Literature DB >> 17996683

Intranasal administration of CpG oligonucleotides induces mucosal and systemic Type 1 immune responses and adjuvant activity to porcine reproductive and respiratory syndrome killed virus vaccine in piglets in vivo.

Linghua Zhang1, Xingshan Tian, Fengzhen Zhou.   

Abstract

Oligonucleotides containing CpG motifs (CpG ODN) are strong adjuvants for immune responses, particularly in mice. Recently, it has been showed that CpG ODN is a promising mucosal adjuvant in mice, but data on mucosal immune responses induced by CpG ODN in piglets are scarce. We have previously demonstrated that CpG ODN is a potent adjuvant to pseudorabies attenuated virus (PRV) vaccine when administered subcutaneously (SC) in newborn piglets. Herein, we evaluated intranasal (IN) delivery of CpG ODN with porcine reproductive and respiratory syndrome (PRRS) killed virus vaccine (PRRSV) to determine its potential as a mucosal adjuvant to a commercial vaccine. CpG ODN augmented systemic (IgG in serum, Peripheral blood mononuclear cells (PBMC) proliferation) and mucosal (IgA in feces, nasal and oral secretions) immune responses against antigen. CpG ODN stimulated both T-helper type1 (Type 1) (IgG2) and Type 2 (IgA) responses when delivered intranasally. Results from this study indicate that stimulatory CpG ODN may be effective as a mucosal adjuvant with commercial vaccine in husbandry animals.

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Year:  2007        PMID: 17996683     DOI: 10.1016/j.intimp.2007.09.012

Source DB:  PubMed          Journal:  Int Immunopharmacol        ISSN: 1567-5769            Impact factor:   4.932


  7 in total

1.  An innovative approach to induce cross-protective immunity against porcine reproductive and respiratory syndrome virus in the lungs of pigs through adjuvanted nanotechnology-based vaccination.

Authors:  Basavaraj Binjawadagi; Varun Dwivedi; Cordelia Manickam; Kang Ouyang; Jordi B Torrelles; Gourapura J Renukaradhya
Journal:  Int J Nanomedicine       Date:  2014-03-24

2.  Assessment of the efficacy of two novel DNA vaccine formulations against highly pathogenic Porcine Reproductive and Respiratory Syndrome Virus.

Authors:  Luping Du; Fengjiao Pang; Zhengyu Yu; Xiangwei Xu; Baochao Fan; Kehe Huang; Kongwang He; Bin Li
Journal:  Sci Rep       Date:  2017-02-03       Impact factor: 4.379

3.  Adjuvanted poly(lactic-co-glycolic) acid nanoparticle-entrapped inactivated porcine reproductive and respiratory syndrome virus vaccine elicits cross-protective immune response in pigs.

Authors:  Basavaraj Binjawadagi; Varun Dwivedi; Cordelia Manickam; Kang Ouyang; Yun Wu; Ly James Lee; Jordi B Torrelles; Gourapura J Renukaradhya
Journal:  Int J Nanomedicine       Date:  2014-01-24

4.  Entrapment of H1N1 Influenza Virus Derived Conserved Peptides in PLGA Nanoparticles Enhances T Cell Response and Vaccine Efficacy in Pigs.

Authors:  Jagadish Hiremath; Kyung-il Kang; Ming Xia; Mohamed Elaish; Basavaraj Binjawadagi; Kang Ouyang; Santosh Dhakal; Jesus Arcos; Jordi B Torrelles; X Jiang; Chang Won Lee; Gourapura J Renukaradhya
Journal:  PLoS One       Date:  2016-04-19       Impact factor: 3.240

5.  Chitosan-DNA nanoparticles enhanced the immunogenicity of multivalent DNA vaccination on mice against Trueperella pyogenes infection.

Authors:  Ting Huang; Xuhao Song; Jie Jing; Kelei Zhao; Yongmei Shen; Xiuyue Zhang; Bisong Yue
Journal:  J Nanobiotechnology       Date:  2018-01-29       Impact factor: 10.435

Review 6.  Evidence for a common mucosal immune system in the pig.

Authors:  Heather L Wilson; Milan R Obradovic
Journal:  Mol Immunol       Date:  2014-09-18       Impact factor: 4.407

7.  CpG DNA facilitate the inactivated transmissible gastroenteritis virus in enhancing the local and systemic immune response of pigs via oral administration.

Authors:  Jian Lin; Chongzhi Tu; Chunxiao Mou; Xiaojuan Chen; Qian Yang
Journal:  Vet Immunol Immunopathol       Date:  2016-02-20       Impact factor: 2.046

  7 in total

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