| Literature DB >> 31726376 |
Milena Nasi1, Elena Bianchini2, Sara De Biasi3, Lara Gibellini3, Anita Neroni3, Marco Mattioli3, Marcello Pinti4, Anna Iannone2, Anna Vittoria Mattioli5, Anna Maria Simone6, Diana Ferraro7, Francesca Vitetta8, Patrizia Sola8, Andrea Cossarizza9.
Abstract
The role of damage-associated molecular patterns in multiple sclerosis (MS) is under investigation. Here, we studied the contribution of circulating high mobility group box protein 1 (HMGB1) and mitochondrial DNA (mtDNA) to neuroinflammation in progressive MS. We measured plasmatic mtDNA, HMGB1 and pro-inflammatory cytokines in 38 secondary progressive (SP) patients, 35 primary progressive (PP) patients and 42 controls. Free mtDNA was higher in SP than PP. Pro-inflammatory cytokines were increased in progressive patients. In PP, tumor necrosis factor-α correlated with MS Severity Score. Thus, in progressive patients, plasmatic mtDNA and pro-inflammatory cytokines likely contribute to the systemic inflammatory status.Entities:
Keywords: Damage-associated molecular patterns; High mobility group box protein 1; Mitochondrial DNA; Pro-inflammatory cytokines; Progressive multiple sclerosis
Year: 2019 PMID: 31726376 DOI: 10.1016/j.jneuroim.2019.577107
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478