| Literature DB >> 28795351 |
Eric Wakshull1, Valerie Quarmby1, Hanns-Christian Mahler2, Hongwen Rivers3, Dhananjay Jere2, Meg Ramos4, Piotr Szczesny5, Karoline Bechtold-Peters6, Sharmila Masli7, Swati Gupta8.
Abstract
Therapeutic breakthroughs in a number of retinal degenerative diseases have come about through the development of biotherapeutics administered directly into the eye. As a consequence of their use, we have gained more insight into the immune privileged status of the eye and the various considerations that development, manufacturing, and use of these drugs require. It has been observed that therapeutic proteins injected into the vitreous can elicit an immune response resulting in the production of anti-drug antibodies (ADAs) which can have clinical consequences. This review includes discussion of the anatomy, physiology, and specific area of the eye that are targeted for drug administration. The various immunologic mechanisms involved in the immune responses to intraocularly administered protein are discussed. This review entails discussion on chemistry, manufacturing, and control (CMC) and formulation-related issues that may influence the risk of immunogenicity. Based on the available immunogenicity profile of the marketed intraocular drugs and their reported adverse events, the animal models and the translational gap from animals to human are discussed. Thus, the objective of this review article is to assess the factors that influence immunogenicity in relation to intraocular administration and the steps taken for mitigating immunogenicity risks.Entities:
Keywords: immunogenicity; intraocular administration; ocular biotherapeutics
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Year: 2017 PMID: 28795351 DOI: 10.1208/s12248-017-0128-y
Source DB: PubMed Journal: AAPS J ISSN: 1550-7416 Impact factor: 4.009