April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
The Innate Immune Response to Subretinal RPE Allografts
Author Affiliations & Notes
  • T. M. Holmes
    Clinical Research Centre, University College Dublin, Dublin, Ireland
  • K. P. Kennelly
    Clinical Research Centre, University College Dublin, Dublin, Ireland
    Ophthalmology, Mater Misericordiae University Hospital, Dublin, Ireland
  • D. M. Wallace
    Ophthalmology, Mater Misericordiae University Hospital, Dublin, Ireland
  • D. J. Keegan
    Clinical Research Centre, University College Dublin, Dublin, Ireland
    Ophthalmology, Mater Misericordiae University Hospital, Dublin, Ireland
  • Footnotes
    Commercial Relationships  T.M. Holmes, None; K.P. Kennelly, None; D.M. Wallace, None; D.J. Keegan, None.
  • Footnotes
    Support  HRB Ireland RP/2007/202
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 832. doi:
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    • Get Citation

      T. M. Holmes, K. P. Kennelly, D. M. Wallace, D. J. Keegan; The Innate Immune Response to Subretinal RPE Allografts. Invest. Ophthalmol. Vis. Sci. 2010;51(13):832.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To identify the components of the innate immune response in subretinal retinal pigmented epithelium transplants. To date all cell-based therapies have been accompanied by significant donor cell loss. The mechanism for this loss is currently unknown. Subretinal transplants have developed into one of the most promising potential treatments for currently incurable retinal disorders such as age related macular degeneration and retinitis pigmentosa. We postulate that the innate immune system plays a major role in graft failure.

Methods: : Subretinal allogeneic transplants of 105 cells from a C57BL/10.RIII.H-2r mouse derived SV40 T +ve RPE cell line were performed in healthy C57BL/6 mice and harvested at post operative day (POD) 1, 3, 7 and 28 days, sham treatments were also applied (n=4 animals/timepoint). Eyes were fixed and snap frozen for immunocytochemistry. Frozen sections were processed and immunostained for macrophage markers CD11b & F4/80 and neutrophil marker Gr-1. Glial fibrillary acidic protein (GFAP) immunostaining was used to identify the graft site. Donor cells were visualized using a SV40 T antibody.

Results: : The subretinal bolus at POD 1&3 comprised largely of SV40T +ve donor cells. CD11b, F480 and Gr1 cells increased as a proportion of the bolus from POD 1 to predominate over SV40 T cells by POD 7. These innate immune cells infiltrated primarily from the outer retina. Co-localization of SV40 T +ve cells was only seen at POD 7 predominately with F4/80, to a lesser degree with CD11b and not at all with Gr-1 labelled cells. By POD 28 the subretinal bolus was no longer in evidence and no inflammatory cells could be detected. From POD 3 to 28, graft sites in shams and transplants could be detected by GFAP up-regulation.

Conclusions: : Subretinal RPE allografts are subjected to rapid attack by cells of the innate immune system, which infiltrate the graft by POD 1. This culminates in massive graft cell loss and colocalization of surviving graft cells with macrophages by POD 7. We have identified a mechanism of rapid graft cell loss, which will have to be overcome for long term graft survival in future cell-based therapies.

Keywords: retina • inflammation • cell survival 
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