Differential protein expression in endothelial cells exposed to serum from patients with acute graft‐vs‐host disease, depending on steroid response

Author:

Martinez‐Sanchez Julia123ORCID,Palomo Marta123,Pedraza Alexandra4,Moreno‐Castaño Ana Belén23,Torramade‐Moix Sergi2,Rovira Montserrat5,Salas María Queralt5,Cid Joan6,Escolar Gines23,Penack Olaf7,Carreras Enric13,Diaz‐Ricart Maribel23

Affiliation:

1. Josep Carreras Leukaemia Research Institute Hospital Clínic de Barcelona, Universitat de Barcelona Barcelona Spain

2. Hemostasis and Erythropathology Laboratory, Hematopathology, Department of Pathology, Centre de Diagnòstic Biomèdic (CDB) Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona Barcelona Spain

3. Barcelona Endothelium Team Barcelona Spain

4. Blood Bank Department Hematopoietic Transplantation Unit, Banc de Sang i Teixits, Hospital Clínic Barcelona Spain

5. Hematology Department Bone Marrow Transplantation Unit, Institut Clínic de Malalties Hemato‐Oncològiques (ICMHO), Hospital Clínic Barcelona Spain

6. Apheresis & Cellular Therapy Unit, Department of Hemotherapy and Hemostasis ICMHO, Hospital Clínic de Barcelona, IDIBAPS, Universitat de Barcelona Barcelona Spain

7. Hematology, Oncology and Tumorimmunology Department Charité‐Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany

Abstract

AbstractGraft‐versus‐host disease (GVHD) is a complication of allogeneic haematopoietic cell transplantation. Endothelial injury is crucial as pathophysiological substrate for GVHD. GVHD first‐line treatment is high‐dose corticosteroids, although some patients are steroid‐refractory. Through the present study, we compared the endothelial proteomic profiles in response to serum from steroid‐refractory acute GVHD (SR‐aGVHD) and steroid‐sensitive acute GVHD (SS‐aGVHD) patients. Blood samples from SR‐aGVHD (n = 4) and SS‐aGVHD (n = 8) patients were collected at aGVHD diagnosis. Endothelial cell cultures were exposed (48 h) to patients' serum. Protein extraction and proteomic analysis were performed. Differences were statistically evaluated by multivariate analysis. Forty‐four proteins contributed to separate all samples into the two study groups, among which 15 participated significantly (p < 0.05), 10 exhibiting a fold change >1.2. Differentially expressed proteins were mainly associated with oxidative phosphorylation (Cytochrome C oxidase subunit 6B1, CX6B1), inflammation and angiogenesis (Apolipoprotein D, APOD), cell survival (Rapamycin‐insensitive companion of mTOR, RICTR), and oxidative stress (Riboflavin kinase, RIFK). This pilot study used a novel approach to distinguish the aGVHD response to steroid treatment. The proteins differentially expressed could constitute potential biomarkers for steroid‐treatment response. These findings signify a step forward to identify the mechanisms of response to steroids, of high clinical relevance considering the SR‐aGVHD elevated mortality.

Funder

Deutsche Forschungsgemeinschaft

Deutsche Krebshilfe

Fundació la Marató de TV3

Generalitat de Catalunya

Instituto de Salud Carlos III

Stiftung Charité

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

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