The tumor microenvironment of benign and malignant salivary gland tumors

被引:0
|
作者
Wai, Katherine C. [1 ,2 ,3 ]
Okholm, Trine Line H. [1 ,2 ,3 ]
Ha, Patrick K. [1 ,3 ]
Marquez, Diana M. [1 ,2 ,3 ]
Tenvooren, Iliana [1 ,2 ,3 ]
Jones, Kyle B. [1 ,2 ,3 ,4 ,5 ]
Spitzer, Matthew H. [1 ,2 ,3 ,6 ,7 ,8 ]
机构
[1] Univ Calif San Francisco, Dept Otolaryngol Head & Neck Surg, San Francisco, CA USA
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA USA
[3] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
[4] Univ Calif San Francisco, Dept Orofacial Sci, San Francisco, CA USA
[5] Genentech Inc, Pharm Tech Cell & Gene Therapy, South San Francisco, CA USA
[6] Parker Inst Canc Immunotherapy, San Francisco, CA USA
[7] Chan Zuckerberg Biohub, San Francisco, CA USA
[8] Univ Calif San Francisco, Dept Otolaryngol Head & Neck Surg, 513 Parnassus Ave HSW 1501A, San Francisco, CA 94143 USA
关键词
CyTOF; immunology; salivary gland cancer; salivary gland tumor; single-cell; FREE SURVIVAL; T-CELLS; CANCER; CARCINOMA; PATTERNS; REVEAL;
D O I
10.1002/hed.27716
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
BackgroundTreatment of salivary gland tumors (SGTs) remains challenging. Little is known about the immune landscape of SGTs. We aimed to characterize the tumor microenvironment in benign and malignant SGTs.MethodsEleven benign and nine malignant tumors were collected from patients undergoing curative intent surgery. Specimens were analyzed using mass cytometry by time-of-flight. Immune cell populations were manually gated, and T cells were clustered using the FlowSOM algorithm. Population frequencies were compared between high-grade and low-grade malignancies, corrected for multiple hypothesis testing.ResultsThere were trends towards increased CD4+ and CD8+ T cells among malignant tumors. High-grade malignancies exhibited trends towards higher frequencies of CD8+ PD-1+ CD39+ CD103+ exhausted T cells, CD4+ FoxP3+ TCF-1+ CD127- Tregs, and CD69+ CD25- CD4+ T cells compared to low-grade malignancies.ConclusionSGTs exhibit significant immunologic diversity. High-grade malignancies tended to have greater infiltration of exhausted CD8+ T cells and Tregs, which may guide future studies for immunotherapy strategies.
引用
收藏
页码:1625 / 1636
页数:12
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