CLINICAL IMMUNOLOGY

Lidia Fernández-Paredesa, Armanda Casrouge, Jérémie Decalf et al. 
Clinical Immunology
DOI: 10.1016/j.clim.2017.05.019

Abstract:

Delay in the diagnosis of multiple sclerosis (MS) stems from the lack of specific clinical and analytical markers to assist in the early diagnosis and prediction of progressive course. We propose a decision-tree model that better defines early at onset MS patients and those with the progressive form by analysing a 12-biomarkers panel in serum and CSF samples of patients with MS, other neurological diseases (OND) and healthy contols. Thus, patients at onset of neurological disease were first classified by serum IL-7 levels < 141 pg/ml (OR = 6.51, p < 0.001). Combination of IL-7 and IP-10 indicated risk for a specific MS clinical form, where IL-7 < 141 and IP-10 < 570 pg/ml were associated with the highest risk for PP-MS (OR = 22, p = 0.01). Unexpectedly, both PP-MS and RR-MS patients shared significantly decreased prototypical biomarkers of inflammation and tissue regeneration in CSF than OND suggesting a defective intrinsic immune response playing a role at the beginning of the disease.