Whitcup S M, Butler K M, Caruso R, de Smet M D, Rubin B, Husson R N, Lopez J S, Belfort R, Pizzo P A, Nussenblatt R B
Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, MD 20892.
Am J Ophthalmol. 1992 Jan 15;113(1):1-7. doi: 10.1016/s0002-9394(14)75744-7.
To assess the safety and antiretroviral activity of 2',3'-dideoxyinosine, we enrolled 43 children with symptomatic (Centers for Disease Control class P-2) human immunodeficiency virus infection in a Phase I-II study and monitored them prospectively for the development of ocular complications secondary to HIV infection or drug toxicity. Follow-up ranged from 12 to 103 weeks with a median follow-up of 71 weeks. Three of 43 children (7.0%) developed peripheral atrophy of the retinal pigment epithelium during treatment with 2',3'-dideoxyinosine. The two children with the most severe retinal atrophy were enrolled in the study at the highest dosage studied (540 mg/m2/day). In contrast to findings in children, no retinal atrophy in HIV-infected adults treated with 2',3'-dideoxyinosine has been evident to date.