Retinal Degenerative Diseases XIX: Mechanisms and Experimental Therapy

Ash, John D., Pierce, Eric, Anderson, Robert E.

  • 出版商: Springer
  • 出版日期: 2024-07-15
  • 售價: $15,220
  • 貴賓價: 9.5$14,459
  • 語言: 英文
  • 頁數: 588
  • 裝訂: Quality Paper - also called trade paper
  • ISBN: 3031276833
  • ISBN-13: 9783031276835
  • 海外代購書籍(需單獨結帳)

商品描述

This book contains the proceedings of the XVIII International Symposium on Retinal Degeneration (RD2018). A majority of those who spoke and presented posters at the meeting contributed to this volume. The blinding diseases of inherited retinal degenerations have no treatments, and age-related macular degeneration has no cures, despite the fact that it is an epidemic among the elderly, with 1 in 3-4 affected by the age of 70. The RD Symposium focused on the exciting new developments aimed at understanding these diseases and providing therapies for them. Since most major scientists in the field of retinal degenerations attend the biennial RD Symposia, they are known by most as the "best" and "most important" meetings in the field.

The volume presents representative state-of-the-art research in almost all areas of retinal degenerations, ranging from cytopathologic, physiologic, diagnostic and clinical aspects; animal models; mechanisms of cell death; candidate genes, cloning, mapping and other aspects of molecular genetics; and developing potential therapeutic measures such as gene therapy and neuroprotective agents for potential pharmaceutical therapy.

While advances in these areas of retinal degenerations were described, there will be many new topics that either are in their infancy or did not exist at the time of the last RD Symposium. These include the role of inflammation and immunity, as well as other basic mechanisms, in age-related macular degeneration, several new aspects of gene therapy, and revolutionary new imaging and functional testing that will have a huge impact on the diagnosis and following the course of retinal degenerations, as well as to provide new quantitative endpoints for clinical trials.

The retina is an approachable part of the central nervous system (CNS), and there is a major interest in neuroprotective and gene therapy for CNS diseases and neurodegenerations, in general. It should be noted that withsuccessful and exciting initial clinical trials in neuroprotective and gene therapy, including the restoration of sight in blind children, the retinal degeneration therapies are leading the way towards new therapeutic measures for neurodegenerations of the CNS. Many of the successes recently reported in these areas of retinal degeneration sprang from collaborations established at previous RD Symposia, and many of those were reported at the RD2016 meeting and included in the current volume. We anticipate the excitement of those working in the field and those afflicted with retinal degenerations is reflected in the volume.

商品描述(中文翻譯)

本書包含第十八屆國際視網膜退化症研討會(RD2018)的會議紀錄。大多數在會議上發言和展示海報的人士均對本書作出了貢獻。遺傳性視網膜退化症的致盲疾病目前尚無治療方法,而年齡相關性黃斑變性則沒有治癒辦法,儘管這在老年人中已成為流行病,70歲時約有1/3至1/4的人受到影響。RD研討會專注於旨在理解這些疾病並提供治療的新進展。由於大多數視網膜退化症領域的主要科學家參加每兩年舉行一次的RD研討會,因此這些會議被大多數人認為是該領域“最佳”和“最重要”的會議。

本書呈現了幾乎所有視網膜退化症領域的代表性尖端研究,涵蓋了細胞病理學、生理學、診斷和臨床方面;動物模型;細胞死亡機制;候選基因、克隆、定位及其他分子遺傳學方面;以及開發潛在治療措施,如基因治療和神經保護劑,以用於潛在的藥物治療。

雖然這些視網膜退化症領域的進展已被描述,但仍有許多新主題要麼處於起步階段,要麼在上次RD研討會時並不存在。這些主題包括炎症和免疫的作用,以及其他基本機制在年齡相關性黃斑變性中的角色,幾個基因治療的新方面,以及革命性的成像和功能測試,這將對視網膜退化症的診斷和病程追蹤產生巨大影響,並為臨床試驗提供新的定量終點。

視網膜是中樞神經系統(CNS)中一個可接觸的部分,對於CNS疾病和神經退化症的神經保護和基因治療有著極大的興趣。值得注意的是,隨著神經保護和基因治療的成功和令人興奮的初步臨床試驗,包括恢復盲童視力,視網膜退化症的治療正在引領CNS神經退化症的新療法。最近在這些視網膜退化症領域報告的許多成功案例源於之前RD研討會上建立的合作關係,其中許多在RD2016會議上報告並納入本書。我們預期在該領域工作的研究人員和受到視網膜退化症影響的患者的興奮感會在本書中有所體現。