June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Corneal inflammation after penetrating keratoplasty and miniature keratoprosthesis implantation
Author Affiliations & Notes
  • Alja Crnej
    Massachusetts Eye and Ear Infirmary, Boston, MA
  • Susanne Eiglmeier
    Schepens Eye Research Institute, Boston, MA
  • Masahiro Omoto
    Schepens Eye Research Institute, Boston, MA
  • Thomas H Dohlman
    Schepens Eye Research Institute, Boston, MA
  • Claes H Dohlman
    Massachusetts Eye and Ear Infirmary, Boston, MA
  • Reza Dana
    Schepens Eye Research Institute, Boston, MA
  • Footnotes
    Commercial Relationships Alja Crnej, None; Susanne Eiglmeier, None; Masahiro Omoto, None; Thomas Dohlman, None; Claes Dohlman, None; Reza Dana, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 4023. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Alja Crnej, Susanne Eiglmeier, Masahiro Omoto, Thomas H Dohlman, Claes H Dohlman, Reza Dana; Corneal inflammation after penetrating keratoplasty and miniature keratoprosthesis implantation. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):4023.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: To compare corneal inflammation after syngeneic and allogeneic penetrating keratoplasty (PK) and miniature Keratoprosthesis (m-KPro) implantation.

Methods: BALB/c (syngeneic) or C57BL/6 (allogeneic) corneas were transplanted onto BALB/c host beds as part of PK or m-KPro implantation. Corneal inflammation was assessed by determining the frequencies of CD45+ leukocytes, CD4+ T cells, CD11b+ dendritic cells, and Gr-1+ granulocytes/monocytes by flow cytometry at 2, 4, and 8 weeks post-transplantation. In addition, expression of the pro-inflammatory cytokines TNFα and IL-1β was analyzed using Real-Time qPCR at 8 weeks post-transplantation.

Results: Cell frequencies in the syngeneic and allogeneic m-KPro groups were higher compared to the syngeneic and allogeneic PK groups, respectively, at all time points. However, after week four, frequencies of all immune cells were higher in the alloPK group as compared to the synKPro group. The expression of TNFα was higher in synKPro, alloPK, and alloKPro groups compared to the naïve and synPK groups at eight weeks. The expression of IL-1β was significantly higher in both KPro groups as compared to PK groups.

Conclusions: Although m-KPro device augments the inflammatory response in cornea after its implantation, allogenicity is greater contributor to inflammation. We suggest using syngeneic or decellularized corneal tissue as a Boston-KPro carrier. Results also suggest that after second standard graft failure, B-KPro should have greater likelihood of success than further regraft.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×