Thrombocyte apheresis cassettes as a novel source of viable peripheral blood mononuclear cells. Issue 7 (14th March 2020)

• Record Type: Journal Article
• Authors: Cunningham, Sarah; Buchele, Vera; Brox, Regine; Strasser, Erwin; Hackstein, Holger
• Is Part Of: Transfusion. Volume 60:Issue 7(2020)
• Page Start: 1500
• Page End: 1507
• Publication Date: 2020-03-14
• Subjects: Hematology -- Periodicals; Blood -- Transfusion -- Periodicals; Blood Group Antigens -- Periodicals; Blood Preservation -- Periodicals; Blood Transfusion -- Periodicals; 615
• DOI: 10.1111/trf.15756
• Languages: English
• ISSNs: 0041-1132

Abstract

Abstract : BACKGROUND: Traditionally, white blood cells (WBCs) are collected from buffy coats or freshly drawn blood. However, the increasing demand for peripheral blood mononuclear cells (PBMCs) in the research phases of immunological therapy development makes it necessary to identify alternative sources of these cells. STUDY DESIGN AND METHODS: Leukapheresis products are cost intensive and not offered by all blood banks. Therefore, thrombocyte apheresis cassettes (TACs), plateletpheresis waste products, were investigated as a possible low‐cost and easily accessible blood source for research laboratories. The recovery rate, phenotype, and functionality of WBC subsets from TAC are unknown and were investigated in comparison to frequently used blood resources via flow cytometry. RESULTS: On average, TACs provide 30.3 × 10 6 /mL PBMCs, situating themselves between peripheral whole blood (WB; 5.35 × 10 6 /mL) and leukoreduction system chamber (LRSC; 163.9 × 10 6 /mL) yields. Frequencies of CD14, CD3, CD4, CD8, CD56, CD19, and CD11c positive cells in TACs correlate with normal proportions of WBC populations. Stimulation of TAC‐derived PBMCs by lipopolysaccharide (LPS) and resiquimod (R848) showed no significant differences in expression levels of human leukocyte antigen (HLA)‐DR, DQ, DP, and CD86 or cytokine secretion compared to other blood source derived PBMC. Following stimulation with LPS or R848, comparable levels of tumor necrosis factor‐α, interleukin‐10, and interleukin‐1β could be measured between TAC, LRSC, and WB. Additionally, TAC‐derived T cells retained their proliferation capability and were able to produce interferon‐γ following T‐cell receptor stimulation. CONCLUSION: TACs provide a cost‐effective source of viable and functional human blood cells that can readily be used for clinical and laboratory investigations after plateletpheresis preparation.