Roy J, Blazar B R, Ochs L, Weisdorf D J
Department of Medicine and Pediatrics, University of Minnesota, Minneapolis, USA.
Transplantation. 1995 Aug 27;60(4):343-8. doi: 10.1097/00007890-199508270-00008.
Although acute graft-versus-host disease (GVHD) is a common complication after allogeneic bone marrow transplantation (BMT), the specific pathophysiology of tissue damage has not been elucidated. We have previously described an infiltrate of CD2+, CD8+, alpha/beta receptor+ T lymphocytes, and the upregulation of ICAM-1 in tissues with acute GVHD. We hypothesized that these infiltrating lymphocytes may secrete cytokines that could contribute to tissue damage. In the current study, we used reverse transcription (RT) polymerase chain reaction (PCR) to explore the mRNA expression of candidate inflammatory cytokines IL-1 alpha, IL-2, IL-4, IL-6, TNF-alpha, and interferon-gamma (IFN-gamma) in peripheral blood mononuclear cells (PBMC) and skin biopsies of allogeneic BMT patients with GVHD and controls. In post-BMT control PBMC (n = 10); IL-2 RNA was infrequent (20% of samples) but was significantly more frequently detectable (71%; P < 0.05) after development of acute GVHD (n = 7). IL-4 expression was also more common in PBMC from patients with acute GVHD (57% vs. 30%; P < 0.05). Consistent with the PBMC data, IL-2 and IL-4 RNA were also more frequently detectable in skin biopsies with GVHD (n = 10): 70% of samples expressed IL-2 vs. 25% of normal controls (n = 8; P < 0.05); 60% had detectable IL-4 RNA vs. 0% of controls (P < 0.05). IFN-gamma detectability (40% vs. 12%; P < 0.05) was also more frequent in GVH skin. For both PBMC and skin, IL-1 alpha expression was infrequent in GVHD and controls, whereas TNF-alpha and IL-6 were expressed in nearly all samples. These data suggest that upregulated expression of IL-2, IL-4, and IFN-gamma may be part of the inflammatory cascade of human acute GVHD, while IL-1 alpha, TNF-alpha, and IL-6 are not discriminatory for the inflammation observed at the time of initial GVHD diagnosis.
尽管急性移植物抗宿主病(GVHD)是异基因骨髓移植(BMT)后常见的并发症,但组织损伤的具体病理生理学尚未阐明。我们之前曾描述过在急性GVHD组织中有CD2 +、CD8 +、α/β受体 + T淋巴细胞浸润以及细胞间黏附分子-1(ICAM-1)上调。我们推测这些浸润的淋巴细胞可能分泌有助于组织损伤的细胞因子。在当前研究中,我们使用逆转录(RT)聚合酶链反应(PCR)来探究候选炎性细胞因子白细胞介素-1α(IL-1α)、白细胞介素-2(IL-2)、白细胞介素-4(IL-4)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)在患有GVHD的异基因BMT患者及对照者的外周血单个核细胞(PBMC)和皮肤活检组织中的mRNA表达。在BMT后对照PBMC(n = 10)中;IL-2 RNA很少见(20%的样本),但在急性GVHD发生后(n = 7)其检出频率显著更高(71%;P < 0.05)。IL-4表达在急性GVHD患者的PBMC中也更常见(57%对30%;P < 0.05)。与PBMC数据一致,在有GVHD的皮肤活检组织(n = 10)中IL-2和IL-4 RNA也更常被检测到:70%的样本表达IL-2,而正常对照(n = 8)中为25%(P < 0.05);60%有可检测到的IL-4 RNA,而对照中为0%(P < 0.05)。在GVH皮肤中IFN-γ的可检测性(40%对12%;P < 0.05)也更频繁。对于PBMC和皮肤两者,在GVHD和对照中IL-1α表达均很少见,而TNF-α和IL-6在几乎所有样本中均有表达。这些数据表明IL-2、IL-4和IFN-γ表达上调可能是人类急性GVHD炎性级联反应的一部分,而IL-1α、TNF-α和IL-6对于初始GVHD诊断时观察到的炎症并无鉴别意义。