TLR9-based immunotherapy for the treatment of allergic diseases

被引:30
作者
Farrokhi, Shokrollah [1 ]
Abbasirad, Narjes [1 ]
Movahed, Ali [2 ]
Khazaei, Hossein Ali [3 ]
Pishjoo, Masoud [4 ]
Rezaei, Nima [5 ]
机构
[1] Bushehr Univ Med Sci, Persian Gulf Trop Med Res Ctr, Dept Immunol Asthma & Allergy, Bushehr, Iran
[2] Bushehr Univ Med Sci, Dept Biochem, Bushehr, Iran
[3] Zahedan Univ Med Sci, Clin Immunol Res Ctr, Dept Immunol & Hematol, Zahedan, Iran
[4] Zahedan Univ Med Sci, Clin Immunol Res Ctr, Zahedan, Iran
[5] Univ Tehran Med Sci, Res Ctr Immunodeficiencies, Tehran, Iran
关键词
allergic diseases; immunotherapy; TLR9; Toll-like receptors; TOLL-LIKE-RECEPTORS; CPG OLIGODEOXYNUCLEOTIDES; IMMUNOSTIMULATORY DNA; IMMUNE-RESPONSE; CLINICAL-EFFICACY; CELL-ACTIVATION; CUTTING EDGE; MURINE MODEL; EAT DIRT; RECOGNITION;
D O I
10.2217/imt-2016-0104
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toll-like receptors (TLRs), a family of pattern recognition receptors expressed on many cell types of innate immunity, recognize the pathogen-associated molecular patterns of microbes. The hygiene hypothesis suggests that a reduced microbial exposure in early childhood increases the susceptibility to allergic diseases due to deviation in development of the immune system. TLRs are key roles in the right and healthy direction of adaptive immunity with the induction of T-helper 2 toward Th1 immune responses and regulatory T cells. TLR ligand CpG-ODN-based immunomodulation is independent of allergen and it mainly affects innate immune system. While, CpG-oligodeoxynucleotide- based vaccination is allergen specific and induces adaptive immune system. The use of agonists of TLR9 in two distinct strategies of immunotherapy, immunomodulation and vaccination, could be presented as the curative method for the treatment of allergic diseases.
引用
收藏
页码:339 / 346
页数:8
相关论文
共 75 条
[61]  
Spiegelberg HL, 2002, CURR OPIN MOL THER, V4, P64
[62]  
Sur S, 1999, J IMMUNOL, V162, P6284
[63]   TLR signaling pathways [J].
Takeda, K ;
Akira, S .
SEMINARS IN IMMUNOLOGY, 2004, 16 (01) :3-9
[64]   Toll-like receptors [J].
Takeda, K ;
Kaisho, T ;
Akira, S .
ANNUAL REVIEW OF IMMUNOLOGY, 2003, 21 :335-376
[65]   Preferentially the R-stereoisomer of the mycoplasmal lipopeptide macrophage-activating lipopeptide-2 activates immune cells through a toll-like receptor 2-and MyD88-dependent signaling pathway [J].
Takeuchi, O ;
Kaufmann, A ;
Grote, K ;
Kawai, T ;
Hoshino, K ;
Morr, M ;
Muhlradt, PF ;
Akira, S .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :554-557
[66]   Cutting edge: Role of Toll-like receptor 1 in mediating immune response to microbial lipoproteins [J].
Takeuchi, O ;
Sato, S ;
Horiuchi, T ;
Hoshino, K ;
Takeda, K ;
Dong, ZY ;
Modlin, RL ;
Akira, S .
JOURNAL OF IMMUNOLOGY, 2002, 169 (01) :10-14
[67]   Differential roles of TLR2 and TLR4 in recognition of gram-negative and gram-positive bacterial cell wall components [J].
Takeuchi, O ;
Hoshino, K ;
Kawai, T ;
Sanjo, H ;
Takada, H ;
Ogawa, T ;
Takeda, K ;
Akira, S .
IMMUNITY, 1999, 11 (04) :443-451
[68]  
Tulic Meri K., 2009, Allergology International, V58, P565, DOI 10.2332/allergolint.09-OA-0108
[69]   Amb a 1-immunostimulatory oligodeoxynucleotide conjugate immunotherapy decreases the nasal inflammatory response [J].
Tulic, MK ;
Fiset, PO ;
Christodoulopoulos, P ;
Vaillancourt, P ;
Desrosiers, M ;
Lavigne, F ;
Eiden, J ;
Hamid, Q .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2004, 113 (02) :235-241
[70]   Toll-like receptors and innate immunity [J].
Uematsu, Satoshi ;
Akira, Shizuo .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2006, 84 (09) :712-725