Trousdale M D, Nóbrega R, Wood R L, Stevenson D, dos Santos P M, Klein D, McDonnell P J
Doheny Eye Institute, Los Angeles, CA 90033, USA.
Invest Ophthalmol Vis Sci. 1995 Dec;36(13):2740-8.
To achieve a better understanding of the pathogenic processes associated with human adenovirus (Ad)-induced ocular disease.
Growth curves of Ad5 and Ad14 were performed in cell cultures derived from rabbit and human corneal epithelium (CE) and corneal keratocytes (CK). For in vivo studies, rabbit eyes were inoculated intrastromally and topically with 10(6) plaque-forming units per eye of Ad5 and ultraviolet light-inactivated (UV-1) Ad5 or Ad14, and the clinical features of the eyes were evaluated by biomicroscopic slit lamp examinations. Duration and quantitation of virus in tear samples were monitored. Humoral response was evaluated by enzyme-linked immunosorbent assay and serum neutralization titrations. Histopathologic and immunocytochemical staining of frozen corneal tissues was performed to determine the expression of major histocompatibility complex (MHC) class I and II and the presence of CD4+ and CD8+ T lymphocytes and CD18+ cells after the immunopathologic response elicited by virus inoculation.
Both Ad5 and Ad14 replicated in all human cell cultures studied. In cells of rabbit origin, Ad5 replicated in cultured CE and CK cells, whereas Ad14 replication appeared restricted. Virus titers in ocular samples from Ad5-inoculated eyes peaked on postinoculation days 3 through 4, with approximately a 100-fold increase in infectious virus in comparison to initial titers. The duration of Ad5 shedding was 8.9 +/- 2.4 days. Ad5, Ad5 UV-I, and Ad14 induced seroconversion and subepithelial opacities. CD4+ and CD8+ T lymphocytes and CD18+ cells were present in these intrastromal immune cell infiltrates. Expression of MHC class I and II was observed in keratocytes and immune cells; MHC class I also was expressed on CE cells in inflamed areas.
Ad5 is capable of replicating in both CE and CK cells of the rabbit eye. The presence of Ad antigens within the corneal stroma originating from infectious virus (Ad5), UV-inactivated virus (Ad5), or nonreplicating infectious virus (Ad14) can elicit indistinguishable immunopathologic responses in the stroma composed of CD4+, CD8+, and CD18+ cells.
更好地了解与人类腺病毒(Ad)引起的眼部疾病相关的致病过程。
在源自兔和人角膜上皮(CE)及角膜基质细胞(CK)的细胞培养物中进行Ad5和Ad14的生长曲线测定。对于体内研究,给兔眼基质内和局部接种每只眼10⁶ 个空斑形成单位的Ad5以及紫外线灭活(UV-1)的Ad5或Ad14,通过生物显微镜裂隙灯检查评估眼部的临床特征。监测泪液样本中病毒的持续时间和定量。通过酶联免疫吸附测定和血清中和滴定评估体液反应。对冷冻角膜组织进行组织病理学和免疫细胞化学染色,以确定在病毒接种引发免疫病理反应后主要组织相容性复合体(MHC)I类和II类的表达以及CD4⁺和CD8⁺ T淋巴细胞及CD18⁺细胞的存在情况。
Ad5和Ad14在所有研究的人类细胞培养物中均能复制。在兔源细胞中,Ad5在培养的CE细胞和CK细胞中复制,而Ad14的复制似乎受到限制。接种Ad5的眼的眼部样本中的病毒滴度在接种后第3至4天达到峰值,与初始滴度相比,感染性病毒增加了约100倍。Ad5排出的持续时间为8.9±2.4天。Ad5、Ad5 UV-I和Ad14诱导血清转化和上皮下混浊。这些基质内免疫细胞浸润中存在CD4⁺和CD8⁺ T淋巴细胞及CD18⁺细胞。在基质细胞和免疫细胞中观察到MHC I类和II类的表达;在炎症区域的CE细胞上也表达了MHC I类。
Ad5能够在兔眼的CE细胞和CK细胞中复制。源自感染性病毒(Ad5)、紫外线灭活病毒(Ad5)或非复制性感染性病毒(Ad14)的角膜基质内Ad抗原的存在可在由CD4⁺、CD8⁺和CD18⁺细胞组成的基质中引发难以区分的免疫病理反应。