Abstract A159: Agonistic CD40 antibody therapy induces formation of tertiary lymphoid structures in glioma and inhibits the response to immune-checkpoint blockade

L. Hooren, A. Vaccaro, Maria Georganaki, Mohanraj Ramachandran, Hua Huang, J. Lau, A. Smits, M. Essand, A. Dimberg
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Abstract

Cancer immunotherapy of glioma, the most common primary brain tumor in adults, is constrained by an immunosuppressive microenvironment. Tertiary lymphoid structures (TLSs) are ectopic lymphoid structures that mediate immune responses and provide a local site for tumor antigen presentation. Here, we show for the first time that TLSs are present in human low-grade glioma and that they can be induced in murine glioma models. Agonistic CD40 antibodies induced lymphotoxin α expression in B cells and enhanced the formation of TLSs in mice bearing orthotopic GL261 or CT-2A gliomas. TLSs consisting of B cells, T-cells and antigen presenting cells formed around CD31+ vessels proximal to the tumor tissue and adjacent to the meninges. Agonistic CD40 antibody treatment improved the CD8+ T-cell / Treg ratio in tumor-bearing mice, but there was no survival benefit. A decreased CD69 activation status on CD8+ T-cells, an increase of B cells with a CD1d+CD5+ regulatory phenotype and a high infiltration of Tregs in TLSs indicate that agonistic CD40 antibodies induce an immunosuppressive microenvironment in glioma. Consistent with this, the efficacy of both PD-1 and CTLA-4 checkpoint blockade was significantly decreased by co-administration of agonistic CD40 antibodies. These results demonstrate that TLSs are present and can be induced in glioma, but that they at least under certain conditions are associated with immunosuppression, shedding light on new mechanisms of immune regulation in the brain microenvironment. Citation Format: Luuk van Hooren, Alessandra Vaccaro, Maria Georganaki, Mohanraj Ramachandran, Hua Huang, Joey Lau, Anja Smits, Magnus Essand, Anna Dimberg. Agonistic CD40 antibody therapy induces formation of tertiary lymphoid structures in glioma and inhibits the response to immune-checkpoint blockade [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A159.
摘要:激动性CD40抗体治疗诱导胶质瘤中三级淋巴结构的形成并抑制对免疫检查点封锁的反应
神经胶质瘤是成人最常见的原发性脑肿瘤,其免疫治疗受到免疫抑制微环境的限制。三级淋巴样结构(TLSs)是异位淋巴样结构,介导免疫反应并提供肿瘤抗原呈递的局部部位。在这里,我们首次表明TLSs存在于人类低级别胶质瘤中,并且它们可以在小鼠胶质瘤模型中诱导。在原位GL261或CT-2A胶质瘤小鼠中,激动性CD40抗体诱导淋巴素α在B细胞中的表达,并增强TLSs的形成。由B细胞、t细胞和抗原提呈细胞组成的TLSs在肿瘤组织近端和脑膜附近的CD31+血管周围形成。激动性CD40抗体治疗提高了荷瘤小鼠的CD8+ t细胞/ Treg比率,但没有生存益处。CD8+ t细胞上CD69激活状态的降低,CD1d+CD5+调节性表型的B细胞的增加以及tls中Tregs的高浸润表明,激动性CD40抗体在胶质瘤中诱导了免疫抑制微环境。与此一致的是,PD-1和CTLA-4检查点阻断的有效性在联合使用激动性CD40抗体后显著降低。这些结果表明,TLSs在胶质瘤中存在并可被诱导,但至少在某些条件下它们与免疫抑制有关,从而揭示了脑微环境中免疫调节的新机制。引文格式:Luuk van Hooren, Alessandra Vaccaro, Maria Georganaki, Mohanraj Ramachandran, Hua Huang, Joey Lau, Anja Smits, Magnus Essand, Anna Dimberg。激动性CD40抗体治疗诱导胶质瘤中三级淋巴结构的形成并抑制对免疫检查点封锁的反应[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫,2019;7(2增刊):摘要nr A159。
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