Superantigens: The good, the bad, and the ugly

被引:55
作者
Torres, BA
Kominsky, S
Perrin, GQ
Hobeika, AC
Johnson, HM
机构
[1] Univ Florida, Dept Microbiol & Cell Sci, Gainesville, FL 32611 USA
[2] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
来源
EXPERIMENTAL BIOLOGY AND MEDICINE | 2001年 / 226卷 / 03期
关键词
superantigens; autoimmunity; cancer; prophylactic vaccination;
D O I
10.1177/153537020122600303
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Increasing evidence suggests that superantigens play a role in immune-mediated diseases. Superantigens are potent activators of CD4(+) T cells, causing rapid and massive proliferation of cells and cytokine production. This characteristic of superantigens can be exploited in diseases where strong immunologic responses are required, such as in the B16F10 animal model of melanoma. Superantigen administration is able to significantly enhance ineffective anti-tumor immune responses, resulting in potent and long-lived protective anti-tumor immunity. However, superantigens are more well-known for the role they play in diseases. Studies using an animal model for neurologic demyelinating diseases such as multiple sclerosis show that superantigens can induce severe relapses and activate autoreactive T cells not involved in the initial bout of disease. This may also involve epitope spreading of disease. Superantigens have also been implicated in acute diseases such as food poisoning and TSS, and in chronic diseases such as psoriasis and rheumatoid arthritis. Viral superantigens are also involved in the disease process, including superantigens derived from human immunodeficiency virus and mouse mammary tumor virus. Finally, immunotherapies that ameliorate the role played by superantigens in disease are discussed.
引用
收藏
页码:164 / 176
页数:13
相关论文
共 117 条
[21]   Human natural killer (NK) cells present staphylococcal enterotoxin B (SEE) to T lymphocytes [J].
DOrazio, JA ;
SteinStreilein, J .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1996, 104 (02) :366-373
[22]   In vivo tumor transfection with superantigen plus cytokine genes induces tumor regression and prolongs survival in dogs with malignant melanoma [J].
Dow, SW ;
Elmslie, RE ;
Willson, AP ;
Roche, L ;
Gorman, C ;
Potter, TA .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (11) :2406-2414
[23]   INTERFERON BETA-1B IS EFFECTIVE IN RELAPSING-REMITTING MULTIPLE-SCLEROSIS - CLINICAL-RESULTS OF A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL [J].
DUQUETTE, P ;
GIRARD, M ;
DESPAULT, L ;
DUBOIS, R ;
KNOBLER, RL ;
LUBLIN, FD ;
KELLEY, L ;
FRANCIS, GS ;
LAPIERRE, Y ;
ANTEL, J ;
FREEDMAN, M ;
HUM, S ;
GREENSTEIN, JI ;
MISHRA, B ;
MULDOON, J ;
WHITAKER, JN ;
EVANS, BK ;
LAYTON, B ;
SIBLEY, WA ;
LAGUNA, J ;
KRIKAWA, J ;
PATY, DW ;
OGER, JJ ;
KASTRUKOFF, LF ;
MOORE, GRW ;
HASHIMOTO, SA ;
MORRISON, W ;
NELSON, J ;
GOODIN, DS ;
MASSA, SM ;
GUTTERIDGE, E ;
ARNASON, BGW ;
NORONHA, A ;
REDER, AT ;
MARTIA, R ;
EBERS, GC ;
RICE, GPA ;
LESAUX, J ;
JOHNSON, KP ;
PANITCH, HS ;
BEVER, CT ;
CONWAY, K ;
WALLENBERG, JC ;
BEDELL, L ;
VANDENNOORT, S ;
WEINSHENKER, B ;
WEISS, W ;
REINGOLD, S ;
PACHNER, A ;
TAYLOR, W .
NEUROLOGY, 1993, 43 (04) :655-661
[24]   GENES ENCODING LIGANDS FOR DELETION OF V-BETA-11 T-CELLS COSEGREGATE WITH MAMMARY-TUMOR VIRUS GENOMES [J].
DYSON, PJ ;
KNIGHT, AM ;
FAIRCHILD, S ;
SIMPSON, E ;
TOMONARI, K .
NATURE, 1991, 349 (6309) :531-532
[25]   Both T and B cells shed infectious mouse mammary tumor virus [J].
Dzuris, JL ;
Golovkina, TV ;
Ross, SR .
JOURNAL OF VIROLOGY, 1997, 71 (08) :6044-6048
[26]   AIDS - A SYNDROME OF IMMUNE DYSREGULATION, DYSFUNCTION, AND DEFICIENCY [J].
EDELMAN, AS ;
ZOLLAPAZNER, S .
FASEB JOURNAL, 1989, 3 (01) :22-30
[27]   TOXICITY OF INTERFERON AND INTERLEUKIN [J].
FENT, K ;
ZBINDEN, G .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1987, 8 (03) :100-105
[28]  
FESTENSTEIN H, 1973, TRANSPLANT REV-DENMA, V15, P62
[29]   2 TYPES OF MOUSE T-HELPER CELL .4. TH2 CLONES SECRETE A FACTOR THAT INHIBITS CYTOKINE PRODUCTION BY TH1 CLONES [J].
FIORENTINO, DF ;
BOND, MW ;
MOSMANN, TR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (06) :2081-2095
[30]   LINKAGE OF MLS GENES TO ENDOGENOUS MAMMARY-TUMOR VIRUSES OF INBRED MICE [J].
FRANKEL, WN ;
RUDY, C ;
COFFIN, JM ;
HUBER, BT .
NATURE, 1991, 349 (6309) :526-528