Department of Pediatrics, Mie University Graduate School of Medicine, Edobashi, Tsu, Mie, Japan.
Haematologica. 2013 Jan;98(1):41-9. doi: 10.3324/haematol.2012.069815. Epub 2012 Jun 24.
Although there are National Institutes of Health consensus criteria for the global assessment of chronic graft-versus-host disease, no validated biomarkers have been established for this disease. Furthermore, whereas the role of T cells, B cells, and dendritic cells in chronic graft-versus-host disease has been established, the contribution of monocytes has not been clearly addressed. Using an enzyme-linked immunospot assay, we measured the spot-forming cells for interferon-γ, interleukin-4, interleukin-10, and interleukin-17 in unstimulated peripheral blood of patients following allogeneic hematopoietic stem cell transplantation. Other immunological examinations, including skin biopsy, were also done. Fifty-seven patients were enrolled. Interleukin-10 spot-forming cells were evaluable for therapeutic monitoring in 16 patients with chronic graft-versus-host disease. The number of interleukin-10 spot-forming cells in patients with active chronic graft-versus-host disease was significantly higher than the number in those with no or inactive chronic graft-versus-host disease. Interleukin-10 was predominantly produced by monocytes. CD29 expression on monocytes in patients with active chronic graft-versus-host disease was elevated. The level of plasma fibronectin, a ligand of CD29, correlated with the number of interleukin-10 spot-forming cells. Immunohistochemical analysis of the skin in active chronic graft-versus-host disease showed that infiltrating CD29(+) monocytes might produce interleukin-10. A novel biomarker, interleukin-10 spot-forming cells, shows promise as both a diagnostic and prognostic indicator for chronic graft-versus-host disease, and may allow for early intervention prior to the onset of the disease. Measurement of interleukin-10 spot-forming cells would be helpful in clinical trials and in patients' management.
尽管有美国国立卫生研究院关于慢性移植物抗宿主病整体评估的共识标准,但尚未为该病确立经过验证的生物标志物。此外,尽管已经确定 T 细胞、B 细胞和树突状细胞在慢性移植物抗宿主病中的作用,但单核细胞的作用尚未得到明确解决。我们使用酶联免疫斑点测定法,测量了异基因造血干细胞移植后患者外周血未刺激时干扰素-γ、白细胞介素-4、白细胞介素-10 和白细胞介素-17 的斑点形成细胞。还进行了其他免疫学检查,包括皮肤活检。共纳入 57 例患者。在 16 例慢性移植物抗宿主病患者中,可评估白细胞介素-10 斑点形成细胞进行治疗监测。处于活动期慢性移植物抗宿主病患者的白细胞介素-10 斑点形成细胞数量明显高于无或不活动期慢性移植物抗宿主病患者。白细胞介素-10 主要由单核细胞产生。处于活动期慢性移植物抗宿主病患者的单核细胞上的 CD29 表达增加。血浆纤维连接蛋白(CD29 的配体)水平与白细胞介素-10 斑点形成细胞的数量相关。慢性移植物抗宿主病活动期皮肤的免疫组织化学分析显示,浸润的 CD29(+)单核细胞可能产生白细胞介素-10。一种新的生物标志物,白细胞介素-10 斑点形成细胞,有望成为慢性移植物抗宿主病的诊断和预后指标,并可能在疾病发作前进行早期干预。白细胞介素-10 斑点形成细胞的测量将有助于临床试验和患者管理。