دورية أكاديمية

Broad protective immune responses elicited by bacterium-like particle-based intranasal pneumococcal particle vaccine displaying PspA2 and PspA4 fragments

التفاصيل البيبلوغرافية
العنوان: Broad protective immune responses elicited by bacterium-like particle-based intranasal pneumococcal particle vaccine displaying PspA2 and PspA4 fragments
المؤلفون: Jingcai Lu, Jieshi Guo, Dandan Wang, Jinfei Yu, Tiejun Gu, Chunlai Jiang, Wei Kong, Yongge Wu
المصدر: Human Vaccines & Immunotherapeutics, Vol 15, Iss 2, Pp 371-380 (2019)
بيانات النشر: Taylor & Francis Group, 2019.
سنة النشر: 2019
المجموعة: LCC:Immunologic diseases. Allergy
LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: pneumococcal surface protein a (pspa), bacterium-like particles (blp), s. pneumoniae, intranasal vaccine, Immunologic diseases. Allergy, RC581-607, Therapeutics. Pharmacology, RM1-950
الوصف: Streptococcus pneumoniae is an infectious pathogen mainly infecting host bodies through the respiratory system. An effective pneumococcal vaccine would be targeted to the mucosa and provide not only protection against invasive infection but also against colonization in the respiratory system. In the present work, we applied bacterium-like particles (BLPs) as an adjuvant for the development of a PspA mucosal vaccine, in which the PspA protein was displayed on the surface of BLPs. Intranasal immunization with the PspA-BLP pneumococcal vaccine, comprised of PspA2 from pneumococcal family 1 and PspA4 from pneumococcal family 2, not only induced a high level of serum IgG antibodies but also a high level of mucosal SIgA antibodies. Analysis of binding of serum antibodies to intact bacteria showed a broad coverage of binding to pneumococcal strains expressing PspA from clade 1 to 5. Immunization with the PspA-BLP vaccine conferred protection against fatal intranasal challenge with both PspA family 1 and family 2 pneumococcal strains regardless of serotype. Therefore, the PspA-BLP pneumococcal vaccine was demonstrated to be a promising strategy for mucosal immunization to enhance both systemic and mucosal immune responses.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2164-5515
2164-554X
21645515
Relation: https://doaj.org/toc/2164-5515; https://doaj.org/toc/2164-554X
DOI: 10.1080/21645515.2018.1526556
URL الوصول: https://doaj.org/article/dd4974adf44d4bfa8babfa5474966862
رقم الأكسشن: edsdoj.4974adf44d4bfa8babfa5474966862
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21645515
2164554X
DOI:10.1080/21645515.2018.1526556