{"title":"玻璃体内抗血管内皮生长因子药物的免疫原性和眼内炎症的可能性","authors":"Hyeong Min Kim MD, MSc , Se Joon Woo MD, PhD","doi":"10.1016/j.curtheres.2024.100742","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Concerns of intraocular inflammation associated with intravitreal administration of anti-VEGF drugs have been risen and the exact mechanism is not yet elucidated.</p></div><div><h3>Objective</h3><p>To explore the relationship between immunogenicity and intraocular inflammation in intravitreal anti-VEGF drugs.</p></div><div><h3>Methods</h3><p>This review examines the immunogenicity of individual intravitreal anti-VEGF drugs and their potential link to intraocular inflammation.</p></div><div><h3>Results</h3><p>We suggest that the main cause of intraocular inflammation is the presence of pre-existing and treatment-induced antidrug antibodies, along with considerations related to the molecular structure, which includes the drug's format and size.</p></div><div><h3>Conclusions</h3><p>Researchers and clinicians involved in the advancement of new anti-VEGF drugs should take into consideration the factors related to intraocular inflammation that have been discussed.</p></div>","PeriodicalId":10920,"journal":{"name":"Current Therapeutic Research-clinical and Experimental","volume":null,"pages":null},"PeriodicalIF":1.6000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0011393X24000122/pdfft?md5=726046823de302fc9e832324390aa5ae&pid=1-s2.0-S0011393X24000122-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Immunogenicity and Potential for Intraocular Inflammation of Intravitreal Anti-VEGF Drugs\",\"authors\":\"Hyeong Min Kim MD, MSc , Se Joon Woo MD, PhD\",\"doi\":\"10.1016/j.curtheres.2024.100742\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Concerns of intraocular inflammation associated with intravitreal administration of anti-VEGF drugs have been risen and the exact mechanism is not yet elucidated.</p></div><div><h3>Objective</h3><p>To explore the relationship between immunogenicity and intraocular inflammation in intravitreal anti-VEGF drugs.</p></div><div><h3>Methods</h3><p>This review examines the immunogenicity of individual intravitreal anti-VEGF drugs and their potential link to intraocular inflammation.</p></div><div><h3>Results</h3><p>We suggest that the main cause of intraocular inflammation is the presence of pre-existing and treatment-induced antidrug antibodies, along with considerations related to the molecular structure, which includes the drug's format and size.</p></div><div><h3>Conclusions</h3><p>Researchers and clinicians involved in the advancement of new anti-VEGF drugs should take into consideration the factors related to intraocular inflammation that have been discussed.</p></div>\",\"PeriodicalId\":10920,\"journal\":{\"name\":\"Current Therapeutic Research-clinical and Experimental\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0011393X24000122/pdfft?md5=726046823de302fc9e832324390aa5ae&pid=1-s2.0-S0011393X24000122-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Therapeutic Research-clinical and Experimental\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0011393X24000122\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Therapeutic Research-clinical and Experimental","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0011393X24000122","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
Immunogenicity and Potential for Intraocular Inflammation of Intravitreal Anti-VEGF Drugs
Background
Concerns of intraocular inflammation associated with intravitreal administration of anti-VEGF drugs have been risen and the exact mechanism is not yet elucidated.
Objective
To explore the relationship between immunogenicity and intraocular inflammation in intravitreal anti-VEGF drugs.
Methods
This review examines the immunogenicity of individual intravitreal anti-VEGF drugs and their potential link to intraocular inflammation.
Results
We suggest that the main cause of intraocular inflammation is the presence of pre-existing and treatment-induced antidrug antibodies, along with considerations related to the molecular structure, which includes the drug's format and size.
Conclusions
Researchers and clinicians involved in the advancement of new anti-VEGF drugs should take into consideration the factors related to intraocular inflammation that have been discussed.
期刊介绍:
We also encourage the submission of manuscripts presenting preclinical and very preliminary research that may stimulate further investigation of potentially relevant findings, as well as in-depth review articles on specific therapies or disease states, and applied health delivery or pharmacoeconomics.
CTR encourages and supports the submission of manuscripts describing:
• Interventions designed to understand or improve human health, disease treatment or disease prevention;
• Studies that focus on problems that are uncommon in resource-rich countries;
• Research that is "under-published" because of limited access to monetary resources such as English language support and Open Access fees (CTR offers deeply discounted English language editing);
• Republication of articles previously published in non-English journals (eg, evidence-based guidelines) which could be useful if translated into English;
• Preclinical and clinical product development studies that are not pursued for further investigation based upon early phase results.