bioRxivImmunologyPreprint
SiteCELL enables on-site PBMCs purification and cryopreservation for immune single cell profiling of diverse ancestries
Aarón Espinosa‐Jaime, Octavio Zambada-MorenoiD, José Antonio Corona-GómeziD, M. Ortega, Marcela Hernández-CoronadoiD, Bárbara dos Santos DiasiD, Larissa Alvez Diniz, Laura LeadeniD, Guilherme Cesar Martelossi CebinelliiD, Doménica MarcheseiD, Adolfo Rojas-HidalgoiD, Emiliano VicencioiD, Diego Pérez-StuardoiD, Sebastián Urquiza-ZurichiD, Marisol Espitia Fajardo, Alicia ColomboiD, Gerardo DonosoiD, Tamara MéndeziD, Carla GalloiD, Hugo Guerrero‐CazaresiD, Carla Daniela Robles‐EspinozaiD, Patrícia A. PossikiD, Guillermo BarretoiD, Lucía SpangenbergiD, Ricardo A. VerdugoiD, , Carlos Ortiz‐RamíreziD
Abstract
Single cell genomics has improved our knowledge of immune function and heterogeneity. In recent years, the steady increase in the number of cells and individuals profiled as part of large multinational projects has enabled the characterization of cellular differences across human populations and ancestries. However, methods for collecting and processing peripheral blood mononuclear cells (PBMCs) for downstream single cell sequencing are difficult to implement in remote and rural settings. This has resulted in a lack of representation of underserved communities across the Global South in current initiatives. Hence, we developed SiteCELL, a method that enables purification and cryopreservation of PBMCs from whole blood at the site of collection using minimal laboratory equipment and without electricity. By comparing matched samples of purified PBMCs, we showed that SiteCELL performs as well as ficoll density gradient (FDG), both in laboratory and rural settings. This method ensures accurate recovery of cell type proportions and excels in reducing stress and minimizing variability across sampling batches. These advantages make it particularly well suited for implementation in challenging settings across countries, thereby enabling the inclusion of underrepresented ancestries in cellular atlases.
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