2016
DOI: 10.1016/j.vaccine.2016.04.052
|View full text |Cite
|
Sign up to set email alerts
|

Heat killed Saccharomyces cerevisiae as an adjuvant for the induction of vaccine-mediated immunity against infection with Mycobacterium tuberculosis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
10
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 11 publications
(10 citation statements)
references
References 29 publications
0
10
0
Order By: Relevance
“…While certain pathogenic yeasts have developed immuneevading strategies, such as epitope-masking to control the production and exposure of highly antigenic cell wall proteins (Candida albicans) (58) or epigenetic switching to selectively silence their expression (Plasmodium species, Pneumocystis species, and Trypanosoma) (59), the high cell wall antigenicity other yeast such Saccharomyces cerevisiae make them prime candidates for the creation of vaccine adjuvants (60). The yeast cell wall compiles multiple highly antigenic components in a single location enabling a multi-pronged immune activation, namely through the recognition of β-glucans by dectin-1 and CR3 leading to activation of other inflammatory cells and T-cell responses (58,59,61). The mucosal and systemic immunity triggered by oral vaccine delivery could be enhanced with the incorporation of yeasts, potentially leading to higher baseline antibody levels following fewer doses.…”
Section: The Impact Of Yeasts On the Immune Systemmentioning
confidence: 99%
See 3 more Smart Citations
“…While certain pathogenic yeasts have developed immuneevading strategies, such as epitope-masking to control the production and exposure of highly antigenic cell wall proteins (Candida albicans) (58) or epigenetic switching to selectively silence their expression (Plasmodium species, Pneumocystis species, and Trypanosoma) (59), the high cell wall antigenicity other yeast such Saccharomyces cerevisiae make them prime candidates for the creation of vaccine adjuvants (60). The yeast cell wall compiles multiple highly antigenic components in a single location enabling a multi-pronged immune activation, namely through the recognition of β-glucans by dectin-1 and CR3 leading to activation of other inflammatory cells and T-cell responses (58,59,61). The mucosal and systemic immunity triggered by oral vaccine delivery could be enhanced with the incorporation of yeasts, potentially leading to higher baseline antibody levels following fewer doses.…”
Section: The Impact Of Yeasts On the Immune Systemmentioning
confidence: 99%
“…Because most yeasts trigger a rapid immune response, disease applications where treatment efficacy and immune stimulation can function synergistically are preferred (58)(59)(60). Due to the low transfection efficiency, it is generally advised to restrict yeast-encapsulated gene-editing therapies to the GI tract alone (24,47,66).…”
Section: Disease Targets For Oral Yeast Systemsmentioning
confidence: 99%
See 2 more Smart Citations
“…Booster vaccines stimulate pre-existing antigen specific immune cells to induce a greater, more rapid response similar to that expected during infection. BCG priming in mice is already able to eliminate approximately 90% of the mycobacterial burden, suggesting it may be difficult to observe boosting, using this host and microbiological endpoint [32, 33]. Boosting BCG with a second vaccine will hopefully result in faster and stronger immune responses than what is seen with BCG alone.…”
Section: Boosting Bcg? a MIX Of The Old And The Newmentioning
confidence: 99%