- Research article
- Open Access
Enhancement of experimental cutaneous leishmaniasis by Leishmania extract: identification of a disease-associated antibody specificity
BMC Research Notesvolume 8, Article number: 197 (2015)
Both Leishmania braziliensis and Leishmania amazonensis induce cutaneous disease when injected in the skin of BALB/c mice. However, L. amazonensis may also visceralize in that strain of mice, infecting mainly the liver and spleen. In addition, whereas BALB/c mice die with a progressive cutaneous disease when infected by L. amazonensis, the infection by L. braziliensis is spontaneously cured. In a previous work, we have found that intravenous injections of L. amazonensis amastigote extract (LaE) potentiated a L. braziliensis infection in BALB/c mice, and that this infection-promoting activity could be inhibited by the addition of protease inhibitors to the extract.
In order to detect markers of disease evolution, in the present work we analyzed the specificity of the anti-L. amazonensis antibody response of L. braziliensis-infected BALB/c mice injected intravenously with saline or LaE, supplemented or not with protease inhibitors, by the Western blot technique.
IgG1 antibodies recognizing an antigen with apparent molecular weight of 116 kDa were specifically detected in BALB/c mice that had been turned susceptible to L. braziliensis infection by injections of LaE.
A Th2 immune response (IgG1 antibody-producing) against this 116 kDa antigen, therefore, could be associated with susceptibility to severe Leishmania infection.
Leishmania parasites proliferate either as extracellular promastigotes, in the sand-fly vector, or as intracellular amastigotes, inside the phagolysosome of mammalian macrophages. Depending on the Leishmania species or isolate, and on the nature of the host immune response, the infection can cause distinct forms of disease, ranging from self-limiting cutaneous lesions to lethal visceral illness [1–3]. The leishmaniases are difficult to treat, and parasite resistance against the currently available drugs is increasing .
Although Leishmania braziliensis causes a serious health problem in South America , leading in some cases to mutilating nasal and/or oral lesions (reviewed in ), few experimental studies on the characterization of its antigens, and on the immune response against them, have been performed [7–9]. Contrasting to what can be observed in L. braziliensis-infected individuals, some L. amazonenis-infected individuals develop a progressive form of leishmaniasis, with multiple, heavily parasitized cutaneous nodules (diffuse cutaneous leishmaniasis), which is clearly associated with a failure of the patients’ immune system to mount a parasite-specific Th1 immune response [10, 11].
In the mouse, it has been shown that antibodies of the IgG1 isotype are produced mainly during a Th2 immune response, and IgG2a antibodies are produced mainly during Th1 immune responses . In murine leishmaniasis models, the Th2 immune response has been associated with disease susceptibility, whereas the Th1 immune response has been associated to disease resistance . Similarly to human beings, different species of Leishmania cause distinct diseases in mice. The genetic background of the mouse also affects the outcome of the infection [14–17].
A study on amastigote antigens, using the Western blot technique, demonstrated that antibodies from infected, healthy individuals and from leishmaniasis patients reacted with different parasites antigens . Along the same line, a Leishmania infantum recombinant antigen, the k39, has been shown to discriminate antibodies from infected, asymptomatic individuals from those of patients with overt visceral leishmaniasis [19, 20]. Antibodies, therefore, may serve as markers of active disease in leishmaniasis. Prospective studies would need to be carried out in order to ascertain whether some antibodies produced by asymptomatic, Leishmania-infected individuals could be markers of resistance or susceptibility to the development of disease.
Our research group has shown that BALB/c mice, which are usually resistant to L. braziliensis , become susceptible if they are intravenously injected with a soluble extract of amastigotes of Leishmania amazonensis (and not of L. braziliensis), and that the supplementation of the extract with serine-protease inhibitors reduces this effect .
In order to identify possible antigenic markers of susceptibility to disease associated with the biologically active L. amazonensis extract, in the present work the specificity of the anti-Leishmania antibody response was assessed by Western blot in L. braziliensis-infected BALB/c mice intravenously injected with the L. amazonensis extract. The extract was supplemented or not with protease inhibitors and was injected one week before the infection and every two weeks thereafter. Antibodies against an antigen with an apparent molecular weight of 116 kDa were only detected in the sera of the mice injected with the biologically active extract (and not in the sera of the mice injected with the protease inhibitors-treated, biologically inactive extract).
Specific pathogen-free, 8-12 week-old, male BALB/c mice were maintained at the animal facilities of the Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Bahia, and provided with rodent diet and water ad libitum. All procedures performed on the animals were approved (protocol number 004/2004) and conducted in accordance with norms of the Ethical Committee in Laboratory Animal Utilization of the Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Parasites and amastigote extract
The MHOM/Br87/Ba125 L. amazonensis and MHOM/Br/3456 L.braziliensis strains were used. Their infectivities were maintained by regular inoculations of promastigotes in susceptible BALB/c mice and golden hamsters, respectively. Promastigotes, derived from tissue amastigotes, were cultured at 23 °C in Schneider’s medium (Sigma Chemical Co., Saint Louis, MO, USA), pH 7.2, supplemented with 50 μg/mL of gentamycin and 10 % of heat-inactivated fetal bovine serum (FBS; HIFCS, Gibco Laboratories, Grand Island, NY, USA) for L. amazonensis, or 20 % FBS for L. braziliensis. L. amazonensis axenic amastigotes were obtained by the differentiation of stationary-phase promastigotes in axenic cultures. They were left to differentiate in Falcon flasks containing 2 × 107 promastigotes/mL in Schneider’s medium supplemented with 5 % fetal bovine serum, pH 5.4, at 32 °C and 5 % CO2. After 5 days, more than 98 % of cells were morphologically undistinguishable from amastigotes, as described elsewhere . The amastigotes were washed three times in ice-cold sterile saline, resuspended in ice-cold saline and lysed by exposition to ultrasound (10 times for 1 min on ice). The lysates were centrifuged at 16,000 g for 10 min at 4 °C, the supernatants filtered on membranes with 0.22 μm-diameter pores (Millipore, São Paulo, Brazil) and immediately stored at -70 °C in small aliquots. These filtered saline supernatants are called in this report L. amazonensis extract (LaE). They were shown to be free of bacterial endotoxin by the Limulus amebocyte enzyme assay (Biowittaker, MD, USA), and their protein content was determined by Lowry’s method . Part of the prepared LaE was supplemented with protease inhibitors (10 mM phenylmethanesulfonyl fluoride, 5.7 mM N-p-tosyl-L-phenylalanine chloromethy l kNap-tosyl-L-lysyl chloromethyl ketone etone, 5.4 mM N-p-tosyl-L-lysine chloromethyl ketone hydrochloride, and 5.9 mM 4-nitrophenyl hepta-O-acetyl-1-thio-beta-lactoside; Sigma Chemical Co., St Louis, MO, USA).
Injection of mice with Leishmania extract
Animals from groups of 4 to 5 BALB/c mice received four 0.2-mL i.v. injections of either LaE or LaE with protease inhibitors. The injections were separated by an interval of two weeks, starting one week before the mice were infected as described below. Each injection contained 200 μg of protein. Control groups of mice received four 0.2-mL injections of either saline or saline plus protease inhibitors.
Murine model of cutaneous leishmaniasis
Ten million L. braziliensis promastigotes, obtained from stationary-phase culture, were subcutaneously inoculated into one of the hind footpads of BALB/c mice, seven days after the first injection of the LaE. The hind pad thicknesses were weekly measured with a digital caliper and the lesion sizes estimated by subtracting the thickness of the uninfected pad from the thickness of the infected pad. Tissue parasitism was estimated as described below.
Evaluation of parasite load
Parasite loads in the footpads were estimated by limiting dilution  six weeks after infection. Briefly, the infected footpads were macerated in Schneider’s medium and centrifuged at 50 g for 10 min, at 4 °C. The supernatants were re-centrifuged at 1540 g for 10 min at 4 °C and the pellets were resuspended in Schneider’s medium, supplemented with 50 μg.mL−1 of gentamycin, and 20 % FBS. The suspension was serially diluted in 10-fold dilutions and distributed in triplicates in 96-well culture plates. The number of viable parasites in each footpad was estimated from the reciprocal of the highest dilution at which promastigotes could be detected after a 7-day culture at 23 °C, and was expressed as parasites per milligram of tissue.
Determination of antibody specificity by Western blot
Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of LaE was performed on 12 % polyacrylamide gels using a Mini Protean II apparatus (Bio-Rad, California, USA). Wells were loaded with LaE containing 20 μg/mL of protein, resuspended in SDS-sample buffer and boiled for 4 min, and the electrophoresis carried out as described elsewhere . Proteins were electrophoretically transferred from the gel to nitrocellulose membranes. The nitrocellulose membranes were cut into vertical strips and blocked for 12 h with 0.15 M phosphate-buffered saline, pH 7.2 (PBS) containing 10 % FBS, at 4 °C. Incubation with mouse sera (diluted 1:1000 in PBS containing 0.05 % of Tween 20 and 10 % of FBS) was carried out during 1 h at room temperature with mechanical agitation. After five 1-min washes in PBS, the membranes were incubated during 1 h with appropriately diluted horseradish peroxidase-conjugated anti-mouse IgG1 or IgG2a (Sigma Chemical Co., Saint Louis, MO, USA) in PBS containing 0.05 % Tween 20 and 5 % FBS, at room temperature. The nitrocellulose strips were finally incubated with a mixture of 3’3-diaminobenzidine (Sigma Chemical Co., Saint Louis, MO, USA) and H2O2 in PBS. Naïve mouse sera were used as negative controls.
When the distribution of the data was found to be Gaussian by the D’Agostino and Pearson’s method, comparisons among the groups were performed by ANOVA followed by the Newman-Keuls’s method. When the distribution was found to be non-Gaussian, comparisons among the groups were performed by the Kruskal-Wallis method followed by the Dunn’s post test. Results were considered significant when P ≤ 0.05. The GraphPad Prism program, version 5, was used to perform the calculations.
Lesion size and parasite burden in experimentally infected mice
In a previously published work, we have shown that injection of LaE together with protease inhibitors abolished the enhancing effect of the LaE on the Leishmania infection in BALB/c mice . We, therefore, have analysed in the present work not only the antibodies present in the sera of saline-injected mice, but also the antibodies present in the sera of a group of mice that had been injected with LaE plus protease inhibitors.
As in previously published work, the four biweekly intravenous injections of LaE significantly increased the size of the lesions caused by L. braziliensis in BALB/c mice (Fig. 1a), whereas the group of mice that received LaE in the presence of protease inhibitors did not differ significantly from the control group (mice that received saline; Fig. 1a).
The number of parasites in the foot pad lesion of BALB/c mice, infected with L. braziliensis, that received four biweekly LaE i.v. injections, was significantly higher than those in animals injected with saline (Fig. 1b). The infected footpads of the mice injected with protease inhibitors-treated LaE had on average 100-fold fewer parasites than the footpads of the mice injected with untreated LaE. The group of mice that received LaE in the presence of protease inhibitors did not differ significantly from the control group in terms of parasite load (Fig. 1b).
Although differences between the groups of mice treated with LaE and LaE plus protease inhibitors, both in terms of lesion size and tissue parasitism, could be clearly seen (Fig. 1), they were not statistically significant.
Specificity of the antibody response against L. amazonensis amastigote antigens
One protein with apparent molecular weight of 28 kDa, and three proteins with apparent molecular weights from 45 to 54 kDa were only detected by the IgG1 antibodies from mice injected with LaE, regardless of its supplementation with protease inhibitors (Fig. 2). Additional antigens were recognized only by the sera of the mice treated with the unsupplemented extract. These sera stained from 6 to 12 or more bands (Fig. 2, lanes 12 to 16). On the other hand, the sera of the mice injected with protease inhibitor-supplemented extract specifically stained only 4 or 5 bands (Fig. 2, lanes 7 to 11). An antigen with apparent molecular weight of 116 kDa was recognized by all sera of the mice injected with unsupplemented LaE (Fig. 2, lanes 12 to 16), and by none of the sera from the mice injected with the protease inhibitor-supplemented extract (Fig. 2, lanes 7 to 11). The recognition pattern of the serum from a particular mouse injected with unsupplemented extract (Fig. 2, lane 15) only differed from the recognition patterns of the sera from mice treated with the protease inhibitor-supplemented extract (Fig. 2, lanes 7 to 11) by the recognition of that particular antigen.
Similar antigens were recognized by IgG2a antibodies of the L. braziliensis-infected BALB/c mice, injected or not with LaE, supplemented or not with protease inhibitors (Fig. 3). Three antigens with apparent molecular weights ranging from 34 to 38 kDa reacted with IgG2a antibodies only from the sera of mice treated with LaE, supplemented or not with protease inhibitors (Fig. 3). No difference in antigen recognition was observed with IgG2a antibodies from animals that received unsupplemented LaE and animals that received LaE supplemented with protease inhibitors (Fig. 3, lanes 7 to 16).
The transformation from promastigotes to amastigotes provides the necessary adaptations for the Leishmania to survive in the mammalian environment, including mechanisms to evade or subvert the host immune response, such as the escape to a safe, protease-free intracellular vacuole and the production of immunomodulatory molecules [27–29]. In this study, the presence of a L. braziliensis infection-enhancing activity in soluble extracts of L. amazonensis amastigotes, as observed previously in our laboratory [22, 30], was confirmed: larger numbers of parasites were found in the foot pad of L. braziliensis-infected BALB/c mice that received LaE than in those from animals injected only with saline (Fig. 1). In the present work, the LaE was injected in a relatively large amount by the intravenous route. In a previously published work , similar results were obtained when the intradermal route was used.
It has been reported that the injection of LaE together with protease inhibitors reverts its infection-enhancing effects . In fact, it has been shown that Leishmania amazonensis serine proteases may be disease-aggravating components of a crude anti-leishmaniasis vaccine . Thus, in the present work we compared the specificity of the humoral immune response of the mice injected only with LaE (susceptible to L. braziliensis infection) with that of the response of mice injected with a mixture of LaE and protease inhibitors (relatively resistant to the development of L. braziliensis infection).
As shown herein, the nature of the humoral immune response against L. amazonensis antigens differed in L. braziliensis-infected mice rendered susceptible by the intravenous injection of LaE from those of relatively resistant mice (injected with LaE supplemented with protease inhibitors or with saline). Quite interestingly, these differences were most evident for IgG1 antibodies (Fig. 2), and not for IgG2a antibodies (Fig. 3), a fact which is consistent with the LaE acting through the promotion of a Th2-dependent immune response. This confirm previous results showing increased production of IL-4 by lymph node cells of LaE-injected mice and the absence of infection-enhancing effect of this extract in IL-4-knockout mice .
The observed differences in the production of IgG1 antibodies were both quantitative (antibodies of infected BALB/c mice injected only with saline, or even with protease inhibitor-supplemented LaE, reacted with fewer peptides than antibodies from mice injected with unsupplemented LaE), and qualitative: a 116 kDa protein band of L. amazonensis amastigotes was exclusively recognized by sera of unsupplemented LaE-treated BALB/c mice. It is possible that the presence of IgG1 antibodies against one or more of these antigens could be a marker of an infection-promoting immune response induced by L. amazonensis. These antigens could in fact lead to the generation and maintenance of a predominant Th2 immune response that would hinder an otherwise effective Th1 response, allowing the progression of the disease. It would be interesting to find out if sera from patients with diffuse cutaneous leishmaniasis differ from those of patients with localized cutaneous leishmaniasis caused by L. amazonensis by the presence of antibodies against these antigens.
A Th2 immune response against the protein with apparent MW of 116 kDa might be one of the many escape mechanisms that have evolved during the thousands of years of interaction of the parasite with the mammalian hosts’ immune system. For instance, other Leishmania molecules, such as the kinetoplastid membrane protein 11 (KMP-11) , the Leishmania-homologue of activated C kinase (LACK) , the lipophosphophoglycan  and the Gp63  have been shown, in different situations, either in vitro or in vivo, to enhance the Leishmania infection.
The expression of a serine protease with an apparent molecular weight of 115 kDa by L. amazonensis has been described by Silva-Lopez and collaborators . In an electrophoretic-zymographic study performed by our research group, a protein with the same apparent molecular weight and with protease activity was found in a L. amazonensis extract and not in a L. braziliensis extract (Oliveira & Navarro, unpublished data). It is possible that this serine protease is the protein recognized only by antibodies from mice with severe leishmaniasis, which had been injected with LaE without serine protease inhibitors in the present work. L. amazonensis serine protease activity has been shown to enhance the Leishmania infection, but the responsible protein has not been identified [22, 32].
Another interesting fact observed in the present work was that the untreated L. braziliensis-infected animals produced antibodies, mainly of the IgG2a isotype, recognizing cross-reactive L. amazonensis antigens (Fig. 3, columns 1-5). This is in accordance to the fact that these animals preferentially produce a Th1-dependent immune response [22, 32]. These cross-reactive antibodies could be useful for identifying, in Leishmania DNA libraries, genes encoding recombinant proteins able to elicit potentially protective Th1 immune responses.
It is possible that antibodies against the 116 kDa protein are produced during the human infection and could be used as markers of disease susceptibility. This possibility is amenable to investigation by seroepidemiological studies.
In summary, we investigated the pattern of antigen recognition by antibodies from BALB/c mice that were rendered susceptible to L. braziliensis infection by intravenous injections of a L. amazonensis extract. We found that a protein with a molecular weight of approximately 116 kDa was specifically recognised by antibodies from those mice. No protein with this molecular weight possessing infection-enhancing activity has been described in the literature so far. The immune response against this protein, therefore, might be detrimental to the development of a protective immune response.
L. amazonensis amastigote extract
Almeida RP, Barral-Neto M, de Jesus AMR, de Freitas LAR, Carvalho EM, Barral A. Biological behavior of Leishmania amazonensis isolated from humans with cutaneous, mucosal, or visceral leishmaniasis in BALB/c mice. Am J Trop Med Hyg. 1996;54:178–84.
Handman E. Leishmaniasis: current status of vaccine development. Clin Microbiol Rev. 2001;14:229–43.
Leopoldo PT, Machado PR, Almeida RP, Schrifer A, Giudice A, de Jesus AR, et al. Differencial effects of antigens from L. braziliensis isolates from disseminated and cutaneous leishmaniasis on in vitro cytokine production. BMC Infect Dis. 2006;25:75–80.
Davidson RN. Visceral leishmaniasis in clinical practice. J Infect. 1999;2:112–6.
Belli AA, Milles MA, Kelly JM. A putative Leishmania panamensis/Leishmania braziliensis hybrid is a causative agent of human cutaneous leishmaniasis in Nicaragua. Parasitology. 1994;109:435–42.
Grimaldi Jr G, Tesh RB. Leishmaniases of the New World: current and implications for future research. Clin Microbiol. 1993;6:230–50.
Williams KM, Sacci JB, Anthony RL. Identification and recovery of Leishmania antigen displayed on the surface membrane of mouse peritoneal macrophages infected in vitro. J Immunol. 1986;136:1853–8.
Silveira TG, Kemmelmeier C. Leishmania braziliensis: isolation of carbohydrate-containing antigen and possibility of its use in the immunodiagnosis of American cutaneous leishmaniasis. Rev Inst Med Trop Sao Paulo. 1995;37:245–52.
Carmelo E, Martinez E, González AC, Piñero JE, Patarroyo ME, Del Castillo A, et al. Antigenicity of Leishmania braziliensis histone H1 during cutaneous leishmaniasis: localization of antigenic determinants. Clin Diag Lab Immunol. 2002;9:808–11.
Petersen EA, Neva FA, Oster CN, Dias HB. Specific inhibition of lymphocyte proliferation responses by adherent suppressor cells in diffuse cutaneous leishmaniasis. N Engl J Med. 1982;306:387–92.
Castes M, Agnelli A, Verde O, Rondon AJ. Characterization of the cellular immune response in American cutaneous leishmaniasis. Clin Immunol Immunopathol. 1983;27:176–86.
Stevens TL, Bossie A, Sanders VM, Fernandez-Botran R, Coffman RL. Regulation of antibody isotype secretion by subsets of antigen-specific helper T cells. Nature. 1988;334:255–8.
Maekawa Y, Himeno K, Ishikawa H, Hisaeda H, Sakai T, Dainichi T, et al. Switch of CD4+ T cell differentiation from Th2 to Th1 by treatment with cathepsin B inhibitor in experimental leishmaniasis. J Immunol. 1998;161:2120–7.
Alexander J, Blackwell JM. The immunological significance of genetically determined cross reactivity between taxonomically distinct Leishmania species. In: Riou JA, editor. Leishmania, taxonomie et phylogenèse: application éco-épidemiologiques. Montpellier: Institut Méditerranéen d’Etudes Epidémiologiques et Ecologiques; 1986. p. 185–91.
Afonso LC, Scott P. Immune responses associated with susceptibility of C57BL/10 mice to Leishmania amazonensis. Infect Immun. 1993;61:2952–9.
Lemos LV, Ascenção SJ, Correia STM, Sampaio TVP, Rodrigues-de-Freitas LA. Different Leishmania species determine distinct profiles of immune and histopathological responses in CBA mice. Microbes Infect. 2000;2:1807–15.
Souza VL, Veras PS, Welby-Borges M, Silva TM, Leite BR, Ferraro RB, et al. Immune and inflammatory responses to Leishmania amazonensis isolated from different clinical forms of human leishmaniasis in CBA mice. Mem Inst Oswaldo Cruz. 2011;106:23–31.
Mary C, Lamouroux D, Quilici M. Western blot analysis of antibodies to Leishmania infantum antigens: potential of the 14-kDa and 16-kDa antigens for diagnosis and epidemiologic purpose. Am J Trop Med Hyg. 1992;47:764–71.
Burns JJM, Shreffler WG, Benson DR, Ghalib HW, Badaro R, Reed SG. Molecular characterization of a kinesin-related antigen of Leishmania chagasi that detects specific antibody in African and American visceral leishmaniasis. Proc Natl Acad Sci U S A. 1993;90:775–9.
Badaró R, Benson D, Eulálio MC, Freire M, Cunha S, Netto EM, et al. rK39: a cloned antigen of Leishmania chagasi that predicts active visceral leishmaniasis. J Infect Dis. 1996;173:758–61.
De Krey GK, Lima HC, Titus RG. Analysis of the immune response of mice infection with Leishmania braziliensis. Infec Immun. 1998;66:827–9.
Silva VM, Larangeira DF, Oliveira PR, Sampaio RB, Biointervention Student Group, Suzart P, et al. Enhancement of experimental cutaneous leishmaniasis by leishmania molecules with serine protease activity. I. Requirement of IL-4. Infect Immun. 2011;79:1236–43.
Teixeira MC, De-Jesus SR, Sampaio RB, Pontes-De-Carvalho LC, Dos-Santos WC. A sample and reproducible method to obtain large numbers of axenic amastiotes of different Leishmania species. Parasitol. 2002;88:963–8.
Lowry OH, Rosenbrough NJ, Faar AL, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem. 1951;193:265–75.
Lima HC, Bleyenberg JA, Titus RG. A simple method for quantifying Leishmania in tissues of infected animals. Techniques. 1997;13:80–2.
Laemmli UK. Cleavage of structural protein during the assembly of the head of bacteriophage T4. Nature. 1970;227:680–5.
Reiner SL, Locksley RM. The regulation of immunity to Leishmania major. Ann Rev Immunol. 1995;13:151–77.
Bogdan C, Rollinghoff M. The immune response to Leishmania: mechanisms of parasite control and evasion. Intern J Parasit. 1998;28:121–34.
Hassani K, Olivier M. Immunomodulatory impact of Leishmania-induced macrophage exosomes: a comparative proteomic and functional analysis. PLoS Negl Trop Dis. 2013;7, e2185.
de Araújo CF, Silva VM, Cronemberger-Andrade A, Aragão-França LS, Rocha VC, Santos PS, et al. Leishmania braziliensis and Leishmania amazonensis amastigote extracts differ in their enhancement effect on Leishmania infection when injected intradermally. BMC Res Notes. 2014;7:70.
de Matos Guedes HL, Pinheiro RO, Chaves SP, De-Simone SG, Rossi-Bergmann B. Serine proteases of Leishmania amazonensis as immunomodulatory and disease-aggravating components of the crude LaAg vaccine. Vaccine. 2010;28:5491–6.
Lacerda ID, Cysne-Finkelstein L, Nunes PM, De-Luca PM, Genestra SM, Leon PLL, et al. Kinetoplastid membrane protein-11 exacerbates infection with Leishmania amazonensis in murine macrophages. Mem Inst Oswaldo Cruz. 2012;107:238–45.
Julia V, Rassoulzadegan M, Glaichenhaus N. Resistance to Leishmania major induced by tolerance to a single antigen. Science. 1996;274:421–3.
Srivastava S, Pandey SP, Jha MK, Chandel HS, Saha B. Leishmania expressed lipophosphoglycan interacts with Toll-like receptor (TLR)-2 to decrease TLR-9 expression and reduce anti-leishmanial responses. Clin Exp Immunol. 2013;172:403–9.
Gómez MA, Olivier M. Proteases and phosphatases during Leishmania-macrophage interaction: paving the road for pathogenesis. Virulence. 2010;1:314–8.
Silva-Lopez RE, Coelho MG, De-Simone SG. Characterization of an extracellular serine protease of Leishmania (Leishmania) amazonensis. Parasitol. 2005;131:85–96.
We acknowledge financial support from the Fundação de Apoio à Pesquisa do Estado da Bahia—FAPESB and the Conselho Nacional de Desenvolvimento Científico e Tecnológico—CNPq.
The authors declare that they have no competing interests.
LPC, VMGS and PRSO designed the experiments; VMGS, PRSO, CFA and ICN conducted the experiments; LPC, VMGS and PRSO analyzed the data; LPC and VMGS wrote the paper. All authors read and approved the final manuscript.