AUTHOR=van der Pan Kyra , de Bruin-Versteeg Sandra , Damasceno Daniela , Hernández-Delgado Alejandro , van der Sluijs-Gelling Alita J. , van den Bossche Wouter B. L. , de Laat Inge F. , Díez Paula , Naber Brigitta A. E. , Diks Annieck M. , Berkowska Magdalena A. , de Mooij Bas , Groenland Rick J. , de Bie Fenna J. , Khatri Indu , Kassem Sara , de Jager Anniek L. , Louis Alesha , Almeida Julia , van Gaans-van den Brink Jacqueline A. M. , Barkoff Alex-Mikael , He Qiushui , Ferwerda Gerben , Versteegen Pauline , Berbers Guy A. M. , Orfao Alberto , van Dongen Jacques J. M. , Teodosio Cristina TITLE=Development of a standardized and validated flow cytometry approach for monitoring of innate myeloid immune cells in human blood JOURNAL=Frontiers in Immunology VOLUME=13 YEAR=2022 URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2022.935879 DOI=10.3389/fimmu.2022.935879 ISSN=1664-3224 ABSTRACT=
Innate myeloid cell (IMC) populations form an essential part of innate immunity. Flow cytometric (FCM) monitoring of IMCs in peripheral blood (PB) has great clinical potential for disease monitoring due to their role in maintenance of tissue homeostasis and ability to sense micro-environmental changes, such as inflammatory processes and tissue damage. However, the lack of standardized and validated approaches has hampered broad clinical implementation. For accurate identification and separation of IMC populations, 62 antibodies against 44 different proteins were evaluated. In multiple rounds of EuroFlow-based design-testing-evaluation-redesign, finally 16 antibodies were selected for their non-redundancy and separation power. Accordingly, two antibody combinations were designed for fast, sensitive, and reproducible FCM monitoring of IMC populations in PB in clinical settings (11-color; 13 antibodies) and translational research (14-color; 16 antibodies). Performance of pre-analytical and analytical variables among different instruments, together with optimized post-analytical data analysis and reference values were assessed. Overall, 265 blood samples were used for design and validation of the antibody combinations and