MEM INST OSWALDO CRUZ, RIO DE JANEIRO, 104 (Suppl.I) July 2009
PAGES: 187-198 DOI: 10.1590/S0074-02762009000900025 Full paper
Back to the future in Chagas disease: from animal models to patient cohort studies, progress in immunopathogenesis research

Julio ScharfsteinI, +; Juliana de Assis Silva GomesII; Rodrigo Correa-OliveiraII

IInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
IIInstituto de Pesquisa René Rachou-Fiocruz, Belo Horizonte, MG, Brasil

Abstract

Despite the wealth of information generated by trans-disciplinary research in Chagas disease, knowledge about its multifaceted pathogenesis is still fragmented. Here we review the body of experimental studies in animal models supporting the concept that persistent infection by Trypanosoma cruzi is crucial for the development of chronic myocarditis. Complementing this review, we will make an effort to reconcile seemingly contradictory results concerning the immune profiles of chronic patients from Argentina and Brazil. Finally, we will review the results of molecular studies suggesting that parasite-induced inflammation and tissue damage is, at least in part, mediated by the activities of trans-sialidase, mucin-linked lipid anchors (TLR2 ligand) and cruzipain (a kinin-releasing cysteine protease). One hundred years after the discovery of Chagas disease, it is reassuring that basic and clinical research tends to converge, raising new perspectives for the treatment of chronic Chagas disease.

Tryanosoma cruzi is a taxon composed of genetically diversified subpopulations of clonal origin in the order Kinetoplatida. Operationally referred as T. cruzi strains or isolates, these parasites display marked phenotypic variability, with different multiplication rates, tissue tropisms and susceptibilities to drug treatment (Zingales et al. 1999, Macedo et al. 2002). In the late 1970s, Michael Miles and co-workers described zymodeme differences in parasites isolated from domestic (Z2) versus sylvatic (Z1/Z3) transmission cycles (Miles et al. 1978). After refinement of zymodeme classification (Tibayrenc & Ayala 1987), the usage of probes for the 24S alpha RNA ribosomal sequences (rRNA) and the highly conserved mini-exon gene (Souto & Zingales 1993, Souto et al. 1996) established that the T. cruzi species were derived from two main filogenetic ancestral lineages, which diverged 10-40 million years ago (Briones et al. 1999). Isolates bearing the genotypic markers corresponding to zymodemes Z1 and Z2, now referred to as Tc1 and TcII, circulate predominantly in the sylvatic and domestic cycles, respectively. It was subsequently found that T. cruzi II can be subclassified into five groups, designated IIa to IIe (Brisse et al. 2000). More recently, a third ancestor lineage (TcIII) was also characterised (De Freitas et al. 2006).

Renewed efforts were made to determine if infection by the major parasite lineages is associated with particular clinical forms of Chagas disease. For reasons that are still unclear, studies in North and Central America have linked chronic chagasic myocardiopathy (CARD) to infection with the TcI lineage (Añez et al. 2004, Ruíz-Sánchez et al. 2005) whereas members of the TcII lineage were associated with heart disease in the Southern Cone of South America (Solari et al. 2001, Coronado et al. 2006). In another report, the reactivation of cerebral forms of Chagas disease in a patient with HIV/AIDS (Burgos et al. 2005) was associated with T. cruzi clones of the TcIIb group, whereas congenital Chagas disease was linked to infection by TcIId clones (Burgos et al. 2007). More recently, Venegas et al. (2009) investigated the association between T. cruzi clones belonging to the TcI and TcII lineages with the severity of cardiac disease. Using the Z-IIb (TcIIb) and Z-hybrid (TcIId and TcIIe) probes to characterise the genotypes of T. cruzi clones circulating in the peripheral blood of 37 chagasic patients, these workers found remarkably higher frequencies of Z-IIb T. cruzi clones in the group of non-cardiac patients. In contrast, the distribution of sublineage Z-I clones was similar in both groups of patients. Based on these observations, Venegas et al. (2009) suggested that Z-IIb and Z-hybrid T. cruzi are efficiently cleared from cardiac tissues by potent immune effector responses. However, this clearance induces collateral heart immunopathology, at least in patients that are living in the Southern Cone of South America, which also suggests a relationship with host genetics. It remains to be determined whether Z-I clones and Z-IIb/Z-hybrid clones are equally competent in invading and thriving in cardiac tissues, and if so, whether these parasites are differentially susceptible to immune clearance by functionally distinct sets of TEM (Macedo & Pena 1998, Andrade 1999, Vago et al. 2000). These are major points that have led researchers to evaluate if the development of chronic myocardiopathy relates to parasite persist-ence in heart tissues.

Tissue parasitism and chronic myocarditis in experimental models

Several decades ago, pathologists were intrigued by the findings that myocardial specimens from chronic chagasic patients often displayed diffused inflammatory infiltrates and evidence of extensive fibrosis in heart tissues in spite of the fact that pseudocysts were rarely detected in such specimens (Andrade et al. 1994). In the mid 1970s, two alternative hypotheses were raised to account for these seemingly contradictory results. One school of thought suggested that microvascular lesions in the chronically infected myocardium might build up over the years, creating microcirculatory abnormalities that ultimately induce hypoxia, inflammation and fibrosis in susceptible chagasic patients (Rossi 1990, Morris et al. 1990, Mengel & Rossi 1992). While not excluding a role for microvascular pathology, some groups contended that T. cruzi antigens might induce myocardial tissue damage and fibrosis through the activation of parasite-specific effector T cells. In contrast, the proponents of the autoimmunity hypothesis (Ribeiro-dos-Santos & Hudson 1981, Kierszenbaum 1986, Rizzo et al. 1989) argued that self-reactive (anti-heart) lymphocytes could account for the diffused inflammation and fibrosis observed in patients with severe chronic myocardiopathy. Ribeiro-dos-Santos et al. (1992) addressed this question using an animal model that closely resembled human CCM: Balb/C mice chronically infected with T. cruzi Colombiana. After developing a heterotypic ear model of syngeneic neonatal heart transplantation, these investigators demonstrated that adoptively transferred CD4+ T cells originating from chronically infected mice rejected the transplanted heart. Although the authors interpreted these findings as an indication that autoreactive CD4+ T cells promote chronic myocardiopathy (Ribeiro-dos-Santos et al. 1992), these conclusions were subsequently challenged by Tarleton et al. (1994); using two different experimental models, i.e., C5BL/6 and C3H mice infected with T. cruzi strains (Brazil, Y and Sylvio), these investigators showed that T cell-mediated rejection of neonatal heart depended on graft invasion by viable parasites. Although not formally excluding a secondary role for self-reactive T lymphocytes (Ribeiro-dos-Santos 2001, Soares et al. 2001, Girones & Fresno 2003, Leon & Engman 2003, Cunha-Neto et al. 2006), these observations suggested that development of chronic myocardiopathy might result from the collateral tissue damage and inflammation induced by IFN-? and TNF-?-producing anti-parasite effector T cells (Zhang & Tarleton 1996, Tarleton 2003).

TS antigens provide dominant epitopes for effector CD8+ T cells

Previously identified as surface targets of antibodies (Affranchino et al. 1989, Duthie et al. 2005), the polymorphic trans-sialidase (TS) antigens induce T cell responses in T. cruzi-infected or vaccinated mice as well as in chronic chagasic patients (Kahn & Wleklinsky 1997, Wizel et al. 1997, 1998, Fujimura et al. 2001, Garg & Tarleton 2002, Tzelepis et al. 2008). In an early study focusing on class II major histocompatibility complex (MHC)-restricted CD4+ T cell responses to TS antigens, Kahn and Wlekinski (1997) showed evidence that the simultaneous expression of individual antigens from the polymorphic TS family may limit the availability of processed epitopes from each protein antigen below the threshold level required to stimulate a protective IFN? response against the parasite. Years later, this issue was re-examined in light of indications that class I MHC-restricted effector CD8+ T cells targeting TS antigens are indispensable for the effective control of intracellular infection in vivo (Garg & Tarleton 2002). Similar to the response to viruses and other pathogens that replicate in the host cell cytoplasm, T. cruzi proteins (amasti-gotes and trypomastigotes) released in the cytoplasm of infected host cells must undergo proteolytic processing by proteasomes before being transported from the cytoplasm to the endoplasmic reticulum, where they bind to MHC-class I molecules en route to the cell surface. In viral infection, it is well established that the cytotoxic CD8+ T cells usually kill infected host cells by targeting a few immunodominant epitopes. Given the far greater complexity of the eukaryotic T. cruzi genome (12,000 genes), immunologists initially argued that class I MHC-restricted epitopes were generated by the intracellular processing of a large number of parasite antigens. However, analysis of the TCR specificity of CD8+ T cells in mice and humans suggests that this is not the case: multiple studies suggest that immune clearance by the CD8+ T cell subset is heavily dependent on recognition of TS epitopes (Wizel et al. 1997, Tzelepis et al. 2008). Using a panel of 324 peptides, 156 of which were derived from 1,430 TS genes in the annotated T. cruzi genome, Martin et al. (2006) identified 7 H2Kb-restricted TS "immunodominant" epitopes that were capable of promptly eliciting IFN-? secretion and served as in vivo targets for cytolytic CD8+ T cells. Of note, subdominant specificities included epitopes from few non-TS proteins (e.g., cruzipain, mucin-associated surface proteins, ?-galatosyl-furanosyl transferase and GP63), all of which able to generate HKb-restricted epitopes for CD8+ T cells. Notably, these non-TS peptides only elicited IFN-? responses (ELISPOT) ex vivo in CD8+ T cells from 40-60% of Brazil strain-infected B6 mice; furthermore, their frequencies were 4-20-fold lower as compared to those of T cells recognising TS epitopes, whether measured in acutely or chronically infected mice. Also noteworthy, the non-TS peptides were only capable of eliciting type-1 cytokine secretion after overnight incubation with CD8+ T cells, while the immunodominant TS peptides elicited secretion of the type 1 cytokine after 5 h of cultivation. Complementing their study, Martin et al. (2006) used peptide/Kb tetra-mers to compare the magnitude, kinetics and dominance patterns of CD8+ T cell responses in mice infected with the Brazil, Y and CL strains. In mice infected with the Brazil parasite strain, the kinetics of the dominant anti-TS-CD8+ T cell responses paralleled those of the tissue parasite load, i.e., it was low at early stage of infection, peaked at 19-24 days post-infection and decreased in the post-acute phase. Not surprisingly, the hierarchy of immunodominant TS epitopes recognised by effector CD8+ T cells was influenced by parasite strain, suggesting that the efficiency of parasite clearance in natural infection may vary for different parasite clones (Martin et al. 2006, Tzelepis et al. 2008). Although the mechanisms leading to the selection of immunodominant TS epitopes are unknown, a comparative analysis of the TCR repertoire of experienced CD8+ T cell responses in infected mice heterozygous for class I MHC molecules (Tzelepis et al. 2008) suggested that immunodominance of TS epitopes is established at the level of antigen-presenting cells (APCs), most likely due to interference/competition of TS dominant agonists on the loading of class I MHC binding by subdominant peptides, thus possibly analogous to mechanisms involved in the generation of class II MHC-restricted epitopes (Kahn & Wleklinsky 1997). By focusing effector CD8+ T cell responses on a limited range of dominant TS epitopes, the immune system can efficiently reduce the massive parasite burden observed in the acute phase, bringing it down to levels that are compatible with host survival. Moreover, considering that naturally infected hosts are often infected by multiple parasite clones, stochastic expression of TS antigens by amastigotes and/or trypomastigotes may allow for parasite escape (Scharfstein & Morrot 1999), hence driving the evolutionary diversification of TS family proteins (Martin et al. 2006).

Although the concept of immunodominance provides a useful framework for investigating the pathogenic role of subdominant T cell specificities during the post-acute and chronic stages of the natural infection (discussed further below), it is not obvious why TS-specific TC1 fail to clear the infection in mice experimentally infected by T. cruzi clones or by parasite strains (less heterogenous than in natural infection). Grisotto et al. (2001) addressed this question by examining the phenotype of CD8+ T cells in secondary lymphoid tissues of mice infected in laboratory settings. Their study revealed that TCR and CD8 molecules were downregulated in memory CD8+ T cells isolated from the spleen but not in CD8+ T cells isolated from the draining lymph nodes of chronically infected mice. Notably, splenic CD8+ memory (resting) T cells cultivated with T. cruzi-infected macrophages were readily activated (secretion of type 1 cytokines), suggesting that the down-regulation of TCR (?,?) and CD8 molecules does not hamper their capacity to control the infection. In a subsequent work, Leavey and Tarleton (2003) compared the functional status (ex-vivo cytolytic and IFN-? responses) of effector CD8+ T cells isolated from muscle tissues of mice chronically infected with T. cruzi with those retrieved from the spleen. These authors noted that effector CD8+ T cells trafficking through the muscle tissues were severely impaired, whereas the effector function of CD8+ T cells isolated from the spleen of the same chronically infected mice was preserved. It is still unclear how the muscle tissue damage/inflammation suppresses Tc1 function ex vivo in such a selective way. Since there is no evidence of overt intracellular parasite outgrowth in the heart of chronically infected mice, it is possible that effector/memory CD8+ T cells (TEM) recruited to the heart might transiently exert their cytolytic function. In other words, collateral tissue damage in muscle tissues might be minimised if the activity of Tc1 is subjected to tight temporal control. More recently, studies by Mariano et al. (2008) showed that regulatory T (CD4+CD25+GITR+Foxp3+) cells migrate into the heart of infected mice. Notably, these authors showed that treatment with anti-CD25 or anti-GITR resulted in increased mortality, while only anti-GITR enhanced tissue parasitism and inflammation, leading to increased frequencies of intracardiac CD4+, CD8+ and CCR5+ leukocytes as well as upregulated TNF-? production. Collectively, these studies suggest that Treg signalling through GITR may have broad implications for the pathogenesis of Chagas disease, affecting heart inflammation, parasite replication and ultimately, host resistance against the infection.

More recently, Bustamante et al. (2008) investigated in greater detail how the memory T cell compartment is affected by T. cruzi persistence in tissues of chronically infected mice. Remarkably, they reported that parasite eradication through aggressive anti-parasite treatment (with benznidazole) leads to the re-emergence of central memory CD8+ T cells (TCM), a functional subset that possesses a higher protective capacity as compared to the dominant, but short-lived, CD8+ TEM-like population of chronically infected mice. Another important inference derived from the above study was that long-term host exposure to T. cruzi does not lead to the exhaustion of the dominant T cell specificities, at least in the mouse model. Additional studies are required to determine if the depressed generation of TCM may reflect dysfunctions associated with parasitism of the thymus and/or secondary lymphoid tissues (De Meis et al. 2008).

Role of CCR5 in the pathogenesis of experimental infection

Chemokines are small, 8-11-kDa proteins that regulate the trafficking of leukocytes by binding to cognate seven transmembrane G protein-coupled receptors (GPCR) expressed at the surface of a variety of cells, including endothelial cells and leukocytes (Proudfoot 2002). In the past decade, studies in experimental models of T. cruzi infection have revealed that chemokines are produced by infected macrophages and by cardiomyocytes, both in vitro (Villalta et al. 1998, Machado et al. 2000) and in vivo (Talvani et al. 2000, Aliberti et al. 2001, Petray et al. 2002, Hardison et al. 2006). Studies on the role of CCR5, the receptor for the chemokines CCL3 (MIP1-?), CCL4 and CCL5 (RANTES), are of particular interest in light of human studies showing that heart disease is attenuated in chagasic patients displaying a single point mutation in the CCR5 promoter, the association being linked to lower expression levels of CCR5 on their leukocytes (Calzada et al. 2001). Based on observations made in the C3H/HeJ model of infection, Marino et al. (2004) reported that CD8+ T cells expressing CCR5 predominated in the heart inflammatory infiltrates. Interestingly, mice treated with CR1/CCR5 antagonist (Met-RANTES) displayed increased survival rates associated with decreased frequencies of intracardiac CD4+ and CD8+ T cells, diminished deposition of fibronectin in heart tissues and attenuated myocarditis. In another study, Machado et al. (2005) showed that CCR5 expression on CD8+ T cells was positively modulated by T. cruzi infection. Consistent with this observation, mRNA and protein for the CCR5 ligands CCL3, CCL4 and CCL5 were detected in the hearts of infected mice in association with CD4+ and CD8+ T cells. Analysis of the outcome of acute infection in CCR5-deficient C57Bl/6 mice showed that T cell migration to the heart was impaired, and these mice were susceptible to acute infection, implying that CCR5 and its ligands play a central role in the control of T cell influx in this mouse-inbred strain. Hardison et al. (2006) reported similar findings in acutely infected CCR5-deficient C57Bl/6 mice, but these mice were not refractory to chronic inflammation. In contrast to their results, Medeiros et al. (2009) recently reported that Met-RANTES ameliorated cardiac damage in mice chronically infected with the Colombian strain. Accordingly, Met-RANTES significantly decreased the numbers of intracardiac CD4+ T cells, without significantly affecting recruitment of CD8+ T and F4/80+ macrophages to the myocardium. In spite of the discrepant results generated by CCR5-deficient C57Bl/6 mice, the results obtained after pharmacological intervention with Met-RANTES and patient cohort studies suggest that CCR5 may play an important role in chronic immunopathology.

Functional characterisation of TS-specific CD8+ T cells from chronic chagasic patients

Although the research conducted in experimental models of Chagas disease strongly suggest that tissue parasitism is a prerequisite for the development of chronic myocardiopathy, the introduction of more sensitive techniques for parasite detection in human myocardial specimens, such as PCR, revealed that tissue parasitism was underestimated by classical histochemistry (Jones et al. 1993). The link between parasite persistence in tissues and disease activity was substantiated by studies showing that chronic patients displaying the CARD display parasite DNA in the heart, but not in oesophageal tissues, whereas reciprocally, the patients that exclusively develop gastrointestinal abnormalities showed the presence of parasite DNA in oesophageal tissues, but not in the heart (Jones et al. 1993, Vago et al. 1996). The conclusions of these studies were further substantiated by immunohistochemical analysis of chronic myocardium specimens showing a positive correlation between the density of mononuclear cell infiltration in the myocardium and presence of local depots of parasite antigens (Higuchi et al. 1997, Palomino et al. 2000, Benvenuti et al. 2008). While not excluding the contribution of IFN-?-producing CD4+ T cells and activated macrophages on the development of chronic myocarditis in humans, TNF-?- and IFN-?-producing CD8+ T cells were identified as the predominant subset of mononuclear cells infiltrating the myocardium (Reis et al. 1993, Higuchi et al. 1997). Due to logistical obstacles, the analysis of the epitope specificity of intracardiac CD8+ T cells from CARD patients was limited to an isolated study, involving a small cohort of patients with CARD that bear the highly prevalent HLA-A0201 allele (Fonseca et al. 2005). According to this study, CD8+ T cell lines derived from the heart tissues of CARD patients recognised two non-TS proteins, i.e., the FL-160 and cruzipain (Fonseca et al. 2005). Given the difficulties in obtaining heart tissues from a large number of chagasic patients, immunologists sought to characterise the epitope specificity of CD8+ T cells by analysing the immune profiles of T cells from the patients' peripheral blood. Taking advantage of structural information obtained about TS antigens, Laucella et al. (2004) used tetramer staining and ELISPOT to characterise class I MHC-restricted peptides derived from ASP-1, ASP-2 and TSA-1, in patients bearing the highly prevalent HLA-A.21 allele. Patients from non-endemic areas displayed very low frequencies of IFN-?-producing memory CD8+ T cells for TS peptides, although the frequencies of responses to HLA-A201-restricted influenza peptides in these chagasic patients were fairly well preserved. As conceded by the authors, it was somewhat disappointing that severe CARD patients exhibited virtually undetectable responses to the TS peptides (Laucella et al. 2004). Notably, however, a markedly different response profile was found in HLA-A2.1-positive individuals that continued to live in areas of active transmission of T. cruzi: these chronic chagasic patients displayed fairly higher frequencies of TS-specific CD8+ T cell responses as compared to those of patients from Buenos Aires (Laucella et al. 2004). The authors believed that these seemingly conflicting data were an indication that multiple exposures to parasites might account for the increased frequencies of TS-specific CD8+ T cells observed in patients living in this high transmission area. Considering that the spectrum of T. cruzi genotypes present in patients that have left endemic areas in the last 11-20 years might be narrower than those in area of active transmission (which may display more divergent TS epitopes), it will be useful to know if the T. cruzi organisms that are currently circulating in areas of active transmission may comprise TS sequences that are more closely related to the raw T. cruzi genome sequencing reads that were used to generate their peptide panel.

Given that TS peptides elicited poor responses in CD8+ T cells from the Buenos Aires cohort, additional assays were performed with parasite lysates (amastigotes). Although limited to a small number (n = 9) of patients, the amastigote lysates induced high-frequency type 1 responses by CD4+ and CD8+ T cells (6/9 patients). Intriguingly, the T cell recall assays performed with patients with severe cardiac disease showed that amastigote lysates did not induce a high frequency of IFN-?-producing T cells. However, there is a potential caveat in the design of CD8+ T cell recall assays performed with PBMCs stimulated by amastigote lysates, or for that matter, for the recall assays performed with epimastigote (Epi) extracts (Gomes et al. 2003, Laucella 2004, Souza et al. 2007): since we don't know how these soluble parasite Ags are cross-presented to class I MHC-restricted CD8+ T cells, it is possible that qualitative/quantitative differences in the APC function of cells present in peripheral blood might account for the seemingly discrepant response profiles of CD8+ T cells from indeterminate (IND) versus CARD patients. Alternatively, amastigotes may express TLRs (Ropert & Gazzinelli 2007, Medeiros et al. 2007) that preferentially suppress cytokine signalling in APCs from CARD patients through the induction of SOCS proteins, a regulatory pathway that limits the extent of TLR signalling by inhibiting type-I IFN signalling (Baetz et al. 2004).

In an effort to circumvent the above-mentioned complications, Albareda et al. (2006) used Brazil-infected dendritic cells (DCs) to study the maturation and migratory properties of the memory T cell compartment of chagasic patients. Their data showed a significant increase in total TEM (CD45RA-CCR7-) in subjects with mild heart disease as compared with uninfected controls. Furthermore, they found that T. cruzi-specific memory CD8+ T cells derived from patients with none or mild heart dysfunctions were enriched in early-differentiated (CD27+CD28+) cells that were more responsive (IFN-? production) than T cells from patients with more severe cardiac disease. Based on these findings, these authors proposed that persistent infection could lead to a gradual exhaustion of the responsive CD8+ T cell population. Although the results obtained by Albareda et al. (2006) suggested that there is a more general dysfunction in the CD8+ T memory compartment, the source of T cells (PBMCs) was depleted of monocytes to ensure that Ag presentation was strongly dependent on the ex vivo-infected DCs. According to earlier studies by Gomes et al. (2003), recently extended by Souza et al. (2007), the cytokine profile of Ag-stimulated T cells from chronic patients is modulated by inflammatory and anti-inflammatory cytokines produced by infected monocytes. Notably, IND patients displayed a higher ratio of monocytes expressing IL-10 than TNF-? (Souza et al. 2007). Although the exposure of monocytes to live T. cruzi leads to an increase in the frequency of CD80+ monocytes irrespective of the clinical stage, monocytes from patients with the cardiac form display decreased frequencies and intensities of CD86 expression compared to infected monocytes from individuals with the indeterminate clinical form. Conversely, exposure of lymphocytes to T. cruzi-infected monocytes led to an increase in surface expression of CTL4 by T cells from IND, but not CARD, patients compared to normal control individuals. As will be discussed, Costa et al. (2009) have recently demonstrated an association between a functional IL-10 gene polymorphism (-1082G/A), which leads to lower expression levels of IL-10, and the worsening of cardiac function in chronic Chagas disease. Hence, it is conceivable that IL-10-secreting cells are underrepresented in the monocyte-depleted populations of PBMCs that Albareda et al. (2006) have used to measure memory T cell responses elicited by Brazil strain-infected DCs. Conversely, it is also possible that the depletion of TNF-?-producing monocytes from the PBMCs of chronic chagasic patients (Buenos Aires cohort) might have reduced the T cell stimulatory properties of Brazil-infected DCs, hence accounting for the low responsiveness observed under these conditions. Although these systemic regulatory interactions may not necessarily occur in the infected heart, it is tempting to speculate that chronic heart pathology is influenced by the balance between TNF-?/IL-10-producing macrophages and/or IL-10-producing CD4+ FOXP3+ regulatory T cells, recently identified in higher frequencies in IND patients (Araujo et al. 2007).

Although the above studies collectively appoint IL-10 as a counter-modulator of chronic heart disease, it is still unclear if the T cell-dependent tissue damage is ultimately caused by parasite-specific CD8+ T cells and/or by TH1 CD4+ T cells. Focusing their analysis on the TCR specificity of CD8+ T cells, Alvarez et al. (2008) have recently conducted a large screen of TS peptides that bind to the six most common HLA supertypes, which cover one or more HLA allele in 95% of the human population irrespective of ethnicity. Their results indicated that the promiscuous TS-binding epitopes for HLA-A02, HLA-A03 and HLA A24 are the primary targets of memory CD8+ T cells in chronic chagasic patients. Positive responses were detected in 13 out of 25 asymptomatic subjects. This approach suggested that a specific set of class I MHC-restricted peptides can be used to measure the frequency and functional activity of T. cruzi-specific CD8+ T cells in a wide range of chagasic patients (with different ethnic backgrounds) without having to conduct HLA typing. As pointed out by the authors, the frequencies of IL-2-secreting, TS-specific CD8+ T cells were markedly reduced in chronically infected patients. Considering that parasite load is extremely low in chronically infected individuals, the authors proposed that long-term parasite persistence may drive the parasite/TS- specific T cell population towards the IL-2-deficient mono-functional IFN-?-T cell-responsive profile, thus impairing the self-renewal capacity. T cell assays performed with amastigote lysates suggested that the frequencies of IL-2-secreting CD4+ T cells were likewise reduced. Longitudinal studies are required to determine if the IL-12 deficiency might differentially affect the T regulatory cell compartment (CD4+ FOXP3 Treg) (Araujo et al. 2007) of IND and CARD patients.

Cohort studies using Epi-Ag link TH1 responses to severity of heart disease

Although the results from cohort studies performed with chagasic patients in Brazil, Guatemala and Argentina seemed conflicting, some of these discrepancies may be reconciled by considering the peculiarities of the experimental design used in different studies. For example, different sources of parasite antigens were used to stimulate peripheral blood T cells in vitro, while the Brazilian group used Epis (Epi, CL strain), the studies with the Argentinian cohorts involved amastigote lysates (Brazil strain), TS-derived peptides and T. cruzi (Brazil)-infected DCs (Gomes et al. 2003, Laucella et al. 2004, Albareda et al. 2006). Given that Epi (insect stage developmental form) do not express appreciable levels of the stage-specific TS antigens (e.g., ASP-1, ASP-2 and TSA-1), we may infer that the epitope specificity of Epi-stimulated TH1 cells studied in Minas Gerais (MG) are exclusively directed against cross-reactive structures present either in amastigotes/trypomastigotes (Gomes et al. 2003, Araujo et al. 2007, Souza et al. 2007). Considering that expression of TS proteins is developmentally regulated (i.e., these surface antigens are upregulated in trypomastigotes and amastigotes, but not in Epis), it is unlikely that TS specificities significantly contribute to the pool of CD4+ or CD8+ T cells activated by Epi lysates in studies reported by Gomes et al. (2003). Viewed against this background, the analysis of the T cell immune response profiles of the cohorts from the Brazilian study (MG) initially involved PBMCs derived from 131 patients, either grouped as IND (41 patients) or CARD (70). The recall assays involved Ag stimulation (Epi or Trypo) ex vivo (1-6 days). Kinetic studies revealed that, irrespective of the source of Ag stimuli used, IFN-? production by CD3+CD4+ T cells started at day 3 and peaked at day 6, while IL-10 production (by monocytes) had an early onset. Based on the levels of IFN-? production elicited by antigen-stimulated CD4+ T cells, it was possible to categorise the patients in high or low-responsiveness groups. Notably, high numbers of IFN-?-producing T cells were found in 83% of CARD patients and 59% of the IND group. Interestingly, the low IFN-? production of IND patients was linked to upregulated frequencies of IL-10-producing monocytes, which were already detectable at earlier stages of the in vitro culture. The observation that monocytes derived from chronic chagasic patients showed upregulated secretion of IL-10, further validated by the recent work of Souza et al. (2007), supports the concept that IL-10 might counterbalance TH1-induced immunopathology in the hearts of IND patients. As already mentioned, the severity of cardiac function abnormalities in Chagas disease (Costa et al. 2009) was recently linked to the 1082G/A polymorphism of the IL-10 promoter (Turner et al. 1997a, b), of which the phenotype is low IL-10 production. In a recent study, Araujo et al. (2007) found that patients with the IND form of the disease display a higher percentage of CD4+CD25high T cells expressing FOXP3 and IL-10 compared to the CARD form. In other recent study, D' Ávila et al. (2009) reported an imbalance between IFN-? and IL-10 levels in the sera of patients with the CARD form. Collectively, these studies suggest that upregulated expression of IL-10 by IND patients might effectively counterbalance IFN-? production by Ag-stimulated T cells.

Admittedly, additional studies are required to substantiate the hypothesis that pathogenic TH1 clones might contribute to the development of chronic myocardiopathy. As previously documented, the recognition of cross-reactive Epi antigens by human T cells may likely include CD4+ T and CD8+ T cell clones that recognise subdominant (non-TS related) class II MHC and class I MHC-restricted epitopes from cruzipain (Arnholdt et al. 1993, Morrot et al. 1997, Fonseca et al. 2005), the major cysteine protease of T. cruzi (Cazzulo et al. 1997). Expressed by all developmental forms of T. cruzi (Scharfstein et al. 1986, Murta et al. 1990), cruzipain has an N-terminal catalytic domain linked to a long and highly antigenic carboxy-terminal extension (GP25) (Scharfstein et al. 1983, 1985). Progress in the structural characterisation of the oligosaccharide chains revealed the presence of sulphated residues (Barbosa et al. 2005) that are essential for cruzipain recognition by IgG antibodies from the serum of chagasic patients (Acosta et al. 2008). Viewed against this background, it is possible that differences in clonal frequencies of B lymphocytes present in the peripheral blood of IND and CARD patients might affect the efficiency of BCR-driven internalisation and processing of cruzipain epitopes for class II MHC-restricted CD4+ T cells. Admittedly, additional cohort studies are required to characterise the TCR repertoire and frequency of CD4+ TH1 and Tc1 clones stimulated by Epi Ags in CARD and IND patients.

Chemokine receptors discriminate TEM phenotypes in chagasic patients

Although conceding that the peripheral blood-derived T cells, which are responsive to Epi-Ag, may not necessarily reach the myocardium, the demonstration of intracardiac MCH-class I-restricted, cruzipain-specific CD8+ T cells in CARD patients displaying the HLA.A0201 allele (Fonseca et al. 2005) implies that T cells with subdominant (i.e., non-TS) specificities are recruited to the damaged chagasic heart.

Given that chemokine receptors CXCR3 and CCR5 were previously defined as markers for type-1 inflammatory T cells in the peripheral blood of multiple sclerosis patients (Misu et al. 2001), Gomes et al. (2005) investigated the percentage of chemokine receptors/cytokines on CD4+ and CD8+ T cells from CARD and IND patients. The percentages of CD4+ and CD8+ T cells co-expressing CCR5 and IFN-?, CXCR3 and IFN-? or CXCR3 and TNF-? were higher in CARD than in IND individuals; on the other hand, the percentage of CD4+ or CD8+ T cells co-expressing CCR3 and IL-10 or co-expressing CCR3 and IL-4 were lower in CARD individuals than in IND individuals. In addition, a significantly positive correlation between the expression of CCR5 or CXCR3 and IFN-? was observed in CARD individuals, contrasting with a significantly positive correlation between the expression of CCR3 and IL-4 and of CCR3 and IL-10 in IND patients. These results are consistent with the notion that excessive type-1 immune responses by CARD patients might favour development of chronic heart pathology.

The pro-inflammatory role of extracellular T. cruzi

In spite of evidence suggesting that tissue parasitism is a prerequisite for the development of chronic myocarditis, it is uncertain if parasite pro-inflammatory molecules play a crucial role in the determination of pathogenic outcome. During the chronic stage, the release of intracellular parasites (spontaneous host cell death and/or resulting from CTL-mediated killing) must be a sporadic event, because the heart tissues are only scarcely parasitised. Once released in interstitial tissues, the extracellular amastigotes tend to cluster in the proximity of the primary infection foci. If viable, the amastigotes can eventually re-infect neighbouring host cells (Ley et al. 1988, Scharfstein & Morrot 1999, Fernandes & Mortara 2004). In contrast, the flagellated trypomastigotes rapidly move away from the primary foci of infection, hence spreading tissue parasitism. Early studies predicted that T. cruzi may induce cumulative microvascular lesions in the heart (Morris et al. 1990, Rossi 1990, Tanowitz et al. 1990), but the molecular mechanisms underlying heart vasculopathy in T. cruzi-infected animals remained elusive for many years. More recently, however, Tanowitz et al. (2005) presented evidence that myocardial up-regulation of endothelin-1 may contribute to the pathogenesis of Chagas disease. In another interesting finding, it was recently proposed that T. cruzi may modulate host-parasite equilibrium through the production of parasite-derived thromboxane molecules (Ashton et al. 2007). In spite of progress made by the above-mentioned groups, it is still unclear how the parasites induce endothelin-1 and/or produce thromboxane and whether these effects are critical for the development of chronic myocardiopathy. Early efforts to understand the molecular basis of endothelial cell responses to T. cruzi focused on the desialylation, at that time attributed to TS enzymes (Libby et al. 1986). More recently, however, Dias et al. (2008) demonstrated that the recombinant (catalytically inactive) TS bound to endothelial cell-surface molecules containing endothelial ?2,3-linked sialic acid, inducing NF-?B activation, expression of adhesion molecules and blocking endothelial cell apoptosis induced by growth factor deprivation. Noteworthy in this context, TS binding to endothelial cells may render these cells sensitive to antibody-mediated cellular cytotoxicity (ADCC), as originally proposed by Ribeiro-dos-Santos and Hudson (1981). Although ultrastructural studies performed in acutely infected animals suggested that ADCC may drive chagasic microangiopathy (Andrade et al. 1994), it remains to be determined if this mechanism may also account for the extensive cardiac microcirculatory abnormalities observed in the chronic stage of human infection (Higuchi et al. 1999, Tanowitz et al. 2005).

Given that the heart microcirculation of chronically infected animals is not easily accessible to intravital microscopy, Monteiro et al. (2006) studied the mechanisms linking parasite-induced interstitial oedema to T cell developmental pathways using the mouse model of subcutaneous infection (Monteiro et al. 2006, Schmitz et al. 2009). While activation of the complement system is classically associated with induction of the adaptive system, it was only recently recognised that the kinin proteolytic system is another example of a proteolytic web that modulates the adaptive branch of cellular immunity (Monteiro et al. 2006, 2008, Scharfstein et al. 2007). Classically viewed as vasoactive autacoids, the nonapeptides bradykinin (BK) and lysyl-bradykinin are released from a moiety of their parental glycoproteins, high or low-molecular-weight kininogens, by the action of tissue or plasma kallikrein. The characterisation of the major cysteine protease of T. cruzi as a microbial kinin-releasing enzyme ("kininogenase") (Del Nery et al. 1997) was the starting point of investigations that appointed a role for the kinin system in the immuno-pathogenesis of experimental Chagas disease (Monteiro et al. 2008, Scharfstein et al. 2008). Although soluble kininogens are not efficiently processed by cruzipain, the interactions of plasma-borne kininogens with sulphated glycosaminoglycans displayed at cell surfaces render the kinin-precursor molecules sensitive to proteolytic processing by cruzipain (Lima et al. 2002). Once liberated, kinins swiftly bind to the bradykinin B2 receptor (B2R), a GPCR subtype that is constitutively expressed by a wide range of cell types, including cardiomyocytes, endothelial cells and DCs (Aliberti et al. 2003, Monteiro et al. 2006). The long-range signalling activity of the released kinins is prevented by the action of kinin-degrading metallopeptidases, such as angiotensin converting enzyme and neutral endopeptidase. Alternatively, the kinin peptides released from kininogens are metabolised by carboxypeptidase M/N, generating the C-terminally truncated des-Arg-BK ligands of B1R, a GPCR that is upregulated in inflamed/damaged tissues.

Studies performed earlier in this decade revealed that tissue culture trypomastigotes (TCTs) can invade a broad range of resting or activated non-phagocytic cells, respectively via the signalling of B2R (Scharfstein et al. 2000) or through the signalling of the inducible B1R pathway (Todorov et al. 2003). Although TCTs are also able to invade host cells through the signalling of alternative GPCR specificities (Andrade & Scharfstein, unpublished observations), it is conceivable that the parasites may exploit the fact that B1R is upregulated in inflamed/injured tissues to opportunistically invade heart cells (Todorov et al. 2003). Whether or not it is acting as a parasite virulence factor, it is now well established that the proteolytic release of kinins in infected tissues has a profound impact on the mechanisms that integrate inflammation and innate/adaptive immunity (Scharfstein et al. 2007). Support for this concept came from analysis of the susceptible phenotype of B2R-deficient mice acutely infected (i.p. route) by the Dm28 strain of T. cruzi (Dm28c) (Monteiro et al. 2008). Based on previous work (Aliberti et al. 2003, Monteiro et al. 2006), these authors predicted that kinins generated in infected peripheral and/or secondary lymphoid tissues might have acted as TH1-directing natural adjuvants, thereby coordinating the generation of immunoprotective T cells. Indeed, analysis of the cytokine profiles of anti-parasite T cell responses in the spleen and heart tissues revealed that B2R-deficient C57Bl/6 mice failed to generate high frequencies of immunoprotective IFN-?-producing CD4+ T and CD8+ effector T cells. Surprisingly, the Ag-specific CD4+ T cells from susceptible B2R-/- mice secreted high levels of IL-17 (Monteiro et al. 2008). Analysis of the in vitro interaction of Dm28 TCTs with conventional CD11+ DCs (splenic) disclosed that the kinin "danger" signals released by cruzipain potently induce the maturation of immature DCs from wild-type mice, but not DCs isolated from B2R-/- mice. Adoptive transfer of wild-type splenic CD11c+ DCs into susceptible B2R-/- mice reverted the susceptible phenotype of the recipient mice, while rescuing their ability to generate high frequencies of immunoprotective (type-1) T cells and reciprocally suppressing IL-17 responses, at the expense of kinin system activation (Monteiro et al. 2008). In summary, these studies suggested that the parasites rely on cruzipain to liberate the TH1-directing kinin danger signal from plasma-borne kininogens diffusing through infected lymphoid and/or peripheral tissues (Scharfstein et al. 2007).

It is well established that tissue sentinel cells, such as mast cells and DCs, sense tissue injury and pathogen threat through alarm signals conveyed by endogenous signals and/or microbial signatures. Further insight on the mechanisms underlying the pro-inflammatory phenotype of TCTs came from a comparison of the dynamics of inflammation in wild-type versus TLR2, TLR4 and B2R-deficient mice infected via the s.c route (Monteiro et al. 2006). As also documented in a more recent paper (Schmitz et al. 2009), Dm28c TCT induce interstitial oedema via an intricate mechanism involving sequential activation of TLR2, CXCR2 and B2R. Using paw oedema responses as a read out for inflammation, Monteiro et al. (2006) showed that glycosylphosphatidylinositol-linked mucin (tGPI-mucin), a potent TLR2 ligand shed by TCTs (Almeida & Gazzinelli 2001, Roppert & Gazzinelli 2007), is rapidly "sensed" by innate sentinel cells (e.g., tissue resident macrophages) via TLR2 activation. Following the secretion of neutrophil-attracting CXC chemokines (MIP-2/KC), the macrophages activate the endothelium/neutrophils, hence linking TLR2-dependent innate recognition of the pathogen to the CXR2/neutrophil-dependent inflammation, which in this model is manifested as a slight increase in vascular permeability (Schmitz et al. 2009). Owing to the diffusion of plasma proteins, the concentration of blood-borne kininogens (cruzipain substrate) suddenly rises in peripheral sites of infection. Further downstream, cruzipain liberates vasoactive kinins from kininogens, thus amplifying interstitial oedema through the sequential activation of the endothelium lining via B2R and B1R (Todorov et al. 2003, Schmitz et al. 2009). As documented by Monteiro et al. (2006), the rise in kinin levels in peripheral tissues converts immature DCs into IL-12-producing APCs, which migrate to draining LNs, where they subsequently activate T cells, inducing and/or sustaining TH1 polarisation.

As discussed above, TCTs evoke interstitial oedema via mechanisms involving cooperate activation of the TLR2 and the kinin/B2R pathway (Monteiro et al. 2008, Schmitz et al. 2009). It is presently unknown if parasite clones from the major filogenetic lineages express variable levels of tGPI-mucin (Nakayasu et al. 2009), other TLR ligands (Ouaissi et al. 2002, Mathieu-Daudé et al. 2007) and/or cruzipain isoforms (Lima et al. 2001). If so, parasite clones may display differential power to activate microvascular beds via the TLR2/CXCR2/cruzipain > kinin/B2R/B1R pathway. If true, we may also predict that such processes may account for differential rates of leukocyte transmigration through the endothelium. Under these hypothetical conditions, the parasites may directly modulate lymphocyte function through the lectin activity of TS molecules (Todeschini et al. 2002a, b) or down-modulate macrophage microbicidal function as result of internalisation of apoptotic neutrophils and/or lymphocytes (Freire-de-Lima et al. 2000, Dos Reis et al. 2005). In either case, we may predict that the differential activation of endothelium/neutrophils via the TLR2 > B2R/B1R axis may have an impact on the host-parasite equilibrium.

Future studies may determine if the vascular permeability increases induced by extracellular T. cruzi forms can lead to the rapid diffusion of anti-parasite and/or autoreactive IgG antibody specificities present in chagasic serum into extravascular cardiac tissues. Although sporadic, these events may render the heart conduction system more vulnerable to the pathological effects of serum IgG auto-antibodies, such as those that cross-react with the R13 tope of T. cruzi ribosomal protein P2? and the peptide ESDEARRCYN from the second extracellular loop of the human ?1-adreno receptors (Smulski et al. 2006).

Conclusive remarks

Although the multifactorial nature of pathogenic determinants of Chagas disease leaves no room for simple-minded conclusions, the body of literature reviewed in this article may provide readers with a reasonable perspective of the current trends and challenges of pathogenesis research. While the bulk of human and animal studies suggest that T cell-dependent control of intracellular parasite outgrowth depends predominantly on the targeting of epitopes encoded by TS family genes, it is conceivable that the development of severe myocardiopathy may result from deficient regulation of type-1 effector T cells that recognise hitherto uncharacterised subdominant epitopes. Another promising line of research in immunopathogenesis relies on knowledge about the activation pathways that interconnect parasite-induced inflammation and innate/adaptive immunity. The dissection of the pro-inflammatory role of parasite factors, such as TS antigens, lipid anchors and proteolytic enzymes, provides a new framework for investigations of the impact of genetic diversification of T. cruzi clones on the pathogenic outcome.

 

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Received 20 May 2009
Accepted 17 June 2009
Financial support: CNPq, FAPERJ, FAPEMIG

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