Yadav Ruchi, Hakobyan Narek, Wang Jen-Chin
Department of Internal Medicine, Brookdale University Hospital Medical Center, Brooklyn, NY 11212, USA.
Department of Hematology/Oncology, Brookdale University Hospital Medical Center, Brooklyn, NY 11212, USA.
Int J Mol Sci. 2023 Aug 7;24(15):12502. doi: 10.3390/ijms241512502.
The Philadelphia chromosome-negative (Ph-) myeloproliferative neoplasms (MPNs), which include essential thrombocythemia (ET), polycythemia vera (PV), and myelofibrosis (MF), are enduring and well-known conditions. These disorders are characterized by the abnormal growth of one or more hematopoietic cell lineages in the body's stem cells, leading to the enlargement of organs and the manifestation of constitutional symptoms. Numerous studies have provided evidence indicating that the pathogenesis of these diseases involves the dysregulation of the immune system and the presence of chronic inflammation, both of which are significant factors. Lately, the treatment of cancer including hematological malignancy has progressed on the agents aiming for the immune system, cytokine environment, immunotherapy agents, and targeted immune therapy. Immune checkpoints are the molecules that regulate T cell function in the tumor microenvironment (TME). The first line of primary immune checkpoints are programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1), and cytotoxic T-lymphocyte antigen-4 (CTLA-4). Immune checkpoint inhibitor therapy (ICIT) exerts its anti-tumor actions by blocking the inhibitory pathways in T cells and has reformed cancer treatment. Despite the impressive clinical success of ICIT, tumor internal resistance poses a challenge for oncologists leading to a low response rate in solid tumors and hematological malignancies. A Phase II trial on nivolumab for patients with post-essential thrombocythemia myelofibrosis, primary myelofibrosis, or post-polycythemia myelofibrosis was performed (Identifier: NCT02421354). This trial tested the efficacy of a PD-1 blockade agent, namely nivolumab, but was terminated prematurely due to adverse events and lack of efficacy. A multicenter, Phase II, single-arm open-label study was conducted including pembrolizumab in patients with primary thrombocythemia, post-essential thrombocythemia or post-polycythemia vera myelofibrosis that were ineligible for or were previously treated with ruxolitinib. This study showed that pembrolizumab treatment did not have many adverse events, but there were no pertinent clinical responses hence it was terminated after the first stage was completed. To avail the benefits from immunotherapy, the paradigm has shifted to new immune checkpoints in the TME such as lymphocyte activation gene-3 (LAG-3), T cell immunoglobulin and mucin domain 3 (TIM-3), T cell immunoglobulin and ITIM domain (TIGIT), V-domain immunoglobulin-containing suppressor of T cell activation (VISTA), and human endogenous retrovirus-H long terminal repeat-associating protein 2 (HHLA2) forming the basis of next-generation ICIT. The primary aim of this article is to underscore and elucidate the significance of next-generation ICIT in the context of MPN. Specifically, we aim to explore the potential of monoclonal antibodies as targeted immunotherapy and the development of vaccines targeting specific MPN epitopes, with the intent of augmenting tumor-related immune responses. It is anticipated that these therapeutic modalities rooted in immunotherapy will not only expand but also enhance the existing treatment regimens for patients afflicted with MPN. Preliminary studies from our laboratory showed over-expressed MDSC and over-expressed VISTA in MDSC, and in progenitor and immune cells directing the need for more clinical trials using next-generation ICI in the treatment of MPN.
费城染色体阴性(Ph-)骨髓增殖性肿瘤(MPN),包括原发性血小板增多症(ET)、真性红细胞增多症(PV)和骨髓纤维化(MF),是长期存在且广为人知的病症。这些疾病的特征是身体干细胞中一种或多种造血细胞谱系异常生长,导致器官肿大并出现全身症状。大量研究已提供证据表明,这些疾病的发病机制涉及免疫系统失调和慢性炎症的存在,这两个都是重要因素。最近,包括血液系统恶性肿瘤在内的癌症治疗在针对免疫系统、细胞因子环境、免疫治疗药物和靶向免疫治疗的药物方面取得了进展。免疫检查点是调节肿瘤微环境(TME)中T细胞功能的分子。主要免疫检查点的第一线是程序性细胞死亡蛋白1(PD-1)/程序性细胞死亡配体1(PD-L1),以及细胞毒性T淋巴细胞相关抗原4(CTLA-4)。免疫检查点抑制剂疗法(ICIT)通过阻断T细胞中的抑制途径发挥其抗肿瘤作用,并彻底改变了癌症治疗。尽管ICIT在临床上取得了令人瞩目的成功,但肿瘤内在抗性给肿瘤学家带来了挑战,导致实体瘤和血液系统恶性肿瘤的缓解率较低。针对原发性血小板增多症后骨髓纤维化、原发性骨髓纤维化或真性红细胞增多症后骨髓纤维化患者进行了一项关于纳武单抗的II期试验(标识符:NCT02421354)。该试验测试了一种PD-1阻断剂即纳武单抗的疗效,但由于不良事件和缺乏疗效而提前终止。进行了一项多中心、II期、单臂开放标签研究,纳入了不符合芦可替尼治疗条件或先前接受过芦可替尼治疗的原发性血小板增多症、原发性血小板增多症后或真性红细胞增多症后骨髓纤维化患者使用派姆单抗。这项研究表明,派姆单抗治疗没有太多不良事件,但没有相关的临床反应,因此在第一阶段完成后终止。为了从免疫治疗中获益,范式已转向TME中的新免疫检查点,如淋巴细胞激活基因3(LAG-3)、T细胞免疫球蛋白和粘蛋白结构域3(TIM-3)、T细胞免疫球蛋白和ITIM结构域(TIGIT)、含V结构域免疫球蛋白的T细胞激活抑制剂(VISTA),以及形成下一代ICIT基础的人类内源性逆转录病毒-H长末端重复序列相关蛋白2(HHLA2)。本文的主要目的是强调并阐明下一代ICIT在MPN背景下的重要性。具体而言,我们旨在探索单克隆抗体作为靶向免疫治疗的潜力以及针对特定MPN表位的疫苗开发,以增强肿瘤相关免疫反应。预计这些基于免疫治疗的治疗方式不仅会扩展,还会加强现有的MPN患者治疗方案。我们实验室的初步研究表明,MDSC中MDSC过表达和VISTA过表达,以及祖细胞和免疫细胞中也有过表达,这表明需要更多使用下一代ICI治疗MPN的临床试验。