Studies of Adenovirus-Induced Eye Disease in the Rabbit Model

作者: M D Trousdale , D Stevenson , D Klein , R L Wood , P M dos Santos

DOI:

关键词: CD8AdenoviridaeAntigenPathologyBiologyMajor histocompatibility complexCorneal epitheliumVirusMHC class IImmune system

摘要: Purpose. To achieve a better understanding of the pathogenic processes associated with human adenovirus (Ad)-induced ocular disease. Methods. Growth curves Ad5 and Ad14 were performed in cell cultures derived from rabbit corneal epithelium (CE) keratocytes (CK). For vivo studies, eyes inoculated intrastromally topically 10 6 plaque-forming units per eye ultraviolet light-inactivated (UV-I) or Ad14, clinical features evaluated by biomicroscopic slit lamp examinations. Duration quantitation virus tear samples monitored. Humoral response was enzyme-linked immunosorbent assay serum neutralization titrations. Histopathologic immunocytochemical staining frozen tissues to determine expression major histocompatibility complex (MHC) class I II presence CD4 + CD8 T lymphocytes CD18 cells after immunopathologic elicited inoculation. Results. Both replicated all studied. In origin, cultured CE CK cells, whereas replication appeared restricted. Virus titers Ad5-inoculated peaked on postinoculation days 3 through 4, approximately 100-fold increase infectious comparison initial titers. The duration shedding 8.9 ± 2.4 days. Ad5, UV-I, induced seroconversion subepithelial opacities. present these intrastromal immune infiltrates. Expression MHC observed ; also expressed inflamed areas. Conclusions. is capable replicating both eye. Ad antigens within stroma originating (Ad5), UV-inactivated nonreplicating (Ad14) can elicit indistinguishable responses composed , cells.

参考文章(18)
I K Gipson, S M Grill, A technique for obtaining sheets of intact rabbit corneal epithelium. Investigative Ophthalmology & Visual Science. ,vol. 23, pp. 269- 273 ,(1982)
T Araullo-Cruz, Y J Gordon, E Romanowski, An ocular model of adenovirus type 5 infection in the NZ rabbit. Investigative Ophthalmology & Visual Science. ,vol. 33, pp. 574- 580 ,(1992)
T Araullo-Cruz, Y J Gordon, E G Romanowski, Topical HPMPC Inhibits Adenovirus Type 5 in the New Zealand Rabbit Ocular Replication Model Investigative Ophthalmology & Visual Science. ,vol. 35, pp. 4135- 4143 ,(1994)
G A Prince, H S Ginsberg, The molecular basis of adenovirus pathogenesis. Infectious agents and disease. ,vol. 3, pp. 1- 8 ,(1994)
Ray Jui-Fong Tsai, Scheffer C. G. Tseng, Substrate modulation of cultured rabbit conjunctival epithelial cell differentiation and morphology. Investigative Ophthalmology & Visual Science. ,vol. 29, pp. 1565- 1576 ,(1988)
A B Tullo, P G Higgins, An outbreak of adenovirus type 4 conjunctivitis. British Journal of Ophthalmology. ,vol. 64, pp. 489- 493 ,(1980) , 10.1136/BJO.64.7.489
Won Ryang Wee, Xun Wei Wang, Peter J. McDonnell, Effect of Artificial Tears on Cultured Keratocytes in Vitro Cornea. ,vol. 14, pp. 273- 279 ,(1995) , 10.1097/00003226-199505000-00008
Masaharu Kotani, Yasuko Yamamura, Takuya Tamatani, Fujiko Kitamura, Masayuki Miyasaka, Generation and characterization of monoclomal antibodies against rabbit CD4, CD5 and CD11a antigens☆ Journal of Immunological Methods. ,vol. 157, pp. 241- 252 ,(1993) , 10.1016/0022-1759(93)90093-M
H. S. Ginsberg, L. L. Moldawer, P. B. Sehgal, M. Redington, P. L. Kilian, R. M. Chanock, G. A. Prince, A mouse model for investigating the molecular pathogenesis of adenovirus pneumonia. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 88, pp. 1651- 1655 ,(1991) , 10.1073/PNAS.88.5.1651