免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Characterization of the tumor-infiltrating lymphocyte landscape in sinonasal mucosal melanoma.
Characterization of the tumor-infiltrating lymphocyte landscape in sinonasal mucosal melanoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
我们的结果表明,高密度的 CD3+和 CD8+ TIL 是 SNMM 生存的强阳性预后生物标志物。有必要开展病例数更大的前瞻性研究来证实我们的发现。
TIL(肿瘤浸润淋巴细胞)(TILs)是多种癌症的重要预后生物标志物。TIL亚群与免疫检查点分子如程序性细胞死亡配体1(PD-L1)之间的相互作用是免疫治疗的一个有前景的靶点。然而,鼻腔鼻窦黏膜黑色素瘤(SNMM)中的TIL景观尚未得到充分表征,TIL亚群和PD-L1表达的预后价值仍不确定。在此,我们研究了SNMM中TIL亚群(CD3+、CD4+、CD8+、CD20+)和PD-L1表达模式,并评估了它们对无复发生存和总生存期的预后价值。
对27例原发性SNMM患者的肿瘤组织进行了CD3、CD4、CD8、CD20和PD-L1的免疫组化染色。获取患者病史,并回顾性分析TIL亚组或PD-L1表达与AJCC肿瘤分期、总生存期和无复发生存期之间的关联。
原发肿瘤中CD3+和CD8+ TILs高的患者,其生存期显著长于CD3+和CD8+ TILs数量低的SNMMs患者。CD3+高和CD8+ TILs高与较低的T3分期和5年生存率提高相关。肿瘤细胞中PD-L1阳性与晚期肿瘤分期相关。
Tumor-infiltrating lymphocytes (TILs) are important prognostic biomarkers in several types of cancers. The interplay between TIL subgroups and immune checkpoint molecules like programmed cell death ligand 1 (PD-L1) is a promising target for immunotherapy. However, the TIL landscape in sinonasal mucosal melanoma (SNMM) has not been sufficiently characterized yet and the prognostic value of TIL subgroups and PD-L1 expression remains uncertain. Here, we investigated subsets of TILs (CD3+, CD4+, CD8+, CD20+) and PD-L1 expression patterns in SNMM and assessed their prognostic value for recurrence-free and overall survival.
Immunohistochemical staining for CD3, CD4, CD8, CD20 and PD-L1 was performed on tumor tissue from 27 patients with primary SNMM. Patient history was obtained and associations between TIL subgroups or PD-L1 expression and AJCC tumor stage, overall survival, and recurrence-free survival were retrospectively analyzed.
Patients with high CD3+ and CD8+ TILs in the primary tumor survived significantly longer than patients with SNMMs with a low number of CD3+ and CD8+ TILs. High CD3+ and high CD8+ TILs were associated with the lower T3 stage and increased 5-year survival. PD-L1 positivity in tumor cells was associated with advanced tumor stage.
Our results indicate that high densities of CD3+ and CD8+ TILs are strong positive prognostic biomarkers for survival in SNMM. Prospective studies with larger case numbers are warranted to confirm our findings.
MEMBER ACCOUNT
登录成功会直接打开下一页。