Division of Pathology, Yokohama City University Medical Center Hospital, Yokohama, Japan.
Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Pathol Int. 2022 Jan;72(1):25-34. doi: 10.1111/pin.13176. Epub 2021 Oct 13.
Pneumocyte injury is a crucial factor influencing the severity of interstitial lung disease (ILD). In this study, we investigated the potential of hepatocyte nuclear factor α (HNF4α) as an immunohistochemical marker to detect pneumocyte injury and as a prognostic marker. Surgical lung biopsy specimens were collected from 309 patients with different types of ILDs (61 idiopathic pulmonary fibrosis (IPF), 173 non-IPF, and 75 unclassifiable ILD). HNF4α expression were examined and the frequency of positive cells (per mm ) was calculated. HNF4α was strongly expressed in regenerating pneumocytes present on fibroblastic foci, Masson bodies/organizing alveoli. In the non-IPF and unclassifiable ILD groups, cases with high frequency expression showed significantly poorer outcome. Particularly, in the unclassifiable ILD group, the prognostic impact was more significant (death due to ILD, log-rank test, p < 0.0001), with a 10-year survival rate (hazard ratio 11.1, Wald test, p = 0.0003), as compared to the non-IPF group (log-rank test, p = 0.0269; hazard ratio 2.7, Wald test, p = 0.0334). Multivariable analysis focusing on the unclassifiable ILD group confirmed that the frequent HNF4α expression was an independent prognostic factor (hazard ratio 28.6; Wald test, p = 0.0033). Thus, HNF4α can be utilized as an immunohistochemical marker for pneumocyte injury and have prognostic impact particularly in unclassifiable ILD.
肺细胞损伤是影响间质性肺疾病(ILD)严重程度的关键因素。在这项研究中,我们研究了肝细胞核因子α(HNF4α)作为一种免疫组织化学标志物,用于检测肺细胞损伤和作为预后标志物的潜力。收集了来自 309 例不同类型 ILD(61 例特发性肺纤维化(IPF)、173 例非 IPF 和 75 例无法分类的 ILD)患者的手术肺活检标本。检查了 HNF4α的表达,并计算了阳性细胞(每毫米)的频率。HNF4α在成纤维细胞灶上存在的再生型肺细胞、Masson 体/有组织肺泡中强烈表达。在非 IPF 和无法分类的 ILD 组中,高频率表达的病例显示出明显较差的结果。特别是在无法分类的 ILD 组中,预后影响更为显著(ILD 死亡,对数秩检验,p<0.0001),10 年生存率(危险比 11.1,Wald 检验,p=0.0003),与非 IPF 组相比(对数秩检验,p=0.0269;危险比 2.7,Wald 检验,p=0.0334)。针对无法分类的 ILD 组的多变量分析证实,频繁的 HNF4α 表达是一个独立的预后因素(危险比 28.6;Wald 检验,p=0.0033)。因此,HNF4α可作为肺细胞损伤的免疫组织化学标志物,特别是在无法分类的 ILD 中具有预后影响。