The number of intratumoral dendritic cells and ζ-chain expression in T cells as prognostic and survival biomarkers in patients with oral carcinoma

IF 5.1 2区 医学 Q1 ONCOLOGY Cancer Pub Date : 2001-05-31 DOI:10.1002/1097-0142(20010601)91:11<2136::AID-CNCR1242>3.0.CO;2-Q
Torsten E. Reichert M.D., Ph.D., Claudia Scheuer Ph.D., Roger Day Sc.D., Wilfried Wagner M.D., Ph.D., Theresa L. Whiteside Ph.D.
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引用次数: 171

Abstract

BACKGROUND

Dendritic cells (DCs) are antigen-presenting cells with a unique ability to cross prime T cells and generate strong antitumor responses. This study evaluates the presence and prognostic significance of DCs as well as functional T cells, which accumulate in the microenvironment in patients with oral squamous cell carcinoma (OSCC).

METHODS

Immunohistochemistry for S-100 positive or p55 positive DCs and for T-cell receptor (TcR)-associated ζ-chain expression in tumor-infiltrating lymphocytes (TILs) was performed in 132 paraffin embedded specimens from patients with primary OSCC. The median clinical follow-up for the patients was 50 months. The numbers of intratumoral DCs or TILs expressing the ζ chain were determined microscopically and compared with clinical and pathohistologic prognostic parameters, including disease stage, T stage or tumor grade, lymph node involvement, as well as disease free survival and overall survival.

RESULTS

Immunostaining identified DCs in the epithelial compartment of the tumors (S-100 positive) as well as interdigitating reticular DCs (p55 positive) in peritumoral areas. Based on S-100 staining, intratumoral DC infiltrates were low (<10 DCs per high-power field [HPF]) in 20% of OSCC specimens, intermediate (10–20 DCs per HPF) in 42% of OSCC specimens, and high (>20 DCs per HPF) in 37% of OSCC specimens. The number of S-100 positive DCs was positively and significantly correlated with that of p55 and of TILs with normal ζ-chain expression. A low number of infiltrating S-100 positive DCs was more predictive of poor survival (hazard ratio, 7.95) than lymph node involvement (hazard ratio, 3.36) or late T stage (hazard ratio, 2.92). A significant but weaker association of p55 positive DC infiltration with survival was observed. Low density of DCs and low or absent expression of the ζ chain in TILs correlated with each other and predicted the poorest survival and the greatest risk.

CONCLUSIONS

The number of DCs infiltrating the tumor is a highly significant prognostic parameter in patients with OSCC. Furthermore, the absence or paucity of DCs is strongly linked to abnormalities in the TcR-associated ζ chain in TILs. The two biomarkers, ζ-chain expression in TILs and the number of S-100+ DCs in the tumor, independently predict overall survival, disease free survival, and time to disease recurrence in patients with OSCC. Cancer 2001;91:2136–47. © 2001 American Cancer Society.

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口腔癌患者肿瘤内树突状细胞数量和T细胞中ζ-链表达作为预后和生存的生物标志物
树突状细胞(dc)是一种抗原呈递细胞,具有独特的能力与原T细胞交叉并产生强烈的抗肿瘤反应。本研究评估了口腔鳞状细胞癌(OSCC)患者微环境中积累的dc和功能性T细胞的存在及其预后意义。方法对132例原发性OSCC患者石蜡包埋标本进行S-100阳性或p55阳性dc和肿瘤浸润淋巴细胞(TILs)中t细胞受体(TcR)相关的β -链表达的免疫组织化学检测。患者的中位临床随访时间为50个月。显微镜下测定肿瘤内表达ζ链的dc或til的数量,并与临床和病理组织学预后参数进行比较,包括疾病分期、T期或肿瘤分级、淋巴结受累、无病生存期和总生存期。结果免疫染色在肿瘤上皮间室中发现dc (S-100阳性),在肿瘤周围区域发现交错网状dc (p55阳性)。S-100染色显示,在20%的OSCC标本中,肿瘤内DC浸润为低浸润(每高倍视野[HPF] 10个DC),在42%的OSCC标本中为中等浸润(每高倍视野10 - 20个DC),在37%的OSCC标本中为高浸润(每高倍视野20个DC)。S-100阳性dc的数量与p55和正常ζ-链表达的TILs的数量呈显著正相关。与淋巴结受累(风险比为3.36)或T期晚期(风险比为2.92)相比,浸润性S-100阳性dc数量少更能预测生存率差(风险比为7.95)。p55阳性DC浸润与存活有显著但较弱的相关性。低密度的DCs和低或不表达的ζ链在TILs相互关联,并预测最低的生存和最大的风险。结论浸润肿瘤的dc数量是影响OSCC患者预后的重要指标。此外,dc的缺失或缺乏与TILs中tcr相关的ζ链的异常密切相关。这两个生物标志物,肿瘤中til中的ζ-链表达和S-100+ dc的数量,独立预测OSCC患者的总生存期、无病生存期和疾病复发时间。癌症2001;91:2136-47。©2001美国癌症协会。
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来源期刊
Cancer
Cancer 医学-肿瘤学
CiteScore
13.10
自引率
3.20%
发文量
480
审稿时长
2-3 weeks
期刊介绍: The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society. CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research
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