2011, Number 2
<< Back Next >>
Rev Med MD 2011; 2.3 (2)
Decrease of pro-inflammatory cytokines and regulation of Toll-like receptors 2 and 4 expression in neutrophils and monocytes after the administration of a symbiotic on patients with infection by HIV
González-Hernández LA, Fafutis-Morris M, Montes-Salcedo KE, Valle-Gutiérrez LG, Andrade-Villanueva JF
Language: Spanish
References: 19
Page: 60-66
PDF size: 539.89 Kb.
ABSTRACT
Background: The human immunodeficiency virus (HIV) induces an immune dysfunction propitiating the onset of HIV
associated enteropathy. Neither the benefits nor the safety of the use of probiotics on patients with HIV have been studied.
Objective: To assess whether the intestinal microbiota modification with the use of symbiotic regulates the TLR 2 and 4
expression in peripheral blood monocytes and neutrophils. Moreover, to provide evidence of a diminution of plasmatic proinflammatory
cytokines.
Methods: Randomized clinical trial, double blind, performed in the Unit of HIV/AIDS in Guadalajara's “Fray Antonio
Alcalde” Civil Hospital and the Centro de investigación en Inmunología y Dermatología in the Health sciences campus of the
University of Guadalajara during 2008 to 2010. 20 patients were included and distributed in 4 groups of 5 individuals with
infection by HIV-1 without retroviral treatment and no admission criteria (Stage ≥ B), with CD4
+T cells > 350 cells/µ L. The
group A was assigned to received the symbiotic, the group B a probiotic, the group C a prebiotic, and the group D a placebo. The
concentrations of cytokines in plasma were quantified (IL-1β, IL-10 and TNF-α) and the TLR 2 and 4 expression in monocytes
and neutrophils through flow cytometry.
Results: In the group A, was observed a decrease in the concentration of IL-6 (p‹ 0.05). For the IL-1β, IL-10 and TNF-α
concentrations, no significant difference was observed. The TLR-4 expression in neutrophils and monocytes presented an
increase. However, it was not a statistical difference (p=0.056). In the group B, no significant statistical differences were
observed for IL-6, TNF-α, IL-1β and IL-10. The TLR-2 presented a significant statistical increase in expression in neutrophils
(p=‹ 0.016), but with no significant changes in monocytes. In the groups C and D, there was no significance on the
concentration of IL-1β, IL-10 and TNF-α. However, the placebo group had a significant negative correlation, between T cells
CD4
+and IL-6 concentration (r =-1.0, p =0.01).
Conclusions: The use of symbiotic diminishes the levels of IL-6 on patients with HIV who have not yet developed AIDS
showing safety on use.
REFERENCES
1.Sodora DL, Silvestri G. Immune activation and AIDS pathogenesis. AIDS 2008,22:439-446.
2.Sumpter B, Dunham R, Gordon S, Engram J, Hennessy M, Kinter A, et al. Correlates of preserved CD4(+) T cell homeostasis during natural, nonpathogenic simian immunodeficiency virus infection of sooty mangabeys: implications for AIDS pathogenesis. J Immunol 2007,178:1680-1691.
3.Lin WW, Karin M. A cytokine-mediated link between innate immunity, inflammation, and cancer. J Clin Invest 2007,117:1175-1183.
4.Levy JA. Prospects for an AIDS vaccine: encourage innate immunity. AIDS 2004,18:2085-2086.
5.Heidemann J, Domschke W, Kucharzik T, Maaser C. Intestinal microvascular endothelium and innate immunity in inflammatory bowel disease: a second line of defense? Infect Immun 2006,74:5425-5432.
6.Lester RT, Yao XD, Ball TB, McKinnon LR, Kaul R, Wachihi C, et al. Toll-like receptor expression and responsiveness are increased in viraemic HIV-1 infection. AIDS 2008,22:685-694.
7.Sartor RB. Microbial influences in inflammatory bowel diseases. Gastroenterology 2008,134:577-594.
8.Schacker TW, Brenchley JM, Beilman GJ, Reilly C, Pambuccian SE, Taylor J, et al. Lymphatic tissue fibrosis is associated with reduced numbers of naive CD4+ T cells in human immunodeficiency virus type 1 infection. Clin Vaccine Immunol 2006,13:556-560.
9.Centlivre M, Sala M, Wain-Hobson S, Berkhout B. In HIV-1 pathogenesis the die is cast during primary infection. AIDS 2007,21:1-11.
10.Goldin BR, Gorbach SL. Clinical indications for probiotics: an overview. Clin Infect Dis 2008,46 Suppl 2:S96-100; discussion S144-151.
11.Hoffman FA, Heimbach JT, Sanders ME, Hibberd PL. Executive summary: scientific and regulatory challenges of development of probiotics as foods and drugs. Clin Infect Dis 2008,46 Suppl 2:S53-57.
12.Senok AC, Ismaeel AY, Botta GA. Probiotics: facts and myths. Clin Microbiol Infect 2005,11:958-966.
13.Parvez S, Malik KA, Ah Kang S, Kim HY. Probiotics and their fermented food products are beneficial for health. J Appl Microbiol 2006,100:1171-1185.
14.Mohamadzadeh M, Olson S, Kalina WV, Ruthel G, Demmin GL, Warfield KL, et al. Lactobacilli activate human dendritic cells that skew T cells toward T helper 1 polarization. Proc Natl Acad Sci U S A 2005,102:2880-2885.
15.Abreu MT. Toll-like receptor signalling in the intestinal epithelium: how bacterial recognition shapes intestinal function. Nat Rev Immunol 2010,10:131-144.
16.Walker WA. Mechanisms of action of probiotics. Clin Infect Dis 2008,46 Suppl 2:S87-91; discussion S144-151.
17.Shida K, Nanno M. Probiotics and immunology: separating the wheat from the chaff. Trends Immunol 2008,29:565-573.
18.Brenchley JM, Douek DC. The mucosal barrier and immune activation in in HIV pathogenesis. Curr Opin HIV AIDS 2008,3:356-361.
19.Tsai CS, Chen DL, Lin SJ, Tsai JC, Lin TC, Lin CY, et al. TNF-alpha inhibits toll-like receptor 4 expression on monocytic cells via tristetraprolin during cardiopulmonary bypass. Shock 2009,32:40-48.