Literature DB >> 23598485

Group A streptococcal vaccines: paving a path for accelerated development.

James B Dale1, Vincent A Fischetti, Jonathan R Carapetis, Andrew C Steer, Samba Sow, Rajesh Kumar, Bongani M Mayosi, Fran A Rubin, Kim Mulholland, Joachim Maria Hombach, Florian Schödel, Ana Maria Henao-Restrepo.   

Abstract

Group A streptococci (GAS) are important causes of morbidity and mortality worldwide. These organisms cause a wide spectrum of disease, ranging from uncomplicated sore throat to invasive, life-threatening infections, as well as immune complications such as acute rheumatic fever (ARF), rheumatic heart disease (RHD) and acute post-streptococcal glomerulonephritis (APSGN). Vaccine prevention of GAS infections and their immunological complications has been a goal of researchers for decades. Several vaccine candidates against GAS infection are in various stages of pre-clinical and clinical development, including M protein-based vaccines (N-terminal vaccine candidates and M protein conserved region vaccines), and non-M protein vaccine candidates representing conserved GAS antigens. Some of the obstacles to GAS vaccine development are related to the complexity of the global epidemiology of GAS infections, the limitation in the criteria for selection of antigens to include in combination vaccines as well as the issues around autoimmunity and vaccine safety, among others. Overcoming these obstacles will require collaborative efforts to develop innovative strategies that address key steps in the pre-clinical and clinical development process, as well as clearly defining the global burden of GAS diseases and the molecular epidemiology of infections. Specific recommendations are presented for an accelerated plan leading to the introduction of a broadly protective vaccine designed for deployment in low-, middle-, and high-income countries.
Copyright © 2012 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23598485     DOI: 10.1016/j.vaccine.2012.09.045

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


  29 in total

1.  Streptococcus pyogenes emm Types and Clusters during a 7-Year Period (2007 to 2013) in Pharyngeal and Nonpharyngeal Pediatric Isolates.

Authors:  F Koutouzi; A Tsakris; P Chatzichristou; E Koutouzis; G L Daikos; E Kirikou; N Petropoulou; V Syriopoulou; A Michos
Journal:  J Clin Microbiol       Date:  2015-04-15       Impact factor: 5.948

2.  Group A Streptococcus T Antigens Have a Highly Conserved Structure Concealed under a Heterogeneous Surface That Has Implications for Vaccine Design.

Authors:  Paul G Young; Jeremy M Raynes; Jacelyn M Loh; Thomas Proft; Edward N Baker; Nicole J Moreland
Journal:  Infect Immun       Date:  2019-05-21       Impact factor: 3.441

Review 3.  Acute rheumatic fever and rheumatic heart disease.

Authors:  Jonathan R Carapetis; Andrea Beaton; Madeleine W Cunningham; Luiza Guilherme; Ganesan Karthikeyan; Bongani M Mayosi; Craig Sable; Andrew Steer; Nigel Wilson; Rosemary Wyber; Liesl Zühlke
Journal:  Nat Rev Dis Primers       Date:  2016-01-14       Impact factor: 52.329

Review 4.  Position statement of the World Heart Federation on the prevention and control of rheumatic heart disease.

Authors:  Bo Remenyi; Jonathan Carapetis; Rosemary Wyber; Kathryn Taubert; Bongani M Mayosi
Journal:  Nat Rev Cardiol       Date:  2013-04-02       Impact factor: 32.419

5.  A systematic and functional classification of Streptococcus pyogenes that serves as a new tool for molecular typing and vaccine development.

Authors:  Martina Sanderson-Smith; David M P De Oliveira; Julien Guglielmini; David J McMillan; Therese Vu; Jessica K Holien; Anna Henningham; Andrew C Steer; Debra E Bessen; James B Dale; Nigel Curtis; Bernard W Beall; Mark J Walker; Michael W Parker; Jonathan R Carapetis; Laurence Van Melderen; Kadaba S Sriprakash; Pierre R Smeesters
Journal:  J Infect Dis       Date:  2014-05-05       Impact factor: 5.226

6.  SpyAD, a moonlighting protein of group A Streptococcus contributing to bacterial division and host cell adhesion.

Authors:  Marilena Gallotta; Giovanni Gancitano; Giampiero Pietrocola; Marirosa Mora; Alfredo Pezzicoli; Giovanna Tuscano; Emiliano Chiarot; Vincenzo Nardi-Dei; Anna Rita Taddei; Simonetta Rindi; Pietro Speziale; Marco Soriani; Guido Grandi; Immaculada Margarit; Giuliano Bensi
Journal:  Infect Immun       Date:  2014-04-28       Impact factor: 3.441

7.  Potential coverage of a multivalent M protein-based group A streptococcal vaccine.

Authors:  James B Dale; Thomas A Penfound; Boubou Tamboura; Samba O Sow; James P Nataro; Milagritos Tapia; Karen L Kotloff
Journal:  Vaccine       Date:  2013-01-31       Impact factor: 3.641

8.  Group A streptococcus expresses a trio of surface proteins containing protective epitopes.

Authors:  Shannon E Niedermeyer; Thomas A Penfound; Claudia Hohn; Yi Li; Ramin Homayouni; Jingnan Zhao; James B Dale
Journal:  Clin Vaccine Immunol       Date:  2014-07-30

9.  Streptococcus pyogenes Employs Strain-dependent Mechanisms of C3b Inactivation to Inhibit Phagocytosis and Killing of Bacteria.

Authors:  Garima Agrahari; Zhong Liang; Kristofor Glinton; Shaun W Lee; Victoria A Ploplis; Francis J Castellino
Journal:  J Biol Chem       Date:  2016-03-04       Impact factor: 5.157

10.  Epidemiology Analysis of Streptococcus pyogenes in a Hospital in Southern Taiwan by Use of the Updated emm Cluster Typing System.

Authors:  Chuan Chiang-Ni; Po-Xing Zheng; Shu-Ying Wang; Pei-Jane Tsai; Woei-Jer Chuang; Yee-Shin Lin; Ching-Chuan Liu; Jiunn-Jong Wu
Journal:  J Clin Microbiol       Date:  2015-11-11       Impact factor: 5.948

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.