dengue-1 envelope protein domain iii along with pelc and cpg oligodeoxynucleotides synergistically enhances immune responsesdengue-1包膜蛋白域三世pelc和cpg oligodeoxynucleotides协同增强免疫反应.pdfVIP
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dengue-1 envelope protein domain iii along with pelc and cpg oligodeoxynucleotides synergistically enhances immune responsesdengue-1包膜蛋白域三世pelc和cpg oligodeoxynucleotides协同增强免疫反应
Dengue-1 Envelope Protein Domain III along with PELC
and CpG Oligodeoxynucleotides Synergistically
Enhances Immune Responses
1. 1. 1 1 1
Chen-Yi Chiang , Ming-Hsi Huang , Chun-Hsiang Hsieh , Mei-Yu Chen , Hsueh-Hung Liu ,
1 1 1 1,2 1,2 1,2
Jy-Ping Tsai , Yi-Shiuan Li , Ching-Yun Chang , Shih-Jen Liu , Pele Chong , Chih-Hsiang Leng *,
Hsin-Wei Chen1,2*
1 National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Miaoli, Taiwan, 2 Graduate Institute of Immunology, China Medical
University, Taichung, Taiwan
Abstract
The major weaknesses of subunit vaccines are their low immunogenicity and poor efficacy. Adjuvants can help to overcome
some of these inherent defects with subunit vaccines. Here, we evaluated the efficacy of the newly developed water-in-oil-
in-water multiphase emulsion system, termed PELC, in potentiating the protective capacity of dengue-1 envelope protein
domain III. Unlike aluminum phosphate, dengue-1 envelope protein domain III formulated with PELC plus CpG
oligodeoxynucleotides induced neutralizing antibodies against dengue-1 virus and increased the splenocyte secretion of
IFN-c after in vitro re-stimulation. The induced antibodies contained both the IgG1 and IgG2a subclasses. A rapid
anamnestic neutralizing antibody response against a live dengue virus challenge was elicited at week 26 after the first
immunization. These results demonstrate
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