Kashima Jumpei, Hishima Tsunekazu, Okuma Yusuke, Horio Hirotoshi, Ogawa Masumi, Hayashi Yukiko, Horiguchi Shin-Ichiro, Motoi Toru, Ushiku Tetsuo, Fukayama Masashi
Department of Pathology, Tokyo Metropolitan Cancer and Infectious diseases Center Komagome Hospital, Tokyo, Japan.
Department of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Front Oncol. 2022 Jan 25;11:808396. doi: 10.3389/fonc.2021.808396. eCollection 2021.
CD70 - a ligand protein of CD27 on lymphocytes - is expressed in a large spectrum of malignancies. It is an attractive target for antibody-based therapy and several clinical trials are currently being conducted. However, there is no evidence regarding the expression of CD70 and its relationship with expression of programmed death ligand-1 (PD-L1) and CD27+ tumor-infiltrating lymphocytes (TIL) in formalin-fixed paraffin-embedded (FFPE) tissues of thymic tumors. FFPE tissues of thymic squamous cell carcinoma (TSCC) (operative specimens, n = 31; biopsy specimens, n = 11), thymoma (n = 60), thymic carcinoid (n = 3), and lung squamous cell carcinoma (LSCC) (n = 30) were analyzed immunohistochemically. Immunoreactivity for CD70 was semi-quantitatively scored according to the proportion of positive tumor cells. Moreover, the densities of CD27-positive intratumoral TIL (iTIL) and stromal TIL of TSCC were assessed and survival was compared. Most TSCC cases (87%; 27/31) were CD70-positive. In contrast, all thymoma and thymic carcinoid cases were CD70-negative. In LSCC cases, CD70-positivity was significantly lower than TSCC cases (20%; 6/30). Biopsy and resected specimens obtained from the same patients demonstrated a consistent staining pattern (6/6 patients). The proportion of CD70-positive TSCC was comparable with those of CD5 (87%) and CD117 (90%). Correlation between CD70 and PD-L1 expression score was observed. There was no significant difference in survival between the CD70-high and CD70-low expression groups. Meanwhile, patients with CD27-positive iTIL-high tumors exhibited better survival than those with iTIL-low tumors. This tendency was weaker in the CD70-high subset. CD70 immunohistochemistry is useful in diagnosing TSCC. CD70 may prevent anti-tumor immunity CD27. Immunotherapy targeting the CD70-CD27 axis may be a promising option for the treatment of TSCC.
CD70(淋巴细胞上CD27的配体蛋白)在多种恶性肿瘤中表达。它是基于抗体治疗的一个有吸引力的靶点,目前正在进行多项临床试验。然而,关于胸腺肿瘤的福尔马林固定石蜡包埋(FFPE)组织中CD70的表达及其与程序性死亡配体-1(PD-L1)和CD27+肿瘤浸润淋巴细胞(TIL)表达的关系尚无证据。对胸腺鳞状细胞癌(TSCC)(手术标本,n = 31;活检标本,n = 11)、胸腺瘤(n = 60)、胸腺类癌(n = 3)和肺鳞状细胞癌(LSCC)(n = 30)的FFPE组织进行免疫组织化学分析。根据阳性肿瘤细胞的比例对CD70的免疫反应性进行半定量评分。此外,评估了TSCC的CD27阳性肿瘤内TIL(iTIL)和基质TIL的密度,并比较了生存率。大多数TSCC病例(87%;27/31)为CD70阳性。相比之下,所有胸腺瘤和胸腺类癌病例均为CD70阴性。在LSCC病例中,CD70阳性率显著低于TSCC病例(20%;6/30)。从同一患者获得的活检和切除标本显示出一致的染色模式(6/6例患者)。CD70阳性TSCC的比例与CD5(87%)和CD117(90%)的比例相当。观察到CD70与PD-L1表达评分之间存在相关性。CD70高表达组和低表达组之间的生存率无显著差异。同时,CD27阳性iTIL高的肿瘤患者比iTIL低的肿瘤患者表现出更好的生存率。这种趋势在CD70高表达亚组中较弱。CD70免疫组织化学对TSCC的诊断有用。CD70可能会阻止CD27的抗肿瘤免疫。靶向CD70-CD27轴的免疫治疗可能是治疗TSCC的一个有前景的选择。