Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathies

被引:5
|
作者
Panicucci, Chiara [1 ]
Baratto, Serena [1 ]
Raffaghello, Lizzia [1 ]
Tonin, Paola [2 ]
D'Amico, Adele [3 ]
Tasca, Giorgio [4 ]
Traverso, Monica [5 ,6 ]
Fiorillo, Chiara [5 ,6 ]
Minetti, Carlo [5 ,6 ]
Previtali, Stefano Carlo [7 ,8 ]
Pegoraro, Elena [9 ]
Bruno, Claudio [1 ]
机构
[1] IRCCS Ist Giannina Gaslini, Ctr Translat & Expt Myol, Via Gerolamo Gaslini 5, I-16147 Genoa, Italy
[2] Univ Verona, Neurol Clin, Verona, Italy
[3] IRCCS Bambino Gesu Childrens Hosp, Unit Neuromuscular & Neurodegenerat Disorders, Rome, Italy
[4] Fdn Policlin Univ A Gemelli IRCCS, Unita Operat Complessa Neurol, Rome, Italy
[5] IRCCS Ist Giannina Gaslini, Pediat Neurol & Neuromuscular Disorders Unit, Genoa, Italy
[6] Univ Genoa, Genoa, Italy
[7] IRCSS San Raffaele Sci Inst, Neuromuscular Repair Unit, Inspe, Milan, Italy
[8] IRCSS San Raffaele Sci Inst, Div Neurosci, Milan, Italy
[9] Univ Padua, ERN Neuromuscular Ctr, Dept Neurosci, Padua, Italy
关键词
sarcoglycanopathy; DAMPS; Duchenne muscular dystrophy; limb-girdle muscular dystrophies; inflammation; MAJOR HISTOCOMPATIBILITY COMPLEX; MUSCULAR-DYSTROPHY; CLASS-I; EXPRESSION; PATHOLOGY; CELLS; MICE; LIFE;
D O I
10.5414/NP301393
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aim: Since the immune system plays a role in the pathogenesis of several muscular dystrophies, we aim to characterize several muscular inflammatory features in alpha- (LGMD R3) and gamma-sarcoglycanopathies (LGMD R5). Materials and methods: We explored the expression of major histocompatibility complex class I molecules (MHCI), and we analyzed the composition of the immune infiltrates in muscle biopsies from 10 patients with LGMD R3 and 8 patients with LGMD R5, comparing the results to Duchenne muscular dystrophy patients (DMD). Results: A consistent involvement of the immune response was observed in sarcoglycanopathies, although it was less evident than in DMD. LGMD R3-R5 and DMD shared an abnormal expression of MHCI, and the composition of the muscular immune cell infiltrate was comparable. Conclusion: These findings might serve as a rationale to fine-tune a disease-specific immunomodulatory regimen, particularly relevant in view of the rapid development of gene therapy for sarcoglycanopathies.
引用
收藏
页码:310 / 318
页数:9
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