TY - JOUR T1 - Multidimensional scaling in Euclidean space of cytokine responses to document hyperinflammation in cystic fibrosis cells JF - European Respiratory Journal JO - Eur Respir J DO - 10.1183/13993003.congress-2021.PA3693 VL - 58 IS - suppl 65 SP - PA3693 AU - Nurlan Dauletbaev AU - Wided Akik AU - Anne-Christin Hauschild AU - Thomas Damm AU - Assel Suleimenova AU - Ainash Oshibayeva AU - Zhanna Kalmatayeva AU - Claus Vogelmeier AU - Larry Lands Y1 - 2021/09/05 UR - http://erj.ersjournals.com/content/58/suppl_65/PA3693.abstract N2 - Introduction: Studies of hyperinflammation in Cystic Fibrosis (CF) frequently yield complex high-dimensional data due to comparisons of CF cells with wildtype or treated controls, and multiple cytokine analyses. This warrants utilization of computational approaches beyond traditional statistics. We previously (Pediatr Pulmonol 2020;55/S2:56) utilized unsupervised clustering to assess a single-cytokine response in CF cells over two culture conditions.The Aim: of this study was to evaluate a composite cytokine response in CF cells under two culture conditions, in comparison with a known hyperinflammatory control.Methods: CFF16HBEge (delF508 CFTR) and 16HBE14o- (wildtype CFTR) were the cell models, tested either under submerged conditions or after differentiation at the air-liquid interface. The BEAS2B cells (wildtype CFTR) provided hyperinflammatory control data points, as per our previous work (Am J Respir Crit Care Med 2020;201:A2918). Basal and stimulated secretions of nine cytokines were quantified by multiplex ELISA (Millipore). The combined dataset, including the hyperinflammatory control, comprised 720 data points. All data points were log2 transformed and scaled to yield an Euclidean distance matrix for the multidimensional scaling (MDS) analysis.Results: The MDS analysis demonstrated proximity (i.e., similarity) of the composite inflammatory response of differentiated CFF16HBEge to that of the hyperinflammatory control.Conclusion: The developed workflow and MDS analysis support the presence of hyperinflammation in differentiated CF airway epithelial cells.Funding: Internal funds, DZL, Krieble Found., Gosselin Found., RSR-QC. ND, WA, ACH: co-first authorsFootnotesCite this article as: European Respiratory Journal 2021; 58: Suppl. 65, PA3693.This abstract was presented at the 2021 ERS International Congress, in session “Prediction of exacerbations in patients with COPD”.This is an ERS International Congress abstract. No full-text version is available. Further material to accompany this abstract may be available at www.ers-education.org (ERS member access only). ER -