Key result
MHC class-I expression differed significantly among neuromuscular diseases (p<0.001), being highly expressed in all idiopathic inflammatory myopathies but also present in 15 non-IIM cases.
Why the study?
The study was conducted to assess MHC class-I expression in different neuromuscular diseases.
Observational (n=54)
p-value: p=<0.001
MHC class-I expression is significantly different among neuromuscular diseases but cannot solely distinguish idiopathic inflammatory myopathies from non-IIMs.
MHC-I cannot solely distinguish IIMs; leaves open its integration into multimodal diagnostic algorithms for neuromuscular diseases.
BACKGROUND: Major histocompatibility complex (MHC) class-1 antigen is a glycoprotein expressed in all nucleated cells. The aim of this study was to assess MHC class-I expression in different neuromuscular diseases. METHODS: The authors reviewed the data of 54 patients with neuromuscular diseases. Anti MHC class-I antibody was performed on the frozen muscle tissues using immunohistochemistry. MHC class-I was scored based on its expression on muscle fibers (0: normal, 1: expression <5 fibers, 2: expression in 5-10 fibers, 3: expression in >10 fibers). The pattern was only assessed in cases with MHC class-I scored 3 as: (1: Sarcocapillary, 2: Sarcocapillary and necrotic fibers, 3: Perifascicular). The relationship between MHC class-I expression and neuromuscular diseases was statistically analyzed. RESULTS: The mean age of the patients was 39.1 ± 18.5 years. Around 50% of patients showed normal CK levels and 5% of the cases showed elevated CK levels. There was a significance difference in MHC class-I expression between cases with normal and elevated CK levels when MHC class-I score was 3 (p= 0.020). There was a significant difference in MHC class-I expression among different neuromuscular diseases (p<0.001). All cases with idiopathic inflammatory myopathies (IIMs) have expressed MHC class-I in more than 10 fibers. MHC class-I was expressed in 15 cases of non-IIMs. CONCLUSION: MHC class-I cannot be solely used as a biomarker to distinguish IIMs from non-IIMs. The presence of MHC class-I molecules in non-IIMs might be related to immunoproteasomes mechanism. Further studies, with different muscle proteins expression and genomic sequencing, must be conducted to understand the role of MHC Class-I in neuromuscular diseases.
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Kurdi et al. (2021) conducted an observational in Neuromuscular diseases (n=54). Idiopathic inflammatory myopathies (IIMs) vs. Non-IIMs was evaluated on MHC class-I expression (p=<0.001). MHC class-I expression differed significantly among neuromuscular diseases (p<0.001), being highly expressed in all idiopathic inflammatory myopathies but also present in 15 non-IIM cases.
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