Molecular Imaging Program at Stanford (MIPS), Department of Radiology, Stanford University School of Medicine, Stanford, CA.
Molecular Imaging Research Center of Harbin Medical University, Harbin, China.
Blood Adv. 2022 Aug 23;6(16):4782-4792. doi: 10.1182/bloodadvances.2022007403.
Allogeneic hematopoietic cell transplantation (HCT) is a well-established and potentially curative treatment for a broad range of hematological diseases, bone marrow failure states, and genetic disorders. Acute graft-versus-host disease (GvHD), mediated by donor T cells attacking host tissues, still represents a major cause of morbidity and mortality following allogeneic HCT. Current approaches to diagnosis of gastrointestinal acute GvHD rely on clinical and pathological criteria that manifest at late stages of disease. New strategies allowing for GvHD prediction and diagnosis, prior to symptom onset, are urgently needed. Noninvasive antibody-based positron emission tomography (PET) (immunoPET) imaging of T-cell activation post-allogeneic HCT is a promising strategy toward this goal. In this work, we identified inducible T-cell costimulator (ICOS) as a potential immunoPET target for imaging activated T cells during GvHD. We demonstrate that the use of the Zirconium-89-deferoxamine-ICOS monoclonal antibody PET tracer allows in vivo visualization of donor T-cell activation in target tissues, namely the intestinal tract, in a murine model of acute GvHD. Importantly, we demonstrate that the Zirconium-89-deferoxamine-ICOS monoclonal antibody PET tracer does not affect GvHD pathogenesis or the graft-versus-tumor (GvT) effect of the transplant procedure. Our data identify ICOS immunoPET as a promising strategy for early GvHD diagnosis prior to the appearance of clinical symptoms.
同种异体造血细胞移植(HCT)是一种成熟且具有潜在治愈作用的治疗方法,可用于治疗广泛的血液系统疾病、骨髓衰竭状态和遗传疾病。由供体细胞 T 细胞攻击宿主组织引起的急性移植物抗宿主病(GvHD)仍然是同种异体 HCT 后发病率和死亡率的主要原因。目前用于诊断胃肠道急性 GvHD 的方法依赖于临床表现和病理学标准,这些标准在疾病的晚期才会出现。迫切需要新的策略来预测和诊断 GvHD,即在症状出现之前。同种异体 HCT 后 T 细胞活化的免疫 PET(immunoPET)成像等非侵入性基于抗体的正电子发射断层扫描(PET)是实现这一目标的有前途的策略。在这项工作中,我们确定了诱导性 T 细胞共刺激分子(ICOS)作为 GvHD 期间成像活化 T 细胞的潜在 immunoPET 靶标。我们证明,使用锆-89-去铁胺-ICOS 单克隆抗体 PET 示踪剂可以在急性 GvHD 的小鼠模型中可视化靶组织(即肠道)中供体细胞 T 细胞的活化。重要的是,我们证明锆-89-去铁胺-ICOS 单克隆抗体 PET 示踪剂不会影响 GvHD 发病机制或移植程序的移植物抗肿瘤(GvT)效应。我们的数据表明,ICOS immunoPET 是一种在出现临床症状之前进行早期 GvHD 诊断的有前途的策略。