» Articles » PMID: 18982345

Intravitreal Administration of the Anti-TNF Monoclonal Antibody Infliximab in the Rabbit

Overview
Specialty Ophthalmology
Date 2008 Nov 5
PMID 18982345
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Tumor necrosis factor (TNF) is known to play an important role in various immune-mediated ocular diseases; intravenous administration of the anti-TNF monoclonal antibody infliximab has proved beneficial in such cases. Since intravitreal injection (when available) is a substitute for systemic administration of various drugs targeting the eye, we aimed to evaluate the safety of intravitreal injection of infliximab in the rabbit eye.

Methods: Seven groups of New Zealand white rabbits (four animals in each group) received a single unilateral intravitreal injection (0.1 ml) of increasing doses of infliximab (namely 1, 2, 5, 8, 10 or 20 mg infliximab [Remicade]) or a sham injection respectively. Slit-lamp biomicroscopy, fundoscopy and electrophysiology recordings, i.e. scotopic, photopic and flicker responses, were performed at baseline and after 1, 5, 10, 15, 30 and 45 days. Infliximab-injected eyes were compared with sham-injected and with uninjected fellow eyes (n = 28). Animals were euthanized on day 45 for histopathological examination of the retinas.

Results: Clinical examination and electrophysiological testing were consistently unremarkable after either sham or 1 mg or 2 mg infliximab injections. In contrast, electrophysiological recordings were significantly reduced in a dose-dependent manner from day 1 through day 45, after 5, 8, 10 and 20 mg infliximab injections. Flicker responses were the most sensitive in detecting the lower toxic dose of 5 mg. Histopathological findings were similar in uninjected and sham-injected eyes, as well as after 1 mg or 2 mg infliximab injections. Consistent with the functional abnormalities, retinal deformities and diffuse edema were observed after injection of 5 mg or higher doses of infliximab.

Conclusions: Intravitreal infliximab may be safely administered up to a dose of 2 mg in the rabbit eye. Such doses can be used in the design of future clinical trials assessing the effects of infliximab for selected patients with immune-mediated ocular conditions.

Citing Articles

The prophylactic value of TNF-α inhibitors against retinal cell apoptosis and optic nerve axon loss after corneal surgery or trauma.

Paschalis E, Zhou C, Sharma J, Dohlman T, Kim S, Lei F Acta Ophthalmol. 2023; 102(3):e381-e394.

PMID: 37803488 PMC: 10997738. DOI: 10.1111/aos.15786.


A Review of Systemic Biologics and Local Immunosuppressive Medications in Uveitis.

Mehta N, Emami-Naeini P J Ophthalmic Vis Res. 2022; 17(2):276-289.

PMID: 35765634 PMC: 9185190. DOI: 10.18502/jovr.v17i2.10804.


A comprehensive review of intravitreal immunosuppressants and biologicals used in ophthalmology.

Hasan N, Chawla R, Shaikh N, Kandasamy S, Azad S, Sundar M Ther Adv Ophthalmol. 2022; 14:25158414221097418.

PMID: 35602659 PMC: 9121505. DOI: 10.1177/25158414221097418.


Intraocular therapy in noninfectious uveitis.

Modugno R, Testi I, Pavesio C J Ophthalmic Inflamm Infect. 2021; 11(1):37.

PMID: 34632541 PMC: 8502718. DOI: 10.1186/s12348-021-00267-x.


Ocular toxicity of intravitreal golimumab in a rabbit model.

Durmaz Engin C, Cilaker Micili S, Yilmaz O, Bagriyanik H, Ergur B, Onen F Turk J Med Sci. 2020; 50(4):1111-1122.

PMID: 32151118 PMC: 7379407. DOI: 10.3906/sag-1911-11.


References
1.
Ueda T, Ueda T, Fukuda S, Browne R, Jenis E, Spengler R . Lipid hydroperoxide-induced tumor necrosis factor (TNF)-alpha, vascular endothelial growth factor and neovascularization in the rabbit cornea: effect of TNF inhibition. Angiogenesis. 2003; 1(2):174-184. DOI: 10.1023/A:1018377621102. View

2.
Markomichelakis N, Theodossiadis P, Sfikakis P . Regression of neovascular age-related macular degeneration following infliximab therapy. Am J Ophthalmol. 2005; 139(3):537-40. DOI: 10.1016/j.ajo.2004.09.058. View

3.
Yang P, Wiser J, Peairs J, Ebright J, Zavodni Z, Bowes Rickman C . Human RPE expression of cell survival factors. Invest Ophthalmol Vis Sci. 2005; 46(5):1755-64. DOI: 10.1167/iovs.04-1039. View

4.
Fries W, Giofre M, Catanoso M, Lo Gullo R . Treatment of acute uveitis associated with Crohn's disease and sacroileitis with infliximab. Am J Gastroenterol. 2002; 97(2):499-500. DOI: 10.1111/j.1572-0241.2002.05514.x. View

5.
Wegscheider B, El-Shabrawi L, Weger M, Ardjomand N, Hermann J, Aberer E . Adverse skin reactions to infliximab in the treatment of intraocular inflammation. Eye (Lond). 2006; 21(4):547-9. DOI: 10.1038/sj.eye.6702262. View