Vaccines for invasive fungal infections.

F1000 medicine reports Pub Date : 2011-01-01 Epub Date: 2011-07-01 DOI:10.3410/M3-13
Brad Spellberg
{"title":"Vaccines for invasive fungal infections.","authors":"Brad Spellberg","doi":"10.3410/M3-13","DOIUrl":null,"url":null,"abstract":"<p><p>Morbidity and mortality from invasive fungal infections remain unacceptably high despite availability of new antifungal agents, underscoring the need for more effective preventative strategies. Due to our enhanced understanding of the host defense and pathogenetic mechanisms that lead to invasive fungal infections, it should be feasible to develop vaccines targeting these infections. A common immunological theme across many vaccine candidates for invasive fungal infections has been the need to activate a cell-based, pro-inflammatory, Th1 or Th17 immune response to improve phagocytic killing of the fungi. Since neutralization of virulence factor functions has not been required for many active vaccines to function, the antigenic repertoire available for testing should not be limited to virulence factors. With expansion of our fundamental understanding of the immunology of fungal infections, the biggest barrier to development of fungal vaccines is the lack of available capital to translate discoveries made at the bench into biological agents used at the bedside. Continued education on the importance and feasibility of vaccination for such infections, combined with continued development of vaccine antigens and adjuvants, is necessary.</p>","PeriodicalId":88480,"journal":{"name":"F1000 medicine reports","volume":"3 ","pages":"13"},"PeriodicalIF":0.0000,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/df/77/medrep-03-13.PMC3155210.pdf","citationCount":"33","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"F1000 medicine reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3410/M3-13","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2011/7/1 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 33

Abstract

Morbidity and mortality from invasive fungal infections remain unacceptably high despite availability of new antifungal agents, underscoring the need for more effective preventative strategies. Due to our enhanced understanding of the host defense and pathogenetic mechanisms that lead to invasive fungal infections, it should be feasible to develop vaccines targeting these infections. A common immunological theme across many vaccine candidates for invasive fungal infections has been the need to activate a cell-based, pro-inflammatory, Th1 or Th17 immune response to improve phagocytic killing of the fungi. Since neutralization of virulence factor functions has not been required for many active vaccines to function, the antigenic repertoire available for testing should not be limited to virulence factors. With expansion of our fundamental understanding of the immunology of fungal infections, the biggest barrier to development of fungal vaccines is the lack of available capital to translate discoveries made at the bench into biological agents used at the bedside. Continued education on the importance and feasibility of vaccination for such infections, combined with continued development of vaccine antigens and adjuvants, is necessary.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
侵袭性真菌感染的疫苗。
尽管有新的抗真菌药物可用,侵袭性真菌感染的发病率和死亡率仍然高得令人无法接受,强调需要更有效的预防策略。由于我们对导致侵袭性真菌感染的宿主防御和致病机制的理解增强,开发针对这些感染的疫苗应该是可行的。在侵袭性真菌感染的许多候选疫苗中,一个共同的免疫学主题是需要激活基于细胞的、促炎的、Th1或Th17免疫反应,以改善真菌的吞噬杀伤。由于许多活疫苗并不需要毒力因子功能的中和,因此可供检测的抗原库不应局限于毒力因子。随着我们对真菌感染免疫学的基本理解的扩大,真菌疫苗开发的最大障碍是缺乏可用的资金来将实验室的发现转化为床边使用的生物制剂。有必要继续开展关于此类感染接种疫苗的重要性和可行性的教育,同时继续开发疫苗抗原和佐剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Cannabis and psychosis: what causes what? Stronger evidence is needed before accepting that cannabis plays an important role in the aetiology of schizophrenia in the population. Advances in lens implant technology. Polyclonal free light chains: a biomarker of inflammatory disease or treatment target? CORRIGENDUM TO: Neuromodulation for treatment-resistant depression
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1