Altered expression of CXCR3 and CCR6 and their ligands in HTLV-1 carriers and HAM/TSP patients

J Med Virol. 2017 Aug;89(8):1461-1468. doi: 10.1002/jmv.24779. Epub 2017 Mar 10.

Abstract

Recruitment of leukocytes by chemokines and chemokine receptors to CNS plays a crucial role in the induction of inflammatory response in HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). In the present study, chemokine and chemokine receptors involved in trafficking of lymphocytes to the CNS were measured in HAM/TSP patients, HTLV-1 asymptomatic carriers (ACs), and healthy controls. The PVL, CCR6, and CXCR3 mRNA expression, and CXCL9 and CXCL10 protein levels were measured in all subjects. The PVL of HAM/TSP patients was higher than that of ACs (P = 0.02). CCR6 expression was higher in HAM/TSP patients and in ACs compared to the healthy controls (P = 0.005 and P = 0.04, respectively). A significant difference was observed in CCR6 expression when a combination of HAM/TSP patients and ACs were compared to the healthy individuals (P = 0.005). Furthermore, there was a significantly lower CXCR3 expression between HAM/TSP and control groups (P = 0.001), and between the ACs and healthy controls (P = 0.001). However, the increased CXCR3 expression in ACs compared to HAM/TSP patients was not significant. Furthermore, the CXCL10 protein levels in HAM/TSP patients was higher than in controls (P = 0.012), and CXCL9 protein levels was also higher in the HAM/TSP and ACs groups than in the controls (P = 0.001 and P = 0.004, respectively). In conclusion, it seems that decreased expression of CXCR3 and higher expression of CCR6 were associated with HTLV-1 infection, what indicate that these alterations may favor virus dissemination but not disease manifestation.

Keywords: CCR6; CXCR3; HAM/TSP; HTLV-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Carrier State / pathology*
  • Female
  • Gene Expression Profiling
  • HTLV-I Infections / pathology*
  • Humans
  • Male
  • Middle Aged
  • Proteome / analysis
  • RNA, Messenger / analysis
  • Receptors, CCR6 / analysis*
  • Receptors, CXCR3 / analysis*
  • Young Adult

Substances

  • CCR6 protein, human
  • CXCR3 protein, human
  • Proteome
  • RNA, Messenger
  • Receptors, CCR6
  • Receptors, CXCR3