Tumor Immune Microenvironment Heterogeneity at the Invasion Front and Tumor Center in Oral Squamous Cell Carcinoma as a Perspective of Managing This Cancer Entity

被引:6
作者
Mamilos, Andreas [1 ,2 ,3 ]
Lein, Alexander [4 ]
Winter, Lina [1 ,2 ,3 ]
Ettl, Tobias [5 ]
Kuenzel, Julian [6 ]
Reichert, Torsten E. E. [5 ]
Spanier, Gerrit [5 ]
Brochhausen, Christoph [1 ,2 ,3 ,7 ]
机构
[1] Univ Regensburg, Inst Pathol, D-93053 Regensburg, Germany
[2] Univ Regensburg, Cent Biobank Regensburg, D-93053 Regensburg, Germany
[3] Univ Hosp Regensburg, D-93053 Regensburg, Germany
[4] Med Univ Vienna, Dept Otorhinolaryngol Head & Neck Surg, A-1090 Vienna, Austria
[5] Univ Hosp Regensburg, Dept Oral & Maxillofacial Surg, D-93053 Regensburg, Germany
[6] Univ Hosp Regensburg, Dept Otorhinolaryngol, D-93053 Regensburg, Germany
[7] Heidelberg Univ, Univ Med Ctr Mannheim, Inst Pathol, D-68167 Mannheim, Germany
关键词
head and neck cancer; OSCC; immune microenvironment; pathology; immunohistochemistry; spatial distribution; topology; INFILTRATING LYMPHOCYTES; HEAD; NECK; MACROPHAGES; RECURRENT; SURVIVAL; CAVITY; POLARIZATION; TILS;
D O I
10.3390/jcm12041704
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Evaluating the tumor microenvironment and its influence on clinical management and therapy response is becoming increasingly important. However, only a few studies deal with the spatial distribution of immune cells within the tumor. This study aimed to describe the topology of immune cells in the microenvironment of oral squamous cell carcinoma (OSCC) sectioned by tumor invasion front and tumor center and to test their prognostic relevance regarding patient survival. Methods: A total of 55 OSCC patient specimens were collected retrospectively. The cancer tissue was immunohistochemically stained using an automated tissue stainer Ventana Benchmark Ultra (Roche) and analyzed using discrete expression marker profiles on immune cells. We investigated CD4+ lymphocytes, CD8+ lymphocytes, CD68+ macrophages, CD163+ macrophages, and M1 macrophages regarding their spatial distribution. Results: The statistical analysis revealed that the quantity and distribution of CD4+ (p = 0.007), CD8+ (p < 0.001), CD68+ (p < 0.001), CD163+ cells (p = 0.004), and M1 (p < 0.001) macrophages were significantly higher at the invasion front compared to the tumor center in all observed cases. However, high and low immune cell counts in the tumor center and invasion front were not associated with overall survival. Conclusion: Our results show two distinct immune microenvironments of the tumor center compared to the invasion front. Future studies are needed to explore how these results can be leveraged to improve patient therapy and outcome.
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页数:13
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