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  1. 福島医学会
  2. Fukushima Journal of Medical Science
  3. Vol.62 (2016)

Protection from lethal herpes simplex virus type 1 infection by vaccination with a UL41-deficient recombinant strain

https://fmu.repo.nii.ac.jp/records/2001912
https://fmu.repo.nii.ac.jp/records/2001912
f620cd90-2848-445c-88c1-15c40725fcb6
名前 / ファイル ライセンス アクション
FksmJMedSci_62_p36.pdf FksmJMedSci_62_p36.pdf (386.3 KB)
Item type デフォルトアイテムタイプ(フル)fmu(1)
公開日 2016-07-06
タイトル
タイトル Protection from lethal herpes simplex virus type 1 infection by vaccination with a UL41-deficient recombinant strain
言語 en
作成者 Koshizuka, Tetsuo

× Koshizuka, Tetsuo

en Koshizuka, Tetsuo

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Ishioka, Ken

× Ishioka, Ken

en Ishioka, Ken

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Kobayashi, Takahiro

× Kobayashi, Takahiro

en Kobayashi, Takahiro

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Ikuta, Kazufumi

× Ikuta, Kazufumi

en Ikuta, Kazufumi

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Suzutani, Tatsuo

× Suzutani, Tatsuo

en Suzutani, Tatsuo

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権利情報
権利情報 © 2016 The Fukushima Society of Medical Science
内容記述
内容記述タイプ Abstract
内容記述 The UL41 gene of herpes simplex virus type 1 (HSV-1) encodes a virion host shut off protein which is involved in immune evasion. The growth and virulence of HSV-1 is markedly reduced by the deletion of UL41. In this report, the UL41-deleted recombinant HSV-1 strain VR∆41 was evaluated as a prophylactic live attenuated vaccine against lethal HSV-1 infection in a mouse model. Intraperitoneal (i.p.) inoculation with the VR∆41 strain clearly inhibited lethal wild-type HSV-1 (VR-3 strain) infection after both i.p. and intracerebral (i.c.) inoculations. Vaccination with the VR∆41 strain was safer than VR-3 vaccination and was able to protect against a wild-type challenge to the same degree as VR-3 vaccination. In contrast, i.p. inoculation with ultraviolet-irradiated VR-3 induced resistance against i.p. infection, but not against i.c. Although replication of the VR∆41 strain in mice was greatly reduced compared to that of the VR-3 strain, VR∆41 strain maintained the ability to spread to the central nervous system (CNS) from a peripheral inoculation site. These results indicated that the VR∆41 strain evoked a potent immune reaction through viral protein expression within CNS without the induction of lethal encephalitis. The entry of antigens into the CNS was essential for the establishment of protective immunity against the lethal HSV encephalitis. We concluded that only a live attenuated vaccine is able to afford a prophylactic effect against CNS infection with HSV. In order to fulfill this requirement, UL41-deleted viruses provide a strong candidate for use as a recombinant live vaccine.
出版者
出版者 The Fukushima Society of Medical Science
言語
言語 eng
書誌情報 en : Fukushima Journal of Medical Science

巻 62, 号 1, p. 36-42, 発行日 2016
関連情報
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.5387/fms.2015-24
関連情報
識別子タイプ PMID
関連識別子 26983589
関連情報
識別子タイプ ICHUSHI
関連識別子 2017326463
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 0016-2590
収録物識別子
収録物識別子タイプ EISSN
収録物識別子 2185-4610
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA0065246X
主題
主題Scheme Other
主題 herpes simplex virus
主題
主題Scheme Other
主題 UL41 gene
主題
主題Scheme Other
主題 vaccine
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