Systemic immunosuppression in limbal stem cell transplantation: best practices and future challenges.

Can J Ophthalmol

Department of Ophthalmology and Vision Sciences, University of Toronto, Toronto, Ont.; Toronto Transplant Institute, University Health Network, Toronto, Ont.. Electronic address:

Published: August 2018

AI Article Synopsis

  • The study aimed to assess systemic immunosuppression regimens for patients undergoing ocular surface stem cell transplantation, focusing on their benefits and side effects in treating limbal stem cell deficiency (LSCD).
  • Data were gathered from a systematic review of literature between 1980 and 2015, revealing that the most common intervention was keratolimbal allograft and that immunosuppressive treatments evolved from oral cyclosporine to combinations like mycophenolate mofetil and tacrolimus.
  • Successful long-term management yielded stable ocular surfaces in 70%-80% of patients, but adverse effects such as hypertension and diabetes were noted, highlighting the need for further randomized studies to define optimal immunosuppressive strategies.

Article Abstract

The objective of this study was to evaluate systemic immunosuppression regimens used for patients undergoing ocular surface stem cell transplantation, including their benefits and adverse effects in the adjunctive management of limbal stem cell deficiency (LSCD). A systematic literature review was conducted using the MEDLINE and EMBASE databases (1980-2015). Data were collected on surgical intervention(s), type of immunosuppressive agent(s), duration of immunosuppression, percentage with stable ocular surface at last follow-up, mean follow-up time, and demographics. Data were also collected on adverse ocular and systemic outcomes. Sixteen reports met the inclusion criteria. There were no randomized controlled studies. Three studies were noncomparative prospective case series, whereas the majority were retrospective case series. Bilateral severe LSCD was the most common disease (50%), and keratolimbal allograft was the most common intervention (80%). Immunosuppressive regimens showed a progression from early studies using oral cyclosporine to later studies using combinations of mycophenolate mofetil and tacrolimus. Most studies included a course of high-dose systemic corticosteroids. For patients adherent to long-term systemic immunosuppression, stable ocular surface rates of 70%-80% at last follow-up were reported. Adverse effects included hypertension, diabetes mellitus, and biochemical abnormalities managed with pharmacotherapy or discontinuation of offending agents. There were no cases of mortality related to immunosuppression. However, the current literature does not elucidate which immunosuppressive regimen is most efficacious for different categories of LSCD or graft types. Evidence-based guidelines for systemic immunosuppression in limbal allograft therapy would benefit from randomized controlled and/or additional prospective studies. Long-term immunosuppression would benefit from close collaboration between ophthalmologists and transplant specialists to individualize treatments.

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http://dx.doi.org/10.1016/j.jcjo.2017.10.040DOI Listing

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