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Protective immune responses in mice induced by intramuscular and intranasal immunization with a Mycoplasma pneumoniae P1C DNA vaccine

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成果类型:
期刊论文
作者:
Zhu, Cuiming;Wu, Yimou;Chen, Sufang;Yu, Minjun;Zeng, Yanhua;...
通讯作者:
Wang, Shiping
作者机构:
[Wang, Shiping; Zhu, Cuiming] Cent S Univ, Xiangya Sch Med, Changsha 410078, Hunan, Peoples R China.
[Wu, Yimou; Xiao, Jinhong; Yu, Minjun; You, Xiaoxing; Zeng, Yanhua; Chen, Sufang] Univ S China, Dept Microbiol & Immunol, Hengyang 421001, Peoples R China.
通讯机构:
[Wang, Shiping] C
Cent S Univ, Xiangya Sch Med, Changsha 410078, Hunan, Peoples R China.
语种:
英文
关键词:
Mycoplasma pneumoniae;P1 adhesin protein carboxy terminal region;DNA vaccine;immune response;Mycoplasma pneumoniae;région carboxy terminale de l’adhésine P1;vaccin à ADN;réponse immune
期刊:
CANADIAN JOURNAL OF MICROBIOLOGY
ISSN:
0008-4166
年:
2012
卷:
58
期:
5
页码:
644-652
基金类别:
Innovation Team Foundation of Hunan Province [2010-212]; Research Foundation of Education Bureau of Hunan Province, China [09B088]
机构署名:
本校为其他机构
院系归属:
医学院
摘要:
Mycoplasma pneumoniae is an important causative agent of atypical pneumonia. This study was to determine the ability of a DNA expression vector, which encodes the carboxy terminal region of the M. pneumoniae P1 protein (P1C), to induce humoral and cellular immune responses and to protect against M. pneumoniae infection in BALB/c mice. Mice were immunized with pcDNA3.1/P1C by either intramuscular injection (i.m.) or intranasal inoculation (i.n.). Our results showed that p1c DNA immunization generates detectable antibodies specific to M. pneumoni...

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