Extracorporeal photopheresis induces NETosis in neutrophils derived from patients with chronic graft-vs-host disease.

extracorporeal photopheresis (ECP) graft vs host disease (GVHD) neutrophil extracellular traps (NETs)

Journal

Journal of clinical apheresis
ISSN: 1098-1101
Titre abrégé: J Clin Apher
Pays: United States
ID NLM: 8216305

Informations de publication

Date de publication:
Oct 2023
Historique:
revised: 25 05 2023
received: 15 11 2022
accepted: 26 06 2023
pubmed: 13 7 2023
medline: 13 7 2023
entrez: 13 7 2023
Statut: ppublish

Résumé

Extracorporeal photopheresis (ECP) is considered an effective treatment for patients with chronic graft vs host disease (cGVHD) and demonstrates efficacy in ameliorating GVHD. The mechanism by which ECP acts against cGVHD is not fully understood. Preliminary observations have hinted at the potential involvement of neutrophil extracellular traps (NETs) formation in the pathogenesis of cGVHD. We aimed to assess the influence of ECP on the formation of NETs in patients with cGVHD as a potential mechanism in this setting. Patients treated with ECP for cGVHD at the Rabin Medical Center were included in this study. Blood samples were obtained at three different time points: before starting an ECP cycle, at the end of the first day of treatment, and 24 h following the initiation of the ECP treatment cycle. Neutrophils were harvested from all blood samples. NET formation was assessed by measurement of NET-bound specific neutrophil elastase activity and by immunofluorescence staining. Six patients (two females and four males) with cGVHD were included in the study. We observed a significant increase in NET formation among all six patients following ECP. Net-bound specific neutrophil elastase activity was elevated from a median value of 2.23 mU/mL (interquartile range [IQR] 2.06-2.47 mU/mL) at baseline to a median value of 13.06 mU/mL (IQR 10.27-15.97 mU/mL) immediately after the treatment and to a peak median value of 14.73 mU/mL (IQR 9.6-22.38 mU/mL) 24 h following the initiation of the ECP cycle. A qualitative assessment of NET formation using immunofluorescence staining has demonstrated markedly increased expression of citrullinated histone H3, a marker of NET formation, following ECP treatment. Our preliminary data indicate that ECP induces NET formation among patients with cGVHD. The contribution of increased NET formation to the therapeutic effect of cGVHD should be further investigated.

Identifiants

pubmed: 37439388
doi: 10.1002/jca.22073
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

615-621

Informations de copyright

© 2023 The Authors. Journal of Clinical Apheresis published by Wiley Periodicals LLC.

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Auteurs

Idan Goldberg (I)

Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Sackler School Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Internal Medicine F - Recanati, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Galit Granot (G)

Felsenstein Medical Research Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Alona Telerman (A)

Felsenstein Medical Research Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Shirly Partouche (S)

Felsenstein Medical Research Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Tzippy Shochat (T)

Statistical Consulting Unit, Beilinson Hospital, Rabin Medical Centre, Petah Tikva, Israel.

Erez Halperin (E)

Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Anat Gafter-Gvili (A)

Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Sackler School Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Internal Medicine A, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Liat Shargian (L)

Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Sackler School Medicine, Tel Aviv University, Tel Aviv, Israel.

Moshe Yeshurun (M)

Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Sackler School Medicine, Tel Aviv University, Tel Aviv, Israel.

Pia Raanani (P)

Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Sackler School Medicine, Tel Aviv University, Tel Aviv, Israel.

Ofir Wolach (O)

Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Sackler School Medicine, Tel Aviv University, Tel Aviv, Israel.

Vered Yahalom (V)

Sackler School Medicine, Tel Aviv University, Tel Aviv, Israel.
Blood Services & Apheresis Institute, Rabin Medical Center, Petah Tikva, Israel.

Classifications MeSH