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Development and Optimization of an Ex Vivo Model of Corneal Epithelium Damage with 1-Heptanol: Investigating the Influence of Donor Clinical Parameters and MSC-sEV Treatment on Healing Capacity.
Pub Date : 2025-02-04 DOI: 10.1016/j.jtos.2025.02.002
Filippo Bonelli, Seyedmohammad Moosavizadeh, Elisa Fasolo, Alessia Di Nella, Vanessa Barbaro, Ilaria Zorzi, Mauro Krampera, Jana D'Amato Tóthová, Diego Ponzin, Thomas Ritter, Stefano Ferrari, Umberto Rodella

Purpose: To develop and characterize a reproducible human corneal epithelial wound-healing model using 1-heptanol, and to investigate the healing potential of Bone Marrow-derived Mesenchymal Stromal Cell small Extracellular Vesicles (MSC-sEV) and the influence of donor characteristics on epithelial healing.

Methods: Eighty-eight (n=88) human corneoscleral tissues unsuitable for transplantation were employed. Corneal epithelial damage was induced with 1-heptanol and monitored every 24 hours up to 96 hours using fluorescein and trypan blue staining. Histological assessment was performed on untreated and damaged tissues. Damaged areas were measured with FIJI software, and healing rates were calculated. MSC-sEV were isolated with size exclusion chromatography and characterized for their size, morphology and biomarkers. Their impact on healing was assessed in both in vitro scratch assays on cultured human corneal epithelial cells and on ex vivo 1-heptanol-damaged corneas.

Results: Histological analysis revealed detached corneal epithelium in the central area, while other layers remained unaffected. Healing rate peaked at 48 hours post-damage. Trypan blue and Fluorescein staining correlated and the former highlighted a higher initial healing rate than the latter. Diabetic and heart-beating brain-deceased donors showed impaired healing rates. MSC-sEV (79.8 nm, spherical bilayer, positive for TSG101, CD9, CD63, and CD81) significantly improved epithelial wound healing in both in vitro and ex vivo models.

Conclusion: 1-heptanol effectively induces reproducible corneal epithelial damage, and the ex vivo organ-cultured human cornea heals the epithelium within 96 hours. Diabetes and donation from heart-beating brain-deceased donors reduce healing capacity. MSC-sEV boost epithelial repair in damaged corneas.

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引用次数: 0
Pipeline: US FDA Efficacy requirements for treatment of ocular surface disease: drugs vs. medical devices.
Pub Date : 2025-02-04 DOI: 10.1016/j.jtos.2025.02.001
R L E E Kramm, G A R Y D Novack
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引用次数: 0
AZR-MD-001 0.5% selenium sulfide ophthalmic ointment for the treatment of contact lens discomfort: A vehicle-controlled, randomized, clinical trial. AZR-MD-001 0.5%硫化硒眼膏治疗隐形眼镜不适:一项对照、随机、临床试验。
Pub Date : 2024-12-28 DOI: 10.1016/j.jtos.2024.12.009
Fiona Stapleton, Mark Hinds, Jacqueline Tan, Lyndon Jones, Robin Chalmers, Charles Bosworth, Yair Alster

Background: Contact lens discomfort (CLD) is a common problem for CL wearers, and patients with CLD often have changes in meibomian gland function and structure. In a Phase 2 trial AZR-MD-001 0.5% (AZR) ophthalmic ointment improved meibomian gland dysfunction (MGD) in non-lens wearers. The current study evaluated the efficacy and safety of AZR in participants with CLD and concomitant MGD.

Methods: Adults with CLD (Contact Lens Dry Eye Questionnaire-8 >12, range 0-37) and MGD (Meibomian Gland Secretion Score [MGS] ≤12, range 0-45) were randomized (1:1) to AZR:vehicle applied twice-weekly in a three-month multicenter, prospective, double-masked study. Endpoints included difference in change from baseline (CFB) in the number of Meibomian Glands Yielding Liquid Secretion (MGYLS), MGS, the ability to wear their lenses as long as desired, and safety.

Results: At Month 3, AZR (n = 34) significantly increased the MGYLS and MGS versus vehicle (n = 33), with least squares mean difference (LSMD) CFB in MGYLS of 5.0 (SE = 0.47) for AZR and 1.6 (0.45) for vehicle, P < 0.0001; MGS of 13.8 (SE = 0.67) for AZR and 3.8 (SE = 0.68) for vehicle, P < 0.0001. Significantly more participants treated with AZR were able to wear lenses as long as desired (43% vs. 6%, P = 0.0023). The most common treatment-emergent adverse event (TEAE) was eye irritation (61.8% AZR; 0% vehicle). All TEAEs related to treatment were mild/moderate, transient, and did not result in discontinuation.

Conclusion: AZR-MD-001 0.5% significantly improved MGD signs and hours of comfortable CL wear, demonstrating good efficacy, safety, and tolerability in those with CLD.

背景:隐形眼镜不适(CLD)是配戴隐形眼镜的常见问题,患者通常有睑板腺功能和结构的改变。在一项2期试验中,AZR- md -001 0.5% (AZR)眼药膏改善了非晶状体配戴者的睑板腺功能障碍(MGD)。目前的研究评估了AZR对CLD合并MGD患者的疗效和安全性。方法:在一项为期三个月的多中心、前瞻性、双盲研究中,CLD(隐形眼镜干眼症问卷-8 - 12,范围0-37)和MGD(睑板腺分泌评分[MGS]≤12,范围0-45)的成年人随机(1:1)至AZR:每周两次应用载体。终点包括睑板腺分泌液体(MGYLS)数量与基线的变化差异(CFB)、MGS、佩戴隐形眼镜的时间和安全性。结果:在第3个月,AZR (n=34)显著增加了MGYLS和MGS,与对照(n=33)相比,AZR (n=34)的最小二乘平均差(LSMD) CFB在MGYLS中的最小二乘平均差(LSMD)为5.0 (SE = 0.47),对照为1.6(0.45)。结论:AZR- md -001 0.5%显著改善了MGD体征和舒适CL磨损时间,对CLD患者具有良好的疗效、安全性和耐受性。
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引用次数: 0
Readership awareness series – Paper 9: Retraction of a publication 读者意识系列 - 文件 9:撤回出版物
Pub Date : 2024-01-17 DOI: 10.1016/j.jtos.2024.01.008
Mohammad Javed Ali, Ali Djalilian
Abstract not available
无摘要
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引用次数: 0
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The ocular surface
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