CpG oligodeoxynucleotides induce cyclooxygenase-2 in human B lymphocytes: Implications for adjuvant activity and antibody production

被引:25
作者
Bernard, Matthew P.
Phipps, Richard P.
机构
[1] Univ Rochester, Sch Med & Dent, Dept Environm Med, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med & Dent, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[3] Univ Rochester, Sch Med & Dent, Lung Biol & Dis Program, Rochester, NY 14642 USA
关键词
B cells; antibodies; cyclooxygenase-2; CpG; NSAIDs; cox-2-selective inhibitors;
D O I
10.1016/j.clim.2007.07.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Synthetic CpG oligodeoxynucteotides (ODN), similar to DNA sequences found in certain microorganisms, have shown promise as adjuvants for humans by enhancing immune responses. Since antibodies are often indicators of successful vaccination, it is important to understand how CpG ODNs affect human B cells and influence antibody production. Treatment of human B cells with synthetic CpG ODN sequences increased both steady-state Cox-2 mRNA levels and protein expression. B cell receptor stimulation in concert with CpG ODN treatment induced Cox-2 expression and production of prostaglandin E-2, well above that seen with CpG ODN alone. Importantly, CpG-induced human B cell IgM and IgG production was attenuated by dual Cox-1/Cox-2 inhibitors and Cox-2-selective inhibitors. Our findings support a key role for CpG ODN-induced human B cell Cox-2 in the production of IgM and IgG antibodies, revealing that drugs that attenuate Cox-2 activity have the potential to reduce optimal. antibody response to adjuvants/vaccination. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:138 / 148
页数:11
相关论文
共 35 条
[1]   A role for Toll-like receptors in acquired immunity: up-regulation of TLR9 by BCR triggering in naive B cells and constitutive expression in memory B cells [J].
Bernasconi, NL ;
Onai, N ;
Lanzavecchia, A .
BLOOD, 2003, 101 (11) :4500-4504
[2]   IFN-γ mediates CD4+ T-cell loss and impairs secondary antitumor responses after successful initial immunotherapy [J].
Berner, Vanessa ;
Liu, Haiyan ;
Zhou, Qing ;
Alderson, Kory L. ;
Sun, Kai ;
Weiss, Jonathan M. ;
Back, Timothy C. ;
Longo, Dan L. ;
Blazar, Bruce R. ;
Wiltrout, Robert H. ;
Welniak, Lisbeth A. ;
Redelman, Doug ;
Murphy, William J. .
NATURE MEDICINE, 2007, 13 (03) :354-360
[3]   The toll-like receptor repertoire of human B lymphocytes: inducible and selective expression of TLR9 and TLR10 in normal and transformed cells [J].
Bourke, E ;
Bosisio, D ;
Golay, J ;
Polentarutti, N ;
Mantovani, A .
BLOOD, 2003, 102 (03) :956-963
[4]   The cyclooxygenases [J].
Chandrasekharan, NV ;
Simmons, DL .
GENOME BIOLOGY, 2004, 5 (09)
[5]   CpG DNA induces cyclooxygenase-2 expression and prostaglandin production [J].
Chen, YJ ;
Zhang, J ;
Moore, SA ;
Ballas, ZK ;
Portanova, JP ;
Krieg, AM ;
Berg, DJ .
INTERNATIONAL IMMUNOLOGY, 2001, 13 (08) :1013-1020
[6]  
Chuang TH, 2002, J LEUKOCYTE BIOL, V71, P538
[7]   Signal transduction pathways regulating cyclooxygenase-2 expression: potential molecular targets for chemoprevention [J].
Chun, KS ;
Surh, YJ .
BIOCHEMICAL PHARMACOLOGY, 2004, 68 (06) :1089-1100
[8]   Negative selection of human germinal center B cells by prolonged BCR cross-linking [J].
Galibert, L ;
Burdin, N ;
Barthelemy, C ;
Meffre, G ;
Durand, I ;
Garcia, E ;
Garrone, P ;
Rousset, F ;
Banchereau, J ;
Liu, YJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2075-2085
[9]   Host response to infection: the role of CpG DNA in induction of cyclooxygenase 2 and nitric oxide synthase 2 in murine macrophages [J].
Ghosh, DK ;
Misukonis, MA ;
Reich, C ;
Pisetsky, DS ;
Weinberg, JB .
INFECTION AND IMMUNITY, 2001, 69 (12) :7703-7710
[10]  
Graf BA, 1999, EUR J IMMUNOL, V29, P3793, DOI 10.1002/(SICI)1521-4141(199911)29:11<3793::AID-IMMU3793>3.0.CO