研究动态
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细胞毒性 T 淋巴细胞相关 4 蛋白表达与晚期经典霍奇金淋巴瘤的高国际预后评分相关。

Cytotoxic T-lymphocyte-associated 4 protein expression is associated with a high international prognostic score in advanced-stage classical Hodgkin lymphoma.

发表日期:2024 Jul 08
作者: Flora Dameria Pangaribuan, Maria Francisca Ham, Mutiah Mutmainnah, Agnes Stephanie Harahap
来源: MEDICINE & SCIENCE IN SPORTS & EXERCISE

摘要:

所有经典霍奇金淋巴瘤 (CHL) 病例中有 20% 会复发,尤其是在国际预后评分 (IPS) 较高的晚期阶段。细胞毒性T淋巴细胞相关蛋白4(CTLA-4)是一种能够抑制免疫反应并与肿瘤侵袭性相关的调节分子。本研究旨在确定晚期 CHL 和 IPS 中 CTLA-4 表达的关系,将其确定为潜在的治疗靶点。在晚期 CHL 中,IPS 高的组表现出明显更高的平均 CTLA-4 表达。 IPS 低的组 (p = 0.003)。 Hb 水平 < 10.5 g/dl、白细胞计数 > 15,000/μL、淋巴细胞计数 < 8%、白蛋白水平 < 4 g/dl 和第 4 阶段的组表现出较高的 CTLA -4 表达高于其他组,尽管仅白细胞计数和分期显示出统计学显着性(p = 0.004 和 p = 0.020)。结节性硬化症的平均 CTLA-4 表达为 239.84±76.36,混合细胞型为 293.95±147.94,淋巴细胞耗尽型为 271.4±23.56,富含淋巴细胞亚型为 225.2。结果表明,CTLA-4 表达与晚期 CHL IPS 中的不良预后因素相关,支持免疫检查点在癌症进展中发挥作用的观点。© 2024。作者。
Twenty percent of all classical Hodgkin lymphoma (CHL) cases relapse and recur, especially in advanced stages with a high International Prognostic Score (IPS). Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is a regulatory molecule that can inhibit the immune response and is related to tumor aggressiveness. This study aimed to determine the relationship between CTLA-4 expression in advanced-stage CHL and IPS, identifying it as a potential therapy target.In advanced-stage CHL, the group with a high IPS exhibited significantly higher mean CTLA-4 expression compared to the group with a low IPS (p = 0.003).The group with Hb level < 10.5 g/dl, leukocyte count > 15,000/µL, lymphocyte count < 8%, albumin level < 4 g/dl, and stage 4 exhibited higher CTLA-4 expression than the other group, although only leukocyte count and stage showed statistical significance (p = 0.004 and p = 0.020). Mean CTLA-4 expression was 239.84 ± 76.36 for nodular sclerosis, 293.95 ± 147.94 for mixed cellularity, 271.4 ± 23.56 for lymphocyte depleted, and 225.2 for lymphocyte-rich subtypes. The results suggest that CTLA-4 expression is associated with adverse prognostic factors in the IPS for advanced-stage CHL, supporting the notion that immune checkpoints play a role in cancer progression.© 2024. The Author(s).