Printer Friendly

Upregulation of Cardiac IL-10 and Downregulation of IFN-[gamma] in Balb/c [IL-4.sup.-/-]in Acute Chagasic Myocarditis due to Colombian Strain of Trypanosoma cruzi.

1. Introduction

Chagas disease, also known as American trypanosomiasis, is a chronic systemic infectious disease caused by the protozoan Trypanosoma cruzi (T. cruzi), an important public health problem in American continent. According to the World Health Organization (WHO), the disease affects around 7.5 million people worldwide, the majority in Latin America [1,2].

Murine experimental model reproduces human Chagas' disease infections, and genetic background has influences both, triggering a series of reactions that evolve from an acute symptomatic phase to chronic phase [3]. Some variables interfere in Chagas' disease pathogenicity such as the infecting strain and the mouse lineage. Balb/c strain mice are known to be susceptible to T. cruzi infection, present a high parasitemia and the vast majority succumb early to acute infection [4]. Colombian strain has been used in several studies with the purpose of evaluating cardiac function due to its evident myotropism [5]. Prominent myocardial lesions with intense inflammatory process, evolution in parasitemia with peak between 21 and 25 days of postinfection, distinct myotropism with involvement of the skeletal musculature resulting in extensive lesions in the skeletal muscle fibers, electrocardiographic alterations, and resistance to chemotherapeutics such as benznidazole and nifurtimox are characteristics of this strain. [6, 7].

Knockout model is widely used in studies that evaluate direct or indirect implication of certain cytokines in resistance to T. cruzi infection. IL-10 KO mice infected with T. cruzi Y strain had lower serum and tissue parasite load and higher IFN-gamma and nitric oxide production by spleen cells than wild-type mice [8]. Furthermore, IL-10 KO mice infected with the Tulahuen strain, in addition to lower serum parasite load, also showed higher levels of serum TNF-[alpha], IL-12, and IFN-gamma compared with infected [IL-10.sup.+/+] mice [9]. Knockout models for other molecules as B2-microglobulin [10], CD4 or CD8 [11], gamma delta T cells [12],and Fas ligand [13] were also used in studies on Chagas disease.

In acute phase, Chagas disease has variable clinical presentations, from asymptomatic to symptomatic and even fatal in some cases. Parasite proliferation and dissemination by blood or lymphatic vessels characterized this phase, with a parasitemia peak that regresses in some days and tends to be undetectable in chronic phase. Acute phase dissemination affects several cellular types, especially cardiac muscle fibers, with amastigotes nest formation [14], myocarditis, and subsequent collagen deposition between cardiac fibers, causing progressive functional damage. Excessive immune system activation with proinflammatory cytokine production of Th1-type IL-12, TNF-[alpha], and IFN-[gamma] characterizes this phase. On the other hand, cytokines such as IL-10 and TGF-[beta] are activated to modulate immune response with consequent reduction of tissue damage [15, 16].

IL-4 is described as an anti-inflammatory cytokine, prototypic of Th2 profile, and related to susceptibility to protozoa infection, such as cutaneous leishmaniasis [17, 18], although even in models of polarized clinical manifestations, its relation with Th1 response still raises major controversies [19]. IL-4 reduces IFN-[gamma] production [20] controlling Th1 response and preventing excessive tissue inflammation [21]. IL-4 knockout animals tend to have better response to infection by intracellular parasites, and when infected by T. cruzi, they increase Th1-type immune response, resulting in decreased parasitemia and mortality and increased cardiac inflammatory reaction, although these effects are observed in late stages of acute or in chronic phase [21, 22]. On the basis of in vitro testing, two contrasting roles for IL-4 have been described: enhancement of intracellular T. cruzi destruction by macrophages [23] and inhibition of IFN-[gamma]mediated trypanocidal activity [24].

Our group had already pointed out that infected and reinfected animals with Colombian strain present a modulation of immune response leading to higher production of proinflammatory cytokines, such as IFN-[gamma] and TNF-[alpha], resulting in marked myocarditis and lower survival rate [25]. As Balb/c mice are usually good IL-4 producers [26] and due to [IL-4.sup.-/-] relevance in modulating response against infectious and parasitic agents, including chagasic cardiomyopathy, [IL-4.sup.-/-] knockout animals were used to analyze if this cytokine has any influence on immune response modulation in mice infected with T. cruzi Colombian strain, which has marked myotropism in acute phase. We demonstrate that in early stages of acute phase, [IL-4.sup.-/-] knockout animals presented milder myocarditis with lower IFN-[gamma] production and higher in situ IL-10 production, despite Th1 cells increase in splenocyte general repertoire. Our results open perspectives of IL-4 role in chagasic myocarditis initial events in a more complex frame than the dichotomy Th1/Th2.

2. Material and Methods

2.1. Animals and Infection. We evaluated male animals of Balb/c WT and Balb/c [IL-4.sup.-/-] lineages infected with T. cruzi Colombian strain (n = 8) and an uninfected group (n = 6), both aged 10 weeks and weighing 20-25 g. Infections were performed using trypomastigote forms obtained at peak of parasitemia from previously infected Swiss mice (Waynforth and Flecknell, 1992). Briefly, Swiss mice were euthanized and peripheral blood was collected by cardiac puncture. Five microliters of blood was used to quantify parasite number in a hematocytometer, counted in fifty microscopic fields at a final magnification of x400. Inoculum was adjusted to 1000 trypomastigotes/ml. One hundred (100) trypomastigote forms were subcutaneously inoculated. Animals were euthanized

on the 21st day of infection for acute phase. Next, necropsy was performed and the heart was collected through a ventral incision in thoracic cavity. This research was approved by CEUA/UFG.

2.2. Histological Analysis. To evaluate inflammatory infiltrate, slides of cardiac tissue (ventricle) stained with hematoxylin and eosin (HE) were used. Qualitative analysis classified infiltrate as predominantly mononuclear (macrophages and lymphocytes) or polymorphonuclear (neutrophils and eosinophils), according to the cellular type observed in more than 50% of the infiltrate. Semiquantitative analysis classified the inflammatory infiltrate in mild (involvement < 25% of the tissue), moderate (25%-50% of the tissue), or severe (involvement > 50% of the tissue) [25].

Tissue parasitism was quantified under light microscopy by the number of myocardium T. cruzi nests using three slides with serial slices. All infected animals had nests.

For collagen quantification, we used the heart sections stained with sirius red. Slides were analyzed in polarized light microscope at a final magnification of x400 with a semiautomatic interactive image analyzer system, ImageJ[R] (National Institutes of Health, Bethesda, EUA).

2.3. Immunological Analysis

2.3.1. Cardiac Tissue Homogenate Preparation. The heart tissue sections were immersed in PBS solution containing complete protease inhibitor (Sigma, St. Louis, MO, USA) and Nonidet-P40. After that, they were submitted to tissue homogenizer. The homogenate obtained was centrifuged at 14,000 xg for 10 minutes, and the supernatant was maintained for quantification of cytokines and total proteins [25].

2.3.2. Culture of Splenocytes. Mouse splenocytes were collected, maintained in RPMI 1640 medium (GE Healthcare, Uppsala, Sweden) and macerated for cell individualization. These suspended cells were washed three times by centrifugation at 400 x g for 15 min at 8[degrees]C in RPMI 1640. Then, they were counted in a Neubauer chamber and resuspended to 2 x 106 cells/ml in RPMI 1640 medium with addition of 50 mM Hepes (Gibco, Grand Island, NY, USA), 5% of inactivated fetal bovine serum (Gibco, USA), 2 mM L-glutamine (Gibco, USA), 0.05 mM 2[beta]-mercaptoethanol (Gibco, USA), and 40 [micro]g/ml gentamicin (Neoqumica, Anapolis, GO, BR). Then, 2 x [10.sup.6] cells were incubated without stimulus or with 10 [micro]g/ml of concanavalin A in 24-well culture plates (BD Pharmingen, San Diego, CA, USA). Cultures were kept in a moist incubator with 5% C[O.sub.2] at 37[degrees]C for 48 hours. Supernatants were collected and maintained at -70[degrees]C until analysis [25].

2.3.3. TNF-[alpha], IL-12p70, IL-10, IFN-[gamma], and IL-17 Quantification. Cytokine quantification was performed on cardiac homogenate, spleen culture, and serum cells by ELISA (enzyme-linked immunosorbent assay), using antibody pairs from BD commercial kit (Biosciences, USA) and following manufacturer's instructions. Reaction was developed using 3,3',5,5'-tetramethylbenzidine (TMB) peroxidase substrate and read at 450 nm. For cardiac homogenate, results were normalized to total protein concentration, determined by Bradford assay (Bio-Rad, Hercules, CA, USA) of each heart and expressed as picogram of cytokine per gram of tissue (pg/g of tissue).

2.4. Statistical Analyses. The GraphPad Prism 6.0 software (GraphPad Software, USA) was used. Student's t-test was used for analysis between two groups with normal distribution.

Qualitative variables were expressed as percentage and associations were analyzed using the chi-square ([chi square]) test. Results were considered statistically significant when p < 0.05.

3. Results

3.1. Balb/c [IL-4.sup.-/-] Mice Infected with T. cruzi Strain Presented Less Intense Inflammatory Infiltrate in Acute Phase of Infection. Inflammatory cardiac infiltrate in Balb/c WT and Balb/c [IL-4.sup.-/-] mice infected with Colombian strain in acute phase of experimental Chagas disease was analyzed. IL-4 absence had an impact on inflammatory infiltrate reduction, as Balb/c [IL-4.sup.-/-] had predominantly moderate inflammatory infiltrate (p = 0.04, chi-square test, Figure 1). Regarding quantification of heart fibrosis and amastigotes nests, no difference was observed in group comparison (Figure 1).

3.2. Absence of IL-4 Culminates in Lower IFN-[gamma] Cardiac Tissue Production with Similar Expression of TNF-[alpha]. Once infection with T. cruzi Colombian strain leads to lower inflammatory infiltrate in IL-4 knockout animals, we evaluated immune response quality in situ through cardiac homogenate and systemically through serum dosages. As expected, wild-type animal infection triggered increased IFN-[gamma] production in cardiac tissue (noninfected WT vs. infected WT, p = 0.02, t = 2.611). However, in IL-4 absence, IFN-[gamma] expression was significantly reduced, either basal (NI WT vs. NI [IL-4.sup.-/-], p = 0.009, t = 3.315) or after infection with Colombian strain (Inf WT vs. Inf [IL-4.sup.-/-], p = 0.001, t = 4.43). No statistically significant difference was observed in IFN-[gamma] serum levels (data not shown).

However, despite significant IFN-[gamma] reduction in cardiac tissue, TNF-[alpha] expression was similar between WT and [IL-4.sup.-/-], both in uninfected mice (NI WT vs. NI [IL-4.sup.-/-], p > 0.17) and after infection (Inf WT vs. Inf [IL-4.sup.-/-], p > 0.5). In both groups of animals, infection with Colombian strain induced a significant increase in TNF-[alpha] (NI WT vs. Inf WT, p = 0.02, t = 2.61 and NI [IL-4.sup.-/-] vs. Inf [IL-4.sup.-/-], p = 0.002, t = 4.74). Interestingly, TNF-[alpha] systemic levels were significantly elevated in WT-infected animals compared to [IL-4.sup.-/-] animals (p = 0.01, t = 3.08).

To investigate if nonproduction of IFN-[gamma] was due to non-expression of Th1-inducing cytokines, we evaluated in situ expression of IL-12p70. In both groups, infection induced significantly increased IL-12p70 expression in cardiac tissue (NI WT vs. Inf WT, p = 0.04, t = 2.32 and NI [IL-4.sup.-/-] vs. Inf [IL-4.sup.-/-], p = 0.04, t = 2.39), but with no difference between WT and [IL-4.sup.-/-], in situ or systemically (p > 0.05, Figure 2).

3.3. Lower Inflammation and Lower IFN-[gamma] Production in Cardiac Tissue of [IL-4.sup.-/-] Animals Infected with T. cruzi Colombian Strain Are due to Increased IL-10 Production. Once we observed Balb/c mice with IL-4 absence and infected with T. cruzi cardiotropic strain had a significant IFN-[gamma] expression reduction in cardiac tissue, and that this reduction was not due to a decrease in innate immunity cytokine production related to Th1 cell differentiation or function, such as TNF-[alpha] and IL-12p70, we evaluated a possible differential production of IL-10, classically implicated in anti-inflammatory mechanisms.

Our results indicate that T. cruzi Colombian strain infection induced significant IL-10 production, both in WT mice (NI WT vs. Inf WT, p = 0.007, t = 5.29) and Balb/c IL-4-/(NI[IL-4.sup.-/-] vs. Inf [IL-4.sup.-/-], p = 0.001, t = 4.93). Furthermore, in IL-4 absence, significantly higher IL-10 levels were observed in cardiac tissue following infection (Inf WT vs. Inf [IL-4.sup.-/-], p = 0.004, t = 3.42). A significant increase in serum IL-10 between WT and IL-4 [animals.sup.-/-] (p >0.05) was not observed, although both had higher systemic levels after infection (NI WT vs. Inf WT, p = 0.002, t = 4.25 and NI [IL-4.sup.-/-] vs. Inf [IL-4.sup.-/-], p = 0.001, t = 4.89) (Figure 3).

Finally, considering that IL-4 absence could imply alterations of other non-Th1 inflammatory profiles, we assessed Th17 profile through IL-17 in situ expression. No statistical differences were observed in IL-17 cytokine expression between groups, which shows that nonactivation of Th2 profile by IL-4 absence did not lead to Th17 profile activation in a compensatory fashion (Figure 3).

3.4. Cytokine Pattern in Cardiac Tissue Is Not due to Difference in Splenocyte General Repertoire. To assess if observed differences in cardiac tissue cytokine expression of [IL-4.sup.-/-] animals were due to a global difference in lymphocyte repertoire, we stimulated splenocytes with 10 [micro]g/ml of concanavalin A for 48 h and calculated cytokine production (expressed in fold increment related to nonstimulated splenocytes). We demonstrate here that [IL-4.sup.-/-] mouse splenocytes produce significantly increased amounts of IFN-[gamma] (Inf WT vs. Inf [IL-4.sup.-/-], p = 0.02, t = 2.79), TNF-[alpha] (Inf WT vs. Inf [IL-4.sup.-/-], p = 0.009, t = 3.39), IL-17 (Inf WT vs. Inf [IL-4.sup.-/-], p = 0.006, t =5.47), and lower IL-10 production (Inf WT vs. Inf [IL-4.sup.-/-], p = 0.007, t = 576) (Figure 4). This result shows a clear difference between repertoire generated by T. cruzi Colombian strain infection and cytokines expressed at the infection site, more clearly demonstrated by radar plots (Figure 5). These results were calculated using the mean expression of each cytokine in cardiac tissue homogenate or CON-Astimulated splenocytes from Balb/c [IL-4.sup.-/-]-infected mice and expressed as fold change relative to Balb/c WT-infected mice.

4. Discussion

This study is aimed at evaluating IL-4 role in immune response modulation of mice infected with T. cruzi Colombian strain in acute phase of infection. Our results point out the relationship between IL-4 and Th1 cells, classically described as antagonistic. In acute myocarditis triggered by cardiotropic strain of T. cruzi, IL-4 absence implies a general polarization for Th1 in the spleen, but in cardiac tissue, inflammatory balance is significantly regulated by an increase in IL-10, triggering a lower inflammatory infiltrate.

The profile of cytokines released during T. cruzi infection may be associated with a protective or disease susceptible profile. Th1-type response is characterized by IL-2 and IFN-[gamma] secretion, leading to activation of macrophages and cell-mediated response, whereas in Th2 response, synthesis of IL-4, IL-5, and IL-10 is observed, culminating in relevant humoral response. Balance between these cytokines is fundamental to determine which response has to be developed [27, 28].

In our study, IL-4 absence at 21 days of infection did not determine a change in amastigotes nest density in cardiac tissue, using 100 forms of Colombian strain of T. cruzi, a reference strain for chagasic myocarditis studies due to its high heart tropism in Balb/c mice [29, 30]. These results conflict with other studies that demonstrated the potentiating IL-4 effect on infection, since [IL-4.sup.-/-] mice would better control tissue parasitism [21,31]. However, here and in both studies, nest density was small, even though several serial cuts were evaluated. Another study using greater inoculum with Y strain found no difference in parasite load as did our study [32]. Taken together, all these studies show in the early events of T. cruzi infection that intense myocarditis has no direct relation with the amount of amastigote nests that will persist in chronic phase.

In the present study, Balb/c [IL-4.sup.-/-]-infected mice had milder inflammatory infiltration compared to WT Balb/c. No significant differences were observed in intensity of diffuse and focal inflammation in cardiac tissue compared IL-4 KO and WT animals [31]; however, this work evaluated late acute phase in 30 days of infection, where parasitemia is reduced and transition to chronic infection begins, while we evaluate the moment when Colombian strain presents its parasitemia peak, that is, greater parasitic circulation [25].

Fibrosis is a fundamental substrate of Chagas' heart disease and progression to heart failure [33]. However, there is no consensus on the exact moment process takes place. In face of a continuous inflammatory process, it is believed that extracellular matrix increases collagen production evolving to fibrosis, especially secondary to tissue damage. In the present study, difference in collagen deposition was not found, possibly due to the time infection was evaluated, when myocarditis is prominent and fibrosis is not yet fully installed. In chronic phase, it is well established that induction of inflammatory response and death of cardiac fibers contribute to continuous deposition of collagen and consequently fibrosis [1, 34].

IL-4 absence culminated in lower cardiac tissue IFN-[gamma] production; this fact justifies decrease of in situ infiltrate. However, IFN-[gamma] expression is extremely relevant for immunity against intracellular pathogens, including T. cruzi [35]. We believe systemic production of IFN-[gamma] suppressed local decrease of this cytokine, since its levels were well expressed in splenocytes culture in the [IL-4.sup.-/-] group. However, increased IFN-[gamma] and nitric oxide production was demonstrated in mice infected with T. cruzi Tulahuen strain with IL-4 suppression, showing that IL-4 absence is related to a greater proinflammatory state activation in T. cruzi infection [36].

IL-4 absence did not alter TNF-[alpha] in situ production, despite IFN-[gamma] local reduction. TNF-[alpha] is especially synthesized by macrophages, T lymphocytes, and NK cells, with a great diversity of functions including recruitment and activation of macrophages, which stimulate nitric oxide production and intracellular destruction of protozoan, actively participating in the initial proinflammatory response of the disease [37, 38]. Other studies have shown that increased TNF-[alpha] is also associated with increased cardiac damage [39, 40], although treatment with TNF-[alpha] inhibitors, such as etanercept, in chronic phase, aggravates chagasic myocarditis [41], demonstrating that its presence in cardiac tissue has more complex repercussions than conceptual simplification increase is equal to damage. It is important to emphasize that splenocyte production capacity was positively impacted by IL-4 absence, suggesting cardiac tissue-specific control mechanisms.

Among infected animals, there was no difference in IL-12p70 cytokine expression in IL-4 absence. It is known that this cytokine is a fundamental mediator of innate immune response, secreted by mononuclear phagocytes and dendritic cells, and important in stimulating IFN-[gamma] production by NK cells and T lymphocytes [42, 43]. It can be inferred that, in this study, at the beginning of infectious process, the ability to produce IL-12p70 contributes to a Th1 response profile influenced by pathogen itself.

In fact, animals in the present study had no histological evidence of cardiac involvement. We believe this is due to immune response control represented in our study by in situ increase in IL-10 and decrease in IFN-[gamma]. Our data also point out that immune response local regulation associated with a good repertoire of systemic Th1 immune response may have been sufficient to maintain the effectiveness of the response to T. cruzi infection. These data become more consistent, since we observed increased serum and in situ IL-10 with reduced systemic repertoire production, as demonstrated in stimulated culture.

IL-4 absence did not influence IL-17 expression in situ; however, the repertoire in the ex vivo culture increased. IL17 plays an important role in resolution of T. cruzi protozoan infection, and this cytokine is associated with protective and nonpathogenic responses [44-46]. In chagasic patients with heart disease, greater serum IL-17 levels were related to improvement of organ function; therefore, it has protective effect [47]. A study in [IL-17.sup.-/-] animals demonstrated that this cytokine actively participates in inflammatory response in initial phase of disease and its absence during T. cruzi infection results in a reduction in recruitment of defense cells, which favors parasitemia [48]. However, researches are still recent and limited on true role of this cytokine in Chagas' disease.

The relationship between IL-4 functions and Th1 cell differentiation is classically described as antagonistic and widely reported in several models of T lymphocyte differentiation [49-52]. However, we demonstrated in acute myocarditis triggered by T. cruzi cardiotropic strain that IL-4 absence implies a repertorial polarization for Th1, but in cardiac tissue, inflammatory balance is strongly regulated by an increase in IL-10, triggering a lower inflammatory infiltrate. Our results open perspectives of IL-4 role in initial events of chagasic myocarditis in a more complex frame than the dichotomy Th1/Th2.
Abbreviations

CON-A:        Concanavalin A
ELISA:        Enzyme-linked immunosorbent assay
IFN-[gamma]:  Interferon gamma
IL-4:         Interleukin 4
IL-10:        Interleukin 10
IL-17:        Interleukin 17
IL-12p7       Interleukin 12p70
KO:           Knockout for the gene
T. cruzi:     Trypanosoma cruzi
TNF-[alpha]:  Tumor necrosis factor-alpha
TMB:          3,3,5,5 -Tetramethylbenzidine
WT:           Wild type.


https://doi.org/10.1155/2018/3421897

Data Availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

Conflicts of Interest

The authors declare that they have no conflicts of interest. Authors' Contributions

Marcos Vinicius da Silva and Vera Lucia de Almeida equally contributed to this paper.

References

[1] J. A. Marin-Neto, E. Cunha-Neto, B. C. Maciel, and M. V. Simoes, "Pathogenesis of chronic Chagas heart disease," Circulation, vol. 115, no. 9, pp. 1109-1123, 2007.

[2] World Health Organization (WHO), Preventing Mother-to-Child Transmission of Chagas disease: from Control to Elimination, WHO: Neglected tropical disease, 2018.

[3] B. A. Burleigh and N. W. Andrews, "The mechanisms of Trypanosoma cruzi invasion of mammalian cells," Annual Review of Microbiology, vol. 49, no. 1, pp. 175-200, 1995.

[4] T. C. de Araujo-Jorge and S. L. de Castro, Doenga de Chagas: Manual Para Experimentacao Animal, Editora FIOCRUZ, Rio de Janeiro, 2000.

[5] E. E. Federici, W. H. Abelmann, and F. A. Neva, "Chronic and progressive myocarditis and myositis in C3H mice infected with Trypanosoma cruzi," The American Journal of Tropical Medicine and Hygiene, vol. 13, no. 2, pp. 272-280, 1964.

[6] S. G. Andrade and J. B. Magalhaes, "Biodemes and zymodemes of Trypanosoma cruzi strains: correlations with clinical data and experimental pathology," Revista da Sociedade Brasileira de Medicina Tropical, vol. 30, no. 1, pp. 27-35, 1997.

[7] S. G. Andrade, A. R. Pimentel, M. M. de Souza, and Z. A. Andrade, "Interstitial dendritic cells of the heart harbor Trypanosoma cruzi antigens in experimentally infected dogs: importance for the pathogenesis of chagasic myocarditis," The American Journal of Tropical Medicine and Hygiene, vol. 63, no. 1, pp. 64-70, 2000.

[8] I. A. Abrahamsohn and R. L. Coffman, "Trypanosoma cruzi: IL-10, TNF, IFN-[gamma], and IL-12 regulate innate and acquired immunity to infection," Experimental Parasitology, vol. 84, no. 2, pp. 231-244, 1996.

[9] C. A. Hunter, L. A. Ellis-Neyes, T. Slifer et al., "IL-10 is required to prevent immune hyperactivity during infection with Trypanosoma cruzi," The Journal of Immunology, vol. 158, pp. 3311-3316, 1997.

[10] R. L. Tarleton, B. H. Koller, A. Latour, and M. Postan, "Susceptibility of j2-microglobulin-deficient mice to Trypanosoma cruzi infection," Nature, vol. 356, no. 6367, pp. 338-340,1992.

[11] M. E. Rottenberg, M. Bakhiet, T. Olsson et al., "Differential susceptibilities of mice genomically deleted of CD4 and CD8 to infections with Trypanosoma cruzi or Trypanosoma brucei," Infection and Immunity, vol. 61, no. 12, pp. 5129-5133, 1993.

[12] E. C. Santos Lima and P. Minoprio, "Chagas' disease is attenuated in mice lacking y5 T cells," Infection and Immunity, vol. 64, no. 1, pp. 215-221, 1996.

[13] M. F. Lopes, M. P. Nunes, A. Henriques-Pons et al., "Increased susceptibility of Fas ligand-deficient gld mice to Trypanosoma cruzi infection due to a Th2-biased host immune response," European Journal of Immunology, vol. 29, no. 1, pp. 81-89, 1999.

[14] M. d. L. Higuchi, "Chronic chagasic cardiopathy: the product of a turbulent host-parasite relationship," Revista do Instituto de Medicina Tropical de Sao Paulo, vol. 39, no. 1, pp. 53-60, 1997.

[15] J. S. Silva, D. R. Twardzik, and S. G. Reed, "Regulation of Trypanosoma cruzi infections in vitro and in vivo by transforming growth factor [beta] (TGF-[beta])," The Journal of Experimental Medicine, vol. 174, no. 3, pp. 539-545, 1991.

[16] W. Savino, D. M. S. Villa-Verde, D. A. Mendes-da-Cruz et al., "Cytokines and cell adhesion receptors in the regulation of immunity to Trypanosoma cruzi," Cytokine & Growth Factor Reviews, vol. 18, no. 1-2, pp. 107-124, 2007.

[17] R. Hurdayal and F. Brombacher, "The role of IL-4 and IL-13 in cutaneous leishmaniasis," Immunology Letters, vol. 161, no. 2, pp. 179-183, 2014.

[18] J. Alexander and K. Bryson, "T helper (h)1/Th2 and Leishmania: paradox rather than paradigm," Immunology Letters, vol. 99, no. 1, pp. 17-23, 2005.

[19] J. Alexander and F. Brombacher, "T helper1/T helper2 cells and resistance/susceptibility to Leishmania infection: is this paradigm still relevant?," Frontiers in Immunology, vol. 3, p. 80, 2012.

[20] O. M. Martinez, R. S. Gibbons, M. R. Garovoy, and F. R. Aronson, "IL-4 inhibits IL-2 receptor expression and IL-2dependent proliferation of human T cells," The Journal of Immunology, vol. 144, pp. 2211-2215, 1990.

[21] M. B. P. Soares, K. N. Silva-Mota, R. S. Lima, M. C. Bellintani, L. Pontes-de-Carvalho, and R. Ribeiro-dos-Santos, "Modulation of chagasic cardiomyopathy by interleukin-4: dissociation between inflammation and tissue parasitism," The American Journal of Pathology, vol. 159, no. 2, pp. 703-709, 2001.

[22] C. Holscher, G. Kohler, U. Muller, H. Mossmann, G. A. Schaub, and F. Brombacher, "Defective nitric oxide effector functions lead to extreme susceptibility of Trypanosoma cruzi-infected mice deficient in gamma interferon receptor or inducible nitric oxide synthase," Infection and Immunity, vol. 66, no. 3, pp. 1208-1215, 1998.

[23] J. J. Wirth, F. Kierszenbaum, and A. Zlotnik, "Effects of IL-4 on macrophage functions: increased uptake and killing of a protozoan parasite (Trypanosoma cruzi)," Immunology, vol. 66, no. 2, pp. 296-301, 1989.

[24] J. M. Golden and R. L. Tarleton, "Trypanosoma cruzi: cytokine effects on macrophage trypanocidal activity," Experimental Parasitology, vol. 72, no. 4, pp. 391-402, 1991.

[25] J. Reis Machado, M. V. Silva, D. C. Borges et al., "Immunopathological aspects of experimental Trypanosoma cruzi reinfections," BioMed Research International, vol. 2014, Article ID 648715, 9 pages, 2014.

[26] S. R. Paludan, "Interleukin-4 and interferon-y: the quintessence of a mutual antagonistic relationship," Scandinavian Journal of Immunology, vol. 48, no. 5, pp. 459-468, 1998.

[27] M.-J. Pinazo, M. C. Thomas, J. Bustamante, I. C. Almeida, M. C. Lopez, and J. Gascon, "Biomarkers of therapeutic responses in chronic Chagas disease: state of the art and future perspectives," Memorias do Instituto Oswaldo Cruz, vol. 110, no. 3, pp. 422-432, 2015.

[28] W. O. Dutra, C. A. S. Menezes, L. M. D. Magalhaes, and K. J. Gollob, "Immunoregulatory networks in human Chagas disease," Parasite Immunology, vol. 36, no. 8, pp. 377-387, 2014.

[29] E. Camandaroba, T. S. The, D. H. Pessina, and S. G. Andrade, "Trypanosoma cruzi: clones isolated from the Colombian strain, reproduce the parental strain characteristics, with ubiquitous histotropism," International Journal of Experimental Pathology, vol. 87, no. 3, pp. 209-217, 2006.

[30] L. O. Andrade, C. R. S. Machado, E. Chiari, S. D. J. Pena, and A. M. Macedo, "Trypanosoma cruzi: role of host genetic background in the differential tissue distribution of parasite clonal populations," Experimental Parasitology, vol. 100, no. 4, pp. 269-275, 2002.

[31] V. Michailowsky, N. M. Silva, C. D. Rocha, L. Q. Vieira, J. Lannes-Vieira, and R. T. Gazzinelli, "Pivotal role of interleukin-12 and interferon-y axis in controlling tissue parasitism and inflammation in the heart and central nervous system during Trypanosoma cruzi infection," The American Journal of Pathology, vol. 159, no. 5, pp. 1723-1733, 2001.

[32] I. A. Abrahamsohn, A. P. G. da Silva, and R. L. Coffman, "Effects of interleukin-4 deprivation and treatment on resistance to Trypanosoma cruzi," Infection and Immunity, vol. 68, no. 4, pp. 1975-1979, 2000.

[33] E. R. Lopes, E. Chapadeiro, W. L. Tafuri, A. O. Almeida, and D. Abraao, "Peso do coracao e tipo de morte no chagasico," Revista do Instituto de Medicina Tropical de Sao Paulo, vol. 12, pp. 293-297, 1970.

[34] J. A. Torreao, B. M. Ianni, C. Mady et al., "Myocardial tissue characterization in Chagas' heart disease by cardiovascular magnetic resonance," Journal of Cardiovascular Magnetic Resonance, vol. 17, no. 1, p. 97, 2015.

[35] M. d. L. Higuchi, T. de Brito, M. Martins Reis et al., "Correlation between Trypanosoma cruzi parasitism and myocardial inflammatory infiltrate in human chronic chagasic myocarditis: light microscopy and immunohistochemical findings," Cardiovascular Pathology, vol. 2, no. 2, pp. 101-106, 1993.

[36] K. Hiyama, S. Hamano, T. Nakamura, K. Nomoto, and I. Tada, "IL-4 reduces resistance of mice to Trypanosoma cruzi infection," Parasitology Research, vol. 87, no. 4, pp. 269-274, 2001.

[37] J. A. Langermans, M. E. van der Hulst, P. H. Nibbering, and R. van Furth, "Endogenous tumor necrosis factor alpha is required for enhanced antimicrobial activity against Toxoplasma gondii and Listeria monocytogenes in recombinant gamma interferon-treated mice," Infection and Immunity, vol. 60, no. 12, pp. 5107-5112, 1992.

[38] A. A. Rodrigues, A. F. O. Notario, T. L. Teixeira et al., "A high throughput analysis of cytokines and chemokines expression during the course of Trypanosoma cruzi experimental oral infection," Acta Tropica, vol. 157, pp. 42-53, 2016.

[39] A. Haensel, P. J. Mills, R. A. Nelesen, M. G. Ziegler, and J. E. Dimsdale, "The relationship between heart rate variability and inflammatory markers in cardiovascular diseases," Psychoneuroendocrinology, vol. 33, no. 10, pp. 1305-1312, 2008.

[40] E. Cunha-Neto, L. G. Nogueira, P. C. Teixeira et al., "Immunological and non-immunological effects of cytokines and chemokines in the pathogenesis of chronic Chagas disease cardiomyopathy," Memorias do Instituto Oswaldo Cruz, vol. 104, Suppl 1, pp. 252-258, 2009.

[41] A. M. B. Bilate, V. M. Salemi, F. J. Ramires et al., "TNF blockade aggravates experimental chronic Chagas disease cardiomyopathy," Microbes and Infection, vol. 9, no. 9, pp. 1104-1113, 2007.

[42] L. Rogge, L. Barberis-Maino, M. Biffi et al., "Selective expression of an interleukin-12 receptor component by human T helper 1 cells," The Journal of Experimental Medicine, vol. 185, no. 5, pp. 825-832, 1997.

[43] M. S. Cardoso, J. L. Reis-Cunha, and D. C. Bartholomeu, "Evasion of the immune response by Trypanosoma cruzi during acute infection," Frontiers in Immunology, vol. 6, p. 659, 2015.

[44] Y. Miyazaki, S. Hamano, S. Wang, Y. Shimanoe, Y. Iwakura, and H. Yoshida, "IL-17 is necessary for host protection against acute-phase Trypanosoma cruzi infection," The Journal of Immunology, vol. 185, no. 2, pp. 1150-1157, 2010.

[45] P. M. da Matta Guedes, F. R. S. Gutierrez, F. L. Maia et al., "IL-17 produced during Trypanosoma cruzi infection plays a central role in regulating parasite-induced myocarditis," PLoS Neglected Tropical Diseases, vol. 4, no. 2, article e604, 2010.

[46] D. A. Bermejo, S. W. Jackson, M. Gorosito-Serran et al., "Trypanosoma cruzi trans-sialidase initiates a program independent of the transcription factors ROR[gamma]t and Ahr that leads to IL-17 production by activated B cells," Nature Immunology, vol. 14, no. 5, pp. 514-522, 2013.

[47] G. R. Sousa, J. A. S. Gomes, M. P. S. Damasio et al., "The role of interleukin 17-mediated immune response in Chagas disease: high level is correlated with better left ventricular function," PLoS One, vol. 12, no. 3, article e0172833, 2017.

[48] J. Tosello Boari, M. C. Amezcua Vesely, D. A. Bermejo et al., "IL-17RA signaling reduces inflammation and mortality during Trypanosoma cruzi infection by recruiting suppressive IL-10-producing neutrophils," PLoS Pathogens, vol. 8, no. 4, article e1002658, 2012.

[49] C. A. Lazarski, J. Ford, S. D. Katzman, A. F. Rosenberg, and D. J. Fowell, "IL-4 attenuates Th1-associated chemokine expression and Th1 trafficking to inflamed tissues and limits pathogen clearance," PLoS One, vol. 8, no. 8, article e71949, 2013.

[50] M. Lopez-Bravo, M. Minguito de la Escalera, P. M. Dominguez et al., "IL-4 blocks TH1-polarizing/inflammatory cytokine gene expression during monocyte-derived dendritic cell differentiation through histone hypoacetylation," The Journal of Allergy and Clinical Immunology, vol. 132, no. 6, pp. 1409-1419.e13, 2013.

[51] T. R. Mosmann, H. Cherwinski, M. W. Bond, M. A. Giedlin, and R. L. Coffman, "Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins," The Journal of Immunology, vol. 136, pp. 2348-2357, 1986.

[52] E. A. Kurt-Jones, S. Hamberg, J. Ohara, W. E. Paul, and A. K. Abbas, "Heterogeneity of helper/inducer T lymphocytes. I. Lymphokine production and lymphokine responsiveness," The Journal of Experimental Medicine, vol. 166, no. 6, pp. 1774-1787, 1987.

Marcos Vinicius da Silva [ID], (1) Vera Lucia de Almeida, (2) Wendyson Duarte de Oliveira, (2) Natalia Carasek Matos Cascudo, (2) Pollyana Guimaraes de Oliveira, (2) Crislaine Aparecida da Silva [ID], (3) Aline Cristina Souza da Silva [ID], (3) Maria Lulza Gon$alves dos Reis Monteiro [ID](3) Rosana Rosa Miranda Correa, (3) Milton Adriano Pelli Oliveira [ID], (2) Ruy de Sousa Lino-Junior, (2) Mara Rubia Nunes Celes [ID], (2) and Juliana Reis Machado, [ID] (3)

(1) Department of Parasitology, Institute of Natural and Biological Sciences, Federal University of Triangulo Mineiro, 38025180 Uberaba, MG, Brazil

(2) Institute of Tropical Pathology and Public Health of Federal University of Goias, Federal University of Goias, 74605-050 Goiania, Brazil

(3) General Pathology, Institute of Natural and Biological Sciences, Federal University of Triangulo Mineiro, 38025-180 Uberaba, MG, Brazil

Correspondence should be addressed to Juliana Reis Machado; juliana.patologiageral@gmail.com

Received 15 July 2018; Accepted 5 November 2018; Published 28 November 2018

Academic Editor: Daniela Novick

Caption: Figure 1: Morphological analysis of the heart of Balb/c WT and Balb/c [IL-4.sup.-/-] mice infected and not infected with the Colombian strain of T. cruzi in the acute phase of experimental Chagas' disease. (a) Density of amastigote nests in cardiac tissue of infected WT and [IL-4.sup.-/-] mice. Bars represent the mean, and vertical lines represent the standard error. (b) Intensity of cardiac inflammatory infiltrate in infected WT and [IL-4.sup.-/-] mice (p = 0.04, chi-square test). (c) Percentage of collagen fibers in cardiac tissue of infected and uninfected WT and IL-4-/mice. Bars represent the mean, and vertical lines represent the standard error. Histological sections of the WT and [IL- 4.sup.-/-]- infected mice heart. (d, g) HE-stained amastigote nests. (e) Mild inflammatory infiltrate. (h) Moderated inflammatory infiltrate. (f, i) Collagen fibers stained red by sirius red.

Caption: Figure 2: Expression of proinflammatory cytokines in cardiac tissue and serum of Balb/c WT and Balb/c [IL- 4.sup.-/-] mice infected and not infected with the Colombian strain of T. cruzi in the acute phase of experimental Chagas' disease. (a) Tissue IFN- [gamma] production (pg/g). (b) Tissue TNF-[alpha] production (pg/g). (c) Serum levels of TNF-[alpha] (pg/ml). (d) Tissue IL12p70 production (pg/g). Student's i- test. Bars represent the mean, and vertical lines represent the standard error. * Significant differences between infected versus uninfected animals. [#] Significant differences between the WT versus [IL-4.sup.-/-] group.

Caption: Figure 3: Cytokine expression with regulatory profile in cardiac tissue and serum of Balb/c WT and Balb/c [IL- 4.sup.-/-] mice infected and not infected with the T. cruzi Colombian strain in the acute phase of experimental Chagas' disease. (a) Production of IL-10 in cardiac tissue (pg/g) and (b) serum levels of IL-10 (pg/ml). (c) Production of IL-17 in cardiac tissue (pg/g). Student's i-test. Bars represent the mean, and vertical lines represent the standard error. * Significant differences between infected versus uninfected animals. Significant differences between the WT versus [IL-4.sup.-/-] group.

Caption: Figure 4: Cytokine production in splenocytes of WT Balb/c and [IL-4.sup.-/-] Balb/c mice infected with Colombian strain of T. cruzi stimulated with 10 [micro]g/ml of concanavalin A in the acute phase of experimental Chagas' disease. Fold change between nonstimulated versus CON-A stimulated splenocytes. Student's i-test. Bars represent the mean, and vertical lines represent the standard error. * Significant differences between infected versus uninfected animals.

Caption: Figure 5: Radar plot representation of cytokine profile in cardiac tissue and splenocytes. The lines highlight the fold change in cytokine production in [IL-4.sup.-/-] Balb/c (gray line) in relation to WT Balb/c mice (black line). Data were obtained by calculating the ratio between the mean concentrations of each cytokine in the [IL-4.sup.-/-] Balb/c-infected group and WT Balb/c-infected mice.
COPYRIGHT 2018 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Research Article
Author:da Silva, Marcos Vinicius; de Almeida, Vera Lucia; de Oliveira, Wendyson Duarte; Cascudo, Natalia Ca
Publication:Mediators of Inflammation
Geographic Code:3BRAZ
Date:Jan 1, 2018
Words:5999
Previous Article:Naringenin Protects against Acute Pancreatitis in Two Experimental Models in Mice by NLRP3 and Nrf2/HO-1 Pathways.
Next Article:Anti-Inflamm-Ageing and/or Anti-Age-Related Disease Emerging Treatments: A Historical Alchemy or Revolutionary Effective Procedures?
Topics:

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters |