Department of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Department of Clinical Sciences and Advanced Medicine, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Vet Comp Oncol. 2020 Dec;18(4):447-470. doi: 10.1111/vco.12595. Epub 2020 Apr 27.
Key advances in our understanding of immunobiology and the immunosuppressive mechanisms of the tumour microenvironment have led to significant breakthroughs in manipulating the immune system to successfully treat cancer. Remarkable therapeutic responses have occurred with tumours that carry a high mutational burden. In these cases, pre-existing tumour-specific T cells can be rejuvenated via checkpoint inhibition to eliminate tumours. Furthermore, durable remissions have been achieved in haematological malignancies following adoptive transfer of T cells that specifically target cell surface proteins where expression is restricted to the malignancy's cell of origin. Soft tissue sarcomas and bone sarcomas have a paucity of non-synonymous somatic mutations and do not commonly express known, targetable, tumour-specific antigens. Historically, soft tissue sarcomas have been considered immunologically 'cold' and as such, unlikely candidates for immune therapy. Here, we review the immune landscape of canine and feline sarcomas and the immunotherapeutic strategies that have been employed in veterinary clinical trials to improve patient outcome. We also provide insight into immunotherapeutic approaches being used to treat human sarcomas. Together, current data indicates that, rather than a barren immunological wasteland, sarcomas represent a field of opportunities for immunotherapies. Furthermore, we and others would suggest that strategic combinations of immunotherapeutic approaches may hold promise for more effective treatments for high grade soft tissue sarcomas and bone sarcomas.
我们对免疫生物学和肿瘤微环境中免疫抑制机制的理解取得了重大进展,这使得操纵免疫系统成功治疗癌症成为可能。在那些携带高突变负担的肿瘤中,已经出现了显著的治疗反应。在这些情况下,可以通过检查点抑制来恢复预先存在的肿瘤特异性 T 细胞,从而消除肿瘤。此外,在对特定于细胞表面蛋白的 T 细胞进行过继转移后,血液恶性肿瘤也实现了持久缓解,这些细胞表面蛋白的表达仅限于恶性肿瘤的起源细胞。软组织肉瘤和骨肉瘤缺乏非同义体细胞突变,通常不表达已知的、可靶向的肿瘤特异性抗原。从历史上看,软组织肉瘤被认为是免疫“冷”的,因此不太可能成为免疫治疗的候选者。在这里,我们回顾了犬和猫肉瘤的免疫景观以及在兽医临床试验中采用的免疫治疗策略,以改善患者的预后。我们还提供了一些关于正在用于治疗人类肉瘤的免疫治疗方法的见解。综上所述,目前的数据表明,肉瘤代表了免疫治疗的机会领域,而不是贫瘠的免疫学荒地。此外,我们和其他人认为,免疫治疗方法的策略组合可能为高级软组织肉瘤和骨肉瘤的更有效治疗带来希望。