Evidence map›Paper›PMID 41642041›Full record

ArticleTranslational vision science & technology2026

Anti-IL-6 Receptor Antibody Suppresses Visual Dysfunction in AQP4 Peptide-Immunized Mice.

Yoshichika Katsura, Yuko Nakatake-Furuie, Shinichi Onishi, Chie Kato, Shota Miyake, Kenichi Serizawa, Makoto Nakamura

Abstract read
In one paragraph

Article in Translational vision science & technology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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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

7 authors.

Yoshichika KatsuraProduct Research Department, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Yuko Nakatake-FuruieProduct Research Department, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Shinichi OnishiProduct Research Department, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Chie KatoProduct Research Department, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Shota MiyakeProduct Research Department, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Kenichi SerizawaProduct Research Department, Chugai Pharmaceutical Co., Ltd, Kanagawa, Japan.
Makoto NakamuraDepartment of Surgery, Division of Ophthalmology, Kobe University Graduate School of Medicine, Kobe, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To investigate whether an anti-interleukin-6 (IL-6) receptor antibody (MR16-1) can prevent retinal and optic nerve dysfunction, as well as myelitis, in a mouse model of myelitis induced by immunization with aquaporin-4 (AQP4) peptide. Methods: Mice immunized with AQP4 peptide received MR16-1 or vehicle. Retinal function was assessed by electroretinography (ERG), including b-wave, a-wave, and positive scotopic threshold response (pSTR) amplitudes. Histologic analysis evaluated inflammatory cell infiltration and aberrant Müller cell activation (punctate pattern of glial fibrillary acidic protein staining). Blood-retinal barrier (BRB) integrity was assessed using Evans blue dye, IgG leakage, and transendothelial electrical resistance (TEER) in primary mouse retinal microvascular endothelial cells (mRMECs) exposed to mouse serum. Results: AQP4 peptide immunization led to reductions in ERG b-wave and pSTR amplitudes and increased inflammatory cell infiltration, Müller cell alteration, and retinal vascular permeability. MR16-1 treatment significantly mitigated these changes, suppressing reductions in pSTR and b-wave amplitude, preventing inflammation and aberrant Müller cell activation, and reducing vascular leakage. The improvement of a-wave amplitude was not significant. Serum from MR16-1-treated mice did not reduce mRMEC TEER, while serum from AQP4 peptide-immunized mice reduced it. Conclusions: IL-6 receptor blockade with MR16-1 has the potential to suppress AQP4 peptide immunization-related retinal and optic nerve dysfunction and pathology, likely by protecting BRB integrity and suppressing inflammation. These findings support the therapeutic potential of IL-6 inhibition in preserving visual function in neuromyelitis optica spectrum disorder (NMOSD). Translational Relevance: IL-6 receptor blockade may be a viable strategy for preventing visual impairment in patients with NMOSD.

Indexed as

Aquaporin 4Receptors, Interleukin-6Vision DisordersAnimalsBlood-Retinal BarrierDisease Models, AnimalElectroretinographyFemaleImmunizationMiceMice, Inbred C57BLOptic NerveRetinaAqp4 protein, mouseAquaporin 4Receptors, Interleukin-6

Identifiers

PMID41642041
PMCPMC12889182

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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.