The Institute of Optics, University of Rochester, Rochester, NY, 14627, USA; The Center for Visual Science, University of Rochester, Rochester, NY, 14627, USA; The Flaum Eye Institute, University of Rochester, Rochester, NY, 14642, USA.
Clerio Vision Inc., Rochester, NY, 14618, USA.
Exp Eye Res. 2021 Jun;207:108579. doi: 10.1016/j.exer.2021.108579. Epub 2021 Apr 20.
Laser-induced refractive index change (LIRIC) is a new, non-incisional, non-ablative, femtosecond photo-modification technique being developed for vision correction in humans. Prior, exvivo studies showed intra-tissue refractive index change to induce minimal cell death, restricted to the laser focal zone in the corneal stroma, and with no observable damage to the epithelium or endothelium. Here, we used live rabbits to ascertain longer-term consequences of LIRIC in vivo. Specifically, we assessed cell death, fibrosis, corneal nerve distribution, endothelial cell density, and corneal structure for up to 3 months after LIRIC. A +2.5 D gradient-index LIRIC Fresnel lens was inscribed inside 20 applanated corneas of Dutch Belted rabbits, over a circular region of the mid-stroma measuring 4.5 mm in diameter. Twelve additional rabbit eyes were used as applanation-only controls to differentiate the effects of laser treatment and suction applanation on biological and structural parameters. In vivo optical measurements were performed pre-operatively, then immediately, 2, 4, and 12 weeks after the procedure, to measure endothelial cell density and changes in corneal structure. Groups of four rabbits were sacrificed at 4 hours, 2, 4, and 12 weeks after LIRIC for histological determinations; the TUNEL assay was used to evaluate cell death, H&E staining was used to assess inflammatory infiltration, and immunostaining for α-smooth muscle actin (α-SMA) and βIII tubulin (Tuj-1) was performed to assess myofibroblast differentiation and corneal nerve distribution, respectively. Consistent with prior ex vivo data, only minimal cell death was observed in the laser focal zone, with TUNEL-positive cells restricted to the stromal region of refractive index change 4 h after LIRIC. No TUNEL-positive cells were evident anywhere in the cornea 2, 4, or 12 weeks after LIRIC. Applanation-only corneas were completely TUNEL-negative. Neither LIRIC-treated nor applanation-only eyes exhibited α-SMA-positive staining or altered corneal nerve distributions at any of the time points examined. In vivo confocal imaging revealed normal endothelial cell densities in all eyes (whether LIRIC-treated or applanation-only) at all time points. Optical coherence tomography showed suction applanation to cause a temporary decrease in central corneal thickness, which returned to normal within 4 h. Corneas into which LIRIC Fresnel lenses were written while applanated did not undergo major structural or shape changes beyond the temporary thinning already described for suction applanation. The present findings suggest that LIRIC patterns, which generated a clinically-relevant refractive correction in the mid-stromal region of live rabbit corneas, induced little-to-no disruption to corneal structure and biology for 3 months after the procedure. This affirms the relative safety of LIRIC and predicts that compared to traditional laser vision correction surgeries, common post-operative complications such as dry eye, haze, or patient discomfort may be entirely avoided.
激光诱导折射率变化(LIRIC)是一种新的非切口、非消融、飞秒光修饰技术,用于人类视力矫正。先前的离体研究表明,组织内折射率变化可导致最小的细胞死亡,仅限于角膜基质的激光焦域内,并且对上皮或内皮没有观察到可见的损伤。在这里,我们使用活体兔子来确定 LIRIC 在体内的长期后果。具体来说,我们评估了细胞死亡、纤维化、角膜神经分布、内皮细胞密度和角膜结构,直到 LIRIC 后 3 个月。在 20 个荷兰带兔的角膜平面上,用 +2.5 D 梯度指数 LIRIC 菲涅耳透镜在直径为 4.5 毫米的中基质圆形区域内刻写。另外 12 只兔子的眼睛被用作仅平面化对照,以区分激光治疗和抽吸平面化对生物和结构参数的影响。在手术前、手术后立即、2 周、4 周和 12 周进行活体光学测量,以测量内皮细胞密度和角膜结构的变化。在 LIRIC 后 4 小时、2 周、4 周和 12 周时,每组 4 只兔子被处死,进行组织学测定;TUNEL 测定用于评估细胞死亡,H&E 染色用于评估炎症浸润,免疫染色用于评估α-平滑肌肌动蛋白(α-SMA)和βIII 微管蛋白(Tuj-1)用于评估肌成纤维细胞分化和角膜神经分布。与先前的离体数据一致,仅在激光焦域中观察到最小的细胞死亡,TUNEL 阳性细胞仅局限于 LIRIC 后 4 小时的折射率变化的基质区域。LIRIC 后 2、4 或 12 周,角膜的任何部位均未见 TUNEL 阳性细胞。仅平面化的角膜完全呈 TUNEL 阴性。在任何检查时间点,无论是 LIRIC 治疗还是平面化仅治疗的眼睛,都没有观察到 α-SMA 阳性染色或改变的角膜神经分布。体内共聚焦成像显示所有眼睛(无论是否接受 LIRIC 治疗或仅平面化)的内皮细胞密度均正常。光学相干断层扫描显示抽吸平面化会导致中央角膜厚度暂时下降,4 小时内恢复正常。在平面化时写入 LIRIC 菲涅耳透镜的角膜不会发生超出已描述的抽吸平面化引起的暂时变薄的主要结构或形状变化。目前的发现表明,在活体兔角膜的中基质区域生成临床相关折射校正的 LIRIC 图案,在手术后 3 个月内对角膜结构和生物学几乎没有造成破坏。这证实了 LIRIC 的相对安全性,并预测与传统的激光视力矫正手术相比,干眼、混浊或患者不适等常见术后并发症可能完全避免。