CpG ODN signal through Toll-like receptor 9 (TLR9) and trigger a cascade of events that lead to activation of innate and adaptive immune responses. Our current understanding of the immunobiology of host responses to CpG is based largely on studies on peripheral blood mononuclear cells (PBMC) and splenocytes. Little is known regarding CpG-induced responses in other lymphoid tissues. In the present study, we investigated responses induced by CpG in both PBMC and lymph nodes. Cells were isolated from the superficial cervical lymph node (LNC) and blood and then stimulated with CpG ODN (either A-, or B- or C-class ODN). Cytokine production was assayed by ELISA, and lymphocyte proliferation was determined by H-3-thymidine incorporation. NK-like cytotoxicity was analyzed by lysis of Cr-51-labelled target cells. All three classes of CpG induced IFN alpha and IFN-gamma in LNC. In contrast, only A and C-cl ass ODN induced IFN alpha and IFN gamma in PBMC. Moreover, the IFN levels in LNC were 20-40-fold higher than in PBMC. Furthermore, all classes of ODN induced higher IL-12 levels in LNC (five- to six-fold) than in PBMC. Both B and C-class ODN induced good proliferative responses in PBMC and LNC, but the A-class ODN did not induce proliferation of PBMC and only induced moderate proliferation of LNC. A-class ODN induced significant NK-like activity in LNC. Thus, all three classes of CpG ODN induced similar responses in LNC, and these responses were consistently higher than in PBMC. These observations indicate that CpG ODN-induced responses differ between blood and lymph nodes, and suggest that the functional classification of CpG ODN based on PBMC responses may not be directly applicable to cells from other immune tissues. (c) 2006 Elsevier B.V. All rights reserved.
机构:
Thomas Jefferson Univ, Dept Microbiol & Immunol, Bluemle Life Sci Bldg Room 709,233 South 10th St, Philadelphia, PA 19107 USAThomas Jefferson Univ, Dept Microbiol & Immunol, Bluemle Life Sci Bldg Room 709,233 South 10th St, Philadelphia, PA 19107 USA
Melo-Silva, Carolina R.
Sigal, Luis J.
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Thomas Jefferson Univ, Dept Microbiol & Immunol, Bluemle Life Sci Bldg Room 709,233 South 10th St, Philadelphia, PA 19107 USAThomas Jefferson Univ, Dept Microbiol & Immunol, Bluemle Life Sci Bldg Room 709,233 South 10th St, Philadelphia, PA 19107 USA
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Univ Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
Jassies-van der Lee, Annette
Rutten, Victor
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Univ Utrecht, Fac Vet Med, Div Immunol, Dept Infect Dis & Immunol, Utrecht, Netherlands
Univ Pretoria, Fac Vet Sci, Dept Vet Trop Dis, ZA-0110 Onderstepoort, South AfricaUniv Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
Rutten, Victor
Spiering, Rachel
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Univ Utrecht, Fac Vet Med, Div Immunol, Dept Infect Dis & Immunol, Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
Spiering, Rachel
van Kooten, Peter
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Univ Utrecht, Fac Vet Med, Div Immunol, Dept Infect Dis & Immunol, Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
van Kooten, Peter
Willemse, Ton
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Univ Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
Univ Utrecht, Fac Vet Med, Div Immunol, Dept Infect Dis & Immunol, Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands
Willemse, Ton
Broere, Femke
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Univ Utrecht, Fac Vet Med, Div Immunol, Dept Infect Dis & Immunol, Utrecht, NetherlandsUniv Utrecht, Fac Vet Med, Dept Clin Sci Compan Anim, Utrecht, Netherlands