Bordetella bronchiseptica is a potent and safe adjuvant that enhances the antigen-presenting capability of dendritic cells
We previously demonstrated that ( ) antigen (Ag) enhances the Ag-specific immune response. The focus of this study was whether acellular bacterin of could be used as an adjuvant to increase antigen-presenting capability of dendritic cells (DCs) by increasing the level of activation. The metabolic ac...
Saved in:
Published in | The Korean journal of physiology & pharmacology Vol. 24; no. 1; pp. 47 - 52 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
The Korean Physiological Society and The Korean Society of Pharmacology
01.01.2020
대한약리학회 |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | We previously demonstrated that
(
) antigen (Ag) enhances the
Ag-specific immune response. The focus of this study was whether acellular bacterin of
could be used as an adjuvant to increase antigen-presenting capability of dendritic cells (DCs) by increasing the level of activation. The metabolic activity of DCs was increased by
, similar to lipopolysaccharide (LPS). Flow cytometry analysis revealed that
increases the expression of major histocompatibility complex class-2, cluster of differentiation (CD)40, CD54, and CD86 which are closely related to DC-mediated immune responses.
enhanced the production of cytokines related to adaptive immune responses. Furthermore, the survival rate of
-injected groups was 100% at 15 and 20 mg/kg doses, whereas that of LPS-injected groups was only 20%, 0% at 15 and 20 mg/kg doses respectively, and so
is likely to be safer than LPS. Taken together, these results indicate that
can be used as an adjuvant to enhance the antigen-presenting capability of DCs.
is a candidate for producing vaccines, especially in case of DC-mediating efficacy and safety demands. This study provides researchers and clinicians with valuable information regarding the usage of
as a safe bacteria-derived immunostimulating agent for developing efficient vaccines. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1226-4512 2093-3827 |
DOI: | 10.4196/kjpp.2020.24.1.47 |