Volume 13, Issue 1 (Winter 2024)                   aumj 2024, 13(1): 9-16 | Back to browse issues page


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Aghaie T, Gorgani M, Motallebnezhad M, Jazayeri M H. Comparison of the PD-1 expression level in peripheral blood of Multiple Sclerosis and Neuromyelitis Optica patients. aumj 2024; 13 (1) :9-16
URL: http://aums.abzums.ac.ir/article-1-1666-en.html
1- Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.Immunology Research Center, Institute of Immunology and Infectious Disease, Iran University of Medical Sciences, Tehran, Iran.
Abstract:   (762 Views)
Programmed cell death-1 (PD-1) is one of the important co-inhibitory receptors in maintaining tolerance and inhibiting the proliferation and activity of activated immune cells. PD-1: PD-L pathway enhances regulatory T cells proliferation and inhibition of autoreactive T cells and regulates central and peripheral tolerance. This pathway has affected various aspects of the immune system and is of particular importance in a variety of diseases, such as autoimmune diseases. Multiple sclerosis (MS) and Neuromyelitis Optica (NMO) are neurological disorders characterized by inflammation, demyelination by the immune system, and axonal and neuronal damage in the CNS. The clinical manifestations of NMO are very similar to MS and lead to a misdiagnosis. Therefore, the existence of specific diagnostic markers is of particular importance for correct diagnosis. Here, we examined the expression of the PD-1 gene in 40 MS patients, 20 NMO patients, and 15 healthy individuals. Thus, after RNA extraction from human blood and cDNA synthesis, gene expression of PD-1 was investigated using quantitative real-time PCR technique. The results show that the PD-1 mRNA expression in the peripheral blood of the MS group was significantly increased in comparison to that of the NMO group and healthy group (p= 0.0008, p= 0.0024, respectively). However, there was no significant difference in PD-1 mRNA expression between the NMO group and the healthy group.
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Type of Study: Original | Subject: Special
Received: 2023/03/01 | Accepted: 2023/07/18 | Published: 2024/02/29

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