Early changes in IL-21, IL-22, CCL2, and CCL4 serum cytokines after outpatient autologous transplantation for multiple sclerosis: A proof of concept study.
José Carlos Jaime-PérezGrecia A Turrubiates-HernándezLeslie J López-SilvaRosario Salazar-RiojasDavid Gómez-AlmaguerPublished in: Clinical transplantation (2020)
Changes in serum cytokines after autologous hematopoietic stem cell transplantation (AHSCT) in multiple sclerosis (MS) patients were documented. Thirty-six consecutive MS patients who had their Expanded Disability Status Scale (EDSS) scored before AHSCT were prospectively enrolled. Cyclophosphamide (Cy) was infused at 200 mg/kg in two administrations given 10 days apart: the first dose for mobilization, the second as the conditioning regimen. Patients were mobilized with 10 µg/kg/day subcutaneous G-CSF. Serum was collected 14 days before and 14 after AHSCT. IL-6, IL-9, IL-10, IL 17-A, IL-21, IL-22, IL-23, TNF-A, CCL2, CCL3, and CCL4 were measured by magnetic bead-based immunoassay. t Test and Wilcoxon test were used to compare cytokine levels before and after AHSCT. There were 28 women and 8 men with a median age of 46 (15-62) years, median duration of MS was 9.5 (1-32) years, and EDSS score was 5.7 (1.5-8.0). Patients had a decrement of pro-inflammatory IL-21 and IL-22 (p = .003 and p = .028) and an increment of anti-inflammatory CCL2 and CCL4 (p < .001 and p = .039) after AHSCT. Decrease of IL-21 and IL-22 coupled with an increment of CCL2 and CCL4 could reflect the immunomodulatory effect of auto-HSCT and be an early indicator of its efficacy.
Keyphrases
- multiple sclerosis
- liver injury
- liver fibrosis
- end stage renal disease
- ejection fraction
- mass spectrometry
- low dose
- metabolic syndrome
- drug induced
- pregnant women
- ms ms
- prognostic factors
- white matter
- stem cells
- rheumatoid arthritis
- peritoneal dialysis
- adipose tissue
- bone marrow
- acute myeloid leukemia
- skeletal muscle
- patient reported outcomes
- peripheral blood