Mangifera indica L. extract (Vimang) and mangiferin modulate mouse humoral immune responses

被引:82
作者
García, D
Leiro, J [1 ]
Delgado, R
Sanmartín, ML
Ubeira, FM
机构
[1] Univ Santiago de Compostela, Fac Farm, Parasitol Lab, Dept Microbiol & Parasitol, E-15782 Santiago De Compostela, Spain
[2] Univ Santiago de Compostela, Inst Invest & Anal Alimentarios, Parasitol Lab, E-15782 Santiago De Compostela, Spain
[3] Ctr Quim Farmaceut, Farmacol Lab, Ciudad Habana, Havana, Cuba
关键词
microsporidian spores; antibodies; ELISA; CELISA; Mangifera indica extract; mangiferin;
D O I
10.1002/ptr.1338
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The present study investigated the effects of orally administered Vimang (an aqueous extract of Mangifera indica) and mangiferin (the major polyphenol present in Vimang) on mouse antibody responses induced by inoculation with spores of microsporidian parasites. Inoculation induced specific antibody production with an exponential timecourse, peaking after about one month. Vimang significantly inhibited this antibody production from about three weeks post-inoculation, and most markedly by four weeks post-inoculation; by contrast, mangiferin had no significant effect. Determination of Ig isotypes showed that the IgM to IgG switch began about four weeks post-inoculation, with IgG2a predominating. Vimang significantly inhibited IgG production, but had no effect on IgM. Mangiferin did no affect either IgM or IgG2a, but significantly enhanced production of IgG1 and IgG2b. Neither Vimang nor mangiferin enhanced specific antibody secretion by splenic plasma cells from mice inoculated with microsporidian spores, whether administered in vivo before serum extraction or in vitro to the culture medium. Inoculation with spores induced splenomegaly, which was significantly reduced by Vimang and significantly enhanced by mangiferin. These results suggest that components of Mangifera indica extracts may be of potential value for modulating the Immoral response in different immunopathological disorders. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:1182 / 1187
页数:6
相关论文
共 59 条
[1]  
AWE SP, 1988, PHYTOTHER RES, V12, P437
[2]   Interferon-γ is required for lupus-like disease and lymphoaccumulation in MRL-lpr mice [J].
Balomenos, D ;
Rumold, R ;
Theofilopoulos, AN .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) :364-371
[3]   Carrier-dependent suppression of the anti-phosphorylcholine plaque-forming cell response in Trichinella-infected mice is mediated by anti-hapten IgG1 antibodies [J].
Baltar, P ;
Romarís, F ;
Estévez, J ;
Leiro, J ;
Ubeira, FM .
EXPERIMENTAL PARASITOLOGY, 1998, 90 (01) :95-102
[4]   IFN-GAMMA ENHANCES SECRETION OF IGG2A FROM IGG2A-COMMITTED LPS-STIMULATED MURINE B-CELLS - IMPLICATIONS FOR THE ROLE OF IFN-GAMMA IN CLASS SWITCHING [J].
BOSSIE, A ;
VITETTA, ES .
CELLULAR IMMUNOLOGY, 1991, 135 (01) :95-104
[5]  
Braunfuchsová P, 1999, FOLIA PARASIT, V46, P91
[6]   MICROSPORIDIA OF MAMMALS - WIDESPREAD PATHOGENS OR OPPORTUNISTIC CURIOSITIES [J].
CANNING, EU ;
HOLLISTER, WS .
PARASITOLOGY TODAY, 1987, 3 (09) :267-273
[7]   ACTIVATION OF LYMPHOCYTES OF NORMAL AND TUMOR-BEARING MICE BY MANGIFERIN, A NATURALLY-OCCURRING GLUCOSYLXANTHONE [J].
CHATTOPADHYAY, U ;
DAS, S ;
GUHA, S ;
GHOSAL, S .
CANCER LETTERS, 1987, 37 (03) :293-299
[8]   CpG oligodeoxynucleotides act as adjuvants that switch on T helper 1 (Th1) immunity [J].
Chu, RS ;
Targoni, OS ;
Krieg, AM ;
Lehmann, PV ;
Harding, CV .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (10) :1623-1631
[9]   Screening of medicinal plants used by the Garifuna of eastern Nicaragua for bioactive compounds [J].
Coe, FG ;
Anderson, GJ .
JOURNAL OF ETHNOPHARMACOLOGY, 1996, 53 (01) :29-50
[10]   Dynamics of the murine humoral immune response to Neisseria meningitidis group B capsular polysaccharide [J].
Colino, J ;
Outschoorn, I .
INFECTION AND IMMUNITY, 1998, 66 (02) :505-513