Selective inhibition of mitochondrial Kv1.3 prevents and alleviates multiple sclerosis in vivo

Multiple sclerosis (MS) is characterized by invasion of the brain by effector memory T (T<sub>EM</sub>) lymphocytes that have been activated by repeated auto-antigen stimulation. Existing therapies target these and other autoreactive lymphocytes but their side effects include general immunosuppression and toxicity. Because the Kv1.3 potassium channel is highly expressed by chronically activated autoreactive T<sub>EM</sub>s, we investigated whether specific targeting of mitochondrial Kv1.3 using the pharmacological inhibitor PAPTP could selectively kill these T<sub>EM</sub>s in patients and mice with MS. 1 µM PAPTP targeted and reduced the number of autoreactive T<sub>EM</sub>s in blood samples from relapsing-remitting MS (RRMS) patients, leaving other T cell populations unaffected. Remarkably, pre-treatment of the entire T cell population with PAPTP during adoptive transfer of experimental autoimmune encephalomyelitis (EAE) killed T<sub>EM</sub>s and completely prevented disease onset in this mouse model. Moreover, PAPTP selectively eliminated activated T<sub>EM</sub>s and halted EAE progression when administered following disease onset. Our findings reveal the potential of PAPTP as an effective treatment for MS without adverse side effects.

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Publication Details

Journal
EMBO Molecular Medicine
Published
2025-09-29
DOI
https://doi.org/10.1038/s44321-025-00307-2
Citations
5
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
4.03
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article

Selective inhibition of mitochondrial Kv1.3 prevents and alleviates multiple sclerosis in vivo

Paolo Gallo, Valentina Scattolini, Beatrice Angi, Marta Favero et al.
5 citations
EMBO Molecular Medicine
Mitochondrial Function and Pathology
4.03
article

Selective inhibition of mitochondrial Kv1.3 prevents and alleviates multiple sclerosis in vivo

Paolo Gallo, Valentina Scattolini, Beatrice Angi, Marta Favero, Livio Trentin, Diletta Arcidiacono, Marco Puthenparampil, Gregory C. Wilson, Erich Gulbins, Lucia Biasutto, Maguie El Boustani, Michael Donadon, Andrea Mattarei, Alberto Ongaro, Ildikò Szabó, Matthias Soddemann, Tatiana Varanita, Mitra Tavakoli
article en
5 citations

Abstract

Multiple sclerosis (MS) is characterized by invasion of the brain by effector memory T (T<sub>EM</sub>) lymphocytes that have been activated by repeated auto-antigen stimulation. Existing therapies target these and other autoreactive lymphocytes but their side effects include general immunosuppression and toxicity. Because the Kv1.3 potassium channel is highly expressed by chronically activated autoreactive T<sub>EM</sub>s, we investigated whether specific targeting of mitochondrial Kv1.3 using the pharmacological inhibitor PAPTP could selectively kill these T<sub>EM</sub>s in patients and mice with MS. 1 µM PAPTP targeted and reduced the number of autoreactive T<sub>EM</sub>s in blood samples from relapsing-remitting MS (RRMS) patients, leaving other T cell populations unaffected. Remarkably, pre-treatment of the entire T cell population with PAPTP during adoptive transfer of experimental autoimmune encephalomyelitis (EAE) killed T<sub>EM</sub>s and completely prevented disease onset in this mouse model. Moreover, PAPTP selectively eliminated activated T<sub>EM</sub>s and halted EAE progression when administered following disease onset. Our findings reveal the potential of PAPTP as an effective treatment for MS without adverse side effects.

EMBO Molecular MedicineVol. 17(11)
University of Padua (IT), Istituto Oncologico Veneto (IT), Neuroscience Institute (IT), Essen University Hospital (DE), Istituti di Ricovero e Cura a Carattere Scientifico (IT), University of Cincinnati Medical Center (US)
Openalex Percentile: Top 6%
Mitochondrial Function and Pathology
4.03
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