AIM To report the outcome of a series of patients with stem cell deficiency who underwent allo-limbal transplantation and to describe a technique for this procedure.
METHODS Six consecutive patients underwent allo-limbal stem cell transplantation. The primary diagnosis included alkali burn (n=2), trachoma (n=1), chronic rosacea blepharitis and keratoconjunctivitis (n=1), aniridia (n=1), and Stevens–Johnson syndrome (n=1). The limbal rim consisted of peripheral cornea and perilimbal sclera. FK-506 was used postoperatively for immunosuppression.
RESULTS The length of follow up ranged from 3 to 24 months (mean follow up 11.8 (SD 9.3) months). The outcome was considered satisfactory in five of six cases. The corneal surface was completely epithelialised within 2 weeks, and there was a substantial improvement in vision and symptoms. One patient had recurrent epithelial defects related to eyelid abnormalities. No side effects associated with systemic immunosuppression were noted.
CONCLUSION Allo-limbal transplantation, with systemic immunosuppression with FK-506 is useful in reconstruction of the ocular surface with improvement in vision in patients with severe stem cell deficiency.
- limbal stem cell deficiency
- limbal transplantation
Statistics from Altmetric.com
Corneal stem cells are principally located at the sclerocorneal limbus,1 and are indispensable for the maintenance of a healthy corneal surface. Loss of limbal stem cells, or corneal stem cell deficiency, can be partial or total. Limbal stem cell deficiency can be associated with persistent epithelial defects, vascularisation of the cornea, conjunctivalisation of the cornea, corneal scarring, melting, ulceration and perforation of the cornea, corneal calcification, and band keratopathy.2-8 The symptoms of limbal deficiency may include decreased vision, photophobia, tearing, blepharospasm, and recurrent episodes of pain, as well as a history of chronic inflammation with redness. Diagnosis of limbal stem cell deficiency is crucial because patients with these abnormalities generally are poor candidates for conventional corneal transplantation. Lamellar or penetrating keratoplasty provides only a temporary replacement of the host’s corneal epithelium and does not permanently reconstitute the limbal function.9 10 In patients with limbal stem cell deficiency, limbal autotransplantation12-19 or allotransplantation14-23 should be considered for corneal surface reconstruction. This may be combined with or followed by keratoplasty.
Several techniques have been reported for limbal stem cell transplantation. All the procedures share the goal of transplantation of a new source of epithelium for a diseased ocular surface and the removal of the host’s altered corneal epithelium and pannus.12-23 After successful transplantation the host’s cornea (or grafted cornea) will be permanently covered by epithelium from the donor. Although all techniques used in stem cell transplantation are similar in principle the source of donor stem cells can vary. Donor tissue can be obtained from the fellow eye (limbal autograft) in cases of unilateral disease; or from a living related donor or cadaver donor (whole globe or corneoscleral disc) (limbal allograft) when both eyes are affected. Limbal transplantation procedures also vary depending on the carrier tissue used for the transfer of the limbal stem cells. Carrier tissue is needed in limbal transplantation because it is not possible to transfer limbal stem cells alone. Limbal transplants have used either conjunctiva (conjunctival limbal graft) or cornea (keratolimbal graft) as a carrier tissue for limbal stem cells.17
This report describes a modified surgical technique for limbal stem cell transplantation and the outcome of a series of consecutive patients undergoing limbal allograft.
Materials and methods
Patients with severe bilateral ocular surface abnormalities were treated by limbal allograft transplantation. The diagnosis of limbal stem cell deficiency was made clinically based on the ocular history, patient observation immediately after chemical injury and close follow up, presence of corneal neovascularisation, staining of epithelial cells on the corneal surface by fluorescein, limbal inflammation, and limbal abnormalities. Six consecutive patients were included in this study. Demographics and diagnosis are summarised in Table 1. All patients had long standing problems except case 4 who underwent limbal allotransplantation 3 weeks after severe alkali burn. This patient had a non-healing epithelial defect affecting the cornea and bulbar conjunctiva, dense stromal opacity, severe limbal ischaemia of two quadrants, and persistent inflammation.
Preparation of the donor tissue from cadaver eyes
“Fresh” donor eyes were preferred because the success of the procedure depends on the transplantation of healthy limbal stem cells. Donor material was taken from eyes enucleated promptly after death and stored for up to 24 hours at 4°C. Whole eyes were used for two reasons: (1) it allowed for rapid transport of tissue from source centre to our department with processing of tissue required at an eye bank; and (2) it provided better stabilisation of the cornea and sclera during dissection of the limbal sclerocorneal rim. The donor eye was inflated with air (1–2 ml), injected through the stump of the optic nerve, to make the globe firm (Fig 1A). The globe was wrapped around with a strip of wet gauze and held on a Tudor Thomas stand. A vacuum trephine, with a diameter 3 mm smaller than the corneal diameter (that is, average of vertical and horizontal corneal diameter), was used to trephine the donor central cornea into one fourth to one fifth of the stromal depth (approximately 150 μm). Particular attention was paid to proper centration to ensure that a uniform width of peripheral cornea was obtained. Superficial lamellar dissection of the peripheral cornea was then carried out using an angle bevel up blade, and extended into the sclerocorneal junction and 1 mm beyond, into sclera (Fig 1B and C). Approximately 1–2 mm of donor conjunctiva, if present, was maintained. The dissected tissue was divided at one point and excision completed with a curved scissors, by cutting along the outer circumference of the dissected tissue. The limbal tissue to be grafted thus consisted of an open ring of peripheral corneal and limbal epithelium (and conjunctival tissue at places), and superficial corneal, limbal, and scleral stroma.
Preparation of the recipient eye
Good exposure was obtained by opening the lids widely with a speculum, superior and inferior rectus fixation sutures, and a lateral canthotomy (in two cases). A 16 mm Flieringa ring was sutured in place when the procedure was combined with a corneal graft (and lens extraction with implant). A 360° peritomy was done, close to the host limbus. The vascularised conjunctiva was recessed about 5–6 mm to expose the limbus and perilimbal sclera. A superficial keratectomy was done to remove all abnormal epithelium and the superficial fibrovascular scar tissue. This abnormal tissue was stripped off by blunt dissection after a suitable plane was created with a bevel up angle blade (Fig 2). In case 4 there was no pannus covering the host surface.
The anterior edge of the “open ring” (with donor peripheral corneal tissue + limbus + sclera) was placed at the host limbus (Fig3A). Therefore, the donor limbus was slightly posterior to the host limbus, increasing the length of the circumference to be covered. The limbal tissue was sutured with interrupted 10-0 nylon sutures at the corneal and scleral margin. Six to eight sutures were first passed along the inner (corneal) edge of the donor tissue and partial thickness of host corneal stroma. A similar number of sutures were then passed directly opposite to the inner sutures, along the outer (scleral) edge of the donor tissue. These were anchored to the superficial sclera of the host. The tension on these sutures also determined the final tension on the inner sutures. The knots were trimmed and buried. This method invariably left a small gap (approximately 5–8 mm) between the two ends of the donor tissue ring. This was filled with a “spacer” fashioned out of donor corneal stroma or a piece of donor limbal tissue, cut to size, harvested from the other eye of the same donor. This piece usually required a couple of additional sutures along either edge. The host conjunctiva was approximated to the limbus with interrupted 8-0 Vicryl sutures. When a penetrating keratoplasty was required at the time of surgery the limbal tissue was first sutured in place (Fig 3B). The donor graft for penetrating keratoplasty was obtained from the central cornea of the donor whole globe. Subconjunctival antibiotics and corticosteroids are injected at the end of the procedure. All surgeries were performed by one of the authors (HSD).
Topical preservative-free chloramphenicol 0.5% was used four times a day for the first month. Topical preservative-free prednisolone acetate 1% was used four times a day for the first 12 weeks, and slowly tapered during the next months. A low dose of topical corticosteroids (one drop per day) was maintained unless elevation of intraocular pressure occurred. Preservative-free artificial tears every hour and highly viscous methylcellulose four times daily were initially used and tapered after epithelial healing was completed.
Autologous serum eye drops were prepared and given hourly until the epithelialisation was completed, usually within the first week after surgery. To prepare serum eye drops 50 ml blood were obtained by venepuncture and centrifuged for 5 minutes at 1500 rpm. A 20% solution of serum was then prepared with saline in a sterile environment and placed into sterile vials, each of them containing 5 ml of the solution. The vials were kept frozen in a refrigerator at −20°C, and one vial per day was defrosted and used.
Vigorous postoperative immunosuppression with FK-506 was used at least during the first 18 months after surgery. All patients underwent thoracic radiography, blood tests (renal function tests), urine tests, and blood pressure determination before and during FK-506 treatment. The daily total dose was initiated at 0.1–0.2 mg/kg of body weight per day 1 day before surgery, and continued for at least 1 year, trying to maintain the trough level between 3 and 15 ng/ml. The serum levels and patient’s systemic condition (blood pressure, thoracic radiography, blood tests (renal function tests: SMA-12), and urine tests) were checked every week for the first month and every 2–4 weeks later. The FK-506 dosage was increased or decreased if it proved ineffective or caused adverse effects.
The length of follow up ranged from 3 to 24 months, with an average follow up of 11.8 (SD 9.3) months. Histological examination of the host’s corneal pannus confirmed the presence of conjunctival-like epithelium. Postoperatively, in all cases, outgrowths of epithelial sheets from the limbal grafts started within the first 3 days and the whole corneal surface was completely epithelialised within 2 weeks (Fig4). There was no infection, limbal graft failure, or slippage of tissue. The epithelium was stable in five of six patients (that is, there were no recurrence of epithelial defect, see Figs 5 and 6), transparent and smooth (in four of six cases). In case 4 the corneal epithelium was irregular, which was attributed to previous stromal abnormalities and persistent low grade inflammation; stromal melting did not occur, and a penetrating keratoplasty was done 5 months after limbal transplantation. Visual acuity improved in five of six patients, and was very substantial in two of them (cases 3 and 6). Improvement of visual function was only moderate in cases 1, 2, and 4 because of pre-existing abnormalities (see Table 1). Case 5 had a satisfactory reconstruction of the corneal epithelial surface and vision improved to 6/60 shortly after surgery. However, the follow up was complicated with several episodes of epithelial defects associated with eyelid abnormalities. This corneal epithelium could be restored but stromal opacity developed and a repeated corneal graft was done 4 months after limbal transplantation.
Side effects related to FK-506 were not observed. All cases but two (cases 1 and 2) were still taking FK-506 at the time of submission of this paper. In case 1, FK-506 was discontinued 13 months after surgery. He presented with a rejection episode of the limbal graft (intense congestion along scleral edge, oedema of donor tissue, and clouding of tissue) and of the corneal graft (keratic precipitates and stromal oedema) 2 months later. FK-506 orally and topical steroids were recommenced. The rejection settled with complete clearing of limbal and corneal graft tissue. FK-506 was finally discontinued 5 months later. Case 2 had limbal allograft rejection 4 months after surgery, with engorgement of limbal and conjunctival vessels, and the dosage of FK-506 was increased. Three weeks later the vascular engorgement regressed. In this patient immunosuppression was discontinued 18 months after surgery and 6 months later graft rejection did not recur.
The aetiology of limbal stem cell deficiency can beprimary—related to an insufficient stromal microenvironment to support stem cell functions, such as aniridia, congenital erithrokeratodermia, keratitis associated with multiple endocrine deficiencies, neurotrophic (neural and ischaemic) keratopathy, and chronic limbitis, orsecondary—related to external factors that destroys the limbal stem cells such as chemical or thermal injuries, Stevens–Johnson syndrome, ocular rosacea, ocular cicatricial pemphigoid, multiple surgeries or cryotherapies, contact lens wear, or extensive microbial infection.24 In this series most patients (five of six) had secondary limbal stem cell deficiency.
The technique described in this article was a variation of previously described limbal transplantation.20 21 In 1984, Thoft used lenticules of peripheral cornea from a cadaveric donor globe as a source of epithelium (that is, keratoepithelioplasty) but limbal cells were not transplanted.25 The first trials of human limbal stem cell transplant were performed by Kenyon and Tseng in 1989 through limbal autograft transplantation to treat unilateral ocular surface disorders.11 They transplanted conjunctiva and limbus presumably including stem cells, from the good fellow eye to the recipient eye. Since this original report several variations of limbal autografts12-19 26 27 and allografts14-23 28 have been reported with good reconstitution of the corneal epithelium and regression of neovascularisation. Cornea or conjunctiva have been the most commonly used carriers to transplant limbal stem cells. In this study peripheral cornea, perilimbal sclera, and conjunctiva were used as carriers for limbal cells and providers of an adequate microenvironment for their survival and replication. After surgery, autologous serum eye drops were used as described by other authors to promote corneal epithelialisation.20
We performed six limbal allograft transplants to reconstruct corneal surface severely affected by different disorders. All patients had very poor vision and were not manageable with penetrating keratoplasty alone. All cases achieved rapid surface healing restoration of an optically improved surface, resulting in improved visual acuity. In five of six patients visual function improved. However, two patients required penetrating keratoplasty after limbal transplantation for visual rehabilitation. In limbal allografts the surface disorder can recur if there is immunological destruction of the transplanted limbal stem cells. A high rate of immune reactions can be expected because the high immunogenic stimulus of the limbal transplant, related to the relatively abundant of Langerhans cells and HLA-DR antigens.29 They play an important role in the afferent arm of allograft rejection and effective immunosuppression is judged to be absolutely necessary. Several authors had used cyclosporine A as the immunosuppressive agent.16 20 21 23 The use of FK-506, a new agent isolated from the fermentation broth ofStreptomyces tsukubaensis, for immunosuppression in limbal or corneal allografts has not been reported before. FK-506 has been successfully used in organ transplantation30 and uveitis.31-33 This agent has immunosuppressive activities similar to and more potent than those of cyclosporine.34 35 The major side effects of FK-506 are sensation of warmth, hypomagnesaemia, renal dysfunction, glucose intolerance, nausea, vomiting, and disorders of the central nervous system. In this series FK-506 was well tolerated by all patients. One patient had an episode of rejection that could be controlled by increasing the dosage of the drug. Limbal rejection can be suspected with the development of inflammation and/or acute or chronic severe surface disorders.20 Our decision to stop this drug months after surgery was empirical. It is not known whether immunosuppression may not be necessary in some patients undergoing allo-limbal transplantation. Hypothetically, patients receiving HLA matched limbal tissue may not need intense immunosuppression. Tanet al reported three cases who received limbal tissue from living relatives without systemic immunosuppression and no rejection was noted after midterm follow up.19 The duration of systemic immunosuppression in allo-limbal transplantation is yet undefined. Some authors advocate indefinite oral cyclosporine treatment.23 In this series, two patients discontinued FK-506. One of them developed a rejection episode which was controlled, FK-506 was again stopped, and rejection did not recur. Longer follow up and further research is necessary to evaluate whether FK-506 can be stopped, its timing, and the long term outcome of limbal transplantation.
In conclusion, allo-limbal transplantation with corneal, scleral, and conjunctival carriers for ocular surface reconstruction, associated with systemic FK-506 immunosuppression, has a successful midterm outcome and is a valuable option for patients with severe bilateral limbal stem cell deficiency.
Dr Azuara-Blanco is the current Vision Express fellow in cornea and contact lenses.
We are grateful to Dr Richard J Powell and Mrs Myra Sloper for monitoring our patients on FK-506.
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.