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Characteristics of endothelial corneal transplant rejection following immunisation with SARS-CoV-2 messenger RNA vaccine
  1. Maria Phylactou,
  2. Ji-Peng Olivia Li,
  3. Daniel F P Larkin
  1. Cornea and External Diseases, Moorfields Eye Hospital NHS Foundation Trust, London, UK
  1. Correspondence to Maria Phylactou, Cornea and External Diseases, Moorfields Eye Hospital NHS Foundation Trust, London EC1V 2PD, UK; phylactou.maria{at}gmail.com

Abstract

Aim We report two cases of endothelial corneal allograft rejection following immunisation with SARS-CoV-2 messenger RNA (mRNA) vaccine BNT162b2 and describe the implications for management of transplant recipients postvaccination for COVID-19.

Methods A 66-year-old woman with Fuchs endothelial corneal dystrophy (FECD) and a unilateral Descemet’s membrane endothelial keratoplasty (DMEK) transplant received COVID-19 mRNA vaccine BNT162b2 14 days post-transplant. Seven days later, she presented with symptoms and signs of endothelial graft rejection. An 83-year-old woman with bilateral DMEK transplants for FECD 3 and 6 years earlier developed simultaneous acute endothelial rejection in both eyes, 3 weeks post second dose of COVID-19 mRNA vaccine BNT162b2. Rejection in both cases was treated successfully with topical corticosteroids.

Conclusions We believe this is the first report of temporal association between corneal transplant rejection following immunisation against COVID-19 and the first report of DMEK rejection following any immunisation. We hypothesise that the allogeneic response may have been initiated by the host antibody response following vaccination. Clinicians and patients should be aware of the potential of corneal graft rejection associated with vaccine administration and may wish to consider vaccination in advance of planned non-urgent keratoplasties. Patients should be counselled on the symptoms and signs that require urgent review to allow early treatment of any confirmed rejection episode.

  • cornea
  • COVID-19
  • immunology

Data availability statement

Data sharing not applicable as no data sets generated and/or analysed for this study. No data are available.

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Data availability statement

Data sharing not applicable as no data sets generated and/or analysed for this study. No data are available.

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Footnotes

  • Contributors MP, J-POL and DFPL conceived the study and wrote the manuscript. MP and J-POL collected the clinical data. All authors read and approved the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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