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Author | dc.contributor.author | Prados-Rosales, Rafael | |
Author | dc.contributor.author | Carreño, Leandro | |
Author | dc.contributor.author | Cheng, Tingting | |
Author | dc.contributor.author | Blanc, Caroline | |
Author | dc.contributor.author | Weinrick, Brian | |
Author | dc.contributor.author | Malek, Adel | |
Author | dc.contributor.author | Lowary, Todd L. | |
Author | dc.contributor.author | Baena, Andres | |
Author | dc.contributor.author | Joe, Maju | |
Author | dc.contributor.author | Bai, Yu | |
Author | dc.contributor.author | Kalscheuer, Rainer | |
Author | dc.contributor.author | Batista-Gonzalez, Ana | |
Author | dc.contributor.author | Saavedra, Noemi A. | |
Author | dc.contributor.author | Sampedro, Leticia | |
Author | dc.contributor.author | Tomás, Julen | |
Author | dc.contributor.author | Anguita, Juan | |
Author | dc.contributor.author | Hu | |
Admission date | dc.date.accessioned | 2019-03-18T11:56:22Z | |
Available date | dc.date.available | 2019-03-18T11:56:22Z | |
Publication date | dc.date.issued | 2017 | |
Cita de ítem | dc.identifier.citation | PLoS Pathogens, Volumen 13, Issue 3, 2018, | |
Identifier | dc.identifier.issn | 15537374 | |
Identifier | dc.identifier.issn | 15537366 | |
Identifier | dc.identifier.other | 10.1371/journal.ppat.1006250 | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/167092 | |
Abstract | dc.description.abstract | © 2017 Prados-Rosales et al.Currently there are a dozen or so of new vaccine candidates in clinical trials for prevention of tuberculosis (TB) and each formulation attempts to elicit protection by enhancement of cell-mediated immunity (CMI). In contrast, most approved vaccines against other bacterial pathogens are believed to mediate protection by eliciting antibody responses. However, it has been difficult to apply this formula to TB because of the difficulty in reliably eliciting protective antibodies. Here, we developed capsular polysaccharide conjugates by linking mycobacterial capsular arabinomannan (AM) to either Mtb Ag85b or B. anthracis protective antigen (PA). Further, we studied their immunogenicity by ELISA and AM glycan microarrays and protection efficacy in mice. Immunization with either Abg85b-AM or PA-AM conjugates elicited an AM-specific antibody response in mice. AM binding antibodies stimulated transcriptional changes in Mtb. Sera from AM conjugate immunized mice reac | |
Lenguage | dc.language.iso | en | |
Publisher | dc.publisher | Public Library of Science | |
Type of license | dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
Link to License | dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
Source | dc.source | PLoS Pathogens | |
Keywords | dc.subject | Parasitology | |
Keywords | dc.subject | Microbiology | |
Keywords | dc.subject | Immunology | |
Keywords | dc.subject | Molecular Biology | |
Keywords | dc.subject | Genetics | |
Keywords | dc.subject | Virology | |
Título | dc.title | Enhanced control of Mycobacterium tuberculosis extrapulmonary dissemination in mice by an arabinomannan-protein conjugate vaccine | |
Document type | dc.type | Artículo de revista | |
dcterms.accessRights | dcterms.accessRights | Acceso Abierto | |
Cataloguer | uchile.catalogador | SCOPUS | |
Indexation | uchile.index | Artículo de publicación SCOPUS | |
uchile.cosecha | uchile.cosecha | SI | |
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