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The development of vaccines against SARS corona virus in mice and SCID-PBL/hu mice.

Identifieur interne : 000D62 ( PubMed/Corpus ); précédent : 000D61; suivant : 000D63

The development of vaccines against SARS corona virus in mice and SCID-PBL/hu mice.

Auteurs : Masaji Okada ; Yuji Takemoto ; Yoshinobu Okuno ; Satomi Hashimoto ; Shigeto Yoshida ; Yukari Fukunaga ; Takao Tanaka ; Yoko Kita ; Sachiko Kuwayama ; Yumiko Muraki ; Noriko Kanamaru ; Hiroko Takai ; Chika Okada ; Yayoi Sakaguchi ; Izumi Furukawa ; Kyoko Yamada ; Makoto Matsumoto ; Tetsuo Kase ; Daphne E. Demello ; J S M. Peiris ; Pei-Jer Chen ; Naoki Yamamoto ; Yoshiyuki Yoshinaka ; Tatsuji Nomura ; Isao Ishida ; Shigeru Morikawa ; Masato Tashiro ; Mitsunori Sakatani

Source :

RBID : pubmed:15755609

English descriptors

Abstract

We have investigated to develop novel vaccines against SARS CoV using cDNA constructs encoding the structural antigen; spike protein (S), membrane protein (M), envelope protein (E), or nucleocapsid (N) protein, derived from SARS CoV. Mice vaccinated with SARS-N or -M DNA using pcDNA 3.1(+) plasmid vector showed T cell immune responses (CTL induction and proliferation) against N or M protein, respectively. CTL responses were also detected to SARS DNA-transfected type II alveolar epithelial cells (T7 cell clone), which are thought to be initial target cells for SARS virus infection in human. To determine whether these DNA vaccines could induce T cell immune responses in humans as well as in mice, SCID-PBL/hu mice was immunized with these DNA vaccines. As expected, virus-specific CTL responses and T cell proliferation were induced from human T cells. SARS-N and SARS-M DNA vaccines and SCID-PBL/hu mouse model will be important in the development of protective vaccines.

DOI: 10.1016/j.vaccine.2005.01.036
PubMed: 15755609

Links to Exploration step

pubmed:15755609

Le document en format XML

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<div type="abstract" xml:lang="en">We have investigated to develop novel vaccines against SARS CoV using cDNA constructs encoding the structural antigen; spike protein (S), membrane protein (M), envelope protein (E), or nucleocapsid (N) protein, derived from SARS CoV. Mice vaccinated with SARS-N or -M DNA using pcDNA 3.1(+) plasmid vector showed T cell immune responses (CTL induction and proliferation) against N or M protein, respectively. CTL responses were also detected to SARS DNA-transfected type II alveolar epithelial cells (T7 cell clone), which are thought to be initial target cells for SARS virus infection in human. To determine whether these DNA vaccines could induce T cell immune responses in humans as well as in mice, SCID-PBL/hu mice was immunized with these DNA vaccines. As expected, virus-specific CTL responses and T cell proliferation were induced from human T cells. SARS-N and SARS-M DNA vaccines and SCID-PBL/hu mouse model will be important in the development of protective vaccines.</div>
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