新型免疫检查点TIM-3在肿瘤研究中的趋势、热点及临床研究进展:基于文献计量分析

    Trends, frontiers, and clinical trials of TIM-3 in cancer research: a bibliometric analysis

    • 摘要:
      目的: 探讨T细胞免疫球蛋白和黏蛋白结构域蛋白3(TIM-3)在肿瘤研究中的年发文量趋势、研究前沿及热点和临床试验现状。
      方法: 基于Web Of Science Core Collection数据库,利用Microsoft Excel、CiteSpace6.3.R1(Advanced)、VOSviewer,对TIM-3与肿瘤相关的427条数据进行文献计量分析。
      结果: TIM-3在肿瘤领域的相关研究逐年增加;TIM-3与其他免疫检查点在肿瘤中共表达;程序性死亡受体配体1(PD-L1)抗体和程序性死亡受体1(PD-1)治疗为TIM-3相关肿瘤研究较活跃的研究方向。
      结论: TIM-3与PD-1、PD-L1、LAG-3、CTLA-4、TIGHT等其他免疫检查点共表达与肿瘤预后有关;TIM-3使CD8+ T细胞、自然杀伤细胞、树突状细胞等免疫细胞耗竭,抑制抗肿瘤免疫;国内外尚无靶向TIM-3抗肿瘤药物上市,尽管有较多临床试验正在进行,但均处于临床前阶段。

       

      Abstract:
      Objective To investigate the annual publication trends, research frontiers and hotspots, and clinical trial status of T cell immunoglobulin and mucin domain-containing protein 3(TIM-3) in cancer research.
      Methods By using Microsoft Excel, CiteSpace6.3.R1 (Advanced) and VOSviewer, a bibliometric analysis was conducted on 427 articles involving TIM-3 related with tumor based on Web of Science Core Collection database.
      Results The research on TIM-3 in cancer has been increasing each year. TIM-3 is co-expressed with other immune checkpoints in tumors. Programmed death receptor ligand 1 (PD-L1) antibody and programmed death receptor 1 (PD-1) therapy are active research directions in TIM-3-related tumor studies.
      Conclusions The co-expression of TIM-3 with other immune checkpoints such as PD-1, PD-L1, LAG-3, CTLA-4, and TIGHT is associated with tumor prognosis. TIM-3 induces exhaustion of immune cells such as CD8+ T cells, natural killer cells, and dendritic cells, leading to inhibition of anti-tumor immunity. Currently, there are no approved TIM-3-targeted anti-cancer drugs available globally. Although numerous clinical trials are underway, they are still in the preclinical stage.

       

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