XCL1, a serum biomarker in neurological diseases; HTLV-1-associated myelopathy and multiple sclerosis

Microb Pathog. 2023 Jan:174:105962. doi: 10.1016/j.micpath.2022.105962. Epub 2022 Dec 23.

Abstract

The XCL1-XCR1 axis has a potential role in the recruitment of immune cells to the site of inflammation. The present study aimed to examine the relation of XCL1 serum levels with Multiple sclerosis (MS) and HTLV-1-associated myelopathy (HAM), as chronic inflammatory diseases of the central nervous system (CNS). DNA was extracted to evaluate HTLV-1 proviral load (PVL) using real-time PCR. Serum levels of XCL1 was determined by using an ELISA assay. The serum level of XCL1 was significantly higher in patients with HAM than that of asymptomatic carriers (ACs) and healthy controls (HCs) (p < 0.001 and p < 0.0001, respectively) and was also higher in MS patients compared to HCs (p < 0.0001). Moreover, the concentration of XCL1 serum level was significantly different between the ACs and HCs group (p < 0.0001). In conclusion, increased expression of XCL1 might contribute to the migration of autoreactive T cells to the central nervous system and play a critical role in the development and pathogenesis of inflammatory neurological diseases including HAM and MS.

Keywords: Central nervous system; HTLV-1-Associated myelopathy; Human T-lymphotropic virus 1; Inflammation; Multiple sclerosis; XCL1.

MeSH terms

  • Biomarkers
  • Central Nervous System
  • Chemokines, C*
  • Human T-lymphotropic virus 1* / genetics
  • Humans
  • Multiple Sclerosis*
  • Paraparesis, Tropical Spastic*
  • Viral Load

Substances

  • Biomarkers
  • XCL1 protein, human
  • Chemokines, C