Larcher Clara, Geltner Christian, Fischer Helmut, Nachbaur David, Müller Ludwig C, Huemer Hartwig P
Department of Hygiene, Microbiology and Social Medicine, Innsbruck Medical University, Innsbruck, Austria.
J Heart Lung Transplant. 2005 Nov;24(11):1891-901. doi: 10.1016/j.healun.2005.02.014.
In immunocompromised patients, respiratory viruses are likely to lead to lower respiratory tract infections that cause severe morbidity and mortality. We conducted a prospective study from September 2003 to March 2004 to investigate the epidemiology and impact of human metapneumovirus (hMPV) on lung transplant recipients.
We collected 265 nasopharyngeal aspirates and bronchoalveolar lavages: 51 samples originated from immunocompromised adults, 49 from lung transplant recipients, and 2 from a bone marrow recipient. Additionally, 209 samples from hospitalized non-immunocompromised children and 5 samples from immunocompromised children were analyzed for replicating hMPV by a combined cell culture and reverse transcriptase polymerase chain reaction method that includes DNA sequencing of selected isolates.
Twelve samples from lung transplant recipients (25%), 29 from non-immunocompromised children (14%), and 2 from a child with a renal transplant were positive for hMPV. Most of the cases clustered within 2 outbreaks in October/November and March. In immunocompromised patients, hMPV was isolated throughout the entire observation period. The same viral strains circulated in hospitalized children and in lung transplant recipients. A different strain was isolated during the interepidemic period, suggesting that hMPV infections may be transmitted among lung transplant recipients independently from the community outbreak situation. Clinical signs and symptoms varied from no symptoms to severe pneumonia or acute graft rejection. Significantly, the only deaths occurred in the hMPV-positive group. Of interest, identification of replicating hMPV significantly correlated with rejection symptoms present at the time point of sample collection.
Results of the study suggest that hMPV may be added to the list of pathogens that are possibly associated with episodes of allograft rejection.
在免疫功能低下的患者中,呼吸道病毒很可能导致下呼吸道感染,进而引发严重的发病和死亡。我们于2003年9月至2004年3月进行了一项前瞻性研究,以调查人偏肺病毒(hMPV)对肺移植受者的流行病学及影响。
我们收集了265份鼻咽抽吸物和支气管肺泡灌洗样本:51份样本来自免疫功能低下的成年人,49份来自肺移植受者,2份来自一名骨髓移植受者。此外,采用细胞培养和逆转录聚合酶链反应相结合的方法(包括对选定分离株进行DNA测序),对209份来自住院非免疫功能低下儿童的样本和5份来自免疫功能低下儿童的样本进行分析,以检测hMPV复制情况。
12份来自肺移植受者的样本(25%)、29份来自非免疫功能低下儿童的样本(14%)以及2份来自一名肾移植儿童的样本hMPV检测呈阳性。大多数病例集中在10月/11月和3月的2次暴发期间。在免疫功能低下的患者中,在整个观察期内均分离出hMPV。住院儿童和肺移植受者中传播的是相同的病毒株。在两次流行期之间分离出不同的毒株,这表明hMPV感染可能在肺移植受者之间独立传播,与社区暴发情况无关。临床体征和症状从无症状到严重肺炎或急性移植物排斥反应不等。值得注意的是,唯一的死亡病例发生在hMPV阳性组。有趣的是,hMPV复制的检测结果与样本采集时间点出现的排斥症状显著相关。
研究结果表明,hMPV可能应被列入可能与同种异体移植物排斥反应相关的病原体名单。