Sökning: WFRF:(Persson Josefine 1980) >
Intranasal immuniza...
Intranasal immunization with a proteoliposome-derived cochleate containing recombinant gD protein confers protective immunity against genital herpes in mice.
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Del Campo, Judith (författare)
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- Lindqvist, Madelene, 1982 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
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Cuello, Maribel (författare)
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- Bäckström, Malin, 1967 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Core Facilities, Mammalian Protein Expression,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology,Core Facilities, Mammalian Protein Expression
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Cabrerra, Osmir (författare)
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- Persson, Josefine, 1980 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för mikrobiologi och immunologi,Institute of Biomedicine, Department of Microbiology and Immunology
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Perez, Oliver (författare)
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- 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
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(creator_code:org_t)
- Elsevier BV, 2010
- 2010
- Engelska.
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Ingår i: Vaccine. - : Elsevier BV. - 1873-2518 .- 0264-410X. ; 28:5, s. 1193-200
- Relaterad länk:
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https://gup.ub.gu.se...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- The purpose of this study was to investigate the potential of intranasal (IN) immunization with Neisseria meningitides B proteoliposome (AFPL1) and AFPL1-derived cochleate (AFCo1), containing glycoprotein D (gD) of herpes simplex virus type 2 (HSV-2) for induction of protective immunity against genital herpes infection in mice. We could show that IN immunization with both AFPL1 and AFCo1 containing gD induced gD-specific IgG antibody and lymphoproliferative responses. However, IFN-gamma response could only be detected in CD4(+) splenic cells and genital lymph node cells of the AFCo1gD immunized mice upon recall antigen stimulation in vitro. Importantly, IN immunization with AFCo1gD could elicit a complete protection against an otherwise lethal vaginal challenge with HSV-2, while the AFPL1gD immunized mice were only partially protected. Further, we could show that the IFN-gamma response and protective immunity observed after IN immunization with AFCo1gD are mediated via the adaptor molecule myeloid differentiation factor 88. These data may have implications for the development of a mucosal vaccine against genital herpes.
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
- Administration
- Intranasal
- Animals
- Antibodies
- Viral
- immunology
- Antigens
- Bacterial
- immunology
- pharmacology
- CD4-Positive T-Lymphocytes
- immunology
- Female
- Herpes Genitalis
- genetics
- immunology
- prevention & control
- Herpesvirus 2
- Human
- immunology
- Immunization
- Immunoglobulin G
- immunology
- Interferon-gamma
- immunology
- Liposomes
- Mice
- Mice
- Knockout
- Myeloid Differentiation Factor 88
- genetics
- immunology
- Neisseria meningitidis
- Serogroup B
- immunology
- Recombinant Proteins
- genetics
- immunology
- pharmacology
- Viral Envelope Proteins
- genetics
- immunology
- pharmacology
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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