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Revista da Sociedade Brasileira de Medicina Tropical

Print version ISSN 0037-8682On-line version ISSN 1678-9849

Rev. Soc. Bras. Med. Trop. vol.42 no.3 Uberaba May/June 2009

http://dx.doi.org/10.1590/S0037-86822009000300021 

COMMUNICATION COMUNICAÇÃO

 

Boosting the suppressive effects of Ascaris suum components in IFN-γ-deficient mice

 

Potencialização do efeito supressor de componentes do Ascaris suum em camundongos deficientes em IFN-γ

 

 

Valdênia Maria Oliveira SouzaI; Mahasti Sahihi MacedoII

ILaboratory of Immunopathology Keizo Asami, Department of Pharmaceutical Sciences, Federal University of Pernambuco, Recife, PE, Brazil
IIDepartment of Immunology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil

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ABSTRACT

High molecular weight components from Ascaris suum extract suppress ovalbumin-specific immunity in mice. In IFN-γ-deficient mice, ovalbumin-specific delayed-type hypersensitivity reactions are more strongly downregulated by these suppressive components. Here, the cellularity of the delayed-type hypersensitivity reaction in IFN-γ-deficient mice and the increased downregulation induced by Ascaris suum components were analyzed. IL-12p40-dependent neutrophilic influx was predominant. Suboptimal doses of the suppressive fraction from this nematode completely inhibited the hypersensitivity reaction, thus indicating intensification of the immunosuppression under conditions of intense recruitment of IFN-γ-independent neutrophils.

Key-words: Ascaris suum. Delayed-type hypersensitivity. Immunosuppression. IFN-γ-deficient mice. Neutrophil.


RESUMO

Componentes de alto peso molecular do extrato de Ascaris suum suprimem a imunidade específica à ovalbumina em camundongos. Em camundongos geneticamente deficientes de IFN-γ a reação de hipersensibilidade tardia específica para ovalbumina foi mais fortemente prejudicada por estes componentes supressivos. Aqui, a celularidade da reação de hipersensibilidade tardia em camundongos deficientes de IFN-γe o incremento na supressão induzida por componentes do Ascaris suum foram analisados. Influxo neutrofílico, dependente de IL-12p40, foi predominante. Dose sub-ótima da fração supressiva do nematódeo inibiu completamente a reação de hipersensibilidade, indicando uma intensificação da imunossupressão em condições de recrutamento intenso de neutrófilos independente de IFN-γ.

Palavras-chaves: Ascaris suum. Hipersensibilidade tardia. Imunossupressão. Camundongos deficientes em IFN-γ. Neutrófilos.


 

 

Helminth infections inhibit the host's protective Th1-type immune response to non-related pathogenic agents such as virus, parasites and bacterial antigens1 4 11. On the other hand, harmful Th1 or Th2 responses leading to autoimmune encephalomyelitis or enteric allergy, respectively, can be also controlled in the presence of helminth antigens3 15. With regard to the nematode Ascaris suum, the regulatory mechanisms induced by its immunosuppressive components have been the focus of our studies for some time. These components correspond to the high molecular weight fraction, eluted in the first peak (PI), after gel filtration chromatography of the adult Ascaris suum body extract5. In mice, when PI was combined with ovalbumin (OVA) and adjuvant, both OVA-specific Th1 and Th2 immune responses were found to be impaired (lymphoproliferation, delayed-type hypersensitivity (DTH) reactions, IgG2a/IgG1/IgE and IL-2/IFN-γ/IL-4/IL-10 production)5. Using IL-4 or IL-10 knockout mice that were immunized in the same way, we demonstrated the essential role of IL-10 in suppressing the OVA-specific Th2 immune response, while IL-10 plus IL-4 were required for suppressing Th1-related parameters18. In IL-12 or IFN-γ knockout mice, the PI suppressive ability remained intact. Unexpectedly, OVA-immunized IFN-γ-deficient mice developed a very intense OVA-specific DTH reaction, that seemed to be more strongly impaired when these mice received PI18. Thus, in the present study, we investigated the type of infiltrating cell in an OVA-specific DTH and analyzed the intensity of the suppressive effect of PI in the absence of IFN-γ.

For this, C57BL/6 mice that presented targeted disruption of the IFN-γ gene (IFN-γ-/-) and wild-type C57BL/6 mice were subcutaneously immunized with OVA (200µg of protein/animal; Sigma Chemical Co) or OVA (200µg of protein/animal) plus PI (200 or 50µg of protein/animal), emulsified in complete Freund's adjuvant (Sigma Chemical Co), on the base of the tail (0.2ml/animal). PI was obtained after gel filtration chromatography (XK 26/100 column of Sephacryl S-200; Pharmacia, Uppsala, Sweden) on adult Ascaris suum body extract and was concentrated with Centriprep 100 (Amicon, Beverly, MA, USA)5. After eight days, the mice were challenged in the hind footpad with 2% aggregated OVA, and the DTH reaction was measured 24 hours later. Histopathological analyses on footpads (stained with Lunas) from animals in each group were compared. The results represent the mean ± standard error of the mean for 5-7 animals/group. To test the significance between the groups, one-way analysis of variance was used, followed by multiple comparisons using Tukey's method21. Statistical significance was set at p < 0.05. The results were representative of three experiments.

As expected, the anti-OVA DTH reaction in IFN-γ-/- mice was significantly greater than in wild-type mice (Figure 1). The high dose of PI (200µg) completely suppressed DTH in both wild-type and IFN-deficient mice. In contrast, the low dose (50µg) had this same drastic effect only in IFN-γ-/- mice. In wild-type mice, this dose reduced the reaction to half of that obtained in wild-type mice immunized with OVA alone. Analysis on the cellular infiltrate in the footpads showed predominance of neutrophils in OVA-immunized IFN-γ-/- mice, with a few eosinophils, in comparison with intense mononuclear cell infiltrate in the OVA-immunized wild-type mice. Ovalbumin plus PI-immunized IFN-γ-/- mice presented scarce cellular infiltrate (data not shown).

 

 

IL-12 is required for type 1 immune responses and IFN-γ production to develop9. We have shown that almost no DTH reaction is obtained in our immunization model for genetic deficiency of IL-12 production18. Additionally, another IL-12 family member, IL-23, is committed to the Th17-subtype mediated immune response, in which IL-17 is secreted20. The Th17-type immune response elicits acute inflammation/neutrophilic response14 20. IL-12 and IL-23 share the IL-12p40 subunit, which binds respectively to distinct p35 and p19 subunits, while binding to a specific cell receptor12.

Here, we analyzed the role of the IL-12p40 subunit in anti-OVA DTH from IFN-γ-/- mice using an anti-IL-12p40 monoclonal antibody treatment (C17.8; kindly provided by Dr R.L. Coffman, Dynavax Technologies, Berkeley, CA, USA), before immunization with OVA (200µg of protein/animal) or OVA (200µg of protein/animal) plus PI (200µg of protein/animal). Wild-type and IFN-γknockout mice received anti-β-galactosidase monoclonal control antibody (GL117) before similar immunization. IL-12p40 neutralization eliminated the anti-OVA DTH reaction in the footpad of IFN-γ-deficient mice (Figure 2), thus corroborating the regulatory function of IL-12 family cytokines in both mononuclear cells and the neutrophilic influx into the footpad after antigen challenge.

 

 

Replacement of a mononuclear cell by eosinophilic or neutrophilic infiltrate due to lack of IFN-γ has been demonstrated in experimental infection models2 8 19. Here, for OVA immunization, few eosinophils were observed whereas neutrophils were predominant. The pro-inflammatory cytokine TNF-α and neutrophil-attractive chemokines are extensively produced in IFN-γ-/- mice2 8 and could become committed to this type of cell influx. Furthermore, the IL-23-IL-17 axis provides synthesis of attractant chemokines and extracellular matrix proteins relating to neutrophil recruitment14 20.

Induction of IL-10 synthesis by PI has been demonstrated to be the main immunosuppressive mechanism6 13 18. It has been shown that PI downregulates the expression of costimulatory agents (CD40, CD80 and CD86) and major histocompatibility complex II molecules on the surface of dendritic cells and, consequently, reduces the antigen-presenting function of these cells. This effect was mediated by IL-1016. IFN-γ and IL-10 have opposite effects on immune system activation10. It is most likely that, in the absence of IFN-γ, IL-10 induced by PI has a more potent suppressive function, including on TNF-α, IL-12 and IL-23 action. This would explain why low doses of PI are more effective in IFN-γ-deficient mice.

Ascaris species are similar in their capacity to suppress the protective immune response of the host4. In this regard, our results show that PI impaired the IL-12p40-mediated neutrophilic influx. IL-23 action has been related to the protective neutrophil response to infection by extracellular bacterial species20 or intracellular parasites7. On the other hand, Ascaris products have been demonstrated to be a potential therapeutic strategy for inflammatory diseases17 such as lung allergic inflammation and LPS-induced inflammation. We hypothesize that PI could fulfill a control strategy for autoimmune inflammation, mediated independently of IL-12-IFN-γ (arthritis, multiple sclerosis, psoriasis and inflammatory bowel disease), but strikingly related to IL-23-IL-17 synthesis20.

In conclusion, our results indicate that the products from IL-10-inducing Ascaris nematodes exhibit improved immunosuppressive properties in settings in which IFN-γ synthesis is not essential for the inflammatory process. This finding emphasizes that these molecules have wide use as therapeutic tools for different clinical approaches.

 

ACKNOWLEDGEMENTS

We thank by supported by the Research Support Foundation of the State of São Paulo (FAPESP) and Marilú Mazzaro for competent technical assistance.

 

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Address to:
Dra. Valdênia M.O. Souza
Laboratório de Imunopatologia Keizo Asami/UFPE
Av. Prof. Moraes Rego s/n, Cidade Universitária
50670-901 Recife, PE, Brazil
Tel: 55 81 2101-2515; Fax: 55 81 2126-8485
e-mail: valdenia.souza@ufpe.br

Received in 19/11/2007
Accepted in 14/04/2009
Financial support: Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP).

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