Evidence map›Paper›PMID 41268982›Full record

ReviewInvestigative ophthalmology & visual science2025

Can Immune Checkpoint Modulation Redefine Ocular Immunotherapy? Emerging Mechanisms, Challenges, and Translational Opportunities-A Comprehensive Review.

Kai-Yang Chen, Hoi-Chun Chan, Chi-Ming Chan

Abstract readReview
In one paragraph

Review in Investigative ophthalmology & visual science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. 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

3 authors.

Kai-Yang ChenDepartment of General Medicine, Chang Gung Memorial Hospital (Linkou branch), Taoyuan, Taiwan.
Hoi-Chun ChanSchool of Pharmacy, China Medical University, Taichung, Taiwan.
Chi-Ming ChanDepartment of Ophthalmology, Cardinal Tien Hospital, New Taipei City, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors have revolutionized cancer immunotherapy, and their application is now expanding to various conditions, including prevalent medical issues such as uveal melanoma, autoimmune uveitis, and surface squamous neoplasms. The unique immunological challenges in these cases arise from the immune-privileged nature of the eye, which employs immune evasion mechanisms that often lead to an advanced disease at diagnosis. Recent breakthroughs in immune checkpoints have identified critical regulatory molecules, such as PD-1, CTLA-4, TIM-3, LAG-3, and CEACAM1, which are pivotal in modulating ocular immune responses. The use of novel immunotherapeutic strategies to block these pathways presents new opportunities to treat ocular and inflammatory eye disorders. T-cell exhaustion (Tex) is a significant hurdle in ocular immunotherapy that results in immune dysfunction because of prolonged antigen exposure. Strategies to counteract Tex, including combination therapies that pair PD-1 inhibitors with co-stimulatory agonists such as OX40 and CD137, have shown promise in preclinical murine models. Additionally, dual blockade targeting TIM-3 alongside PD-1 has been found to enhance T-cell responses. An integrated approach targeting multiple pathways may yield improved therapeutic outcomes in eye diseases characterized by immune dysregulation. However, several challenges remain in optimizing immune checkpoint therapies for ocular conditions. Future research should prioritize dual objectives: (1) developing IL-10/TGF-β-promoting therapies to mitigate immune-related adverse events (e.g., retinal vasculitis) and (2) validating LAG-3 + tumor-infiltrating lymphocytes as biomarkers for predicting immune checkpoint inhibitor response in uveal melanoma. It is essential to explore effective combinations of checkpoint inhibitors, determine the optimal timing for their use, and establish better criteria for patient selection. As research on immune checkpoint therapies progresses, they have the potential to transform the management of ocular diseases, offering innovative treatment options for patients who previously had limited choices.

Indexed as

Immune Checkpoint InhibitorsImmunotherapyAnimalsHumansMelanomaT-LymphocytesUveal NeoplasmsUveitisImmune Checkpoint Inhibitors

Identifiers

PMID41268982
PMCPMC12663882

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.