = 100), breast cancer (n = 56), prostate cancer (n = 70) and blood donors (n = 159) were analyzed using TK 210 ELISA and TK1 activity by [3H]-deoxythymidine (dThd) phosphorylation assay. The sandwich TK 210 ELISA was highly specific for TK1 protein having a detection limit of 0.12 ng/mL, with a functional sensitivity of 0.25 ng/mL. Within-run CVs ranged from 5.5% to 10% and between-run CVs ranged from 5% to 15%. The ratio of observed to expected dilutional parallelism of 5 serum samples was in the range of 80-120%. Samples exhibited stability through four freeze/thaw cycles and 5 days at 4°C. Further, the ROC curve analysis showed that TK 210 ELISA and [3H]-dThd phosphorylation assay had similar sensitivity (62% vs 59%) in hematological malignancies. However, in the case of breast and prostate cancer sera, TK 210 ELISA had higher sensitivity (59% and 44%) compared to [3H]-dThd phosphorylation assay (47% and 25%) at a specificity of 98%. These data demonstrate that the dual monoclonal antibody based AroCell TK 210 ELISA is a robust, accurate and precise tool for measuring TK1 protein in different malignancies that can improve the clinical applications of TK1 as a biomarker in cancer management.

Identifiants

pubmed: 36201558
doi: 10.1371/journal.pone.0275444
pii: PONE-D-21-30021
pmc: PMC9536554
doi:

Substances chimiques

Antibodies, Monoclonal 0
Biomarkers, Tumor 0
DNA 9007-49-2
Thymidine Kinase EC 2.7.1.21
thymidine kinase 1 EC 2.7.1.21
Thymidine VC2W18DGKR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0275444

Déclaration de conflit d'intérêts

Staffan Eriksson is an inventor of a TK1 patent licensed to DiaSorin Inc and is a shareholder in AroCell AB. The other authors have declared that no competing interest and this does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

K K Jagarlamudi (KK)

R&D Division, AroCell AB, Stockholm, Sweden.

Swinkels L (S)

Future Diagnostics, Wijchen, The Netherlands.

Zupan M (Z)

Blood Transfusion Center, Ljubljana, Slovenia.

Osredkar J (O)

University Medical Centre, Institute of Clinical Biochemistry, Ljubljana, Slovenia.

Venge P (V)

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

Eriksson S (E)

R&D Division, AroCell AB, Stockholm, Sweden.
Department of Anatomy, Physiology and Biochemistry, Swedish University of Agricultural Sciences, Uppsala, Sweden.

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Classifications MeSH