Please wait a minute...

中国生物工程杂志

China Biotechnology
China Biotechnology  2011, Vol. 31 Issue (7): 20-26    DOI:
    
IL-17 as an Adjuvant Enhances Immune Responses of Recombinant Protein Vaccine
LOU Yao-xian1, ZOU Qiang2, JIN Jin2, WANG Xian-zheng2, ZHANG Yi-zhi2, WANG Bin2
1. College of Veterinary Medicine, China Agricultural University, Beijing 100193, China;
2. State Key Laboratory for Agro-Biotechnology, College of Biological Science, China Agricultural University, Beijing 100193, China
Download: HTML   PDF(940KB) HTML
Export: BibTeX | EndNote (RIS)      

Abstract  

Objective: To enhance immune responses to protein vaccine, IL-17 was investigated as a molecular adjuvant to enhance humoral immune responses, especially cellular immune responses to protein vaccine. Methods: C57BL/6 mice were immunized with OVA alone, or with IL-17A by intramuscular injection. The immunization was performed on week 0, 2. The concentration of the anti-OVA IgG, the stimulated index of T lymphocyte proliferation, and the expressions of IFN-γ, IL-4 and IL-17 in CD+4 T cells and IL-17, IFN-γ in CD+8 T cells, and specific in vivo cytotoxic T lymphocyte (CTL) activity were detected on week 3,4. Results: The results showed that IL-17 as a molecular adjuvant for the protein vaccine, OVA, could enhance immune responses, especially the cellular immune responses. IL-17 could not only enhance the humoral responses and T cell proliferation, but also the expressions of IL-17 in CD+4 and CD+8 T cells, and IFN-γ in CD+8 T cells. Accordingly, the level of CTL in vivo was significantly increased. Conclusion: The results demonstrated that IL-17 as a molecular adjuvant enhanced humoral and cellular immune responses to protein vaccine, especially the CD+8 T cell-immunity. The novel functionality of IL-17 on adaptive immunity may lead to develop new protein vaccine targeted to the cellular immune responses.



Key wordsIL-17      Molecular adjuvant      OVA      Protein vaccine      Cellular immune responses     
Received: 31 March 2011      Published: 25 July 2011
ZTFLH:  Q78  
Cite this article:

LOU Yao-xian, ZOU Qiang, JIN Jin, WANG Xian-zheng, ZHANG Yi-zhi, WANG Bin. IL-17 as an Adjuvant Enhances Immune Responses of Recombinant Protein Vaccine. China Biotechnology, 2011, 31(7): 20-26.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2011/V31/I7/20


[1] Dzierzbicka K, Kolodziejczyk A M. Adjuvants--essential components of new generation vaccines. Postepy Biochem, 2006,52(2):204-211.

[2] Korn T, Bettelli E, Oukka M, et al. IL-17 and Th17 Cells. Annu Rev Immunol, 2009,27(1): 485-517.

[3] Murugaiyan G, Mittal A, Weiner H L. Increased osteopontin expression in dendritic cells amplifies IL-17 production by CD+4 T cells in experimental autoimmune encephalomyelitis and in multiple sclerosis. J Immunol, 2008, 181(11): 7480-7488.

[4] Wong C K, Lit L C, Tam L S, et al. Hyperproduction of IL-23 and IL-17 in patients with systemic lupus erythematosus: implications for Th17-mediated inflammation in auto-immunity. Clin Immunol, 2008,127( 3): 385-393.

[5] Kehlen A, Thiele K, Riemann D, et al. Expression, modulation and signalling of IL-17 receptor in fibroblast-like synoviocytes of patients with rheumatoid arthritis. Clin Exp Immunol, 2002,127(3): 539-546.

[6] 张景熙. IL-17与疾病相关的研究进展. 国外医学, 2004,27(1): 52-55. Zhang J X. Foreign Medical Sciences, 2004,27(1): 52-55.

[7] 秦霞, 刘钟滨. 白细胞介素17家族. 同济大学学报(医学版), 2003, 24(6): 519-522. Qin X, Liu Z B. Journal of Tongji University (Medical Science), 2003, 24(6): 519-522.

[8] Garley M, Jablonska E, Grabowska S Z, et al. IL-17 family cytokines in neutrophils of patients with oral epithelial squamous cell carcinoma. Neoplasma, 2009,56(2): 96-100.

[9] Arican O, Aral M, Sasmaz S, et al. Serum levels of TNF-alpha, IFN-gamma, IL-6, IL-8, IL-12, IL-17, and IL-18 in patients with active psoriasis and correlation with disease severity. Mediators Inflamm, 2005,2005(5): 273-279.

[10] Ma D, Zhu X, Zhao P, et al. Profile of Th17 cytokines (IL-17, TGF-beta, IL-6) and Th1 cytokine (IFN-gamma) in patients with immune thrombocytopenic purpura. Ann Hematol, 2008,87(11): 899-904.

[11] Mitsdoerffer M, Lee Y, Kuchroo V K, et al. Proinflammatory T helper type 17 cells are effective B-cell helpers. Proc Natl Acad Sci USA, 2010,107(32):14292-14297.

[12] Awasthi A, Kuchroo V K. IL-17A directly inhibits TH1 cells and thereby suppresses development of intestinal inflammation. Nat Immunol, 2009, 10(6): 568-570.

[13] Lindblad E B. Aluminium adjuvants-in retrospect and prospect. Vaccine,2004, 22(27-28):3658-3668.

[14] Da-Silva C A, Hartl D, Liu W, et al.TLR-2 and IL-17A in chitin-induced macrophage activation and acute inflammation. The Journal of Immunology, 2008,181(6): 4279-4286.

[15] Doreau A, Belot A, Bastid J, et al. Interleukin 17 acts in synergy with B cell-activating factor to influence B cell biology and the pathophysiology of systemic lupus erythematosus. Nat Immunol, 2009,10(7):778-785.

[1] CHEN Yu-qiong,TAN Wen-hua,LIU Hai-feng,CHEN Gen. Protective Effect of miR-29a on Lipopolysaccharide-induced Human Pulmonary Microvascular Endothelial Cells Injury by Targeting PTEN Expression[J]. China Biotechnology, 2021, 41(5): 8-16.
[2] HU Yuan-lei,CHEN Yan-cheng,PU Run,YAO Wei-hao,ZHANG Hong-xiang. Bio-tech Startup Incubation Best Practice in the United Kingdom and Suggestion[J]. China Biotechnology, 2021, 41(4): 100-105.
[3] WU Han-rong,WANG Ying,HUANG Ying-ming,LI Dong-xue,LI Zhi-fei,FANG Zi-han,FAN Lin. Promote the Innovation and Transformation of Biotechnology by Base Platform[J]. China Biotechnology, 2021, 41(12): 141-147.
[4] TANG De-ping,XING Meng-jie,SONG Wen-tao,YAO Hui-hui,MAO Ai-hong. Advance of microRNA Therapeutics in Cancer and Other Diseases[J]. China Biotechnology, 2021, 41(11): 64-73.
[5] YANG Dan,TIAN Hai-shan,LI Xiao-kun. Research Progress of Fibroblast Growth Factor 5[J]. China Biotechnology, 2020, 40(3): 117-124.
[6] CAO Meng,ZHAO Yu-hao,GUO Zhong-ping. A Review of the Global Bio-Therapeutics Development Process from the Perspective of International Nonproprietary Names[J]. China Biotechnology, 2020, 40(1-2): 154-165.
[7] KONG Jian-tao,ZHUANG Ying-ping,GUO Mei-jin. Enhancement of Anti-CD20 Monoclonal Antibody Expression by CHO based on DOE and Amino Acid Supplemental Strategy[J]. China Biotechnology, 2020, 40(12): 41-48.
[8] Heng ZHU,Hai-jiao LIN,Ji-fu ZHANG,Yun ZHANG,Ai-jun SUN,Yun-feng HU. Covalent Immobilization of Marine Candida Rugosa Lipase Using Amino Carrier[J]. China Biotechnology, 2019, 39(7): 71-78.
[9] HU Yuan-lei,YAO Wei-hao,PU Run,ZHANG Hong-xiang. Bio-tech Startup Incubation Best Practice in the United States[J]. China Biotechnology, 2019, 39(12): 103-109.
[10] Ding-hao DENG,Yong-le XIAO,Jian-xue TANG,Xing YANG,Rong GAO. Eukaryotic Expression of Porcine IL-17 Gene and its Bioactivity[J]. China Biotechnology, 2018, 38(8): 10-18.
[11] Ya-fang LI,Ying-hui ZHAO,Sai-bao LIU,Wei WANG,Wei-jun ZENG,Jin-quan WANG,Hong-yan CHEN,Qing-wen MENG. Chicken OV Promoter Expressed HA to Protect Chickens from Lethal Challenge of AIV[J]. China Biotechnology, 2018, 38(7): 67-74.
[12] Qing BI,Lin SUN. Analysis and Comparison of Foreign and Chinese Patent Applications in Chimeric Antigen Receptor T Cell (CAR-T) Technology[J]. China Biotechnology, 2018, 38(4): 107-114.
[13] Xiang HUANG,Jie YANG,Pei-yan HE,Zhi-hui WU,Hui-lan ZENG,Xin-Ning WANG,Jian-wei JIANG. Molecular Mechanism of Inducing 2774-C10 Cell Apoptosis and G1/S Cell Cycle Arrest by Ethanol Extract from Elephantopus mollis H.B.K.[J]. China Biotechnology, 2018, 38(4): 17-23.
[14] Qiao-li LANG,Lin YU,Qi-lin HE,Liang-peng GE,Xi YANG. Construction and Screening of a Phage Display Library of Single Chain Fv Antibody Efficiently from Mouse Immunized with Ovalbumin[J]. China Biotechnology, 2018, 38(11): 25-31.
[15] Jia-wei ZENG,Guo-feng HOU,Ji-ping ZHENG,Nou YANG,Ji-feng ZENG,Gui-ying GUO. The Progress of CRISPR/Cas System Used As Antimicrobials[J]. China Biotechnology, 2018, 38(11): 59-65.