Kandolf R
Institut für Pathologie, Universität Tübingen.
Verh Dtsch Ges Pathol. 1996;80:127-38.
In situ hybridization studies have shown that myocardial enterovirus infections may be detected in acute and chronic enterovirus-induced myocarditis, indicating the possibility of myocardial enterovirus persistence in the human heart. As well, such infections can be observed in patients with dilated cardiomyopathy, a condition which may evolve from chronic myocarditis. The discovery of possible enterovirus persistence in the human heart is supported by the finding in different strains of immunocompetent mice, demonstrating that coxsackievirus B3, typically a cytolytic enterovirus, is capable of evading immunological surveillance in a host-dependent fashion, thus inducing a persistent type of heart muscle infection. Progress is currently being made in unraveling the molecular mechanisms of enterovirus persistence, the diversity of host and virus genetics and their impact on the nature and severity of myocardial injury. Apart from providing an etiologic diagnosis, there are therapeutic implications from in situ demonstration of myocardial enterovirus infection. Evaluation of specific antiviral agents, for example interferons, may lead to the development of new therapeutic strategies capable of providing protection against myocardial enterovirus infection.
原位杂交研究表明,在急性和慢性肠道病毒诱导的心肌炎中可检测到心肌肠道病毒感染,这表明肠道病毒有可能在人类心脏中持续存在。同样,在扩张型心肌病患者中也可观察到此类感染,这种疾病可能由慢性心肌炎演变而来。在不同品系的免疫活性小鼠中的发现支持了肠道病毒可能在人类心脏中持续存在这一观点,这表明柯萨奇病毒B3(一种典型的溶细胞性肠道病毒)能够以宿主依赖的方式逃避免疫监视,从而引发持续性的心肌感染。目前在揭示肠道病毒持续存在的分子机制、宿主和病毒基因的多样性及其对心肌损伤的性质和严重程度的影响方面正在取得进展。除了提供病因诊断外,心肌肠道病毒感染的原位证明还具有治疗意义。评估特定的抗病毒药物,例如干扰素,可能会导致开发出新的治疗策略,从而能够预防心肌肠道病毒感染。