2. Academic Validation
  3. Virus-induced RGMa expression drives neurodegeneration in HTLV-1-associated myelopathy

Virus-induced RGMa expression drives neurodegeneration in HTLV-1-associated myelopathy

  • JCI Insight. 2025 Apr 24;10(11):e184530. doi: 10.1172/jci.insight.184530.
Natsumi Araya 1,  Makoto Yamagishi 2,  Makoto Nakashima 1,  Naomi Asahara 3,  Kazuhiro Kiyohara 3,  Satoko Aratani 1 4,  Naoko Yagishita 1,  Erika Horibe 1,  Izumi Ishizaki 5,  Toshiki Watanabe 6,  Tomoo Sato 1 7,  Kaoru Uchimaru 5,  Yoshihisa Yamano 1 7
Affiliations

Affiliations

  • 1 Department of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kanagawa, Japan.
  • 2 Laboratory of Viral Oncology and Genomics, Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
  • 3 Neuroscience Unit Research Division, Mitsubishi Tanabe Pharma Corporation, Kanagawa, Japan.
  • 4 LSI Medience Co., Tokyo, Japan.
  • 5 Laboratory of Tumor Cell Biology, Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
  • 6 Department of Hematology/Oncology, and.
  • 7 Department of Neurology, St. Marianna University School of Medicine, Kanagawa, Japan.
PMID: 40305434 DOI: 10.1172/jci.insight.184530
Abstract

Human T-lymphotropic virus type 1-associated (HTLV-1-associated) myelopathy (HAM, also known as tropical spastic paraparesis) is a rare neurodegenerative disease with largely elusive molecular mechanisms, impeding targeted therapeutic advancements. This study aimed to identify the critical molecule responsible for neuronal damage in HAM, its source, and the regulatory mechanisms controlling its expression. Utilizing patient-derived cells and established cell lines, we discovered that HTLV-1 Tax, in conjunction with specificity protein 1 (Sp1), enhanced the expression of repulsive guidance molecule A (RGMa), a protein known to contribute to neuronal damage. RGMa expression was specifically upregulated in HTLV-1-infected cells from patients with HAM, particularly in those expressing HTLV-1 Tax. Furthermore, in CD4+ cells from patients with HAM, the level of H3K27me3 methylation upstream of the RGMA gene locus was reduced, making RGMA more prone to constitutive expression. We demonstrated that HTLV-1-infected cells in HAM inflict neuronal damage via RGMa. Crucially, the neutralizing antibody against RGMa, unasnemab (MT-3921), effectively mitigated this damage in a dose-responsive manner, highlighting RGMa's pivotal role in neuronal damage and its potential as a therapeutic target for alleviating neuronal damage in HAM.

Keywords

Infectious disease; Neurodegeneration; Neuroscience; T cells; Transcription.

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