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针对球孢子菌感染的基于T淋巴细胞表位的疫苗的合理设计

Rational Design of T Lymphocyte Epitope-Based Vaccines Against Coccidioides Infection.

作者信息

Hurtgen Brady J, Hung Chiung-Yu

机构信息

Department of Biology, University of Texas at San Antonio, One UTSA Circle, San Antonio, TX, 78249, USA.

Department of Microbiology and Immunology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.

出版信息

Methods Mol Biol. 2017;1625:45-64. doi: 10.1007/978-1-4939-7104-6_4.

Abstract

Coccidioidomycosis is a potentially life-threatening mycosis endemic to the Southwestern USA and some arid regions of Central and South America. A vaccine against Coccidioides infection would benefit over 30-million people who reside in or visit the endemic regions. Vaccine candidates against systemic fungal infections come in many forms. Live attenuated vaccines are derived from disease-causing pathogens and generally stimulate excellent protective immunity. Since attenuated vaccines contain living microbes, there is a degree of unpredictability raising concerns regarding safety and stability. Generation of a subunit vaccine has initiated efforts to design a safe reagent suitable for administration to humans at risk of coccidioidomycosis. Epitope-based vaccines allow for eliciting specific protective immune responses and removal of potentially detrimental sequences to improve safety. This chapter describes methods for the identification of T cell epitopes derived from Coccidioides antigens, design, and production of a recombinant vaccine containing multiple T cell epitopes, and evaluation of its protective efficacy and vaccine immunity against pulmonary Coccidioides infection using a strain of transgenic mice that express a human MHC II molecule.

摘要

球孢子菌病是一种潜在的危及生命的真菌病,在美国西南部以及中美洲和南美洲的一些干旱地区流行。一种针对球孢子菌感染的疫苗将使居住在或前往流行地区的3000多万人受益。针对全身性真菌感染的候选疫苗有多种形式。减毒活疫苗源自致病病原体,通常能激发良好的保护性免疫。由于减毒疫苗含有活微生物,存在一定程度的不可预测性,引发了对安全性和稳定性的担忧。亚单位疫苗的研发已着手设计一种适合给有球孢子菌病风险的人使用的安全试剂。基于表位的疫苗能够引发特异性保护性免疫反应,并去除潜在有害序列以提高安全性。本章描述了从球孢子菌抗原中鉴定T细胞表位的方法、含有多个T细胞表位的重组疫苗的设计和生产,以及使用表达人类MHC II分子的转基因小鼠品系评估其对肺部球孢子菌感染的保护效力和疫苗免疫性的方法。

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