Literature DB >> 18640167

c-di-GMP is an effective immunomodulator and vaccine adjuvant against pneumococcal infection.

Abiodun D Ogunniyi1, James C Paton, Alun C Kirby, Jonathan A McCullers, Jan Cook, Mamoru Hyodo, Yoshihiro Hayakawa, David K R Karaolis.   

Abstract

Cyclic diguanylate (c-di-GMP) is a unique bacterial intracellular signaling molecule capable of stimulating enhanced protective innate immunity against various bacterial infections. The effects of intranasal pretreatment with c-di-GMP, or intraperitoneal coadministration of c-di-GMP with the pneumolysin toxoid (PdB) or pneumococcal surface protein A (PspA) before pneumococcal challenge, were investigated in mice. We found that c-di-GMP had no significant direct short-term effect on the growth rate of Streptococcus pneumoniae either in vitro or in vivo. However, intranasal pretreatment of mice with c-di-GMP resulted in a significant decrease in bacterial load in lungs and blood after serotypes 2 and 3 challenge, and a significant decrease in lung titers after serotype 4 challenge. Potential cellular mediators of these enhanced protective responses were identified in lungs and draining lymph nodes. Intraperitoneal coadministration of c-di-GMP with PdB or PspA before challenge resulted in significantly higher antigen-specific antibody titers and increased survival of mice, compared to that obtained with alum adjuvant. These findings demonstrate that local or systemic c-di-GMP administration stimulates innate and adaptive immunity against invasive pneumococcal disease. We propose that c-di-GMP can be used as an effective broad spectrum immunomodulator and vaccine adjuvant to prevent infectious diseases.

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Year:  2008        PMID: 18640167      PMCID: PMC2647696          DOI: 10.1016/j.vaccine.2008.06.099

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


  48 in total

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2.  Host cellular immune response to pneumococcal lung infection in mice.

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Authors:  O T Avery; C M Macleod; M McCarty
Journal:  J Exp Med       Date:  1944-02-01       Impact factor: 14.307

4.  Pneumococcal surface protein A (PspA) is effective at eliciting T cell-mediated responses during invasive pneumococcal disease in adults.

Authors:  L Baril; J Dietemann; M Essevaz-Roulet; L Béniguel; P Coan; D E Briles; B Guy; G Cozon
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5.  Complete genome sequence of a virulent isolate of Streptococcus pneumoniae.

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6.  Autolysis and autoaggregation in Pseudomonas aeruginosa colony morphology mutants.

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Journal:  J Bacteriol       Date:  2002-12       Impact factor: 3.490

7.  Low CD4 T cell immunity to pneumolysin is associated with nasopharyngeal carriage of pneumococci in children.

Authors:  Qibo Zhang; Linda Bagrade; Jolanta Bernatoniene; Ed Clarke; James C Paton; Tim J Mitchell; Desmond A Nunez; Adam Finn
Journal:  J Infect Dis       Date:  2007-03-06       Impact factor: 5.226

8.  Immunization of healthy adults with a single recombinant pneumococcal surface protein A (PspA) variant stimulates broadly cross-reactive antibodies to heterologous PspA molecules.

Authors:  G S Nabors; P A Braun; D J Herrmann; M L Heise; D J Pyle; S Gravenstein; M Schilling; L M Ferguson; S K Hollingshead; D E Briles; R S Becker
Journal:  Vaccine       Date:  2000-03-06       Impact factor: 3.641

9.  Cyclic di-GMP stimulates protective innate immunity in bacterial pneumonia.

Authors:  David K R Karaolis; Michael W Newstead; Xianying Zeng; Mamoru Hyodo; Yoshihiro Hayakawa; Urvhashi Bhan; Hallie Liang; Theodore J Standiford
Journal:  Infect Immun       Date:  2007-07-23       Impact factor: 3.441

10.  Expression of recombinant proteins in a lipid A mutant of Escherichia coli BL21 with a strongly reduced capacity to induce dendritic cell activation and maturation.

Authors:  Isabelle Cognet; Amélie Benoit de Coignac; Giovanni Magistrelli; Pascale Jeannin; Jean-Pierre Aubry; Karine Maisnier-Patin; Gersende Caron; Sylvie Chevalier; Frédéric Humbert; Thien Nguyen; Alain Beck; Dominique Velin; Yves Delneste; Martine Malissard; Jean-François Gauchat
Journal:  J Immunol Methods       Date:  2003-01-15       Impact factor: 2.303

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  26 in total

1.  Nanoparticulate STING agonists are potent lymph node-targeted vaccine adjuvants.

Authors:  Melissa C Hanson; Monica P Crespo; Wuhbet Abraham; Kelly D Moynihan; Gregory L Szeto; Stephanie H Chen; Mariane B Melo; Stefanie Mueller; Darrell J Irvine
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2.  MPYS is required for IFN response factor 3 activation and type I IFN production in the response of cultured phagocytes to bacterial second messengers cyclic-di-AMP and cyclic-di-GMP.

Authors:  Lei Jin; Krista K Hill; Holly Filak; Jennifer Mogan; Heather Knowles; Bicheng Zhang; Anne-Laure Perraud; John C Cambier; Laurel L Lenz
Journal:  J Immunol       Date:  2011-08-03       Impact factor: 5.422

Review 3.  Rationale, progress and development of vaccines utilizing STING-activating cyclic dinucleotide adjuvants.

Authors:  Thomas W Dubensky; David B Kanne; Meredith L Leong
Journal:  Ther Adv Vaccines       Date:  2013-11

4.  Identification of a novel pneumococcal vaccine antigen preferentially expressed during meningitis in mice.

Authors:  Layla K Mahdi; Hui Wang; Mark B Van der Hoek; James C Paton; Abiodun D Ogunniyi
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5.  Stimulation of innate immunity by in vivo cyclic di-GMP synthesis using adenovirus.

Authors:  Benjamin J Koestler; Sergey S Seregin; David P W Rastall; Yasser A Aldhamen; Sarah Godbehere; Andrea Amalfitano; Christopher M Waters
Journal:  Clin Vaccine Immunol       Date:  2014-09-17

Review 6.  Cyclic di-GMP: the first 25 years of a universal bacterial second messenger.

Authors:  Ute Römling; Michael Y Galperin; Mark Gomelsky
Journal:  Microbiol Mol Biol Rev       Date:  2013-03       Impact factor: 11.056

Review 7.  Structural and mechanistic determinants of c-di-GMP signalling.

Authors:  Tilman Schirmer; Urs Jenal
Journal:  Nat Rev Microbiol       Date:  2009-10       Impact factor: 60.633

8.  Natural STING Agonist as an "Ideal" Adjuvant for Cutaneous Vaccination.

Authors:  Ji Wang; Peiyu Li; Mei X Wu
Journal:  J Invest Dermatol       Date:  2016-06-07       Impact factor: 8.551

9.  MPYS/STING-mediated TNF-α, not type I IFN, is essential for the mucosal adjuvant activity of (3'-5')-cyclic-di-guanosine-monophosphate in vivo.

Authors:  Steven M Blaauboer; Vincent D Gabrielle; Lei Jin
Journal:  J Immunol       Date:  2013-12-04       Impact factor: 5.422

10.  STING-Activating Adjuvants Elicit a Th17 Immune Response and Protect against Mycobacterium tuberculosis Infection.

Authors:  Erik Van Dis; Kimberly M Sogi; Chris S Rae; Kelsey E Sivick; Natalie H Surh; Meredith L Leong; David B Kanne; Ken Metchette; Justin J Leong; Jacob R Bruml; Vivian Chen; Kartoosh Heydari; Nathalie Cadieux; Tom Evans; Sarah M McWhirter; Thomas W Dubensky; Daniel A Portnoy; Sarah A Stanley
Journal:  Cell Rep       Date:  2018-05-01       Impact factor: 9.423

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