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CD8α(2) CD11b(+) Dendritic Cells Present Exogenous Virus-like Particles to CD8(+) T Cells and Subsequently Express CD8α and CD205 Molecules

Recombinant porcine parvovirus virus-like particles (PPV-VLPs) are particulate exogenous antigens that induce a strong, specific cytotoxic T lymphocyte (CTL) response in the absence of adjuvant. In the present report, we demonstrate in vivo that dendritic cells (DCs) present PPV-VLPs to CD8(+) T cel...

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Detalles Bibliográficos
Autores principales: Morón, Gabriel, Rueda, Paloma, Casal, Ignacio, Leclerc, Claude
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193750/
https://www.ncbi.nlm.nih.gov/pubmed/12021304
http://dx.doi.org/10.1084/jem.20011930
Descripción
Sumario:Recombinant porcine parvovirus virus-like particles (PPV-VLPs) are particulate exogenous antigens that induce a strong, specific cytotoxic T lymphocyte (CTL) response in the absence of adjuvant. In the present report, we demonstrate in vivo that dendritic cells (DCs) present PPV-VLPs to CD8(+) T cells after intracellular processing. PPV-VLPs are captured by DCs with a high efficacy, which results in the delivery of these exogenous antigens to 50% of the whole spleen DC population. In vivo, a few hours after injection, PPV-VLPs are presented exclusively to CD8(+) T cells by CD8α(−) DCs, whereas 15 hours later they are presented mainly by CD8α(+) DCs. After PPV-VLPs processing, a fraction of CD11b(+) DCs undergo phenotypic changes, i.e., the up-regulation of CD8α and CD205 and the loss of CD4 molecules on their surface. The failure to detect mRNA coding for CD8α in CD11b(+) DCs suggests that CD8α expression by these cells is not due to de novo synthesis. In recombination-activating gene knockout mice (Rag(−/−)), CD11b(+) DCs did not express CD8α and PPV-VLPs presentation by CD8α(+) DCs was severely diminished. These results indicate that both CD8α(−) and CD8α(+) DCs play an important role in the induction of CTL responses by exogenous antigens, such as VLP.