scholarly journals STAT3 Modulation of Regulatory T Cells in Response to Radiation Therapy in Head and Neck Cancer

2019 ◽  
Vol 111 (12) ◽  
pp. 1339-1349 ◽  
Author(s):  
Ayman J Oweida ◽  
Laurel Darragh ◽  
Andy Phan ◽  
David Binder ◽  
Shilpa Bhatia ◽  
...  

Abstract Background Radioresistance represents a major problem in the treatment of head and neck cancer (HNC) patients. To improve response, understanding tumor microenvironmental factors that contribute to radiation resistance is important. Regulatory T cells (Tregs) are enriched in numerous cancers and can dampen the response to radiation by creating an immune-inhibitory microenvironment. The purpose of this study was to investigate mechanisms of Treg modulation by radiation in HNC. Methods We utilized an orthotopic mouse model of HNC. Anti-CD25 was used for Treg depletion. Image-guided radiation was delivered to a dose of 10 Gy. Flow cytometry was used to analyze abundance and function of intratumoral immune cells. Enzyme-linked immunosorbent assay was performed to assess secreted factors. For immune-modulating therapies, anti–PD-L1, anti-CTLA-4, and STAT3 antisense oligonucleotide (ASO) were used. All statistical tests were two-sided. Results Treatment with anti-CD25 and radiation led to tumor eradication (57.1%, n = 4 of 7 mice), enhanced T-cell cytotoxicity compared with RT alone (CD4 effector T cells [Teff]: RT group mean = 5.37 [ 0.58] vs RT + αCD25 group mean =10.71 [0.67], P = .005; CD8 Teff: RT group mean = 9.98 [0.81] vs RT + αCD25 group mean =16.88 [2.49], P = .01) and induced tumor antigen-specific memory response (100.0%, n = 4 mice). In contrast, radiation alone or when combined with anti-CTLA4 did not lead to durable tumor control (0.0%, n = 7 mice). STAT3 inhibition in combination with radiation, but not as a single agent, improved tumor growth delay, decreased Tregs, myeloid-derived suppressor cells, and M2 macrophages and enhanced effector T cells and M1 macrophages. Experiments in nude mice inhibited the benefit of STAT3 ASO and radiation. Conclusion We propose that STAT3 inhibition is a viable and potent therapeutic target against Tregs. Our data support the design of clinical trials integrating STAT3 ASO in the standard of care for cancer patients receiving radiation.

2009 ◽  
Vol 15 (20) ◽  
pp. 6348-6357 ◽  
Author(s):  
Magis Mandapathil ◽  
Miroslaw J. Szczepanski ◽  
Marta Szajnik ◽  
Jin Ren ◽  
Diana E. Lenzner ◽  
...  

2015 ◽  
Vol 75 (11) ◽  
pp. 2200-2210 ◽  
Author(s):  
Hyun-Bae Jie ◽  
Patrick J. Schuler ◽  
Steve C. Lee ◽  
Raghvendra M. Srivastava ◽  
Athanassios Argiris ◽  
...  

Oral Oncology ◽  
2012 ◽  
Vol 48 (5) ◽  
pp. 409-416 ◽  
Author(s):  
Clarissa A. Wild ◽  
Sven Brandau ◽  
Ramin Lotfi ◽  
Stefan Mattheis ◽  
Xiang Gu ◽  
...  

2005 ◽  
Vol 133 (2) ◽  
pp. P142-P142 ◽  
Author(s):  
C SCHAEFER ◽  
A ALBERS ◽  
K GOTTE ◽  
R NAIM ◽  
T WHITESIDE ◽  
...  

2002 ◽  
Vol 126 (2) ◽  
pp. 180-187
Author(s):  
Scott E. Strome ◽  
Elizabeth Martin ◽  
Dallas Flies ◽  
Dianne Khurana ◽  
Diva Salomao ◽  
...  

2013 ◽  
Vol 19 (23) ◽  
pp. 6585-6596 ◽  
Author(s):  
Patrick J. Schuler ◽  
Malgorzata Harasymczuk ◽  
Bastian Schilling ◽  
Zenichiro Saze ◽  
Laura Strauss ◽  
...  

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