6533b7dbfe1ef96bd1270935

RESEARCH PRODUCT

Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: Clinical and biological results from a prospective multicenter study

P BondesanCorrado TarellaMario PetriniRoberto MutaniSilvia GarbelliMario MelazziniAdriano ChiòVincenzo La BellaMassimo CorboCristina MogliaFrancesca GualandiMario SabatelliStefania MantovaniGianluigi MancardiR ScimèClaudia CaponnettoAndrea CalvoSergio RutellaCaterina BendottiVincenzo SilaniGabriele SicilianoGabriele Mora

subject

medicine.medical_specialtyPhysiologybusiness.industryMonocyteGranulocytemedicine.diseaseGastroenterologyGranulocyte colony-stimulating factorProinflammatory cytokineCellular and Molecular Neurosciencemedicine.anatomical_structureCerebrospinal fluidPhysiology (medical)Internal medicineMulticenter trialImmunologymedicineNeurology (clinical)Bone marrowAmyotrophic lateral sclerosisbusiness

description

Granulocyte colony-stimulating factor (G-CSF) induces a transient mobilization of hematopoietic progenitor cells from bone marrow to peripheral blood. Our aim was to evaluate safety of repeated courses of G-CSF in patients with amyotrophic lateral sclerosis (ALS), assessing disease progression and changes in chemokine and cytokine levels in serum and cerebrospinal fluid (CSF). Twenty-four ALS patients entered an open-label, multicenter trial in which four courses of G-CSF and mannitol were administered at 3-month intervals. Levels of G-CSF were increased after treatment in the serum and CSF. Few and transitory adverse events were observed. No significant reduction of the mean monthly decrease in ALSFRS-R score and forced vital capacity was observed. A significant reduction in CSF levels of monocyte chemoattractant protein-1 (MCP-1) and interleukin-17 (IL-17) was observed. G-CSF treatment was safe and feasible in a multicenter series of ALS patients. A decrease in the CSF levels of proinflammatory cytokines MCP-1 and IL-17 was found, indicating a G-CSF-induced central anti-inflammatory response.

https://doi.org/10.1002/mus.21851