Banga Natasha, Kanade Rohan, Kappalayil Anishka, Timofte Irina, Lawrence Adrian, Bollineni Srinivas, Kaza Vaidehi, Torres Fernando
Lung Transplant Program, UT Southwestern Medical Center, Dallas, Texas, USA.
Clin Transplant. 2025 Jul;39(7):e70219. doi: 10.1111/ctr.70219.
Lung transplant (LT) recipients with high-risk cytomegalovirus (CMV) mismatch donors (donor seropositive, recipient seronegative) have worse early and late outcomes. We sought to describe the outcomes among high-risk mismatch patients managed using proactive monitoring and multimodality prophylaxis and management protocol.
We included patients with single or bilateral lung transplants between January 2012 and December 2016 (n = 324). The patients were classified into two groups: high-risk CMV mismatch (R-/D+): n = 83 (25.6%) and non-high-risk CMV mismatch (n = 241). Post-LT follow-up period ranged from 8 to 12 years. Post-transplant survival was analyzed as the primary outcome variable.
There was no difference in LT recipients' baseline and post-transplant characteristics with and without CMV-mismatch donors. The mismatch group experienced a significantly higher frequency and burden of CMV viremia (p < 0.001) and resistant viremia (p < 0.001). Regardless, the two groups had similar long-term outcomes with no statistically significant difference in CLAD-free survival at 3 years or overall post-transplant survival. On Cox proportional hazard analysis, transplant indication was the only independent predictor of post-transplant survival (p = 0.004).
A proactive multimodality CMV management protocol consisting of antiviral agents (ganciclovir/valganciclovir) and immune augmentation with CMV immune globulin may improve outcomes among high-risk CMV mismatch LT recipients.
接受高风险巨细胞病毒(CMV)错配供体(供体血清学阳性,受体血清学阴性)的肺移植(LT)受者的早期和晚期结局较差。我们试图描述采用主动监测以及多模式预防和管理方案管理的高风险错配患者的结局。
我们纳入了2012年1月至2016年12月期间接受单肺或双肺移植的患者(n = 324)。患者分为两组:高风险CMV错配(R-/D+):n = 83(25.6%)和非高风险CMV错配(n = 241)。LT后的随访期为8至12年。将移植后生存率作为主要结局变量进行分析。
有无CMV错配供体的LT受者的基线和移植后特征没有差异。错配组的CMV病毒血症(p < 0.001)和耐药病毒血症(p < 0.001)的发生率和负担明显更高。尽管如此,两组的长期结局相似,3年无慢性肺移植功能障碍(CLAD)生存率或总体移植后生存率没有统计学上的显著差异。在Cox比例风险分析中,移植指征是移植后生存的唯一独立预测因素(p = 0.004)。
由抗病毒药物(更昔洛韦/缬更昔洛韦)和使用CMV免疫球蛋白增强免疫组成的主动多模式CMV管理方案可能会改善高风险CMV错配LT受者的结局。