TY - JOUR
T1 - OMIP-121
T2 - Immune Phenotyping of Canine Peripheral Leukocytes by Mass Cytometry
AU - Luong, Huyen Thuc Tran
AU - Revets, Dominique
AU - Vercammen, Sofie
AU - de Marco, Ario
AU - de Rooster, Hilde
AU - Cosma, Antonio
N1 - Publisher Copyright:
© 2026 The Author(s). Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry.
© 2026 The Author(s). Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry.
PY - 2026/6/15
Y1 - 2026/6/15
N2 - Dogs are a critical non-rodent species used in preclinical safety studies, particularly, in the pharmaceutical field, due to their physiological, metabolic, and immunological similarities to humans. As such, immunophenotyping of canine peripheral blood mononuclear cells (PBMCs) plays a crucial role in translational research, immune monitoring, and safety evaluations in drug development. However, the limited availability of canine-specific antibodies restricts detailed and accurate immune profiling, which is essential for advancing safety evaluations in drug development. To address this challenge, we developed a 15-marker panel for comprehensive mass cytometry-based immunophenotyping of cryopreserved canine PBMCs. This panel encompasses major leukocyte subsets, including B cells, CD4+ T helper cells, regulatory T cells, CD8+ cytotoxic T cells, memory T cell subsets, natural killer T cells, natural killer cells, dendritic cells, CD4+ monocytes, classical monocytes, and neutrophils. We utilized both extracellular and intracellular markers to facilitate in-depth immune profiling, despite the limited availability of canine-specific antibodies. The panel was thoroughly optimized in terms of marker selection, antibody clone validation, and metal isotope pairing. Additionally, by the use of mass cytometry, several channels remain unoccupied, providing flexibility for future panel expansion.
AB - Dogs are a critical non-rodent species used in preclinical safety studies, particularly, in the pharmaceutical field, due to their physiological, metabolic, and immunological similarities to humans. As such, immunophenotyping of canine peripheral blood mononuclear cells (PBMCs) plays a crucial role in translational research, immune monitoring, and safety evaluations in drug development. However, the limited availability of canine-specific antibodies restricts detailed and accurate immune profiling, which is essential for advancing safety evaluations in drug development. To address this challenge, we developed a 15-marker panel for comprehensive mass cytometry-based immunophenotyping of cryopreserved canine PBMCs. This panel encompasses major leukocyte subsets, including B cells, CD4+ T helper cells, regulatory T cells, CD8+ cytotoxic T cells, memory T cell subsets, natural killer T cells, natural killer cells, dendritic cells, CD4+ monocytes, classical monocytes, and neutrophils. We utilized both extracellular and intracellular markers to facilitate in-depth immune profiling, despite the limited availability of canine-specific antibodies. The panel was thoroughly optimized in terms of marker selection, antibody clone validation, and metal isotope pairing. Additionally, by the use of mass cytometry, several channels remain unoccupied, providing flexibility for future panel expansion.
UR - https://www.scopus.com/pages/publications/105041883182
UR - https://pubmed.ncbi.nlm.nih.gov/42294829/
U2 - 10.1002/cyto.a.70040
DO - 10.1002/cyto.a.70040
M3 - Article
C2 - 42294829
AN - SCOPUS:105041883182
SN - 1552-4922
VL - 109
SP - 393
EP - 412
JO - Cytometry. Part A : the journal of the International Society for Analytical Cytology
JF - Cytometry. Part A : the journal of the International Society for Analytical Cytology
IS - 6
ER -