An open-label pilot study of recombinant granulocyte-colony stimulating factor in Friedreich's ataxia.
Kevin C KempAnastasia GeorgievskayaKelly HaresJuliana RedondoSteven BaileyClaire M RiceNeil J ScoldingChris MetcalfeAlastair WilkinsPublished in: Nature communications (2022)
Friedreich's ataxia (FA) is an inherited progressive neurodegenerative disease for which there is no proven disease-modifying treatment. Here we perform an open-label, pilot study of recombinant human granulocyte-colony stimulating factor (G-CSF) administration in seven people with FA (EudraCT: 2017-003084-34); each participant receiving a single course of G-CSF (Lenograstim; 1.28 million units per kg per day for 5 days). The primary outcome is peripheral blood mononuclear cell frataxin levels over a 19-day period. The secondary outcomes include safety, haematopoietic stem cell (HSC) mobilisation, antioxidant levels and mitochondrial enzyme activity. The trial meets pre-specified endpoints. We show that administration of G-CSF to people with FA is safe. Mobilisation of HSCs in response to G-CSF is comparable to that of healthy individuals. Notably, sustained increases in cellular frataxin concentrations and raised PGC-1α and Nrf2 expression are detected. Our findings show potential for G-CSF therapy to have a clinical impact in people with FA.
Keyphrases
- peripheral blood
- recombinant human
- stem cells
- oxidative stress
- cerebrospinal fluid
- poor prognosis
- clinical trial
- skeletal muscle
- study protocol
- cell therapy
- multiple sclerosis
- type diabetes
- mesenchymal stem cells
- adipose tissue
- phase ii
- anti inflammatory
- bone marrow
- long non coding rna
- climate change
- binding protein
- combination therapy
- glycemic control