Causes of sterile vitritis in the setting of Boston keratoprosthesis
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Summary
An idiopathic inflammation of the vitreous humor, “sterile vitritis”, has been observed in some keratoprosthesis recipients, typically months to years after implantation. Its etiology is unclear. Potential mechanisms include: (i) local tissue destruction and inflammation around the prosthesis, at the point of contact between cornea donor tissue and the device, (ii) microbial cell wall or nucleic acid triggering inflammation, and (iii) a systemic immune response with ocular manifestations.
One or more of these mechanisms likely contributes to each case of idiopathic vitreous inflammation. Tissue remodeling around the keratoprosthesis may create a dynamic space for inorganic or organic debris to enter the eye. Some cases of vitritis may have an infectious origin, despite negative cultures. Continued studies are needed to assess the clinical significance of corneal tissue loss under the front plate and adjacent to the stem. These areas of tissue “gaps” may provide access for organic and inorganic debris to enter the eye and stimulate inflammation.
Keywords
Boston Keratoprosthesis Sterile inflammation Sterile vitritisUrsachen der sterilen Vitritis im Zusammenhang mit Boston-Keratoprothesen
Zusammenfassung
Eine idiopathische Entzündung des Glaskörpers, die sogenannte sterile Vitritis, konnte bei einigen Patienten Monate bis Jahre nach Implantation einer Boston-Keratoprothese beobachtet werden. Die Ätiologie ist unklar. Mögliche Ursachen umfassen: (I) lokale Gewebszerstörungen und -entzündungen im Kontaktbereich zwischen der Spenderkornea und der Keratoprothese, (II) entzündungsauslösende Nukleinsäuren bzw. mikrobielle Zellwände, sowie (III), okuläre Manifestationen einer systemischen Immunantwort.
Bei idiopathischen Glaskörperentzündungen spielen wohl einer oder auch mehrere der genannten Mechanismen eine Rolle. Gewebeumbau im Bereich der Keratoprothese könnte zur Ausbildung eines dynamischen Zwischenraumes führen, der organischen und anorganischen Ablagerungen als Eintrittsweg in das Auge dient. Trotz unauffälliger Kultur könnten einige der Vitritiden einen infektiösen Ursprung haben. Deswegen sind weitere Studien erforderlich, um die klinische Bedeutung der Minimierung des Korneagewebes unter der Frontplatte und in Nähe des Schafts zu untersuchen. Die Bereiche des Gewebeumbaus und der damit assoziierten „Gewebsspalten“ stellen vermutlich die Eintrittswege für organische und anorganische Ablagerungen dar und stimulieren Entzündungsprozesse.
Schlüsselwörter
Boston-Keratoprothese Sterile Entzündung Sterile VitritisNotes
Conflict of interest
The authors declare that there is no conflict of interest.
References
- 1.Aldave AJ, Kamal KM, Vo RC, Yu F. The Boston type I keratoprosthesis: improving outcomes and expanding indications. Ophthalmology. 2009;116(4):640–51.PubMedCrossRefGoogle Scholar
- 2.Aldave AJ, Sangwan VS, Basu S, Basak SK, Hovakimyan A, Gevorgyan O, et al. International results with the Boston type I keratoprosthesis. Ophthalmology. 2012;119(8):1530–8.PubMedCrossRefGoogle Scholar
- 3.Bradley JC, Hernandez EG, Schwab IR, Mannis MJ. Boston type 1 keratoprosthesis: the university of california davis experience. Cornea. 2009;28(3):321–7.PubMedCrossRefGoogle Scholar
- 4.Zerbe BL, Belin MW, Ciolino JB, Group BTKS. Results from the multicenter Boston Type 1 Keratoprosthesis study. Ophthalmology. 2006;113(10):1779.e1–7.Google Scholar
- 5.Pearlman E, Sun Y, Roy S, Karmakar M, Hise AG, Szczotka-Flynn L, et al. Host defense at the ocular surface. Int Rev Immunol. 2013;32(1):4–18.PubMedCentralPubMedCrossRefGoogle Scholar
- 6.Ueta M, Kinoshita S. Innate immunity of the ocular surface. Brain Res Bull. 2010;81(2–3):219–28.PubMedCrossRefGoogle Scholar
- 7.Ueta M, Kinoshita S. Ocular surface inflammation mediated by innate immunity. Eye Contact Lens. 2010;36(5):269–81.PubMedCrossRefGoogle Scholar
- 8.Nouri M, Durand ML, Dohlman CH. Sudden reversible vitritis after keratoprosthesis: an immune phenomenon? Cornea. 2005;24(8):915–9.PubMedCrossRefGoogle Scholar
- 9.Gautam R, Singh RD, Sharma VP, Siddhartha R, Chand P, Kumar R. Biocompatibility of polymethylmethacrylate resins used in dentistry. J Biomed Mater Res B Appl Biomater. 2012;100(5):1444–50.PubMedCrossRefGoogle Scholar
- 10.Lloyd AW, Faragher RG, Denyer SP. Ocular biomaterials and implants. Biomaterials. 2001;22(8):769–85.PubMedCrossRefGoogle Scholar
- 11.Nowzari H, Botero JE, DeGiacomo M, Villacres MC, Rich SK. Microbiology and cytokine levels around healthy dental implants and teeth. Clin Implant Dent Relat Res. 2008;10(3):166–73.PubMedCrossRefGoogle Scholar
- 12.Nowzari H, Yi K, Chee W, Rich SK. Immunology, microbiology, and virology following placement of NobelPerfect scalloped dental implants: analysis of a case series. Clin Implant Dent Relat Res. 2008;10(3):157–65.PubMedCrossRefGoogle Scholar
- 13.Gratton DG, Aquilino SA, Stanford CM. Micromotion and dynamic fatigue properties of the dental implant-abutment interface. J Prosthet Dent. 2001;85(1):47–52.PubMedCrossRefGoogle Scholar
- 14.Teronen O, Konttinen YT, Lindqvist C, Salo T, Ingman T, Lauhio A, et al. Human neutrophil collagenase MMP-8 in peri-implant sulcus fluid and its inhibition by clodronate. J Dent Res. 1997;76(9):1529–37.PubMedCrossRefGoogle Scholar
- 15.Zimmerli W, Sendi P. Pathogenesis of implant-associated infection: the role of the host. Semin Immunopathol. 2011;33(3):295–306.PubMedCrossRefGoogle Scholar
- 16.Howes EL, Cole PW, Adair TM, Cruse VK, Pollycove M. Cellular and vascular responses in acute experimental ocular inflammation. Invest Ophthalmol Vis Sci. 1994;35(12):4031–8.PubMedGoogle Scholar
- 17.Long M, Rack HJ. Titanium alloys in total joint replacement-a materials science perspective. Biomaterials. 1998;19(18):1621–39.PubMedCrossRefGoogle Scholar
- 18.Rajpura A, Kendoff D, Board TN. The current state of bearing surfaces in total hip replacement. Bone Joint J. 2014;96-B(2):147–56.PubMedCrossRefGoogle Scholar
- 19.Goodman SB, Yao Z, Keeney M, Yang F. The future of biologic coatings for orthopaedic implants. Biomaterials. 2013;34(13):3174–83.PubMedCentralPubMedCrossRefGoogle Scholar
- 20.Heuer W, Elter C, Demling A, Neumann A, Suerbaum S, Hannig M, et al. Analysis of early biofilm formation on oral implants in man. J Oral Rehabil. 2007;34(5):377–82.PubMedCrossRefGoogle Scholar
- 21.Iyer G, Pillai VS, Srinivasan B, Falcinelli G, Padmanabhan P, Guruswami S. Modified osteo-odonto keratoprosthesis-the Indian experience-results of the first 50 cases. Cornea. 2010;29(7):771–6.PubMedGoogle Scholar
- 22.Huang Y, Yu J, Liu L, Du G, Song J, Guo H. Moscow eye microsurgery complex in Russia keratoprosthesis in Beijing. Ophthalmology. 2011;118(1):41–6.PubMedCrossRefGoogle Scholar
- 23.Tan XW, Riau A, Shi ZL, Tan AC, Neoh KG, Khor KA, et al. In vitro effect of a corrosive hostile ocular surface on candidate biomaterials for keratoprosthesis skirt. Br J Ophthalmol. 2012;96(9):1252–8.PubMedCentralPubMedCrossRefGoogle Scholar
- 24.Singh R, Dahotre NB. Corrosion degradation and prevention by surface modification of biometallic materials. J Mater Sci Mater Med. 2007;18(5):725–51.PubMedCrossRefGoogle Scholar
- 25.Green JM, Hallab NJ, Liao YS, Narayan V, Schwarz EM, Xie C. Anti-oxidation treatment of ultra high molecular weight polyethylene components to decrease periprosthetic osteolysis: evaluation of osteolytic and osteogenic properties of wear debris particles in a murine calvaria model. Curr Rheumatol Rep. 2013;15(5):325.Google Scholar
- 26.Durand ML, Dohlman CH. Successful prevention of bacterial endophthalmitis in eyes with the Boston keratoprosthesis. Cornea. 2009;28(8):896–901.PubMedCrossRefGoogle Scholar
- 27.Callegan MC, Booth MC, Jett BD, Gilmore MS. Pathogenesis of gram-positive bacterial endophthalmitis. Infect Immun. 1999;67(7):3348–56.PubMedCentralPubMedGoogle Scholar
- 28.Kaper HJ, Busscher HJ, Norde W. Characterization of poly(ethylene oxide) brushes on glass surfaces and adhesion of Staphylococcus epidermidis. J Biomater Sci Polym Ed. 2003;14(4):313–24.PubMedCrossRefGoogle Scholar
- 29.Kingshott P, Wei J, Bagge-Ravn D, Gadegaard N, Gram L. Covalent attachment of poly(ethylene glycol) to surfaces, critical for reducing bacterial adhesion. Langmuir. 2003;19:6912–21.CrossRefGoogle Scholar