- Research article
- Open Access
- Open Peer Review
Differential effects of antigens from L. braziliensis isolates from disseminated and cutaneous leishmaniasis on in vitro cytokine production
- Paulo TG Leopoldo†1,
- Paulo RL Machado2,
- Roque P Almeida2,
- Albert Schriefer2, 3,
- Angela Giudice2,
- Amélia Ribeiro de Jesus2,
- John L Ho4,
- Luiz Henrique Guimarães2,
- Olívia Bacellar†2 and
- Edgar M Carvalho†2Email author
© Leopoldo et al; licensee BioMed Central Ltd. 2006
- Received: 31 October 2005
- Accepted: 25 April 2006
- Published: 25 April 2006
Disseminated leishmaniasis is an emerging infectious disease, mostly due to L. braziliensis, which has clinical and histopathological features distinct from cutaneous leishmaniasis.
In the current study we evaluated the in vitro production of the cytokines IFN-γ, TNF-α, IL-5 and IL-10 by peripheral blood mononuclear cells (PBMC) from 15 disseminated leishmaniasis and 24 cutaneous leishmaniasis patients upon stimulation with L. braziliensis antigens genotyped as disseminated leishmaniasis or cutaneous leishmaniasis isolates.
Regardless of the source of L. braziliensis antigens, PBMC from cutaneous leishmaniasis patients produced significantly higher IFN-γ than PBMC from disseminated leishmaniasis patients. Levels of TNF-α by PBMC from cutaneous leishmaniasis patients were significantly higher than disseminated leishmaniasis patients only when stimulated by genotyped cutaneous leishmaniasis antigens. The levels of IL-5 and IL-10 production by PBMC were very low and similar in PBMCs from both disseminated leishmaniasis and cutaneous leishmaniasis patients. The immune response of each patient evaluated by the two L. braziliensis antigens was assessed in a paired analysis in which we showed that L. braziliensis genotyped as disseminated leishmaniasis isolate was more potent than L. braziliensis genotyped as cutaneous leishmaniasis isolate in triggering IFN-γ and TNF-α production in both diseases and IL-5 only in cutaneous leishmaniasis patients.
This study provides evidence that antigens prepared from genotypically distinct strains of L. braziliensis induce different degrees of immune response. It also indicates that both parasite and host play a role in the outcome of L. braziliensis infection.
- Peripheral Blood Mononuclear Cell
- Cutaneous Leishmaniasis
- Peripheral Blood Mononuclear Cell Culture
- Mucosal Leishmaniasis
Leishmania are obligate intracellular protozoa transmitted to mammals by infected sand flies. Human infection ranges from asymptomatic to tegumentary and visceral disease, with disfiguring and fatal outcomes in the most severe cases . American tegumentary leishmaniasis (ATL) presents a spectrum of clinical manifestations including cutaneous (CL), mucosal (ML), disseminated (DL) and diffuse cutaneous leishmaniasis [2, 3]. DL caused by L. braziliensis is an emerging infectious disease mainly observed in Northeastern Brazil. DL is characterized by numerous acneiform, papular, nodular and ulcerated skin lesions, distributed in two or more body parts [4–7]. Most importantly, compared to only 3% among CL patients develop mucosal leishmaniasis, up to 28% of DL cases develop mucosal lesions, and the majority manifest mucosal disease concurrent with cutaneous lesions at disease presentation .
Previous studies with small numbers of DL patients have suggested that they often present a negative Leishmania skin test and that their lymphocytes produce lower levels of Th1 cytokines upon antigen stimulation than those of CL individuals . In addition to the roles of host genetics and immune responses, evidence has been accumulated on the intra-species variability among Leishmania sp, and its importance in the development of different clinical forms of leishmaniasis [8–12]. Analyses employing techniques like multilocus enzyme electrophoresis (MLEE) and rRNA gene internal transcribed spacers PCR-RFLP (ITR) showed a high degree of polymorphism between isolates of L. braziliensis from different regions. Moreover, our recent analyses of the populations of parasites in the ATL endemic area of Corte de Pedra (CP), northeastern Brazil, revealed polymorphism among L. braziliensis isolates and associations between genotypes and disease outcome .
In this work to discern whether parasite factors influence outcome of infection towards one of these two forms of ATL, we assessed the production of IFN-γ, TNF-α, IL-5 and IL-10 through the stimulation in vitro of peripheral blood mononuclear cells (PBMC) from DL and CL patients with L. braziliensis antigens isolated from DL and CL patients.
The patients enrolled in this study were recruited at the Corte de Pedra Health Post, situated in the southeast region of the State of Bahia, Brazil. The inclusion criteria were diagnosis of CL and DL with the presence of active skin lesions, and age from 10 to 60 years. The exclusion criteria were pregnancy, AIDS and other immunosuppressive conditions, as well as the patient's desire of being excluded from the study. Participants of this study included 15 DL patients presenting with 10 or more mixed-type lesions (acneiform, papular, nodular and/or ulcerated) in two or more body parts (head, trunk, arms and legs), and 24 CL patients presenting with ulcerated lesions localized in a single body part. The diagnosis was confirmed by culture identification of Leishmania in lesion biopsy or in aspirates, or by histopathology typical of leishmaniasis and a positive Leishmania skin test.
This study has been approved by the Ethical Committee of the Hospital Universitário Professor Edgard Santos and informed consent was obtained from all prospectively enrolled patients.
Two promastigotes of L braziliensis, one from a patient with CL and the other from a patient with DL, each genotyped by RAPD protocols were used as antigen sources for the in vitro cytokine induction assays. The molecular genotyping of parasites was made by four RAPD protocols as previously described . Cutaneous leishmaniasis L. braziliensis isolate belonged to CL enriched L. braziliensis clade B of CP, while the DL isolate belonged to the DL enriched clade D of CP. Therefore, they are designated as L. braziliensis genotyped as CL or DL isolates. In a small number of patients experiments were repeated with two other isolates from different patients with CL and DL. The results were similar to these obtained with the original isolates.
Isolation and cultivation of L braziliensis
The isolation of L. braziliensis was made in Navy McNeal Nicoli (NNN) blood agar overlaid with a modified Liver Infusion Tryptose (LIT) supplemented with 10% heat inactivated fetal bovine serum medium (FCS) (Sigma Chemical Co., St. Louis, MO) from samples obtained by needle aspiration of the skin lesions. The cultures from the biphasic medium were expanded for growth in Schneider's insect medium (Sigma), supplemented with 10% heat inactivated FCS at 25°C.
Antigens used for in vitro stimulation of PBMC came from isolates of L. braziliensis from CL and DL patients. Promastigotes in the stationary-phase of growth were washed three times by centrifugation, adjusted to a concentration of 109 in Phosphate Buffered Saline (PBS), and disrupted by eight repeated cycle of freezing (-70°C) and thawing (37°C), followed by ultrasonication. The supernatants were filtered at 0,45 υM Millipore and stored at -20°C until use. The protein content was determined by the Lowry method . After performing a dose curve response to determine the optimal dose, both antigens were used in the concentration (10 μg/ml).
Separation and culture of cells
PBMC were obtained from heparinized venous blood from patients with CL and DL by density centrifugation over a gradient of Ficoll-Hypaque (LSM; Organon Teknika corporation, Durham, NC, USA). PBMC adjusted to a concentration of 3 × 106 cells/ml were suspended in RPMI 1640 medium (GIBCO BRL., Grand Island, NY), 10% heat-inactivated human AB serum, 2 mM L-glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin (GIBCO). The cells were distributed in 24-well plates and stimulated with Leishmania antigens (10 μg/ml) and phytohemaglutinin (PHA) (100 μg/ml, Sigma), and then incubated for 72 hr at 37°C in 5% CO2 .
The supernatants were harvested and stored at -20°C for cytokine determination . Supernatants of cell cultures from CL and DL patients were assayed for IFN-γ, TNF-α, IL-5 and IL-l0 by sandwich ELISA technique (R & D system, Minneapolis, MN) using a mouse anti-human cytokine monoclonal antibody (mAb) as capture antibody. Purified cytokines at varying amounts were used to derive a standard curve (R & D system, Minneapolis, MN). The sensitivities of the cytokine dosage assays were 8 pg/ml (for IFN-γ), 4.4 pg/ml (for TNF-α), 3.9 pg/ml (for IL-5) and 3.9 pg/ml (for IL-10). IL-4 was not measured because of the low sensitivity of the technique in detecting IL-4 in supernatants of PBMC from humans.
Comparison of the levels of cytokine produced by PBMC from CL and DL patients was made by the Mann-Whitney test. The paired analyses were conducted by Wilcoxon paired non-parametric test; significance was determined as p < 0.05 (two tailed).
Disseminated leishmaniasis is an emerging disease predominantly detected in the state of Bahia, Brazil [4, 5, 7]. Although L. amazonensis and L. braziliensis have been reported to be associated with DL in the past, only L. braziliensis has recently been consistently implicated with this disease . Furthermore, we have recently demonstrated that certain L. braziliensis genotypes are more associated with DL in areas of endemicity for ATL . In the current study we evaluated the production of IFN-γ, TNF-α, IL-5 and IL-10 of PBMC from DL and CL patients, showing that DL patients produce less IFN-γ and TNF-α than those with CL upon antigen stimulation, while the two groups of individuals present similar IL-5 and IL-10 secretion. In addition, we found that antigen from parasites of DL origin is a stronger inducer of the above pro-inflammatory cytokines. These data concur with results from previous work in our lab, in which we demonstrated that PBMC from DL stimulated in vitro with antigens of L. amazonensis produced lower levels of pro-inflammatory cytokines than those of CL individuals . Reinforcing these findings, it has been shown that biopsies from CL patients display a higher intensity of IFN-γ expression than those of DL individuals . While lower levels of IFN-γ and TNF-α may contribute to the dissemination of the disease, they may also play a part in the different clinical aspects of the lesions observed in these two clinical forms of L. braziliensis. These pro-inflammatory cytokines may play key roles in the defense mechanism against Leishmania, but may also be involved in the formation of the immune mediated ulcers of CL [16, 17]. Therefore, in contrast to the CL patients who develop large ulcers with infiltration of lymphocytes in the lesions and absent or few parasites, DL individuals present multiple lesions, frequently over 100, in different parts of their body. These lesions are mostly non-ulcerated and small, and the parasites are more easily documented .
Studies performed in Ethiopia on the stimulation of PBMC from CL and diffuse cutaneous leishmaniasis, a disease clinical and pathologically distinct from DL, have shown that PBMC from CL produce more IFN-γ when stimulated with L. aethiopica antigen from CL than by antigen from diffuse cutaneous leishmaniasis. Interestingly, lymphocyte proliferation among control individuals of that endemic area was higher in response to CL antigen than diffuse cutaneous leishmaniasis antigen, supporting the idea that differences in the parasites may contribute to the clinical outcome of infection with L. aethiopica . Unlike L. aethiopica, L. braziliensis does not cause diffuse cutaneous leishmaniasis and is predominantly associated with CL and ML diseases, characterized by a strong type 1 immune response. While indicating phenotypic variability among the strains, the observation that DL-borne L. braziliensis induced significantly higher levels of IFN-γ and TNF-α in cultures of PBMC from CL patients was still surprising. We offer two possible explanations: (1) a bias in the innate immune response, which might be determining the outcome of DL; and (2) an over modulation of production of these cytokines by regulatory T lymphocytes in DL individuals with carryover effects to the in vitro evaluations. Both possibilities are currently being evaluated.
IFN-γ and TNF-α are important cytokines for the outcome of infection in the experimental models of leishmaniasis. Type 1 immune responses are associated with control of infection, while type 2 leads to susceptibility for Leishmania sp . In humans, low IFN-γ production has been associated with parasite dissemination, as exemplified by VL and diffuse cutaneous leishmaniasis [20–23], in which IL-10 acts to down regulate IFN-γ . In contrast to what has been observed in VL and diffuse cutaneous leishmaniasis, we found neither a type 2 immune response nor an increase in IL-10 levels in DL patients [23, 25]. However, it was clear the type 1 immune response is impaired in DL patients.
This study showed that regardless of the source of antigens, CL patients produce more IFN-γ than DL patients. Antigens from L. braziliensis genotyped as a DL isolate was more potent than a CL isolate in promoting IFN-γ and TNF-α production. This finding lends support for distinct intraspecies differences and argues for the role of intraspecies differences and host factors contributing to the clinical outcome following L. braziliensis infection.
We are grateful to Dr. Seth O'Neal for critical review of the manuscript, Elbe Myrtes Silva and Lúcia Reis for secretarial assistance. This work was supported by Fundação de Amparo à Pesquisa do Estado da Bahia (FAPESB) and Brazilian National Research Council (CNPq). Dr Edgar M. Carvalho is senior investigator of CNPq.
- Pearson RD, Sousa AQ: Clinical spectrum of Leishmaniasis. Clin Infect Dis. 1996, 22: 1-13.View ArticlePubMedGoogle Scholar
- Castes M, Tapia FJ: [Immunopathology of American tegumentary leishmaniasis]. Acta Cient Venez. 1998, 49: 42-56.PubMedGoogle Scholar
- Caceres-Dittmar G, Tapia FJ, Sanchez MA, Yamamura M, K Utyemura, Modlin RL, Bloom BR, Convit J: Determination of the cytokine profile in American cutaneous leishmaniasis using the polymerase chain reaction. Clin Exp Immunol. 1993, 91: 500-5.View ArticlePubMedPubMed CentralGoogle Scholar
- Costa JM, Marsden PD, Llanos-Cuentas EA, Netto EM, Carvalho EM, Barral A, Rosa AC, Cuba CC, Magalhaes AV, Barreto AC: Disseminated cutaneous leishmaniasis in a field clinic in Bahia, Brazil: a report of eight cases. J Trop Med Hyg. 1986, 89: 319-23.PubMedGoogle Scholar
- Carvalho EM, Barral A, Costa JM, Bittencourt A, Marsden P: Clinical and immunopathological aspects of disseminated cutaneous leishmaniasis. Acta Trop. 1994, 56: 315-25. 10.1016/0001-706X(94)90103-1.View ArticlePubMedGoogle Scholar
- Galvao CE, Silva AC, Saldanha AC, Silva CM, Costa Mdo R, Costa JM: [Disseminated cutaneous leishmaniasis due to Leishmania viannia braziliensis in the state of Maranhao, Brazil]. Rev Soc Bras Med Trop. 1993, 26: 121-3.View ArticlePubMedGoogle Scholar
- Turetz ML, Machado PR, Ko AI, Alves F, Bittencourt A, Almeida RP, Mobashery N, Johnson WD, Carvalho EM: Disseminated leishmaniasis: a new and emerging form of leishmaniasis observed in northeastern Brazil. J Infect Dis. 2002, 186: 1829-34. 10.1086/345772.View ArticlePubMedGoogle Scholar
- Schriefer A, Schriefer AL, Goes-Neto A, Guimaraes LH, Carvalho LP, Almeida RP, Machado PR, Lessa HA, de Jesus AR, Riley LW, Carvalho EM: Multiclonal Leishmania braziliensis population structure and its clinical implication in a region of endemicity for American tegumentary leishmaniasis. Infect Immun. 2004, 72: 508-14. 10.1128/IAI.72.1.508-514.2004.View ArticlePubMedPubMed CentralGoogle Scholar
- Saravia NG, Weigle K, Navas C, Segura I, Valderrama L, Valencia AZ, Escorcia B, McMahon-Pratt D: Heterogeneity, geographic distribution, and pathogenicity of serodemes of Leishmania viannia in Colombia. Am J Trop Med Hyg. 2002, 66: 738-44.PubMedGoogle Scholar
- Grimaldi G, David JR, McMahon-Pratt D: Identification and distribution of New World Leishmania species characterized by serodeme analysis using monoclonal antibodies. Am J Trop Med Hyg. 1987, 36: 270-87.PubMedGoogle Scholar
- Cupolillo E, Brahim LR, Toaldo CB, de Oliveira-Neto MP, de Brito ME, Falqueto A, de Farias Naiff M, Grimaldi G: Genetic polymorphism and molecular epidemiology of Leishmania (Viannia) braziliensis from different hosts and geographic areas in Brazil. J Clin Microbiol. 2003, 41: 3126-32. 10.1128/JCM.41.7.3126-3132.2003.View ArticlePubMedPubMed CentralGoogle Scholar
- Cupolillo E, Grimaldi G, Momen H: Genetic diversity among Leishmania (Viannia) parasites. Ann Trop Med Parasitol. 1997, 91: 617-26. 10.1080/00034989760716.View ArticlePubMedGoogle Scholar
- Lowry DH, G RN, Farr AL, J RR: Protein measurement with the folin phenol reagent. Journal of Biological Chemistry. 1951, 193: 265-275.PubMedGoogle Scholar
- Carvalho EM, Johnson WD, Barreto E, Marsden PD, Costa JL, Reed S, Rocha H: Cell mediated immunity in American cutaneous and mucosal leishmaniasis. J Immunol. 1985, 135: 4144-8.PubMedGoogle Scholar
- Vieira MG, Oliveira F, Arruda S, Bittencourt AL, Barbosa AA, Barral-Netto M, Barral A: B-cell infiltration and frequency of cytokine producing cells differ between localized and disseminated human cutaneous leishmaniases. Mem Inst Oswaldo Cruz. 2002, 97: 979-83. 10.1590/S0074-02762002000700009.View ArticlePubMedGoogle Scholar
- Follador I, Araujo C, Bacellar O, Araujo CB, Carvalho LP, Almeida RP, Carvalho EM: Epidemiologic and immunologic findings for the subclinical form of Leishmania braziliensis infection. Clin Infect Dis. 2002, 34: E54-8. 10.1086/340261.View ArticlePubMedGoogle Scholar
- Machado P, Araujo C, Da Silva AT, Almeida RP, D'Oliveira A, Bittencourt A, Carvalho EM: Failure of early treatment of cutaneous leishmaniasis in preventing the development of an ulcer. Clin Infect Dis. 2002, 34: E69-73. 10.1086/340526.View ArticlePubMedGoogle Scholar
- Akuffo H, Schurr E, Andersson G, Yamaneberhan T, Britton S: Responsiveness in diffuse versus local cutaneous leishmaniasis is due to parasite differences. Scand J Immunol. 1987, 26: 717-21.View ArticlePubMedGoogle Scholar
- Heinzel FP, Sadick MD, Mutha SS, Locksley RM: Production of interferon gamma, interleukin 2, interleukin 4, and interleukin 10 by CD4+ lymphocytes in vivo during healing and progressive murine leishmaniasis. Proc Natl Acad Sci U S A. 1991, 88: 7011-5. 10.1073/pnas.88.16.7011.View ArticlePubMedPubMed CentralGoogle Scholar
- Carvalho EM, Barral A, Pedral-Sampaio D, Barral-Netto M, Badaro R, Rocha H, Johnson WD: Immunologic markers of clinical evolution in children recently infected with Leishmania donovani chagasi. J Infect Dis. 1992, 165: 535-40.View ArticlePubMedGoogle Scholar
- Bacellar O, Brodskyn C, Guerreiro J, Barral-Netto M, Costa CH, Coffman RL, Johnson WD, Carvalho EM: Interleukin-12 restores interferon-gamma production and cytotoxic responses in visceral leishmaniasis. J Infect Dis. 1996, 173: 1515-8.View ArticlePubMedGoogle Scholar
- Carvalho EM, Bacellar OA, Reed S, Barral A, Rocha H: Visceral leishmaniasis: a disease associated with inability of lymphocytes to activate macrophages to kill leishmania. Braz J Med Biol Res. 1988, 21: 85-92.PubMedGoogle Scholar
- Bomfim G, Nascimento C, Costa J, Carvalho EM, Barral-Netto M, Barral A: Variation of cytokine patterns related to therapeutic response in diffuse cutaneous leishmaniasis. Exp Parasitol. 1996, 84: 188-94. 10.1006/expr.1996.0104.View ArticlePubMedGoogle Scholar
- Bacellar O, D'Oliveira A, Jeronimo S, Carvalho EM: IL-10 and IL-12 are the main regulatory cytokines in visceral leishmaniasis. Cytokine. 2000, 12: 1228-31. 10.1006/cyto.2000.0694.View ArticlePubMedGoogle Scholar
- Carvalho EM, Badaro R, Reed SG, Jones TC, Johnson WD, Jeronimo S, Carvalho EM: Absence of gamma interferon and interleukin 2 production during active visceral leishmaniasis. Cytokine. 1985, 12: 1228-31.Google Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/6/75/prepub
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