# |
PMID |
Sentence |
1 |
10741861
|
Serum antigen-specific antibody (Ab) responses were enhanced when either IL-6 or IL-12 was mucosally administered with a protein antigen, while only IL-12 induced antigen-specific mucosal IgA Ab responses.
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2 |
10741861
|
Mucosal IL-6 and IL-12 also affected the type of Th cell responses induced by CD4+ T cells from mice that received IL-12 secreted larger amounts of IFN-gamma and IL-6 when compared with mice nasally treated with IL-6.
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3 |
10741861
|
Mixed antigen-specific Th1 -and Th2-type CD4+ T cell responses were induced in the systemic compartment by both lymphotactin and the mixture of HNP-1, HNP-2, and HNP-3 defensins.
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4 |
10741861
|
In summary, these studies clearly show that IL-12 and lymphotactin are able to trigger S-IgA Ab responses and provide new avenues for the design of safe and targeted mucosal vaccines.
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5 |
17655941
|
Neither induction of IFN-stimulated genes (ISGs) by HNP1 nor their antiviral activity against fish rhabovirus has been previously reported.
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6 |
22879887
|
Cholera toxin (CT) from Vibrio cholerae and heat labile enterotoxin (LT) from Escherichia coli both modified the human α-defensin (HNP-1) and β- defensin-1 (HBD1), as efficiently as the mammalian mono-ADP-ribosyltransferase-1.
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7 |
22879887
|
Pseudomonas aeruginosa exoenzyme S was inactive on both HNP-1 and HBD1.
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8 |
22879887
|
Neisseria meningitidis NarE poorly recognized HNP-1 as a substrate but it was completely inactive on HBD1.
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9 |
22879887
|
Cholera toxin (CT) from Vibrio cholerae and heat labile enterotoxin (LT) from Escherichia coli both modified the human α-defensin (HNP-1) and β- defensin-1 (HBD1), as efficiently as the mammalian mono-ADP-ribosyltransferase-1.
|
10 |
22879887
|
Pseudomonas aeruginosa exoenzyme S was inactive on both HNP-1 and HBD1.
|
11 |
22879887
|
Neisseria meningitidis NarE poorly recognized HNP-1 as a substrate but it was completely inactive on HBD1.
|
12 |
22879887
|
Cholera toxin (CT) from Vibrio cholerae and heat labile enterotoxin (LT) from Escherichia coli both modified the human α-defensin (HNP-1) and β- defensin-1 (HBD1), as efficiently as the mammalian mono-ADP-ribosyltransferase-1.
|
13 |
22879887
|
Pseudomonas aeruginosa exoenzyme S was inactive on both HNP-1 and HBD1.
|
14 |
22879887
|
Neisseria meningitidis NarE poorly recognized HNP-1 as a substrate but it was completely inactive on HBD1.
|