Evidence map›Paper›PMID 28825191›Full record

ArticleDocumenta ophthalmologica. Advances in ophthalmology2017

Infliximab exerts a dose-dependent effect on retinal safety in the albino rabbit.

Shiri Zayit-Soudry, Igor Vainer, Esther Zemel, Michael Mimouni, Melvin Rabena, Dante J Pieramici, Ido Perlman, Anat Loewenstein

Abstract read
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Article in Documenta ophthalmologica. Advances in ophthalmology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 82% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Shiri Zayit-SoudryDepartment of Ophthalmology, Rambam Health Care Campus, Haifa, Israel. shirizayit@gmail.com.ORCID 0000-0002-8736-1823
Igor VainerRuth and Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel.
Esther ZemelRuth and Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel.
Michael MimouniDepartment of Ophthalmology, Rambam Health Care Campus, Haifa, Israel.
Melvin RabenaCalifornia Retina Consultants and Research Foundation, Santa Barbara, CA, USA.
Dante J PieramiciCalifornia Retina Consultants and Research Foundation, Santa Barbara, CA, USA.
Ido PerlmanRuth and Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel.
Anat LoewensteinDepartment of Ophthalmology, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Technion – Israel Institute of Technology · ILCalifornia Retina Consultants · USRambam Health Care Campus · ILTel Aviv University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo assess the retinal toxicity of an intravitreal injection of infliximab, a monoclonal antibody to tumor necrosis factor α, in a rabbit model. MATERIALS AND

methodsTwo groups of adult albino rabbits (n = 5) received intravitreal injections of infliximab (0.1 ml) in the study eye and balanced salt solution (BSS, 0.1 ml) in the control eye at baseline. Group 1 was administered with 1.5 mg/0.1 ml, and group 2 was injected with 7.5 mg/0.1 ml of infliximab solution. Electroretinography (ERG) was performed at baseline and at 1, 7, 30, and 45 days after the injection. Visual evoked potentials (VEPs) were recorded at 7 and 45 days after the injection. After the last electrophysiological assessment, the rabbits were euthanized and retinal histopathology and immunhistochemistry for glial fibrillary acidic protein (GFAP) were performed.

resultsERG responses demonstrated no significant deficit in retinal function in eyes injected with infliximab. Mean dark-adapted a-wave and b-wave maximal amplitude and semi-saturation constant values at baseline and throughout the 45 days of follow-up after the injection indicated no remarkable difference in outer retinal function between the control and experimental eyes. VEP responses were similar at each time point (7 and 45 days). No difference was seen in retinal histopathology and immunocytochemistry sections in eyes receiving the 1.5 mg/0.1 ml dose compared to the control eyes. However, increased GFAP labeling in retinal Müller cells was detected in rabbit eyes treated with the 7.5 mg/0.1 ml dose.

conclusionsIntravitreal injection of 1.5 mg/0.1 ml infliximab dose has no toxic effect on the integrity (functional or structural) of the retina in rabbits. A higher dose of 7.5 mg/0.1 ml may be slightly toxic as suggested by positive Müller cell GFAP expression. Additional studies of retinal toxicity at higher doses and after multiple injections are needed to establish the retinal safety of intravitreal infliximab therapy in humans.

Indexed as

Angiogenesis InhibitorsAnimalsAntibodies, MonoclonalElectroretinographyEpendymoglial CellsEvoked Potentials, VisualEye DiseasesGlial Fibrillary Acidic ProteinInfliximabIntravitreal InjectionsRabbitsRetinaTumor Necrosis Factor-alphaVitreous BodyAngiogenesis InhibitorsAntibodies, MonoclonalGlial Fibrillary Acidic ProteinInfliximabTumor Necrosis Factor-alphaAngiogenesisAnti-tumor necrosis factor alphaInfliximabRabbitRetinaToxicity

Identifiers

PMID28825191
OpenAlexW2750225631

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.