CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunoarchitectural Pattern and Its Potential Prognostic Value in Mucoepidermoid Carcinoma.
Immunoarchitectural Pattern and Its Potential Prognostic Value in Mucoepidermoid Carcinoma.
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。
尽管 T 淋巴细胞丰富提示其具有高免疫原性,但 CD8+ T 淋巴细胞的保护作用在 MEC 中并不突出。
确定唾液腺黏液表皮样癌(MEC)的肿瘤免疫结构模式(IP),并描述免疫特征,以评估MEC的预后意义及其对免疫治疗的启示。
研究分析41例MEC,利用全切片成像和AI辅助评估肿瘤IP及TIL(肿瘤浸润淋巴细胞)参数。通过CD3和CD8免疫组化评估关键淋巴细胞亚群。
免疫细胞丰富型(I-rich)肿瘤具有较高TIL密度,并与侵袭性肿瘤行为相关;这种关联在组织学高级别MEC中尤其明显,肿瘤内部侵袭边缘区域TIL密度显著增加(p<0.05)。I-rich病例与较短的无病生存期(DFS)相关(Breslow=4.686,p=0.03)。侵袭性MEC病例呈现高度异质性的TIL特征,但未发现任何TIL模式对DFS有显著影响(p>0.05)。
尽管大量T细胞提示MEC具有较高免疫原性,CD8+ T淋巴细胞的保护作用并不突出。I-rich肿瘤似乎更具侵袭性,预后不良的MEC病例也表现出较高TIL异质性。研究肿瘤内部侵袭边缘TIL的作用,可能为未来免疫治疗发现提供新的机制认识。
To define tumor immunoarchitectural patterns (IPs) and characterize the immune profile in salivary gland mucoepidermoid carcinoma (MEC) toward assessing MEC prognostic significance and implications for immunotherapy.
This study analyzed 41 MEC cases, evaluating the tumor IPs and tumor-infiltrating lymphocyte (TIL) parameters by using whole-slide imaging and AI-assisted assessment. Immunohistochemistry of CD3 and CD8 markers was performed to assess key lymphocyte subpopulations.
Immune-rich (I-rich) tumors were characterized by high TIL density and were associated with aggressive tumor behavior, particularly in histological high-grade MEC, with a significant increase in TIL density observed in the inner invasive margin compartment (p < 0.05). I-rich tumor cases were linked to poorer disease-free survival (DFS) (Breslow = 4.686, p = 0.03). Aggressive MEC cases displayed a highly heterogeneous TIL profile, however, no TIL patterns showed a significant impact on DFS (p > 0.05).
Despite the high immunogenicity suggested by the abundance of T lymphocytes, the protective role of CD8+ T lymphocytes was not prominent in MEC. I-rich tumors appeared more aggressive and unfavorable MEC cases exhibited high heterogeneity in their TIL profiles. Interrogating the role of TILs in the inner invasive tumor margin may offer a new mechanistic understanding for future immunotherapy discovery.
MEMBER ACCOUNT
登录成功会直接打开下一页。