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Immunologic Considerations of the Sclera

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The Sclera

Abstract

The sclera has the ability to participate in immunological diseases. The normal sclera contains immunoglobulins, albumin, and many of the classic and alternative pathway components of complement, and has few or no macrophages, Langherhans’ cells, neutrophils, or lymphocytes.

The development of scleritis probably entails the interaction of genetically controlled mechanisms with environmental factors, such as infectious agents (e.g., viruses, mycobacteria) or trauma. This interaction gives rise to an autoimmune process that damages the vessels through immune complex vessel deposition, subsequent complement activation, and neutrophil enzyme release (type III hypersensitivity). Persistent immunological injury leads to a chronic granulomatous response (type IV hypersensitivity) mediated by macrophages, epithelioid cells, multinucleated giant cells, and lymphocytes.

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Correspondence to Maite Sainz de la Maza MD, PhD .

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de la Maza, M.S., Tauber, J., Foster, C.S. (2012). Immunologic Considerations of the Sclera. In: The Sclera. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-6502-8_2

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