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PMID |
Sentence |
1 |
19304955
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Comparative ability of IL-12 and IL-28B to regulate Treg populations and enhance adaptive cellular immunity.
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2 |
19304955
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IL-28B belongs to the newly described interferon lambda (IFNlambda) family of cytokines, and has not yet been assessed for its potential ability to influence adaptive immune responses or act as a vaccine adjuvant.
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3 |
19304955
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We show here that IL-28B, like IL-12, is capable of robustly enhancing adaptive immunity.
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4 |
19304955
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We also show that IL-28B, unlike IL-12, is able to increase the percentage of splenic CD8(+) T cells in vaccinated animals, and that these cells are more granular and have higher antigen-specific cytolytic degranulation compared with cells taken from animals that received IL-12 as an adjuvant.
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5 |
19304955
|
Comparative ability of IL-12 and IL-28B to regulate Treg populations and enhance adaptive cellular immunity.
|
6 |
19304955
|
IL-28B belongs to the newly described interferon lambda (IFNlambda) family of cytokines, and has not yet been assessed for its potential ability to influence adaptive immune responses or act as a vaccine adjuvant.
|
7 |
19304955
|
We show here that IL-28B, like IL-12, is capable of robustly enhancing adaptive immunity.
|
8 |
19304955
|
We also show that IL-28B, unlike IL-12, is able to increase the percentage of splenic CD8(+) T cells in vaccinated animals, and that these cells are more granular and have higher antigen-specific cytolytic degranulation compared with cells taken from animals that received IL-12 as an adjuvant.
|
9 |
19304955
|
Comparative ability of IL-12 and IL-28B to regulate Treg populations and enhance adaptive cellular immunity.
|
10 |
19304955
|
IL-28B belongs to the newly described interferon lambda (IFNlambda) family of cytokines, and has not yet been assessed for its potential ability to influence adaptive immune responses or act as a vaccine adjuvant.
|
11 |
19304955
|
We show here that IL-28B, like IL-12, is capable of robustly enhancing adaptive immunity.
|
12 |
19304955
|
We also show that IL-28B, unlike IL-12, is able to increase the percentage of splenic CD8(+) T cells in vaccinated animals, and that these cells are more granular and have higher antigen-specific cytolytic degranulation compared with cells taken from animals that received IL-12 as an adjuvant.
|
13 |
19304955
|
Comparative ability of IL-12 and IL-28B to regulate Treg populations and enhance adaptive cellular immunity.
|
14 |
19304955
|
IL-28B belongs to the newly described interferon lambda (IFNlambda) family of cytokines, and has not yet been assessed for its potential ability to influence adaptive immune responses or act as a vaccine adjuvant.
|
15 |
19304955
|
We show here that IL-28B, like IL-12, is capable of robustly enhancing adaptive immunity.
|
16 |
19304955
|
We also show that IL-28B, unlike IL-12, is able to increase the percentage of splenic CD8(+) T cells in vaccinated animals, and that these cells are more granular and have higher antigen-specific cytolytic degranulation compared with cells taken from animals that received IL-12 as an adjuvant.
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17 |
20685940
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Unique Th1/Th2 phenotypes induced during priming and memory phases by use of interleukin-12 (IL-12) or IL-28B vaccine adjuvants in rhesus macaques.
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18 |
20685940
|
To that end, we have employed interleukin-12 (IL-12) and IL-28B as adjuvants for DNA vaccination of rhesus macaques.
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19 |
20685940
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Moreover, analysis 3 months after the final immunization revealed the activity of the IL-12 adjuvant to be short lived, while the IL-28B adjuvant continued to exert its influence on the immune system.
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20 |
20685940
|
Unique Th1/Th2 phenotypes induced during priming and memory phases by use of interleukin-12 (IL-12) or IL-28B vaccine adjuvants in rhesus macaques.
|
21 |
20685940
|
To that end, we have employed interleukin-12 (IL-12) and IL-28B as adjuvants for DNA vaccination of rhesus macaques.
|
22 |
20685940
|
Moreover, analysis 3 months after the final immunization revealed the activity of the IL-12 adjuvant to be short lived, while the IL-28B adjuvant continued to exert its influence on the immune system.
|
23 |
20685940
|
Unique Th1/Th2 phenotypes induced during priming and memory phases by use of interleukin-12 (IL-12) or IL-28B vaccine adjuvants in rhesus macaques.
|
24 |
20685940
|
To that end, we have employed interleukin-12 (IL-12) and IL-28B as adjuvants for DNA vaccination of rhesus macaques.
|
25 |
20685940
|
Moreover, analysis 3 months after the final immunization revealed the activity of the IL-12 adjuvant to be short lived, while the IL-28B adjuvant continued to exert its influence on the immune system.
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26 |
21435672
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Here we report the identification and characterization of bovine (bo) interferon lambda 3 (IFN-λ3), a member of the type III IFN family.
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27 |
21435672
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Inoculation of cattle with Ad5-boIFN-λ3 induced systemic antiviral activity and up-regulation of IFN stimulated gene expression in multiple tissues susceptible to FMDV infection.
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28 |
25503988
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IL-28B, a member of the interferon (IFN)-λ family, has variable expression due to single nucleotide polymorphisms (SNPs).
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29 |
25503988
|
While type-I IFNs are well known to modulate adaptive immunity, the impact of IL-28B on B- and T-cell vaccine responses is unclear.
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30 |
25503988
|
In vitro, recombinant IL-28B increased Th1-cytokines (e.g.
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31 |
25503988
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IL-4, IL-5, and IL-13), H1N1-stimulated B-cell proliferation (reduced 70%), and IgG-production (reduced>70%).
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32 |
25503988
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Since IL-28B inhibited B-cell responses, we designed antagonistic peptides to block the IL-28 receptor α-subunit (IL28RA).
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33 |
25503988
|
IL-28B, a member of the interferon (IFN)-λ family, has variable expression due to single nucleotide polymorphisms (SNPs).
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34 |
25503988
|
While type-I IFNs are well known to modulate adaptive immunity, the impact of IL-28B on B- and T-cell vaccine responses is unclear.
|
35 |
25503988
|
In vitro, recombinant IL-28B increased Th1-cytokines (e.g.
|
36 |
25503988
|
IL-4, IL-5, and IL-13), H1N1-stimulated B-cell proliferation (reduced 70%), and IgG-production (reduced>70%).
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37 |
25503988
|
Since IL-28B inhibited B-cell responses, we designed antagonistic peptides to block the IL-28 receptor α-subunit (IL28RA).
|
38 |
25503988
|
IL-28B, a member of the interferon (IFN)-λ family, has variable expression due to single nucleotide polymorphisms (SNPs).
|
39 |
25503988
|
While type-I IFNs are well known to modulate adaptive immunity, the impact of IL-28B on B- and T-cell vaccine responses is unclear.
|
40 |
25503988
|
In vitro, recombinant IL-28B increased Th1-cytokines (e.g.
|
41 |
25503988
|
IL-4, IL-5, and IL-13), H1N1-stimulated B-cell proliferation (reduced 70%), and IgG-production (reduced>70%).
|
42 |
25503988
|
Since IL-28B inhibited B-cell responses, we designed antagonistic peptides to block the IL-28 receptor α-subunit (IL28RA).
|
43 |
25503988
|
IL-28B, a member of the interferon (IFN)-λ family, has variable expression due to single nucleotide polymorphisms (SNPs).
|
44 |
25503988
|
While type-I IFNs are well known to modulate adaptive immunity, the impact of IL-28B on B- and T-cell vaccine responses is unclear.
|
45 |
25503988
|
In vitro, recombinant IL-28B increased Th1-cytokines (e.g.
|
46 |
25503988
|
IL-4, IL-5, and IL-13), H1N1-stimulated B-cell proliferation (reduced 70%), and IgG-production (reduced>70%).
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47 |
25503988
|
Since IL-28B inhibited B-cell responses, we designed antagonistic peptides to block the IL-28 receptor α-subunit (IL28RA).
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48 |
26038748
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Common single nucleotide polymorphisms (SNPs) in the IFNL3, IFNL4 and the IFNL receptor α-subunit genes have been strongly associated with IFN-α-based treatment of chronic hepatitis C virus infection.
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49 |
26270121
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Interleukin-28B Plays a Therapeutic Role on Mouse U14 Cervical Cancer Cells by Down-Regulating CD4+CD25+FoxP3+Regulatory T Cells In Vivo.
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