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<p>Autoreactive T-cells against myelin are implicated in multiple sclerosis (MS) however, the functional relevance of IL2-producing central memory T-cells and IFNɣ-producing effector T-cells have not been assessed. In this study we aimed to t investigate association of IL2 + and IFNγ + myelin reactive memory T-cells with MS severity and progression. Thirty relapsing–remitting MS (RRMS) patients and 32 age-matched healthy subjects (HS) were analyzed. Peripheral Blood Mononuclear Cells (PBMC) responses to proteolipid protein (PLP), myelin basic protein (MBP), and myelin oligodendrocyte glycoprotein (MOG) were assessed using IFNγ/IL2-FluoroSpot assay and correlated with disease severity and progression. Flow cytometry was performed to characterize central (CD45RO+CD62L+) and effector memory (CD45RO+CD62L-) T-cell subsets. Patients showed increased frequency and magnitude of IL2 responses to PLP compared with HS. Higher PLP-induced IL2 responses were in correlation with clinical severity of the last occurring relapse, including EDSS, EDSS change, and longer time from last occurring relapse (<i>p</i> &lt; 0.05). Odds ratios&#xa0;(OR) confirmed associations between IL2-responses and last occurring relapse severity (OR range 5.3–22.5). Flow cytometry confirmed increase of central memory CD4 + and CD8 + T-cells in RRMS, whereas effector memory frequencies were unchanged. In RRMS, circulating PLP-reactive IL2 + central memory T-cells are linked to severity of last occurring relapse, representing an immunological imprint of recent disease activity rather than cumulative burden.</p>

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Myelin-specific IL2 + T-cells are associated with last occurring relapse severity in relapsing–remitting multiple sclerosis

  • 期刊论文

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  • 发表日期：

    2026年2月14日

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  • Rina Zilkha-Falb,
  • Tali Drori,
  • Katya Shwartz,
  • Michael Gurevich

摘要

Autoreactive T-cells against myelin are implicated in multiple sclerosis (MS) however, the functional relevance of IL2-producing central memory T-cells and IFNɣ-producing effector T-cells have not been assessed. In this study we aimed to t investigate association of IL2 + and IFNγ + myelin reactive memory T-cells with MS severity and progression. Thirty relapsing–remitting MS (RRMS) patients and 32 age-matched healthy subjects (HS) were analyzed. Peripheral Blood Mononuclear Cells (PBMC) responses to proteolipid protein (PLP), myelin basic protein (MBP), and myelin oligodendrocyte glycoprotein (MOG) were assessed using IFNγ/IL2-FluoroSpot assay and correlated with disease severity and progression. Flow cytometry was performed to characterize central (CD45RO+CD62L+) and effector memory (CD45RO+CD62L-) T-cell subsets. Patients showed increased frequency and magnitude of IL2 responses to PLP compared with HS. Higher PLP-induced IL2 responses were in correlation with clinical severity of the last occurring relapse, including EDSS, EDSS change, and longer time from last occurring relapse (p < 0.05). Odds ratios (OR) confirmed associations between IL2-responses and last occurring relapse severity (OR range 5.3–22.5). Flow cytometry confirmed increase of central memory CD4 + and CD8 + T-cells in RRMS, whereas effector memory frequencies were unchanged. In RRMS, circulating PLP-reactive IL2 + central memory T-cells are linked to severity of last occurring relapse, representing an immunological imprint of recent disease activity rather than cumulative burden.