LPS |
Pseudomonas aeruginosa
|
Mouse macrophages |
Both LPS and protein components on OMVs from Pseudomonas aeruginosa were responsible for eliciting innate immune response |
32
|
|
Neisseria meningitidis
|
Human monomacrophages, human dendritic cells |
Neisseria meningitidis OMVs with less LPS or less toxic LPS induced weaker cytokine response |
85
|
|
Escherichia coli
|
Human macrophages |
LPS-neutralized OMVs induced weaker inflammatory response |
113
|
OMPs |
Pseudomonas aeruginosa
|
Mouse macrophages |
Both LPS and protein components on OMVs from Pseudomonas aeruginosa were responsible for eliciting innate immune response |
32
|
|
Acinetobacter baumannii
|
Human laryngeal epithelial cells |
Surface-exposed membrane proteins in Acinetobacter baumannii OMVs induced proinflamatory cytokine response |
114
|
Flagellin |
Enterohemorrhagic Escherichia coli
|
Human intestinal epithelial cells |
H7 flagellin was the key IL-8-inducing component of EHEC O157:H7 OMVs |
115
|
|
Pseudomonas aeruginosa
|
Rat renal epithelial cells |
Both LPS and protein components on OMVs from Pseudomonas aeruginosa are responsible for eliciting innate immune response |
32
|
Peptidoglycan |
Helicobacter pylori, Pseudomonas aeruginosa, Neisseria gonorrhoeae
|
Human epithelial cells |
Bacterial OMVs delivered peptidoglycan to cytosolic NOD-1 and activated NF-kB pathway |
116
|
|
Aggregatibacter actinomycetemcomitans
|
Human gingival fibroblasts |
Internalized OMVs from Aggregatibacter actinomycetemcomitans delivered peptidoglycan to NOD-2 receptors |
37
|
CpG DNA |
Moraxella catarrhalis
|
Human tonsillar B cells |
DNA associated with OMV induced full B cell activation by signaling through TLR9 |
117
|