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Dvelopment of novel adjuvant which constructed by DNA origami technology

Dvelopment of novel adjuvant which constructed by DNA origami technology
DNA折纸技术构建的新型佐剂的研制
批准号:
24659836
负责人:
TERAO Yutaka
金额:
$2.41万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Challenging Exploratory Research
财政年份:
2012
资助国家:
日本
项目状态:
已结题
起止时间:
2012-04-01 至 2014-03-31

项目摘要

项目成果

TERAO Yutaka的其他基金

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中文摘要
翻译
近年来,病原微生物获得了耐药性,并在世界范围内蔓延。抗生素在世纪被认为是治疗感染性疾病的“灵丹妙药”,然而抗生素的大量使用导致了耐药微生物的出现。因此,在发展中国家,用基本抗生素治疗大多数婴儿腹泻变得困难。目前,在基础研究的基础上,开发和完善肠源性和全身性免疫激活剂具有重要意义。在这个提议中,我们专注于DNA序列中的CpG基序。CpG基序在病原微生物的基因组中以高频率观察到。它作为一种免疫激活剂,促进抗原特异性免疫反应的产生。本研究以M13 DNA为载体,构建了将GpG基序固定在体外的“DNA折纸”免疫激活剂,旨在获得免疫增强效果。
英文摘要
Recently, pathogenic microorganisms acquired drug-resistance, and they are spreading throughout the world. Antibiotics were presented as "magic bullets" against infectious diseases in the 20th century, however, the heavy usage of antibiotics has led to the appearance of drug-resistant microorganisms. Thus, it has become difficult to treat most infantile diarrhea with basic antibiotics in the developing countries. Now, it is important to develop and improve the enteric and general immune activators on the basis of fundamental investigations. In this proposal, we focus on a CpG motif among the DNA sequence. The CpG motif is observed at high frequency in the genomes of pathogenic microorganisms. It works as an immune activator to boost production of antigen-specific immune responses. In this study, we constructed "DNA origami" immune activators being fixed the GpG motifs to the outside using M13 DNA, aiming to obtain the immunopotentiating effect.
期刊论文(60)
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会议论文
Long-term survival of salivary streptococci on dental devices made of EVA
唾液链球菌在 EVA 制成的牙科器械上长期存活
DOI: --
发表时间: 2012
期刊: Int J. Oral Science
影响因子: --
作者: [Ogawa, T., Yamasaki, S., Honda, M., Terao, Y., Kawabata, S., and Maeda, Y]
通讯作者: Y
Group A streptococcal cysteine proteases, SpeB and Sib35, cleave epithelial junctions
A 组链球菌半胱氨酸蛋白酶、SpeB 和 Sib35,裂解上皮连接
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [Tomoko Sumitomo, Miharu Higashino, Akari Kominami, Masanobu Nakata, Yutaka Terao, and Shigetada Kawabata]
通讯作者: and Shigetada Kawabata
Cysteine proteinase from Streptococcus pyogenes enables to evade innate immunity via degradation of complement factors.
化脓性链球菌的半胱氨酸蛋白酶能够通过降解补体因子来逃避先天免疫。
DOI: --
发表时间: 2013
期刊: Journal of Biological Chemistry
影响因子: 4.8
作者: [Honda-Ogawa M, Ogawa T, Terao Y, Sumitomo T, Nakata M, Ikebe K, Maeda Y, and Kawabata S.]
通讯作者: and Kawabata S.
新潟大学 大学院医歯学総合研究科 微生物感染症学分野
新泻大学医学齿科研究生院微生物感染科
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
39
    Global survey analysis of drug-resistant anti-biogram evolution pattern of MRSA
    • 批准号:
      26305034
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.32万
    • 财政年份:
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    • 负责人:
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    • 依托单位:
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    • 批准号:
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    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
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    • 财政年份:
      2014
    • 负责人:
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    • 依托单位:
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    • 批准号:
      21360437
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $4.58万
    • 财政年份:
      2009
    • 负责人:
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    • 依托单位:
    海外基金