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Vaccination with Klebsiella pneumoniae-derived extracellular vesicles protects against bacteria-induced lethality via both humoral and cellular immunity
Experimental & Molecular Medicine ; : e183-2015.
Article in English | WPRIM | ID: wpr-215493
ABSTRACT
The emergence of multidrug-resistant Klebsiella pneumoniae highlights the need to develop preventive measures to ameliorate Klebsiella infections. Bacteria-derived extracellular vesicles (EVs) are spherical nanometer-sized proteolipids enriched with outer membrane proteins. Gram-negative bacteria-derived EVs have gained interest for use as nonliving complex vaccines. In the present study, we evaluated whether K. pneumoniae-derived EVs confer protection against bacteria-induced lethality. K. pneumoniae-derived EVs isolated from in vitro bacterial culture supernatants induced innate immunity, including the upregulation of co-stimulatory molecule expression and proinflammatory mediator production. EV vaccination via the intraperitoneal route elicited EV-reactive antibodies and interferon-gamma-producing T-cell responses. Three vaccinations with the EVs prevented bacteria-induced lethality. As verified by sera and splenocytes adoptive transfer, the protective effect of EV vaccination was dependent on both humoral and cellular immunity. Taken together, these findings suggest that K. pneumoniae-derived EVs are a novel vaccine candidate against K. pneumoniae infections.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Klebsiella Infections / Bacterial Vaccines / Interferon-gamma / Vaccination / Extracellular Vesicles / Immunity, Cellular / Immunity, Innate / Klebsiella pneumoniae / Mice, Inbred C57BL Limits: Animals / Female / Humans Language: English Journal: Experimental & Molecular Medicine Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Klebsiella Infections / Bacterial Vaccines / Interferon-gamma / Vaccination / Extracellular Vesicles / Immunity, Cellular / Immunity, Innate / Klebsiella pneumoniae / Mice, Inbred C57BL Limits: Animals / Female / Humans Language: English Journal: Experimental & Molecular Medicine Year: 2015 Type: Article