Evidence map›Paper›PMID 36627583›Full record

ArticleBMC ophthalmology2023

Intraocular neutralizing antibodies against aflibercept in patients with age related macular degeneration.

Andrea Gyenes, Lilla István, Fruzsina Benyó, András Papp, Miklós Resch, Noémi Sándor, Mihály Józsi, Zoltán Z Nagy, Illés Kovács, Szilárd Kiss

Open access · goldAbstract read
In one paragraph

Article in BMC ophthalmology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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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

10 authors at 4 institutions in 2 countries.

Andrea GyenesDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
Lilla IstvánDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
Fruzsina BenyóDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
András PappDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
Miklós ReschDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
Noémi SándorDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Mihály JózsiDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Zoltán Z NagyDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary.
Illés KovácsDepartment of Ophthalmology, Semmelweis University, Budapest, Hungary. kovacs.illes@med.semmelweis-univ.hu.
Szilárd KissDepartment of Ophthalmology, Weill Cornell Medical College, New York, USA.
Semmelweis University · HUCornell University · USEötvös Loránd University · HUHungarian Research Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo detect immunoglobulins in aqueous humour of AMD patients after repeated administration of intravitreal aflibercept. PATIENTS AND

methodsTwenty-one patients (age: 77.85 ± 9.21 years) previously treated with intravitreal aflibercept due to wet type age-related macular degeneration (AMD group) and 18 age-matched control subjects (age: 69.75 ± 12.67 years) were included in this study. Patients in the AMD group received a mean of 5 intravitreal injections (min: 1 max: 17) prior to the cataract surgery. Samples of aqueous humour (50 μl) were obtained by anterior chamber paracentesis as the first step of routine cataract surgery. The IgG content of the samples was analysed by an in-house developed ELISA system.

resultsA significant increase in nonspecific IgG levels in the AMD group was detected compared to the control group (13.37 ± 6.65 vs. 9.44 ± 6.55 μg/ml; p = 0.03). In 11 patients, intraocular anti-aflibercept immunoglobulins could be detected (0.05 ± 0.01 μg/ml) which was significantly higher than the limit of detection for anti-aflibercept (0.04 μg/ml; p = 0.001). No correlation was found between the number of injections or the type of CNV and the aqueous level of anti-aflibercept (r = 0.02; p = 0.95).

conclusionAccording to our results, penetration of non-specific systemic antibodies through the impaired blood-retinal barrier is higher in patients with neovascular AMD than in subjects with an intact structural barrier. Evaluation of neutralizing antibodies to anti-VEGF agents in the aqueous humour can lead us to understanding tachyphylaxis and changes in intraocular immune mechanisms due to AMD.

Indexed as

CataractWet Macular DegenerationAgedAged, 80 and overAngiogenesis InhibitorsAntibodies, NeutralizingHumansImmunoglobulin GIntravitreal InjectionsMiddle AgedRanibizumabReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsVascular Endothelial Growth Factor AVisual AcuityAngiogenesis InhibitorsAntibodies, NeutralizingImmunoglobulin GRanibizumabReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsVascular Endothelial Growth Factor AAge related macular degenerationanti-VEGFTreatment

Identifiers

PMID36627583
PMCPMC9830890
OpenAlexW4313892309

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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.