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Induction of protective immunity by vaccination against Chlamydia trachomatis using the major outer membrane protein adjuvanted with CpG oligodeoxynucleotide coupled to the nontoxic B subunit of cholera toxin.

Cheng, Chunmei (författare)
Bettahi, Ilham (författare)
Cruz-Fisher, Maria I (författare)
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Pal, Sukumar (författare)
Jain, Pooja (författare)
Jia, Zhenyu (författare)
Holmgren, Jan, 1944 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
Harandi, Ali M, 1968 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
de la Maza, Luis M (författare)
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 (creator_code:org_t)
Elsevier BV, 2009
2009
Engelska.
Ingår i: Vaccine. - : Elsevier BV. - 1873-2518 .- 0264-410X. ; 27:44, s. 6239-46
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The present study was undertaken to test the efficacy of immunization with the native major outer membrane protein (nMOMP) of Chlamydia trachomatis mouse pneumonitis (MoPn) serovar in combination with a novel immunostimulatory adjuvant consisting of CpG oligodeoxynucleotide (ODN) linked to the nontoxic B subunit of cholera toxin (CTB-CpG) to elicit a protective immune response to C. trachomatis. High levels of Chlamydia-specific IgG antibodies were detected in the sera from BALB/c mice immunized intramuscularly and subcutaneously (i.m.+s.c.) with the nMOMP/CTB-CpG vaccine or with nMOMP adjuvanted with a mixture of CT and CpG ODN (CT+CpG). Further, these immunization schemes gave rise to significant T-cell-mediated Chlamydia-specific immune responses. No Chlamydia-specific humoral or cell-mediated immune responses were detected in the control mice vaccinated with ovalbumin together with either CTB-CpG or CT+CpG. Following an intranasal challenge with C. trachomatis the groups of mice immunized with nMOMP plus CTB-CpG, CT+CpG or live C. trachomatis were found to be protected based on their change in body weight and lung weight as well as number of inclusion forming unit recovered from the lungs, as compared with control groups immunized with ovalbumin plus either adjuvants. Interestingly, IFN-gamma-producing CD4(+), but not CD8(+), T-cells showed a significant correlation with the outcomes of the challenge. In conclusion, nMOMP in combination with the novel adjuvant CTB-CpG elicited a significant antigen-specific antibody and cell-mediated immune responses as well as protection against a pulmonary challenge with C. trachomatis.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)

Nyckelord

Adjuvants
Immunologic
Animals
Antibodies
Bacterial
blood
Bacterial Vaccines
immunology
Body Weight
Cell Proliferation
Chlamydia Infections
immunology
prevention & control
Chlamydia trachomatis
immunology
Cholera Toxin
immunology
Female
Immunity
Cellular
Immunity
Humoral
Immunoglobulin G
blood
Lung
microbiology
pathology
Mice
Mice
Inbred BALB C
Oligodeoxyribonucleotides
immunology
Porins
immunology
Spleen
cytology
immunology
T-Lymphocytes
immunology

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