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爱泼斯坦-巴尔病毒相关癌症与自身免疫:探寻治疗方法

EBV-Associated Cancer and Autoimmunity: Searching for Therapies.

作者信息

Capone Giovanni, Fasano Candida, Lucchese Guglielmo, Calabrò Michele, Kanduc Darja

机构信息

Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari 70126, Italy.

Brain and Language Laboratory, Free University of Berlin, 14195 Berlin, Germany.

出版信息

Vaccines (Basel). 2015 Feb 5;3(1):74-89. doi: 10.3390/vaccines3010074.

Abstract

Epstein-Barr virus (EBV) infects B-, T-, and NK cells and has been associated not only with a wide range of lymphoid malignancies but also with autoimmune diseases such as lupus erythematosus, rheumatoid arthritis and, in particular, multiple sclerosis. Hence, effective immunotherapeutic approaches to eradicate EBV infection might overthrow cancer and autoimmunity incidence. However, currently no effective anti-EBV immunotherapy is available. Here we use the concept that protein immunogenicity is allocated in rare peptide sequences and search the Epstein-Barr nuclear antigen 1 (EBNA1) sequence for peptides unique to the viral protein and absent in the human host. We report on a set of unique EBV EBNA1 peptides that might be used in designing peptide-based therapies able to specifically hitting the virus or neutralizing pathogenic autoantibodies.

摘要

爱泼斯坦-巴尔病毒(EBV)感染B细胞、T细胞和自然杀伤细胞(NK细胞),不仅与多种淋巴系统恶性肿瘤有关,还与自身免疫性疾病相关,如红斑狼疮、类风湿性关节炎,尤其是多发性硬化症。因此,根除EBV感染的有效免疫治疗方法可能会降低癌症和自身免疫性疾病的发病率。然而,目前尚无有效的抗EBV免疫疗法。在此,我们运用蛋白质免疫原性存在于稀有肽序列中的概念,在爱泼斯坦-巴尔核抗原1(EBNA1)序列中寻找病毒蛋白特有的、在人类宿主中不存在的肽段。我们报告了一组独特的EBV EBNA1肽段,这些肽段可用于设计基于肽的疗法,能够特异性地靶向该病毒或中和致病性自身抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/928e/4494242/71049db09c8c/vaccines-03-00074-g001.jpg

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