Enhanced immune response induced by a potential influenza A vaccine based on branched M2e polypeptides linked to tuftsin (Q45076219)

9 December 2017

Enhanced immune response induced by a potential influenza A vaccine based on branched M2e polypeptides linked to tuftsin (English)

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9 December 2017

Xiaoyu Liu

1

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9 December 2017

Jianqiang Guo

2

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9 December 2017

Su Han

3

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9 December 2017

Lihong Yao

4

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9 December 2017

Aijun Chen

5

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9 December 2017

Qi Yang

6

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9 December 2017

Hong Bo

7

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9 December 2017

Pengwei Xu

8

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9 December 2017

Jiyong Yin

9

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9 December 2017

Zhiqing Zhang

10

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9 December 2017

language of work or name

English

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publication date

7 September 2012

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9 December 2017

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9 December 2017

30

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9 December 2017

46

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9 December 2017

6527-6533

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Influenza vaccines: from surveillance through production to protection.

9 December 2017

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Conserved epitopes of influenza A virus inducing protective immunity and their prospects for universal vaccine development

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Influenza A viruses: why focusing on M2e-based universal vaccines

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Protection against H1, H5, H6 and H9 influenza A infection with liposomal matrix 2 epitope vaccines.

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The epitope recognized by a monoclonal antibody in influenza A virus M2 protein is immunogenic and confers immune protection.

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Influenza A vaccine based on the extracellular domain of M2: weak protection mediated via antibody-dependent NK cell activity.

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Scientific barriers to developing vaccines against avian influenza viruses.

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Characterization of immunity induced by M2e of influenza virus

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An influenza A vaccine based on tetrameric ectodomain of matrix protein 2.

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Universal M2 ectodomain-based influenza A vaccines: preclinical and clinical developments.

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Universal influenza A M2e-HBc vaccine protects against disease even in the presence of pre-existing anti-HBc antibodies.

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Matrix protein 2 vaccination and protection against influenza viruses, including subtype H5N1

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Preclinical study of influenza virus A M2 peptide conjugate vaccines in mice, ferrets, and rhesus monkeys

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Potent immunogenicity and efficacy of a universal influenza vaccine candidate comprising a recombinant fusion protein linking influenza M2e to the TLR5 ligand flagellin

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High epitope density in a single recombinant protein molecule of the extracellular domain of influenza A virus M2 protein significantly enhances protective immunity

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Synthetic peptide vaccine design: synthesis and properties of a high-density multiple antigenic peptide system

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Cellular antitumor immune response to a branched lysine multiple antigenic peptide containing epitopes of a common tumor-specific antigen in a rat glioma model

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A strategy for eliciting antibodies against cryptic, conserved, conformationally dependent epitopes of HIV envelope glycoprotein

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An M2e-based multiple antigenic peptide vaccine protects mice from lethal challenge with divergent H5N1 influenza viruses.

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Synthesis and immunological activity of a branched peptide carrying the T-cell epitope of gp43, the major exocellular antigen of Paracoccidioides brasiliensis

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Induction of influenza type A virus-specific resistance by immunization of mice with a synthetic multiple antigenic peptide vaccine that contains ectodomains of matrix protein 2.

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Increase in the immunogenicity of HIV peptide antigens by chemical linkage to polytuftsin (TKPR40)

7 January 2021

1 reference

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Synthesis, conformation, and immunoreactivity of new carrier molecules based on repeated tuftsin-like sequence.

7 January 2021

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Influenza A virus infection engenders a poor antibody response against the ectodomain of matrix protein 2.

7 January 2021

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Therapeutic potential of a fully human monoclonal antibody against influenza A virus M2 protein

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Universal vaccine based on ectodomain of matrix protein 2 of influenza A: Fc receptors and alveolar macrophages mediate protection.

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CD4 T cell responses to influenza infection

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Influenza A virus M2 protein: monoclonal antibody restriction of virus growth and detection of M2 in virions

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inferred from DOI database lookup

7 January 2021

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Identifiers

DOI

10.1016/J.VACCINE.2012.08.054

1 reference

9 December 2017

1 reference