Division of Hematology and Medical Oncology, Department of Medicine, Ellis Fischel Cancer Center, University of Missouri, Columbia, MO, USA.
Division of Hematology & Blood and Marrow Transplantation, Department of Internal Medicine, University of Kentucky, Lexington, KY, USA.
Bone Marrow Transplant. 2023 Aug;58(8):924-935. doi: 10.1038/s41409-023-02001-8. Epub 2023 May 9.
Graft-versus-host disease (GVHD) is the major factor limiting the widespread use of potentially curative allogeneic hematopoietic stem cell transplant (allo-HSCT). Chronic GVHD is characterized by the activation of alloreactive donor immune cells, especially B- and T-cells, leading to tissue damage and pathogenic fibrosis. In this study, we used highly specific next-generation inhibitors of ITK (PCYC-274), BTK (PCYC-804), and ibrutinib-like BTK/ITK inhibitors (PCYC-914 and PCYC-401) in the B10.D2 → BALB/C model of murine sclerodermatous cGVHD. From the third week onward, allogeneic recipients in each group of respective Tec kinase inhibitors were treated three times weekly with inhibitors at doses of 10 and 30 mg/kg or with saline control via oral gavage. Overall, we found that selective BTK inhibition was less effective than combined ITK/BTK or ITK inhibition in lengthening survival and reducing symptoms of cGVHD. ITK inhibition was most efficacious, with PCYC-274 and PCYC-401 demonstrating a nearly 50 percent reduction in GVHD scoring even at the 10 mg/kg dose, while 30 mg/kg of these compounds almost completely ameliorated GVHD symptomology. BTK/ITK and ITK-treated mice showed significant reductions in overall pathology. Significant reductions in dermal thickness and fibrosis were shown for all treatment groups. There was evidence of mixed Th1 and Th2 cytokine profiles in the skin of mice with dermal cGVHD, as both IFN-gamma and IL-4 were upregulated in the allogeneic control group, while kinase inhibition significantly reduced levels of these cytokines. Using an in vitro model of T-cell polarization, Th1 cell production of TNF-alpha and IFN-gamma were partially blocked by ITK. Th2 cell production of IL-4 was almost completely blocked synergistically by ITK and BTK inhibition. BTK-specific inhibition was unable to block either Th1 or Th2 cytokine production. Taken together, these results confirm previous reports that ITK-focused inhibition inhibits Th1 and Th2 cells. Additionally, the compound's effects on T-cell proliferation were tested by CFSE assay. Pure ITK inhibition was most effective at blocking T-cell proliferation, with no proliferation in PCYC-274-treated cells even at 0.1uM. PCYC-401 and PCYC-914 showed some inhibition at lower doses, with complete inhibition evident at 10uM. PCYC-804 was only partially able to block proliferation even at 10uM. In conclusion, we observed substantial benefit for differential inhibition of Tec kinases in GVHD, with ITK being most efficacious and Th1 cells being more resistant to inhibition, matching the previously reported findings of a Th2 to Th1 selective pressure in cells treated with ibrutinib. Our data warrants the further development of ITK and ITK/BTK inhibitors with specific inhibitory ratios to improve the treatment of GVHD and other T-cell mediated diseases.
移植物抗宿主病(GVHD)是限制潜在治愈性同种异体造血干细胞移植(allo-HSCT)广泛应用的主要因素。慢性 GVHD 的特征是同种异体反应性供体细胞免疫细胞的激活,特别是 B 细胞和 T 细胞,导致组织损伤和病理性纤维化。在这项研究中,我们在 B10.D2→BALB/C 小鼠硬皮病 cGVHD 模型中使用了高度特异性的 ITK(PCYC-274)、BTK(PCYC-804)和伊布替尼样 BTK/ITK 抑制剂(PCYC-914 和 PCYC-401)。从第三周开始,每组 Tec 激酶抑制剂的同种异体受体每周接受三次治疗,剂量为 10 和 30mg/kg,或通过口服灌胃给予生理盐水对照。总体而言,我们发现选择性 BTK 抑制在延长存活和减轻 cGVHD 症状方面不如联合 ITK/BTK 或 ITK 抑制有效。ITK 抑制最有效,PCYC-274 和 PCYC-401 甚至在 10mg/kg 剂量下也将 GVHD 评分降低了近 50%,而这些化合物的 30mg/kg 剂量几乎完全改善了 GVHD 症状。BTK/ITK 和 ITK 治疗的小鼠的总体病理学明显减少。所有治疗组的皮肤厚度和纤维化均显著减少。在患有皮肤 cGVHD 的小鼠皮肤中存在混合的 Th1 和 Th2 细胞因子谱的证据,因为同种异体对照组中 IFN-γ和 IL-4 均上调,而激酶抑制显著降低了这些细胞因子的水平。在体外 T 细胞极化模型中,ITK 部分阻断了 TNF-α和 IFN-γ的 Th1 细胞产生。ITK 和 BTK 抑制协同几乎完全阻断了 Th2 细胞产生的 IL-4。BTK 特异性抑制不能阻断 Th1 或 Th2 细胞因子的产生。总之,这些结果证实了之前的报告,即 ITK 靶向抑制抑制 Th1 和 Th2 细胞。此外,通过 CFSE 测定法测试了化合物对 T 细胞增殖的影响。纯 ITK 抑制最有效地阻断 T 细胞增殖,即使在 0.1μM 的 PCYC-274 处理细胞中也没有增殖。PCYC-401 和 PCYC-914 在较低剂量下显示出一定的抑制作用,在 10μM 时完全抑制。PCYC-804 即使在 10μM 时也只能部分阻断增殖。总之,我们观察到 Tec 激酶的差异抑制在 GVHD 中具有显著的益处,其中 ITK 最有效,Th1 细胞对抑制的抵抗力更强,与先前报道的用伊布替尼治疗的细胞中 Th2 向 Th1 的选择性压力相匹配。我们的数据证明了具有特定抑制比的 ITK 和 ITK/BTK 抑制剂的进一步开发,以改善 GVHD 和其他 T 细胞介导疾病的治疗。