Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA.
Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA.
Chest. 2011 Aug;140(2):489-496. doi: 10.1378/chest.10-2065. Epub 2011 Feb 24.
Serum levels of surfactant protein D (SP-D) have been suggested as reflecting epithelial damage in acute lung injury, COPD, and idiopathic pulmonary fibrosis (IPF). However, little is known about SP-D levels in the setting of lung transplantation.
We examined plasma SP-D levels in 104 subjects from a prospective, multicenter cohort study of lung allograft recipients. Plasma SP-D was measured by enzyme-linked immunosorbent assay prior to transplant and daily for 3 days after transplant.
Subjects undergoing transplant for IPF had higher baseline SP-D levels (median, 325 ng/mL) compared with subjects with cystic fibrosis, COPD, and pulmonary hypertension (median, 100, 80, and 82 ng/mL, respectively; P = .0001). Among subjects with IPF undergoing bilateral transplant, SP-D levels declined rapidly postoperatively. In contrast, SP-D levels in subjects undergoing single lung transplant for IPF remained significantly higher than those of bilateral allograft recipients. Among subjects undergoing single lung transplant for IPF, the development of primary graft dysfunction (PGD) was associated with a subsequent rise in SP-D levels, whereas SP-D levels in IPF subjects undergoing bilateral transplant declined, even in the presence of grade 3 PGD. Importantly, single lung allograft recipients without PGD had higher postoperative SP-D levels than bilateral allograft recipients with PGD.
Subjects undergoing lung transplant for IPF have significantly higher baseline plasma SP-D levels compared with those with other diagnoses. Plasma SP-D is likely a biomarker of the air-blood barrier integrity in the native IPF lung, but may be less useful as a biomarker of PGD after transplant.
表面活性蛋白 D(SP-D)的血清水平被认为反映了急性肺损伤、COPD 和特发性肺纤维化(IPF)中的上皮损伤。然而,对于肺移植患者中 SP-D 水平的了解甚少。
我们检测了 104 例来自前瞻性、多中心肺移植受者队列研究的受试者的血浆 SP-D 水平。在移植前和移植后 3 天内每天通过酶联免疫吸附试验测量血浆 SP-D。
与囊性纤维化、COPD 和肺动脉高压患者相比,进行 IPF 移植的患者具有更高的基线 SP-D 水平(中位数 325ng/mL)(分别为 100ng/mL、80ng/mL 和 82ng/mL,P=0.0001)。在接受双侧移植的 IPF 患者中,SP-D 水平在手术后迅速下降。相比之下,接受单侧肺移植的 IPF 患者的 SP-D 水平仍然显著高于双侧肺移植患者。在接受单侧肺移植的 IPF 患者中,原发性移植物功能障碍(PGD)的发生与 SP-D 水平的随后升高相关,而接受双侧移植的 IPF 患者的 SP-D 水平下降,即使存在 3 级 PGD。重要的是,无 PGD 的单侧肺移植受者的术后 SP-D 水平高于有 PGD 的双侧肺移植受者。
与其他诊断相比,因 IPF 而接受肺移植的患者具有显著更高的基线血浆 SP-D 水平。血浆 SP-D 可能是原发性 IPF 肺气血屏障完整性的生物标志物,但在移植后作为 PGD 的生物标志物可能不太有用。