Cholera toxin, LT-I, LT-IIa and LT-IIb: the critical role of ganglioside binding in immunomodulation by Type I and Type II heat-labile enterotoxins

被引:65
作者
Connell, Terry D. [1 ]
机构
[1] Witebsky Ctr Microbiol Pathogenesis & Immunol, Sch Med & Biomed Sci, Dept Microbiol & Immunol, Buffalo, NY 14214 USA
关键词
adjuvant; enterotoxin; ganglioside; immunomodulation; signal transduction;
D O I
10.1586/14760584.6.5.821
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The heat-labile enterotoxins expressed by Vibrio cholerae (cholera toxin) and Escherichia coli (LT-I, LT-IIa and LT-IIb) are potent systemic and mucosal adjuvants. Coadministration of the enterotoxins with a foreign antigen produces an augmented immune response to that antigen. Although each enterotoxin has potent adjuvant properties, the means by which the enterotoxins induce various immune responses are distinctive for each adjuvant. Various mutants have been engineered to dissect the functions of the enterotoxins required for their adjuvanticity. The capacity to strongly bind to one or more specific ganglioside receptors appears to drive the distinctive immunomodulatory properties associated with each enterotoxin. Mutant enterotoxins with ablated or altered ganglioside-binding affinities have been employed to investigate the role of gangliosides in enterotoxin-dependent immunomodulation.
引用
收藏
页码:821 / 834
页数:14
相关论文
共 143 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   In vivo adjuvant-induced mobilization and maturation of gut dendritic cells after oral administration of cholera toxin [J].
Anjuère, F ;
Luci, C ;
Lebens, M ;
Rousseau, D ;
Hervouet, C ;
Milon, G ;
Holmgren, J ;
Ardavin, C ;
Czerkinsky, C .
JOURNAL OF IMMUNOLOGY, 2004, 173 (08) :5103-5111
[3]   Differential binding of Escherichia coli enterotoxins LT-IIa and LT-IIb and of cholera toxin elicits differences in apoptosis, proliferation, and activation of lymphoid cells [J].
Arce, S ;
Nawar, HF ;
Russell, MW ;
Connell, TD .
INFECTION AND IMMUNITY, 2005, 73 (05) :2718-2727
[4]   In vitro induction of immunoglobulin A (IgA)- and IgM-secreting plasma blasts by cholera toxin depends on T-cell help and is mediated by CD154 up-regulation and inhibition of gamma interferon synthesis [J].
Arce, Sergio ;
Nawar, Hesham F. ;
Muehlinghaus, Gwendolin ;
Russell, Michael W. ;
Connell, Terry D. .
INFECTION AND IMMUNITY, 2007, 75 (03) :1413-1423
[5]   Proinflammatory responses in the murine brain after intranasal delivery of cholera toxin: Implications for the use of AB toxins as adjuvants in intranasal vaccines [J].
Armstrong, ME ;
Lavelle, EC ;
Loscher, CE ;
Lynch, MA ;
Mills, KHG .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (09) :1628-1633
[6]   Cholera toxin and heat-labile enterotoxin activate human monocyte-derived dendritic cells and dominantly inhibit ctokine production through a cyclic AMP-dependent pathway [J].
Bagley, KC ;
Abdelwahab, SF ;
Tuskan, RG ;
Fouts, TR ;
Lewis, GK .
INFECTION AND IMMUNITY, 2002, 70 (10) :5533-5539
[7]   Mucosal immunization with HIV-1 peptide vaccine induces mucosal and systemic cytotoxic T lymphocytes and protective immunity in mice against intrarectal recombinant HIV-vaccinia challenge [J].
Belyakov, IM ;
Derby, MA ;
Ahlers, JD ;
Kelsall, BL ;
Earl, P ;
Moss, B ;
Strober, W ;
Berzofsky, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1709-1714
[8]  
Bukowski JF, 2000, EUR J IMMUNOL, V30, P3199, DOI 10.1002/1521-4141(200011)30:11<3199::AID-IMMU3199>3.0.CO
[9]  
2-Y
[10]  
Chen SC, 1999, ADV POLYM TECH, V18, P1, DOI 10.1002/(SICI)1098-2329(199921)18:1<1::AID-ADV1>3.0.CO