Chemokine-mediated cell migration into the central nervous system in progressive multifocal leukoencephalopathy.
HIV
central nervous system
cerebrospinal fluid
chemokines
immune cell migration
multiple sclerosis
natalizumab
progressive multifocal leukoencephalopathy
single-cell RNA sequencing
viral encephalitis
Journal
Cell reports. Medicine
ISSN: 2666-3791
Titre abrégé: Cell Rep Med
Pays: United States
ID NLM: 101766894
Informations de publication
Date de publication:
17 Jun 2024
17 Jun 2024
Historique:
received:
21
02
2024
revised:
10
04
2024
accepted:
02
06
2024
medline:
26
6
2024
pubmed:
26
6
2024
entrez:
25
6
2024
Statut:
aheadofprint
Résumé
Progressive multifocal leukoencephalopathy (PML) has been associated with different forms of immune compromise. This study analyzes the chemokine signals and attracted immune cells in cerebrospinal fluid (CSF) during PML to define immune cell subpopulations relevant for the PML immune response. In addition to chemokines that indicate a general state of inflammation, like CCL5 and CXCL10, the CSF of PML patients specifically contains CCL2 and CCL4. Single-cell transcriptomics of CSF cells suggests an enrichment of distinct CD4
Identifiants
pubmed: 38917802
pii: S2666-3791(24)00326-4
doi: 10.1016/j.xcrm.2024.101622
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
101622Informations de copyright
Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests L.M.-M. reported travel grants from Alexion outside of the submitted work. S.G. was a consultant for Biogen during the initial phases of the study. She is the scientific director for the Myelin Repair Foundation. E.C.-M. was an employee of Biogen during the conduct of the study. G.M.z.H. reported speaker honoraria and consultant/advisor reimbursement from Roche, LFB Pharma, and Alexion. L.K. reported personal fees from Alexion, Bayer, Biogen, Celgene, Sanofi, Horizon, Grifols, Merck Serono, Novartis, Roche, Santhera, and Teva and grants from the German Research Foundation, IZKF Münster, IMF Münster, Biogen, Immunic AG, Novartis, and Merck Serono outside the submitted work. C.C.G. reported grants from DFG SFB/TR128 A09 during the conduct of the study; grants from DFG (single grant GR3946-3/1), IZKF (grant Kl13_010_19), Horizon2020 ReSToRe, Biogen, Roche, and Novartis Pharma; personal fees from MyLan and DIU Dresden International University GmbH; and other from Biogen, Euroimmun, MyLan, and Novartis Pharma outside the submitted work. H.W. reported personal fees from AbbVie, Alexion, Argenx, Biogen, Bristol-Myers Squibb/Celgene, EMD Serono, F. Hoffmann-La Roche Ltd., Fondazione Cariplo, Genzyme, Gossamer Bio, Idorsia, Immunic, Immunovant, Janssen, Lundbeck, Merck, Neurodiem, NexGen, Novartis, PSI CRO, Roche Pharma AG, Sanofi, Swiss Multiple Sclerosis Society TEVA, UCB Biopharma, WebMD Global, and Worldwide Clinical Trials outside the submitted work. He reported grants by the DFG (CRC128 A09 and 445569437) during the conduct of the study and funding by the German Federal Ministry for Education and Research (BMBF), Deutsche Myasthenie Gesellschaft e.V., Alexion, Amicus Therapeutics Inc., Argenx, Biogen, CSL Behring, Roche, Genzyme, Merck, Novartis Pharma, Roche Pharma, and UCB Biopharma outside of the submitted work. N.S. reported grants from DFG and Biogen during the conduct of the study.