Immunosuppressive human anti-lymphocyte autoantibodies specific for the type 1 sphingosine 1-phosphate receptor

被引:13
作者
Liao, Jia-Jun
Huang, Mei-Chuan
Fast, Katharine
Gundling, Katherine
Yadav, Mahesh
Van Brocklyn, James R. [3 ]
Wabl, Matthias R. [2 ]
Goetzl, Edward J. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Med Ctr, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Microbiol Immunol, San Francisco, CA 94143 USA
[3] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
inflammation; chemotaxis; sphingolipid; G protein-coupled; LYMPHOCYTE EGRESS; ANTIBODIES; SPHINGOSINE-1-PHOSPHATE; S1P; ACTIVATION; IDENTIFICATION; SPHINGOLIPIDS; AGONIST; CELLS;
D O I
10.1096/fj.08-124891
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anti-lymphocyte antibodies (Abs) that suppress T-cell chemotactic and other responses to sphingosine 1-phosphate (S1P), but not to chemokines, were found in a lymphopenic patient with recurrent infections. Lymphocyte type 1 S1P receptor (S1P(1)) that transduces S1P chemotactic stimulation was recognized by patient Abs in Western blots of T cells, S1P(1) transfectants, and S1P(1)-hemagglutinin purified by monoclonal anti-hemagglutinin Ab absorption. The amino terminus of S1P(1), but not any extracellular loop, prevented anti-S1P(1) Ab suppression of S1P(1) signaling and T-cell chemotaxis to S1P. Human purified anti-S1P(1) Abs decreased mouse blood lymphocyte levels by a mean of 72%, suppressed mouse T-cell chemotaxis to S1P in vivo, and significantly reduced the severity of dextran sodium sulfate-induced colitis in mice. Human Abs to the amino terminus of S1P(1) suppress T-cell trafficking sufficiently to impair host defense and provide therapeutic immunosuppression.-Liao, J.- J., Huang, M.-C., Fast, K., Gundling, K., Yadav, M., Van Brocklyn, J. R., Wabl, M. R., Goetzl, E. J. Immunosuppressive human anti-lymphocyte autoantibodies specific for the type 1 sphingosine 1-phosphate receptor. FASEB J. 23, 1786-1796 (2009)
引用
收藏
页码:1786 / 1796
页数:11
相关论文
共 36 条
[1]   The sources of a lipid conundrum [J].
Chun, Jerold .
SCIENCE, 2007, 316 (5822) :208-210
[2]   Transduction of multiple effects of sphingosine 1-phosphate (S1P) on T cell functions by the S1P1 G protein-coupled receptor [J].
Dorsam, G ;
Graeler, MH ;
Seroogy, C ;
Kong, Y ;
Voice, JK ;
Goetzl, EJ .
JOURNAL OF IMMUNOLOGY, 2003, 171 (07) :3500-3507
[3]   Type 1 sphingosine 1-phosphate G protein-coupled receptor signaling of lymphocyte functions requires sulfation of its extracellular amino-terminal tyrosines [J].
Fieger, CB ;
Huang, MC ;
Van Brocklyn, JR ;
Goetzl, EJ .
FASEB JOURNAL, 2005, 19 (11) :1926-+
[4]   Regulation of gut inflammation and TH17 cell response by interleukin-21 [J].
Fina, Damele ;
Sarra, Massimiliano ;
Fantini, Massimo C. ;
Rizzo, Angelamaria ;
Caruso, Roberta ;
Caprioli, Flavio ;
Stolfi, Carmine ;
Cardolini, Iris ;
Boirivant, Monica ;
Pallone, Francesco ;
MacDonald, Thomas T. ;
Monteleone, Giovanni .
GASTROENTEROLOGY, 2008, 134 (04) :A256-A256
[5]   Identification of the hydrophobic ligand binding pocket of the S1P1 receptor [J].
Fujiwara, Yuko ;
Osborne, Daniel A. ;
Walker, Michelle D. ;
Wang, De-an ;
Bautista, Debra A. ;
Liliom, Karoly ;
Van Brocklyn, James R. ;
Parrill, Abby L. ;
Tigyi, Gabor .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (04) :2374-2385
[6]  
GILBREATH MJ, 1983, CLIN EXP IMMUNOL, V51, P232
[7]   Full Pharmacological Efficacy of a Novel S1P1 Agonist That Does Not Require S1P-Like Headgroup Interactions [J].
Gonzalez-Cabrera, Pedro J. ;
Jo, Euijung ;
Sanna, M. Germana ;
Brown, Steven ;
Leaf, Nora ;
Marsolais, David ;
Schaeffer, Marie-Therese ;
Chapman, Jacqueline ;
Cameron, Michael ;
Guerrero, Miguel ;
Roberts, Edward ;
Rosen, Hugh .
MOLECULAR PHARMACOLOGY, 2008, 74 (05) :1308-1318
[8]   Activation-regulated expression and chemotactic function of sphingosine 1-phosphate receptors in mouse splenic T cells [J].
Graeler, M ;
Goetzl, EJ .
FASEB JOURNAL, 2002, 16 (14) :1874-1878
[9]   Protein kinase C ε dependence of the recovery from down-regulation of S1P1 G protein-coupled receptors of T lymphocytes [J].
Graeler, MH ;
Kong, Y ;
Karliner, JS ;
Goetzl, EJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (30) :27737-27741
[10]  
Grähler MH, 2005, J IMMUNOL, V174, P1997