Density and location of CD3+ and CD8+ tumor-infiltrating lymphocytes correlate with prognosis of oral squamous cell carcinoma

被引:50
作者
Zhou, Chen [1 ,2 ]
Wu, Yaping [1 ]
Jiang, Lei [1 ]
Li, Zhongwu [3 ]
Diao, Pengfei [1 ]
Wang, Dongmiao [1 ]
Zhang, Wei [4 ]
Liu, Laikui [1 ,4 ]
Wang, Yanling [1 ]
Jiang, Hongbing [3 ]
Cheng, Jie [1 ,3 ]
Yang, Jianrong [1 ,3 ]
机构
[1] Nanjing Med Univ, Jiangsu Key Lab Oral Dis, Nanjing, Jiangsu, Peoples R China
[2] Jiangnan Univ, Affiliated Hosp, Dept Oral & Maxillofacial Surg, Wuxi, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Oral & Maxillofacial Surg, Affiliated Stomatol Hosp, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Dept Oral Pathol, Sch Stomatol, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
CD3; CD8; oral squamous cell carcinoma; prognosis; tumor-infiltrating lymphocytes; BREAST-CANCER; NECK-CANCER; SURVIVAL; HEAD; TIL;
D O I
10.1111/jop.12698
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BackgroundTumor-infiltrating lymphocytes (TILs) are regarded as adaptive immune response of the host to cancer cells and valuable prognostic factors. Here, we sought to characterize the densities and locations of CD3(+) and CD8(+) TILs in primary oral squamous cell carcinoma (OSCC) samples and assess their clinicopathological and prognostic significance. MethodsA total number of 169 OSCC samples from 2 independent patient cohorts (Nanjing cohort, 93 cases; Wuxi cohort, 76 cases) were retrospectively collected. The numbers of CD3(+) and CD8(+) TILs at tumor center (CT) and invasive margin (IM) of OSCC were identified by immunohistochemistry and calculated. The optimal cutoff values for CD3(+) and CD8(+) TILs to stratify patients were determined by X-tile software in Nanjing cohort and further utilized in Wuxi cohort. The associations between CD3(+)/CD8(+) TILs and clinicopathological parameters or patient survival were assessed. The prognostic values of CD3(+)/ CD8(+) TILs were evaluated by Cox regression analyses. ResultsCD3(+) and CD8(+) TILs were identified at both CT and IM and enriched at IM. High density of CD3(+) TILs at IM (CD3 IM) was significantly associated with increased overall and disease-specific survival (P<.05). High density of CD8(+) TILs at CT (CD8 CT) was significantly associated with increased overall but not disease-specific survival. Moreover, CD3 IM and CD8 CT were identified as independent prognostic factors for patient survival. ConclusionsOur findings provide further evidence to support the prognostic values of CD3(+) and CD8(+) TILs for OSCC, suggesting that TIL subsets might be viable biomarkers and therapeutic targets with translational significance.
引用
收藏
页码:359 / 367
页数:9
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