Literature DB >> 19464533

The mast cell activator compound 48/80 is safe and effective when used as an adjuvant for intradermal immunization with Bacillus anthracis protective antigen.

Afton L McGowen1, Laura P Hale, Christopher P Shelburne, Soman N Abraham, Herman F Staats.   

Abstract

We evaluated the safety and efficacy of the mast cell activator compound 48/80 (C48/80) when used as an adjuvant delivered intradermally (ID) with recombinant anthrax protective antigen (rPA) in comparison with two well-known adjuvants. Mice were vaccinated in the ear pinnae with rPA or rPA+C48/80, CpG oligodeoxynucleotides (CpG), or cholera toxin (CT). All adjuvants induced similar increases in serum anti-rPA IgG and lethal toxin neutralizing antibodies. C48/80 induced a balanced cytokine production (Th1/Th2/Th17) by antigen-restimulated splenocytes, minimal injection site inflammation, and no antigen-specific IgE. Histological analysis demonstrated that vaccination with C48/80 reduced the number of resident mast cells and induced an injection site neutrophil influx within 24h. Our data demonstrate that C48/80 is a safe and effective adjuvant, when used by the intradermal route, to induce protective antibody and balanced Th1/Th2/Th17 responses.

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Year:  2009        PMID: 19464533      PMCID: PMC2743390          DOI: 10.1016/j.vaccine.2009.03.069

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  72 in total

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4.  Early recruitment of neutrophils determines subsequent T1/T2 host responses in a murine model of Legionella pneumophila pneumonia.

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5.  Role of mast cell leukotrienes in neutrophil recruitment and bacterial clearance in infectious peritonitis.

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  30 in total

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Review 2.  Inducing Mucosal IgA: A Challenge for Vaccine Adjuvants and Delivery Systems.

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Review 3.  Mast cell plasticity and sphingosine-1-phosphate in immunity, inflammation and cancer.

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Journal:  Mol Immunol       Date:  2014-04-22       Impact factor: 4.407

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5.  Sublingual targeting of STING with 3'3'-cGAMP promotes systemic and mucosal immunity against anthrax toxins.

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Journal:  Vaccine       Date:  2017-03-24       Impact factor: 3.641

Review 6.  Plasticity in mast cell responses during bacterial infections.

Authors:  Cheryl Y Chan; Ashley L St John; Soman N Abraham
Journal:  Curr Opin Microbiol       Date:  2011-11-04       Impact factor: 7.934

7.  Maximal adjuvant activity of nasally delivered IL-1α requires adjuvant-responsive CD11c(+) cells and does not correlate with adjuvant-induced in vivo cytokine production.

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Review 8.  Roles of Mas-related G protein-coupled receptor X2 on mast cell-mediated host defense, pseudoallergic drug reactions, and chronic inflammatory diseases.

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10.  A comparison of non-toxin vaccine adjuvants for their ability to enhance the immunogenicity of nasally-administered anthrax recombinant protective antigen.

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Journal:  Vaccine       Date:  2013-01-23       Impact factor: 3.641

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