Abstract | AIM: METHODS: RESULTS: Clinical and pathological scores showed that ocular inflammation of tacrolimus-treated eyes was markedly less than that of vehicle-treated eyes. The amount of interferon gamma and tumour necrosis factor alpha was considerably inhibited in tacrolimus-treated eyes. The gene expression of monocyte chemattractant protein-1 (MCP-1) and regulated upon activation, normal T cell expressed and secreted ( RANTES) was markedly reduced in tacrolimus-treated eyes. Delayed-type hypersensitivity responses were not impaired in tacrolimus-treated rats. CONCLUSIONS:
Intravitreal injection of tacrolimus was highly effective in suppressing the ongoing process of EAU without any side effects on systemic cellular immunity. This treatment may be useful in the management of patients with severe uveitis.
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Authors | Keiko Oh-i, Hiroshi Keino, Hiroshi Goto, Naoyuki Yamakawa, Kouhei Murase, Yoshihiko Usui, Takeshi Kezuka, Jun-Ichi Sakai, Masaru Takeuchi, Masahiko Usui |
Journal | The British journal of ophthalmology
(Br J Ophthalmol)
Vol. 91
Issue 2
Pg. 237-42
(Feb 2007)
ISSN: 0007-1161 [Print] England |
PMID | 16987901
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Chemokines
- Immunosuppressive Agents
- RNA, Messenger
- Tumor Necrosis Factor-alpha
- Interferon-gamma
- Tacrolimus
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Topics |
- Animals
- Autoimmune Diseases
(drug therapy, immunology, metabolism)
- Cells, Cultured
- Chemokines
(biosynthesis, genetics)
- Eye
(metabolism)
- Female
- Gene Expression Regulation
(drug effects)
- Hypersensitivity, Delayed
- Immunity, Cellular
(drug effects)
- Immunosuppressive Agents
(administration & dosage, adverse effects, therapeutic use)
- Injections
- Interferon-gamma
(biosynthesis)
- Macrophages
(drug effects, metabolism)
- RNA, Messenger
(genetics)
- Rats
- Rats, Inbred Lew
- Retinitis
(drug therapy, immunology, metabolism)
- Tacrolimus
(administration & dosage, therapeutic use, toxicity)
- Treatment Outcome
- Tumor Necrosis Factor-alpha
(biosynthesis)
- Uveitis
(drug therapy, immunology, metabolism)
- Vitreous Body
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