Kneider M, Bergström T, Gustafsson C, Nenonen N, Ahlgren C, Nilsson S, Andersen O
Institute of Clinical Neuroscience and Physiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.
Mult Scler. 2009 Apr;15(4):437-42. doi: 10.1177/1352458508100038. Epub 2009 Feb 27.
Upper respiratory infections were reported to trigger multiple sclerosis relapses. A relationship between picornavirus infections and MS relapses was recently reported.
To evaluate whether human rhinovirus is associated with multiple sclerosis relapses and whether any particular strain is predominant.
Nasopharyngeal fluid was aspirated from 36 multiple sclerosis patients at pre-defined critical time points. Reverse-transcriptase-PCR was performed to detect human rhinovirus-RNA. Positive amplicons were sequenced.
We found that rhinovirus RNA was present in 17/40 (43%) of specimens obtained at the onset of a URTI in 19 patients, in 1/21 specimens during convalescence after URTI in 14 patients, in 0/6 specimens obtained in 5 patients on average a week after the onset of an "at risk" relapse, occurring within a window in time from one week before to three weeks after an infection, and in 0/17 specimens obtained after the onset of a "not at risk" relapse not associated with any infection in 12 patients. Fifteen specimens from healthy control persons not associated with URTI were negative. The frequency of HRV presence in URTI was similar to that reported for community infections. Eight amplicons from patients represented 5 different HRV strains.
We were unable to reproduce previous findings of association between HRV infections and multiple sclerosis relapses. HRV was not present in nasopharyngeal aspirates obtained during "at risk" or "not at risk" relapses. Sequencing of HRV obtained from patients during URTI did not reveal any strain with predominance in multiple sclerosis.
据报道,上呼吸道感染会引发多发性硬化症复发。最近有报道称小核糖核酸病毒感染与多发性硬化症复发之间存在关联。
评估人鼻病毒是否与多发性硬化症复发相关,以及是否有任何特定毒株占主导地位。
在预先确定的关键时间点,从36例多发性硬化症患者中采集鼻咽分泌物。进行逆转录聚合酶链反应以检测人鼻病毒RNA。对阳性扩增产物进行测序。
我们发现,在19例患者上呼吸道感染发作时采集的40份标本中,有17份(43%)存在鼻病毒RNA;在14例患者上呼吸道感染恢复期采集的21份标本中,有1份存在鼻病毒RNA;在5例患者“有风险”复发(在感染前1周内至感染后3周的时间窗口内发生)发作后平均1周采集的6份标本中,有0份存在鼻病毒RNA;在12例患者“无风险”复发(与任何感染无关)发作后采集的17份标本中,有0份存在鼻病毒RNA。15份来自未患过上呼吸道感染的健康对照者的标本均为阴性。上呼吸道感染中鼻病毒存在的频率与社区感染报告的频率相似。来自患者的8个扩增产物代表5种不同的鼻病毒毒株。
我们无法重现先前关于鼻病毒感染与多发性硬化症复发之间关联的研究结果。在“有风险”或“无风险”复发期间采集的鼻咽抽吸物中未发现鼻病毒。对上呼吸道感染期间从患者获得的鼻病毒进行测序,未发现任何在多发性硬化症中占主导地位的毒株。