Insulin-like growth factor-I serum levels and their biological effects on Leishmania isolates from different clinical forms of American tegumentary leishmaniasis
© The Author(s). 2016
Received: 3 December 2015
Accepted: 1 June 2016
Published: 11 June 2016
American tegumentary leishmaniasis (ATL) in Brazil is mostly caused by Leishmania (Viannia) braziliensis, with known forms of the disease being cutaneous (CL), mucosal (ML) and disseminated (DL) leishmaniasis. The development of the lesion in ATL is related both to the persistence of the Leishmania in the skin and to the parasite-triggered immune and inflammatory responses that ensue lesions. In this context one factor with expected role in the pathogenesis is insulin-like growth factor (IGF)-I with known effects on parasite growth and healing and inflammatory processes. In the present study, we addressed the effect of IGF-I on intracellular amastigote isolates from CL, ML and DL patients within human macrophage and we evaluated the IGF-I and IGF-binding protein-3 (IGFBP3) serum levels in patients presenting different clinical forms and controls from the endemic area.
We evaluated biological variability in the responses of intracellular amastigotes of Leishmania isolates derived from CL, ML, and DL patients from an area for ATL in response to IGF-I. Intracellular amastigote growth was evaluated using the human macrophage cell line THP-1. Arginase activity in infected cells was evaluated quantifying the generated urea concentration. Serum samples from patients and controls were assayed using chemiluminescent immunometric assay to determine IGF-I and IGFBP3 levels.
We observed an increase in intracellular parasitism upon IGF-I stimulus in 62.5 % of isolates from CL, in 85.7 % from ML and only 42.8 % from DL cases. In DL, the basal arginase activity was lower than that of CL. We then evaluated the IGF-I and IGFBP3 serum levels in patients, and we observed significantly lower levels in ML and DL than in CL and control samples.
The data suggest that IGF-I is modulated distinctly in different clinical forms of tegumentary leishmaniasis. IGF-I seemingly exerts effect on parasite growth likely contributing to its persistence in the skin in earlier phase. In addition the decreased IGF-I serum levels may affect the modulation of inflammation and lesion healing in chronic phase. In view of potential role of IGF-I in the pathogenesis of ATL we can speculate on therapeutic procedures taking into account the local IGF-I level.
Human leishmaniasis caused by Leishmania (Viannia) braziliensis infection has a broad spectrum of manifestations ranging from an asymptomatic infection to severe destructive ulcerated and inflammatory forms. The main clinical forms are cutaneous leishmaniasis (CL), severe destructive mucosal leishmaniasis (ML) and disseminated leishmaniasis (DL) . Some studies relate the different disease manifestations to the intraspecific variability of L. (V.) braziliensis not only in Brazil but also in Colombia [2–4] but not in another study . Besides, the presence of Leishmania RNA virus 1 in L. (V.) braziliensis has been associated with the development of ML but not in all ML cases . Therefore, the wide spectrum of manifestations caused by L. (V.) braziliensis are still poorly understood.
It is known that the development of the lesion in tegumentary leishmaniasis is related both to the persistence of the Leishmania in the skin and to the parasite-triggered immune and inflammatory responses that result in lesion development [7, 8]. The Th1-type immune response controls the parasite growth  but in chronic and severe lesions such as in mucosal leishmaniasis maintenance of the supposedly beneficial immune response turn into chronic and harmful process [9, 10].
In this context one of elements that may have role in the pathogenesis is insulin-like growth factor (IGF)-I since this factor has effect on both parasite growth  contributing to its persistence and on the healing and inflammatory processes [12–14].
We have been studying the effect of IGF-I on Leishmania and in leishmaniasis, demonstrating its impact on parasite growth and lesion development. IGF-I in cases of L. (L.) amazonensis showed effects increasing the parasite growth and cutaneous leishmaniasis lesion development . In Leishmania-macrophage interaction, IGF-I exerts effect on Leishmania and host cells, mainly inducing arginase expression and activity, leading to alternative activation of the macrophages interfering with inducible nitric oxide synthase expression [11, 15, 16]. Because biological effects may differ in other species and American tegumentary leishmaniasis is mostly caused by L. (V.) braziliensis, we analyzed the effect of this growth factor on this parasite species. Then, we observed complex results related to the source of the parasite isolates. IGF-I induced higher basal arginase activity in promastigote isolates derived from patients with CL and DL; however, arginase activity was already increased under basal conditions in isolates from ML with no further increase upon IGF-I stimulus . In the present study, we addressed the effect of IGF-I on amastigote forms of isolates from CL, ML and DL patients within the THP-1 human macrophage lineage. We used the macrophage lineage rather than macrophages derived from peripheral blood monocytes to avoid variations in cellular response in different individuals. We observed an increase in intracellular parasitism upon IGF-I stimulus in 62.5 % of isolates from CL, in 85.7 % from ML and only 42.8 % from DL cases. Although we observed differences among Leishmania isolates, they do not clearly explain their different clinical manifestations.
Since in addition to the effect on parasite growth, IGF-I has a pleiotropic effect on cell migration , wound healing [12, 13] and inflammatory process , in the present study, we evaluated the IGF-I and IGF-binding proteins-3 (IGFBP3) serum levels in patients presenting different clinical forms, CL, ML and DL and controls from the endemic area. In this analysis, both IGF-I and IGFBP3 levels decreased in ML and DL compared with CL and controls. The data as a whole suggest that IGF-I is modulated in different clinical forms of tegumentary leishmaniasis, and IGF-I seemingly exerts effects on both parasite growth likely contributing to its persistence in the skin and its lower level affecting the modulation of inflammation and lesion healing process. In view of potential role of IGF-I in pathogenesis of tegumentary lesion development we can speculate on therapeutic procedures considering local IGF-I level.
Study design and subjects
The patients included in this study were from Corte de Pedra municipality, Bahia state, Northeastern Brazil, an area with endemic tegumentary leishmaniasis mostly caused by L. (V.) brasiliensis. The patients were approached at the Corte de Pedra Health Post from 2002 through 2007. All participants were volunteers and provided their individual informed consent.
A leishmaniasis diagnosis was made based on a clinical feature of these forms of leishmaniasis along with one of the following criteria: parasite isolation or a positive skin test for Leishmania soluble antigen and the presence of histopathological findings suggestive of leishmaniasis. Patients with CL had a typical ulcerative lesion in the skin; ML patients had a metastatic mucosal nasal lesion that was not contiguous with the primary cutaneous lesion, and DL patients had polymorphic lesions (acneiform, papular, nodular and/or ulcerated) on two or more parts of their body. The exclusion criteria included HIV infection, diabetes mellitus and pregnancy. All patients were evaluated before receiving therapy and during the active disease. The ages ranged from 21 through 65 years. One-hundred fourteen patients were studied, suffering from CL (n = 65), ML (n = 20), DL (n = 29) and 14 endemic control subjects living in the same municipality. The sera were stored at -70 °C until they were analyzed.
Isolates of L. (V.) braziliensis
The 22 isolates of Leishmania were obtained from patients presenting with the following different clinical forms of the disease: cutaneous leishmaniasis (n = 8), mucosal leishmaniasis (n = 7) and disseminated leishmaniasis (n = 7). The isolates were obtained by aspirating the lesion, and the samples were grown in tubes with biphasic medium (LIT/NNN) supplemented with 10 % heat inactivated fetal calf serum (FCS) (Cripion Biotechnology, Brazil) at 26 °C. The parasite isolates were cryopreserved and expanded in Schneider’s insect medium (Sigma), pH 7.2, supplemented with 10 % FCS. Most of the isolates were characterized as L. (V.) braziliensis by isoenzyme electrophoresis and monoclonal antibodies in the Departamento de Bioquimica e Biologia Molecular, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil . The promastigotes used in the experiments were in the stationary phase of growth and had no more than four passages in culture.
THP-1 monocytic cell line and cell culture
The monocytic cell line THP-1 (ATCC) was grown and replicated every 4 days in RPMI 1640 supplemented with 5 % FCS, 100 UI/ml streptomycin, 2 mM L-glutamine, 11 mM sodium bicarbonate and maintained in a humidified atmosphere at 37 °C with 5 % CO2. The viability was assessed by a dye exclusion test using 0.02 % trypan blue in phosphate-buffered saline 0.01 M, pH 7.2 (PBS); to test for infection, 2 × 105 cells in 500 μl in RPMI 1640 with 2 % FCS were distributed in each well of 24-well culture plates in triplicate with sterile, round 13 mm coverslips.
THP-1 monocytes were submitted to 20 ng/ml phorbol 12-myristate 13 acetate (PMA) for 24 h at 37 ° C, 5 % CO2 for differentiation into macrophages . The non-adherent cells were removed, the medium was replaced, and the cells were maintained for 24 h in the same conditions. Infection with Leishmania/macrophage (ratio of 10:1), using isolates from CL, ML and DL of L. (V.) braziliensis, was performed with or without stimulation with IGF-I (50 ng/ml) and incubated at 33 °C, 5 % CO2. After 4 h, the plates were washed with warm PBS to remove non-internalized parasites, and the RPMI 1640 medium with 2.0 % FCS and IGF-I was replaced. After different incubation times, the supernatant was collected and stored at -70 °C for evaluation of arginase activity, and the coverslips were taken for intracellular parasite counting.
Evaluation of intracellular parasite load
The coverslips removed from the plates were stained with Giemsa dyes, and intracellular parasites were counted under a light microscope (Carl Zeiss, Germany). For each experimental condition, 600 cells and intracellular parasites were counted by two independent observers, blinded for experimental conditions. The data are presented as the number of parasites per 100 cells.
The cells and promastigotes were removed from the cultures, lysed and submitted to arginase activity determination . Briefly, to activate the arginase, 50 μl of lysate was treated with the same volume of 5 mM MnCl2, 25 mM Tris-HCl pH 7.4 at 56 °C for 10 min. Then, 25 μl of 0.5 M L-arginine pH 9.7 was added to 25 μl of the activated lysate and incubated at 37 °C for 60 min. The reaction was stopped with 400 μl of H2SO4/H3PO4/H2O (1/3/7, v/v/v). The urea concentration was measured at 540 nm in a spectrophotometer Multiskan MCC/340 P version 2.20 plate reader (Labsystems, Vantaa, Finland) after the addition of 25 μl of 9 % α-isonitrosopropiophenone in 100 % methanol and submitted to 100 °C for 45 min. One unit of enzyme activity was defined as the amount of enzyme that catalyzes the formation of 1 μmol of urea per minute.
Analyzes of circulation IGF-I and IGFBP3 levels
IGF-I and IGFBP3 assays were performed using the IMMULITE® 2000 (DPC-Diagnostics Products Corporation, Los Angeles, CA, USA). This procedure is an automated 2-site sandwich immunoassay with a chemiluminescent immunometric assay. It was configured and calibrated on an instrument at Laboratório de Hormônio do Hospital das Clínicas da Universidade de São Paulo, according to the manufacturer’s instructions.
Statistical analysis was performed using GraphPad Prism5 (GraphPad Software, Inc., San Diego, CA, USA). The isolates results were submitted to ANOVA with post-hoc Student-Newman Keuls test. An alpha error of 5 % (P = 0.05) was considered to determine statistical significance. The IGF-I and IGFBP3 assay results were expressed as medians and percentiles (25–75) and submitted to the Kruskal-Wallis test with the Student Newman-Keuls post-hoc test to statistically compare the groups.
In this study, we initially evaluated the parasitism and the arginase activity of the isolates of L. (V.) braziliensis derived from patients presenting CL (n = 8), ML (n = 7) or DL (n = 7).
We evaluated the parasites as amastigotes within human monocytic cell line THP-1 in the presence or the absence of the growth factor IGF-I. This cell line can be activated by IGF-I . Having perceived differences in the biological parameters in this approach, we then evaluated the IGF-I and IGFBP3 serum levels in patients and in controls living in the same endemic area.
Effect of IGF-I on parasitism in THP-1 with isolates of Leishmania
IGF-I (50 ng/ml)
The above results suggest that IGF-I is beneficial or deleterious depending on the isolates; therefore, we analyzed whether IGF-I serum levels were altered in leishmaniasis patients presenting with different clinical forms of the disease.
Clinical profile of study patients with Leishmaniasis
34 ± 10
43 ± 10
38 ± 12
30 ± 8
Gender distribution of American Tegumentary Leishmaniasis (ATL) patients
95 % CI
The pathogenesis of American tegumentary leishmaniasis currently is considered multifactorial, due to not only specific immune response  but also parasite diversity [4, 17] and other factors related to the host [25, 26]. In this scenario, we have been studying the role of IGF-I in leishmaniasis mainly in vitro and in experimental models of leishmaniasis. The role of IGF-I in human leishmaniasis has not been established.
Based on our previous experimental data, IGF-I can play a role in the progression of Leishmania (Leishmania) amazonensis infection by (i) decreasing NO production in macrophages and allowing parasite multiplication, (ii) modulating immune responses by increasing TGF-β and decreasing IFNγ production in promastigote infected macrophages, and (iii) inducing apoptotic mimicry characterized by exposure of phosphatidyl serine on amastigotes but without leading to death [15, 16]. However, it is unknown whether similar effects of IGF-I would occur in other Leishmania species.
Because tegumentary leishmaniasis in Brazil is mostly caused by L. (V.) braziliensis  and different biological effects may occur upon IGF-I stimulus, we initially studied its effect on promastigotes. Focusing on the increase of arginase activity of the parasite, which was seen as main effect of IGF-I , we confronted more complex outcomes that were dependent on Leishmania isolates, whether coming from patients with CL, ML or DL. IGF-I induced higher basal arginase activity in L. (V.) braziliensis promastigote isolates from CL and DL but not in ML. Conversely, in Leishmania isolate from ML the arginase activity was already increased in basal conditions . In the present study, we analyzed the effect of IGF-I on intracellular amastigotes in sequence.
The intracellular amastigote growth was evaluated here using human macrophage cell line THP-1 rather than macrophages derived from peripheral blood monocytes to avoid the variation in cellular response that would occur if obtained from different individuals. IGF-I induced an increase in parasitism in CL and ML isolates but a decrease in parasitism in DL isolates. In CL and ML these data suggest that the presence of IGF-I may contribute to the persistence of the parasite in the skin. In DL isolates, basal arginase activity was also lower than that of CL. However, arginase activity was similar with and without IGF-I stimulus, leaving mechanisms that need to be further explored.
To proceed with the study of the involvement of IGF-I in different clinical manifestations, IGF-I and IGFBP3 serum levels were evaluated in patients with CL, ML and DL. In CL, both of these levels were similar to those in healthy controls, while in ML and DL, both levels were decreased. Altogether, these data indicate that IGF-I cannot be interpreted as having similar effects in patients presenting different clinical manifestations and that the effects may encompass healing and inflammatory processes beyond parasite growth.
American tegumentary leishmaniasis is characterized by an intense inflammation with a high production of tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-γ), molecules that are necessary to protect the host against Leishmania but can also cause tissue damage even with a scarce number of parasites in the lesions [25, 27]. In the early phase of the disease when patients have a small cutaneous lesion or when is evolving to heal , this T helper type 1 immune response is known to be down modulated . IGF-I is known to be increased in the initial phase of skin injury because this molecule is necessary for epidermis maintenance [30, 31], which would occur also in CL. In CL, because IGF-I is suggested by the present findings to have a parasite growth promoting effect on Leishmania isolates and has its serum level maintained in the level of controls, IGF-I would probably contribute to the progression of parasite growth and establishment of Leishmania in the host skin.
Cutaneous ulcer is the first lesion of tegumentary leishmaniasis that later can be complicated by the appearance of mucosal or disseminated disease. After the initial phase of L. (V.) braziliensis infection, a very strong Th1 immune response occurs that is associated with a decrease in IL-10 production . IFN-γ and TNF-α are also produced in even higher concentrations in ML patients , and this increased production of cytokines may relate to the lower level of IGF-I in patients with ML observed in the present study.
In DL patients, a slight decrease in IFN-γ production was observed when analyzing peripheral blood mononuclear cells, which may result from the migration of activated T cells to the multiple lesions and to the mucosal tissue because up to 40 % of DL patients have mucosal disease . In DL, IFN-γ production is still high that may relate to the decreased IGF-I serum levels found here in this form of the disease.
IGF-I was shown to decrease vascular inflammatory process in mouse model of atherosclerosis . Because the pathogenesis of American tegumentary leishmaniasis is based on an exaggerated immune response [35, 36], a decrease in IGF-I in ML and DL may contribute to the persistence of the inflammatory response and further on the delayed healing of the lesion.
Having pathogenic mechanism involving IGF-I in mind we can speculate the use of IGF-I to stimulate healing and control of inflammation in chronic and severe cases of ATL where IGF-I level is decreased. There are studies on IGF-I use in other dermatological lesions. In diabetes mellitus ulcer it is suggested that the healing is delayed due to a decrease in IGF-I level in the skin  and some approaches have been tried. In diabetes mellitus patients the skin ulcer healed with an increase in local IGF-I level upon the use of hyperbaric oxygen therapy . In experimental diabetes model local use of IGF-I cream has also improved the healing . In ATL IGF-I may increase the parasite growth but it would be in the tissue environment where strong Th1-type immune response is present and thus the parasite growth would be restrained.
In the present study, analyzing the effect of IGF-I on amastigotes of Leishmania isolates from patients and evaluating the IGF-I serum levels, we observed results that suggest IGF-I affecting both parasites and healing and inflammatory processes with IGF-I being modulated differently in distinct clinical forms of ATL. We suggest that in the initial phase of the disease, there are maintained levels of IGF-I that contribute to downregulation of the immune response and for parasite growth/persistence. In the late phase of the infection, with the decrease in IGF-I levels it would allow mainly the persistence of a tissue damage.
In view of potential role of IGF-I in the pathogenesis of ATL we can speculate on therapeutic procedures taking into account the local IGF-I level.
ATCC, American type culture collection; ATL, American tegumentary leishmaniasis; CI, confidence interval; CL, cutaneous leishmaniasis; DL, disseminated leishmaniasis; FCS, fetal calf serum; HIV, human immunodeficiency virus; IFN-γ, interferon gamma; IGF, insulin-like growth factor; IGFBP3, IGF-binding proteins-3; IL-10, interleukin 10; ML, mucosal leishmaniasis; OR, odds ratios; PBS, phosphate-buffered saline; PMA, phorbol 12-myristate 13 acetate; RPMI, Roswell park memorial institute medium; TGF-β, transforming growth factor beta; TNF-α, tumor necrosis factor alpha
This study was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (research fellowship 2008/2209-6 to LDS), Fundação de Amparo à Pesquisa do Estado da Bahia (research fellowship 1780–2007 to CMVV), Conselho Nacional de Pesquisa (fellowship to EMC, ARJ and HG, and grant 484499/2006) and the Soroepidemiology and Immunobiology Laboratory LIM/38 (HC-FMUSP).
Availability of data and material
All data are disclosed as tables and figures in the main document.
LDS, CMVV, ARJ, EMC and HG conceived and designed distinct parts of studies. AM cultivated the isolates and organized the samples; EMC, AS and LHG participated in the field work approaching individuals in endemic area of ATL, selecting and obtaining samples, organizing the data. LDS, CMVV and MDTC performed the experiments; LDS, CMVV, MDTC and HG analyzed and interpreted the data; HG conceived whole study, coordinated the project; LDS, CMVV, EMC and HG drafted and revised the article. All authors read and approved the final manuscript.
LDS and CMVV had equal participation in this study.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All patients were volunteers and provided their individual informed consent, and the study was approved by the Conselho Nacional de Ética e Pesquisa (Ethical Certificate 1583/2002). The use of parasite isolates from patients were approved by the Ethics Committee of Faculdade de Medicina da Universidade de São Paulo (protocol 0792/09).
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