4.6 Article

CSF SERPINA3 Levels Are Elevated in Patients With Progressive MS

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/NXI.0000000000000941

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Funding

  1. Fondo de Investigacion Sanitaria (FIS), Ministry of Science and Innovation, Spain [PI17/00596]
  2. Generalitat de Catalunya Suport Grups de Recerca [2017 SGR 0527]
  3. Red Espanola de Esclerosis Multiple - FIS [RD16/0015/0004]

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This study identified two new biomarkers, Serpina3n and S100A4, which were upregulated during the progressive phases of multiple sclerosis and induced during neuronal differentiation. Levels of SERPINA3 and S100A4 were found to be increased in the cerebrospinal fluid of patients with progressive forms of MS compared to noninflammatory neurologic controls. Additionally, CSF SERPINA3 levels were significantly correlated with CSF neurofilament light chain levels in patients with primary progressive MS.
Objective To identify biomarkers associated with progressive phases of MS and with neuroprotective potential. Methods Combined analysis of the transcriptional and proteomic profiles obtained in CNS tissue during chronic progressive phases of experimental autoimmune encephalomyelitis (EAE) with the transcriptional profile obtained during the differentiation of murine neural stem cells into neurons. Candidate biomarkers were measured by ELISA in the CSF of 65 patients with MS (29 with relapsing-remitting MS [RRMS], 20 with secondary progressive MS, and 16 with primary progressive MS [PPMS]) and 30 noninflammatory neurologic controls (NINCs). Results Integrative analysis of gene and protein expression data identified 2 biomarkers, the serine protease inhibitor Serpina3n and the calcium-binding protein S100A4, which were upregulated in chronic progressive EAE and whose expression was induced during neuronal differentiation. Immunofluorescence studies revealed a primarily neuronal expression of S100A4 and Serpina3n during EAE. CSF levels of SERPINA3, the human ortholog of murine Serpina3n, and S100A4 were increased in patients with MS compared with NINCs (SERPINA3: 1,320 vs 838.6 ng/mL, p = 0.0001; S100A4: 1.6 vs 0.8 ng/mL, p = 0.02). Within the MS group, CSF SERPINA3 levels were significantly elevated in patients with progressive forms, mainly patients with PPMS compared with patients with RRMS (1,617 vs 1,129 ng/mL, p = 0.02) and NINCs (1,617 vs 838.6 ng/mL, p = 0.0001). Of interest, CSF SERPINA3 levels significantly correlated with CSF neurofilament light chain levels only in the PPMS group (r = 0.62, p = 0.01). Conclusion These results point to a role of SERPINA3 as a biomarker associated with the progressive forms of MS, particularly PPMS.

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