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Multiparameter Flow Cytometry Assay for Quantification of Immune Cell Subsets, PD-1 Expression Levels and PD-1 Receptor Occupancy by Nivolumab and Pembrolizumab.
Pluim, Dick; Ros, Willeke; Miedema, Iris H C; Beijnen, Jos H; Schellens, Jan H M.
Afiliación
  • Pluim D; Division of Pharmacology, Netherlands Cancer Institute - Antoni van Leeuwenhoek (NKI-AVL), Amsterdam, The Netherlands.
  • Ros W; Division of Pharmacology, Netherlands Cancer Institute - Antoni van Leeuwenhoek (NKI-AVL), Amsterdam, The Netherlands.
  • Miedema IHC; Division of Pharmacology, Netherlands Cancer Institute - Antoni van Leeuwenhoek (NKI-AVL), Amsterdam, The Netherlands.
  • Beijnen JH; Department of Clinical Pharmacology, Netherlands Cancer Institute - Antoni van Leeuwenhoek (NKI-AVL), Amsterdam, The Netherlands.
  • Schellens JHM; Department of Pharmacy and Pharmacology, Netherlands Cancer Institute - Antoni van Leeuwenhoek (NKI-AVL), Amsterdam, The Netherlands.
Cytometry A ; 95(10): 1053-1065, 2019 10.
Article en En | MEDLINE | ID: mdl-31407460
We report the development and validation of a 12 parameter immunofluorescence flow cytometry method for the sensitive determination of cell concentrations, their expression of PD-1, and PD-1 receptor occupancy. Cell subsets include CD4+ and CD8+ -T-cells, B-cells, natural killer cells, classical-, intermediate- and non-classical monocytes, and myeloid- and plasmacytoid dendritic cells. Cells were isolated from peripheral blood by density gradient centrifugation. The validation parameters included specificity, linearity, limit of quantification, precision, biological within- and between subject variations. The lower limit of quantification was 5.0% of PD-1+ cells. Samples were stable for at least 153 days of storage at -80°C. The clinical applicability of the method was demonstrated in 11 advanced cancer patients by the successful determination of immune cell concentrations, relative number of PD-1+ immune cells, and number of PD-1 molecules per immune cell. Shortly after infusion of nivolumab, receptor occupancy on CD8+ -T-cells was 98%. Similar values were found predose cycle 2, suggesting receptor occupancy remained high throughout the entire cycle. © 2019 International Society for Advancement of Cytometry.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_other_blood_disorders Asunto principal: Inmunoensayo / Anticuerpos Monoclonales Humanizados / Antígeno B7-H1 / Receptor de Muerte Celular Programada 1 / Citometría de Flujo / Nivolumab / Leucocitos Límite: Humans Idioma: En Revista: Cytometry A Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_other_blood_disorders Asunto principal: Inmunoensayo / Anticuerpos Monoclonales Humanizados / Antígeno B7-H1 / Receptor de Muerte Celular Programada 1 / Citometría de Flujo / Nivolumab / Leucocitos Límite: Humans Idioma: En Revista: Cytometry A Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos
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