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A multivalent T-antigen-based vaccine for Group A Streptococcus.
Loh, Jacelyn M S; Rivera-Hernandez, Tania; McGregor, Reuben; Khemlani, Adrina Hema J; Tay, Mei Lin; Cork, Amanda J; M Raynes, Jeremy; Moreland, Nicole J; Walker, Mark J; Proft, Thomas.
Affiliation
  • Loh JMS; Department of Molecular Medicine & Pathology, School of Medical Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand. mj.loh@auckland.ac.nz.
  • Rivera-Hernandez T; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand. mj.loh@auckland.ac.nz.
  • McGregor R; Australian Infectious Diseases Research Centre and School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, QLD, Australia.
  • Khemlani AHJ; Cátedras CONACYT-Unidad de Investigación Médica en Inmunoquímica, Hospital de Especialidades del Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
  • Tay ML; Department of Molecular Medicine & Pathology, School of Medical Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
  • Cork AJ; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • M Raynes J; Department of Molecular Medicine & Pathology, School of Medical Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
  • Moreland NJ; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
  • Walker MJ; Department of Molecular Medicine & Pathology, School of Medical Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
  • Proft T; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.
Sci Rep ; 11(1): 4353, 2021 02 23.
Article in En | MEDLINE | ID: mdl-33623073
ABSTRACT
Pili of Group A Streptococcus (GAS) are surface-exposed structures involved in adhesion and colonisation of the host during infection. The major protein component of the GAS pilus is the T-antigen, which multimerises to form the pilus shaft. There are currently no licenced vaccines against GAS infections and the T-antigen represents an attractive target for vaccination. We have generated a multivalent vaccine called TeeVax1, a recombinant protein that consists of a fusion of six T-antigen domains. Vaccination with TeeVax1 produces opsonophagocytic antibodies in rabbits and confers protective efficacy in mice against invasive disease. Two further recombinant proteins, TeeVax2 and TeeVax3 were constructed to cover 12 additional T-antigens. Combining TeeVax1-3 produced a robust antibody response in rabbits that was cross-reactive to a full panel of 21 T-antigens, expected to provide over 95% vaccine coverage. These results demonstrate the potential for a T-antigen-based vaccine to prevent GAS infections.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Streptococcus pyogenes / Streptococcal Vaccines / Antigens, Bacterial Limits: Animals / Humans Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Streptococcus pyogenes / Streptococcal Vaccines / Antigens, Bacterial Limits: Animals / Humans Language: En Year: 2021 Type: Article