Boise VA Hospital, Idaho Veterans Research and Education Foundation, Boise, Idaho.
Loyola University Chicago - Stritch School of Medicine and Edward Hines, Jr. Veterans Administration Hospital, Chicago, Illinois, USA.
Curr Opin Infect Dis. 2018 Jun;31(3):251-256. doi: 10.1097/QCO.0000000000000451.
To provide an update on recent studies of human adenoviral (HAdV) infections and to explore the mechanisms of viral persistence and the role of persistent infection in disseminated disease in immunocompromised patients.
Human adenoviruses continue to be a problem in ophthalmology clinics and to cause periodic, limited, global outbreaks of respiratory disease. Ad14p1 remains in worldwide circulation and continues to result in miniepidemics of severe respiratory infections. New variants of Ad4 and Ad7 have emerged in both the United States and Asia. The severity of Ad4 infections in outbreaks appears to depend more on preexisting conditions in patients than on genetically determined, viral virulence factors, in contrast to limited evidence of Ad7 mutations that may convey increased viral pathogenesis. Reactivation of persistent adenovirus infection appears to be the primary source of disseminated infections in immunocompromised patients. New studies suggest that establishment of persistent infection and reactivation are related to variations in interferon-mediated control of viral replication.
Innate immune responses can create a state of adenoviral persistence, and repression of these host defenses can result in reactivation and dissemination of infection. A better definition of the molecular mechanisms of immune-mediated control of viral replication might lead to new strategies for treatment of HAdV reactivation and dissemination.
提供有关人类腺病毒(HAdV)感染的最新研究进展,并探讨病毒持续存在的机制以及持续性感染在免疫功能低下患者传播疾病中的作用。
腺病毒在眼科诊所仍是一个问题,并导致周期性、有限的、全球性的呼吸道疾病爆发。Ad14p1 仍在全球范围内传播,并继续导致严重呼吸道感染的小流行。新型 Ad4 和 Ad7 变体在美国和亚洲均有出现。腺病毒 4 型感染的严重程度似乎更多地取决于患者的现有状况,而不是遗传决定的病毒毒力因素,而 Ad7 突变的有限证据可能表明病毒发病机制增加。潜伏性腺病毒感染的再激活似乎是免疫功能低下患者传播性感染的主要来源。新的研究表明,持续性感染的建立和再激活与干扰素介导的病毒复制控制的变化有关。
先天免疫反应可导致腺病毒持续存在,而宿主防御的抑制可能导致感染的再激活和传播。更好地定义免疫介导的病毒复制控制的分子机制可能会为治疗 HAdV 再激活和传播提供新的策略。