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呼吸道病毒感染与肺移植受者供体特异性抗体发展的关系。

Association between Respiratory Virus Infection and Development of Donor-Specific Antibody in Lung Transplant Recipients.

机构信息

Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Division of Transplant Surgery, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Viruses. 2024 Oct 5;16(10):1574. doi: 10.3390/v16101574.

Abstract

Chronic lung allograft dysfunction (CLAD) is the most common cause of long-term lung allograft failure. Several factors, including respiratory virus infection (RVI), have been associated with CLAD development, but the underlying mechanisms of these associations are not well understood. We hypothesize that RVI in lung transplant recipients elicits the development of donor-specific antibodies (DSAs), thus providing a mechanistic link between RVI and CLAD development. To test this hypothesis, we retrospectively evaluated for the presence of HLA antibodies in a cohort of lung transplant recipients with symptomatic RVI within the first four months post-transplant using sera at two time points (at/directly after the transplant and following RVI) and time-matched controls without RVI (post-transplant). We found a trend toward the development of DSAs in those with symptomatic RVI versus controls [6/21 (29%) vs. 1/21 (5%), respectively, = 0.09]. No cases or controls had DSA at baseline. We also found increased rates of CLAD and death among those who developed class II DSA versus those who did not (CLAD: 5/7 (71.4%) vs. 19/34 (54.3%), death: 5/7 (71.4%) vs. 17/35 (48.6%)). Prospective studies evaluating the temporal development of DSA after RVI in lung transplant patients and the subsequent outcomes are warranted.

摘要

慢性肺移植器官功能障碍(CLAD)是肺移植器官长期失功的最常见原因。多种因素,包括呼吸道病毒感染(RVI),与 CLAD 的发生相关,但这些关联的潜在机制尚不清楚。我们假设肺移植受者中的 RVI 会引发供体特异性抗体(DSA)的产生,从而为 RVI 与 CLAD 发展之间提供了一种机制联系。为了验证这一假设,我们通过在移植后 4 个月内出现症状性 RVI 的肺移植受者的血清在两个时间点(移植时/直接在移植后和 RVI 后)以及时间匹配的无 RVI 对照者(移植后),回顾性评估了 HLA 抗体的存在情况。我们发现,与对照组相比,有症状性 RVI 的患者中 DSA 的发展呈趋势性增加[分别为 6/21(29%)和 1/21(5%), = 0.09]。在基线时,没有患者或对照者有 DSA。我们还发现,与未发生 II 类 DSA 的患者相比,发生 II 类 DSA 的患者中 CLAD 和死亡的发生率更高(CLAD:5/7(71.4%)与 19/34(54.3%),死亡:5/7(71.4%)与 17/35(48.6%))。需要进行前瞻性研究,评估肺移植患者 RVI 后 DSA 的时间发展以及随后的结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1487/11512259/c2c4c67b1784/viruses-16-01574-g001.jpg

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