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Eye Hospital > Clinical Care Services > Cornea and anterior segment

How are stem cells used for treating eye disorders?
All eye disorders cannot be treated with stem cells; only the front part of the eye can be treated.

The eye’s outer surface is exposed to the environment, and has a constant turnover of cells to maintain the optical transparency of the cornea. These cells are regenerated from reserve stem cells, known as limbal stem cells, which are found in an area called the limbus. The limbus is a transition zone separating the central transparent cornea and the peripheral area (See diagram of the eye showing the limbus). The function of limbal stem cells is to regenerate the epithelial (surface) cells of the cornea, while also serving as a barrier to ensure that the conjunctival cells do not grow over the cornea and mar its transparency.


Diagram of the eye showing the limbus

Limbal stem cells help regenerate the surface of the cornea when there is any decay or damage. However, in cases of chemical burns, allergic reactions to drugs and auto-immune diseases, the limbal stem cells may become damaged and lose their ability to regenerate new cells. This condition is known as ‘limbal stem cell deficiency’ (LSCD). This deficiency can be made up in two ways: by direct limbal transplants or by culturing the limbal cells in a controlled environment and transplanting them. The raw surface of the eye causes pain, redness and decreased vision.

The damage to the limbal cells may be partial or total; it may be unilateral/in one eye or bilateral/in both eyes. Based on the extent of damage, doctors make a clinical decision whether a graft from the same eye will be sufficient, or whether there is a need to take it from the other eye. There are two types of grafts – allograft and autograft. In allograft the cells used for culturing are taken from a relative or donor, while in autograft the cells for culturing are taken from the patient.

The surgery
The procedure involves a relatively minor surgery to remove the tissue, which is then cultured in a laboratory on a human amniotic membrane. After almost a fortnight it is then transplanted into the patient. Following surgery, the patient is checked in the clinic, with follow-up visits scheduled every 4-6 weeks till it is found satisfactory.

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