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Multistage vaccines containing outer membrane, type III secretion system and inclusion membrane proteins protects against a Chlamydia genital tract infection and pathology

O'Meara, C. P. (författare)
Armitage, C. W. (författare)
Andrew, D. W. (författare)
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Kollipara, A. (författare)
Lycke, Nils Y, 1954 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
Potter, A. A. (författare)
Gerdts, V. (författare)
Petrovsky, N. (författare)
Beagley, K. W. (författare)
Ldwell Hd, Infection (författare)
Immunity, V. P. (författare)
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 (creator_code:org_t)
Elsevier BV, 2017
2017
Engelska.
Ingår i: Vaccine. - : Elsevier BV. - 0264-410X. ; 35:31, s. 3883-3888
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Pathogens with a complex lifecycles can effectively evade host immunity in part due to each developmental stage expressing unique sets of antigens. Multisubunit vaccines incorporating signature antigens reflecting distinct developmental stages (multistage vaccines) have proven effective against viral, bacterial and parasitic infection at preventing pathogen evasion of host immunity. Chlamydia trachomatis is characterized by a biphasic extra/intracellular developmental cycle and an acute/persistent (latent) metabolic state; hence a multistage vaccine may prevent immune evasion and enhance clearance. Here we tested the efficacy of a multistage vaccine containing outer membrane (MOMP and PmpG), type three secretion system (T3SS) (CdsF and TC0873) and inclusion membrane proteins (IncA and TC0500) in mice against an intravaginal challenge with Chlamydia muridarum. Comparison of single (eg. MOMP) and double antigen vaccines (eg. MOMP and PmpG), largely targeting the extracellular stage, elicited significant yet comparable protection against vaginal shedding when compared to unimmunized control mice. Utilization of different adjuvants (ISCOMATRIX - IMX, PCEP/polyl:C/IDR1002 - VIDO, CTA1-DD and ADVAX) and numerous immunization routes (subcutaneous - SQ and intranasal - IN) further enhanced protection against infection. However, a multistage vaccine elicited significantly greater protection against vaginal shedding and upper genital tract pathology than vaccines targeting only extra- or intracellular stages. This indicates that protection elicited by a vaccine targeting extracellular chlamydial antigens could be improved by including chlamydial antigen expressed during intracellular phase. (C) 2017 Elsevier Ltd. All rights reserved.

Ämnesord

NATURVETENSKAP  -- Biologi -- Immunologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Immunology (hsv//eng)

Nyckelord

Chlamydia
Vaccine
ISCOMATRIX
PCEP
CTAl-DD
ADVAX
PLASMODIUM-FALCIPARUM MALARIA
DEVELOPMENTAL CYCLE
TRACHOMATIS
IMMUNITY
IMMUNIZATION
INDUCTION
ADJUVANT
MULTIANTIGEN
EXPRESSION
NYVAC-PF7
Immunology
Medicine
Research & Experimental

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