# The impact of tacrolimus therapy on the outcomes of vernal keratoconjunctivitis: a systematic review and meta-analysis

**Authors:** Reem AlHuthail

PMC · DOI: 10.3389/fmed.2025.1542440 · 2025-07-30

## TL;DR

This study finds that tacrolimus is effective and safe for treating vernal keratoconjunctivitis, with different forms and dosages showing varying levels of effectiveness and safety.

## Contribution

The study provides the first systematic review and meta-analysis evaluating the safety and effectiveness of different tacrolimus dosages and forms for vernal keratoconjunctivitis.

## Key findings

- Tacrolimus significantly reduced objective signs and subjective symptoms of vernal keratoconjunctivitis compared to controls.
- Tacrolimus 0.03% ointment had the lowest risk of treatment-related adverse events.
- Tacrolimus ophthalmic suspension 0.1% showed the most significant improvement in clinical manifestations.

## Abstract

Various preparations of tacrolimus have been implemented for patients with vernal keratoconjunctivitis (VKC). However, there is a lack of evidence regarding the safety and effectiveness of different dosages and forms of tacrolimus for patients with VKC.

The present systematic review and meta-analysis evaluated the safety and effectiveness of various dosages and forms of tacrolimus for patients with VKC.

The literature review was performed through 12 databases on 15 June 2024. All clinical studies comparing the outcomes of different dosages and tacrolimus preparations for VKC were included. Subgroup analysis was performed based on the dosages and formulations of tacrolimus.

The present meta-analysis included 17 articles, encompassing 832 patients with VKC. Of them, 421 patients received tacrolimus, while 411 patients were in the control group. Of the treated patients with tacrolimus, 66 were treated with tacrolimus ophthalmic suspension 0.1%, and 62 were treated with tacrolimus 0.1% ointment. Furthermore, 293 patients were treated with tacrolimus 0.03% ointment. There was a statistically significant (p = 0.02) difference between tacrolimus and the control group regarding the mean score for objective signs with SMD of −0.70 (95%CI:−1.28, −0.13). A statistically significant difference (p < 0.001) was observed between the tacrolimus ophthalmic suspension 0.1% and the control group with an SMD of −1.09 (95%CI:−1.59, −0.59). There was a significantly lower total subjective symptom score among patients treated with tacrolimus with an SMD of −0.86 (95%CI:−1.44, 0.28) and a probability value of 0.004. A statistically significant lower risk of treatment-related adverse events was revealed among patients treated with tacrolimus 0.03% ointment (p = 0.0002) with an RR of 0.16.

Tacrolimus is an effective and safe therapeutic intervention for patients with VKC. It remarkably reduced the total score for objective signs and total subjective symptom score of VKC, with a relatively lower risk of treatment-related adverse events. The improvement of clinical manifestations was significantly associated with tacrolimus ophthalmic suspension 0.1%, while tacrolimus 0.03% ointment was associated with the lowest risk of treatment-related adverse events.

## Linked entities

- **Chemicals:** tacrolimus (PubChem CID 445643)
- **Diseases:** vernal keratoconjunctivitis (MONDO:0019085)

## Full-text entities

- **Genes:** IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** congestion (MESH:D002311), ectasia (MESH:D004108), toxicity (MESH:D064420), edema (MESH:D004487), epithelial keratitis (MESH:D009375), hyperemia (MESH:D006940), corneal infiltration (MESH:D017254), corneal involvement (MESH:C537363), photophobia (MESH:D020795), glaucoma (MESH:D005901), irregular astigmatism (MESH:D001251), irritation (MESH:D001523), VKC (MESH:D003233), graft-versus-host disease (MESH:D006086), allergic eye disorders (MESH:D005128), visual loss (MESH:D014786), cataract (MESH:D002386), uveitis (MESH:D014605), disease (MESH:D004194), itching (MESH:D011537), conjunctival papillary inflammation (MESH:D007249), ocular allergy (MESH:D004342)
- **Chemicals:** macrolide (MESH:D018942), dextrin (-), prostaglandin (MESH:D011453), TCA (MESH:D014238), castor oil (MESH:D002368), histamine (MESH:D006632), FK506 (MESH:D016559), steroid (MESH:D013256), olive oil (MESH:D000069463), cyclosporine (MESH:D016572)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12343550/full.md

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Source: https://tomesphere.com/paper/PMC12343550