Correlation of Multimodal Clinical Imaging With the Whole-Slide- and Superresolution-Based Immunohistological Structure of the Corneal Limbal Stroma.

PURPOSE

To identify structural landmarks in the limbal stroma by anterior segment optical coherence tomography (asOCT), asOCT angiography (asOCTa) and in vivo confocal microscopy (IVCM), and correlate findings with immunofluorescence microscopy (IFM).

METHODS

The corneal limbus of healthy individuals was examined by IVCM, asOCT, and asOCTa. IFM was performed in cadaveric cornea samples sectioned in clinical imaging planes, with putative markers for limbal niche cells (CD90, N-cadherin, SSEA-4), blood/lymphatic vessels (CD31), nerves (acetyl-α-tubulin, β-III tubulin), limbal epithelial progenitor cells (p63), and hyaluronic acid (HA).

RESULTS

On asOCT, asOCTa, and IVCM superficial and deep limbal vessels could be identified that terminated in the marginal corneal arcade (MCA). Limbal stroma appeared as hyperreflective area between superficial and deep limbal blood vessels. The same blood vessel patterns were identified by IFM. HA localization was identical to hyperreflective stromal structures. Nerves and putative niche cells localized around limbal vessels and were in close contact with the basal limbal epithelium at the level of the MCA. Limbal epithelium was hyperreflective and thinned in the elderly (>60 years, 122.6 ± 36.6 µm; <60 years, 139.9 ± 34.4 µm; P = 0.025) resulting in less visible palisades of Vogt on asOCT (>60 years, 82.6% visible; <60 years, 100% visible; P = 0.011).

CONCLUSIONS

Our study proves that limbal vessel plexuses can serve as landmarks to identify corresponding structures in various clinical imaging modalities. The proximity of blood vessels, niche cells, and nerves, confirmed by IFM, may suggest that limbal vascular damage occurs together with niche cell and neural loss. The IFM correlations provided by this study help to detect healthy limbal structures and aid the diagnosis of diseased corneas.