- Open Access
Pentoxifylline immunomodulation in the treatment of experimental chronic pulmonary paracoccidioidomycosis
Fibrogenesis & Tissue Repair volume 8, Article number: 10 (2015)
Pentoxifylline (PTX) is a methylxanthine compound with immunomodulatory and antifibrotic properties. The simultaneous use of PTX and antifungal therapy (itraconazole) has previously been evaluated in an experimental model of pulmonary paracoccidioidomycosis (PCM), a systemic fungal disease caused by the fungus Paracoccidioides brasiliensis (Pb) and characterized by chronic inflammation and lung fibrosis that appears even after a successful course of antifungal therapy. The results revealed prompt and statistically significant reductions in inflammation and fibrosis when compared to itraconazole alone. However, the effect of monotherapy with PTX on the host response to PCM has not been well-documented. Our aim was to determine the effect of PTX on the course of pulmonary lesions and on the local immune response.
At the middle and end of treatment, the Pb-infected-PTX-treated mice exhibited significant reductions in lung density compared to the Pb-infected-non-treated mice as assessed by the quantification of Hounsfield units on high-resolution computed tomography (HRCT) (p <0.05 by Kruskal-Wallis test); additionally, at the end of therapy, the lung areas involved in the inflammatory reactions were only 3 vs. 22 %, respectively, by histomorphometry (p <0.05 by Mann–Whitney test), and this reduction was associated with a lower fungal burden and limited collagen increment in the pulmonary lesions. PTX treatment restored the levels of IFN-γ, MIP-1β, and IL-3 that had been down-regulated by Pb infection. Additionally, IL-12p70, IL-10, IL-13, and eotaxin were significantly increased, whereas Regulated upon Activation, Normal T cell Expressed and Secreted (RANTES) levels were decreased in the lungs of the Pb-infected-PTX-treated mice compared to the non-treated group.
This study showed that PTX therapy administered at an “early” stage of granulomatous inflammation controlled the progress of the PCM by diminishing the pulmonary inflammation and the fungal burden and avoiding the appearance of collagen deposits in the pulmonary lesions.
Pentoxifylline (PTX) is one of the several methylxanthine compounds that have immunomodulatory properties. PTX acts as cAMP-phosphodiesterases inhibitor and exerts its cellular effects on erythrocytes, platelets, endothelial cells, PMNs, macrophages, and fibroblasts . PTX reduces the production of inflammatory cytokines, such as TNF, IL-1α, IL-6, and IL-8, by phagocytes  and prevents their subsequent effects, such as leukocyte adherence, migration, and degranulation . Additionally, PTX has antifibrotic properties; it exerts an antiproliferative effect on fibroblasts and inhibits extracellular matrix synthesis [4, 5].
Because inflammation participates in the pathogenesis and progression of many diseases, the therapeutic use of PTX has been studied alone or as an adjuvant therapy in different conditions, including infectious processes, and has produced positive effects. PTX prevents murine cerebral malaria  and improves the prognosis of this disease in humans [7, 8], decreases leukocyte recruitment into the cerebrospinal fluid in experimental bacterial meningitis , decreases organ damage, and improves survival in humans [10, 11] and in animals with sepsis . Additionally, PTX has been used simultaneously with amphotericin-B to improve survival and to decrease fungal burden in cerebral cryptococcosis .
In a previous study, we evaluated a combined PTX and itraconazole therapy in a chronic experimental model of paracoccidioidomycosis (PCM) , which is a systemic mycosis produced by the thermally dimorphic fungus Paracoccidioides brasiliensis (Pb) that induces granulomatous inflammation and frequently progresses to pulmonary fibrosis [14, 15]. In that study, we reported prompt reductions of pulmonary granulomatous inflammation and fibrosis when compared to itraconazole treatment alone . However, the effect of monotherapy with PTX on the host response to PCM has not been well-documented.
To better understand the effect of the immunomodulatory therapy with PTX on the course of fungal pulmonary lesions, we used an experimental mouse model of PCM to determine the local immune response and compared the lungs of treated versus non-treated Pb-infected mice with high-resolution computed tomography (HRCT), histopathology/histomorphometry, and assessments of the levels of cytokines, chemokines, and growth factors.
PTX decreased the pulmonary density in the Pb-infected mice
Before treatment (week 4), the Pb-infected mice exhibited peribronchial consolidations that were associated with a significant increase in the upper lung densities (−263 ± 29 vs. −426 ± 68 Hounsfield units (HU) in the control mice, p < 0.001). These increases in density were significantly different compared to the control at all periods of evaluation (Fig. 1a, e, i). The pulmonary lesions tended to extend to the central region of the lung, but the increase in lung density was only higher at week 8 (Fig. 1f,j). After 4 weeks of PTX treatment (8 weeks post-infection (p.i)), the peribronchial consolidations decreased and were present in 4/10 infected treated mice (agreement between the radiologists (κ) = 0.8) in contrast to 10/10 mice in the Pb-infected group (κ = 1.0). Although multiple nodules were reported for both groups, the agreement among the radiologists at this time was low (κ = 0.4). At the end of therapy (12 weeks p.i), marked differences between the groups were noticeable (Fig. 1e,g). The infected mice continued to show the same pattern of lesions, but they tended to be more severe. Indeed, at this time, one of the infected animals also presented with atelectasis and another presented with pleural thickness. In contrast, 8/10 of the mice that were treated for 8 weeks with PTX exhibited only small opacities that were referred to as unique nodules (Fig. 1g) accompanied by significant overall reductions in pulmonary density compared with the Pb-infected non-treated mice (−451 ± 68 vs. −269 ± 25 HU; p < 0.001). However, 4 weeks post-treatment, the pulmonary densities were reactivated in all animals (κ = 1; Fig. 1i) and diffused bronchial dilatation was even observed.
The administration of PTX to the healthy non-infected mice did not induce changes in the normal appearance of the lungs or modify the pulmonary densities as expressed in HU at any observation time (Fig. 1c,d,i,j).
PTX decreased the pulmonary inflammation area in the Pb-infected mice
Before the beginning of the PTX treatment at 4 weeks p.i, the Pb-infected mice presented pulmonary nodules and evidence of incipient periarterial inflammation accompanied by dispersed and intense parenchymal inflammation. In the absence of PTX treatment, these histopathological changes remained present and increased to reach their greatest intensities at 8 and 12 weeks p.i. Four weeks after the treatment onset (8 weeks p.i), the lung area occupied by inflammatory reactions was reduced compared to the Pb-infected group, but this difference was only statistically significant at the end of the treatment (12 weeks) when the average lung inflammation diminished to 3 ± 2 % vs. 22 ± 7 % in the non-treated group (p <0.05) (Fig. 2a–c). In the middle of the therapy, PTX decreased the dispersed parenchymal inflammation and the cellularity at the outer regions of the nodules, which prevented their confluence. At the end of the treatment, only two nodules were observed in five lungs (Fig. 2d–f), and only small focal areas of periarterial inflammation composed of lymphoplasmocytic infiltrate remained in the lungs (Fig. 2e).
PTX decreased the fungal burden in the lungs of the Pb-infected mice
In the Pb-infected mice, the morphologies and quantities of the fungi in the lung tissues varied depending on the locations of the lesions and the time of the infection. There were trends toward increases at 8 and 12 weeks p.i. In the nodules, the fungal cells were restricted to the central zone, and large yeasts predominated (10–20 μm; Fig. 2g). In the perivascular lesions, the fungi were more dispersed and frequently presented with perifungal spaces surrounding large mother cells with multiple small buds of less than 2 μm.
The PTX-treated mice exhibited lesser amounts of Pb yeast in the pulmonary lesions as evidenced by pixel counting of the stained yeast, but some small buds, mainly in the periarterial regions, persisted (Fig. 2h,i).
PTX prevented collagen increments in the pulmonary lesions
In the Pb-infected mice, the collagen fibers gradually increased up to 12 weeks in parallel with the inflammation. The collagen depositions arranged themselves as pseudocapsule around the nodules and were more prominent at the periarterial lesions (Fig. 2j). Measurements of the collagen pixels inside the lesions and comparisons between groups revealed that the PTX-treated mice did not exhibit increases in collagen in the pulmonary lesions while the Pb-infected untreated mice did (Fig. 2k,l).
Immunomodulatory effect of PTX at the lung level in healthy and Pb-infected mice
The administration of PTX to healthy non-infected mice increased MIP1a, granulocyte-monocyte colony-stimulating factor (GM-CSF), regulated upon activation, normal T cell expressed and secreted (RANTES), eotaxin, IL-3, IL-4, IL-13, and IL-10 at the middle and end of the therapy and, in some cases, even post-therapy. Pb infection induced the down-regulation of the immune response included reduced expressions of some cytokines during the most chronic periods of infection (8 to 16 weeks). The cytokines included IFN-γ, MIP-1β, TNF-α, IL-3, and IL-9. PTX treatment restored IFN-γ, MIP-1β, and IL-3 levels to normal values (p <0.001) (Fig. 3).
PTX therapy in Pb-infected mice also increased GM-CSF, IL-12p70, IL-10, IL-13, and eotaxin compared to the levels observed in the Pb-infected untreated mice.
RANTES, a chemokine that was up-regulated at all time points post-Pb infection, was normalized to the basal levels by PTX treatment.
In the Pb-infected mice, the pulmonary levels of IL-1α, IL-1β, IL-2, IL-5, IL-6, IL-9, IL-12 (p40), IL-17, MIP-1α, and TNF-α were not modified by PTX treatment
This study showed that PTX therapy administered at an “early” stage of granulomatous inflammation controlled the progress of the PCM and diminished the pulmonary inflammation and the fungal burden and prevented the appearance of collagen deposits in the pulmonary lesions.
In this study, we applied conventional HRCT to follow the development of the pulmonary lesions in the Pb-infected mice and monitored the effects of the therapy. The results of the radiologic evaluations agreed well with the histopathology/histomorphometry; however, in the middle of the therapy (8 weeks p.i), the recognition of the nodules by the radiologists exhibited minimal agreement (κ = 0.4) likely because of the small sizes of the nodules (∽400 um). The HU measurements revealed significant decrease in lung density beginning after 4 weeks of treatment (8 weeks p.i) despite the fact that some pulmonary lesions (nodules) were still present at this time. It is possible that the sizes of the nodules did not significantly change in density in the selected regions of interest (ROIs) that were larger (2000 μm in the upper and central regions and 4000 μm in the lower lung regions).
At the end of the treatment with PTX, small infiltrates were observed around the periarterial spaces. It would be interesting for future studies to evaluate whether the inflammatory cells migrated to the lymphatic vessels around the periarterial spaces. PTX led to an improvement in the immune response and reversed the immunosuppression observed in the Pb-infected group. The PTX treatment restored the levels of IFN-γ that had been down-regulated by Pb infection and increased IL-12p70. These cytokines belong to the Th-1 profile and are recognized for their capacity to accomplish effective responses in PCM . The level of IL-10 was higher in the Pb-infected-PTX-treated mice than in the infected controls, which produced high levels of IL-10 but only until 4 weeks p.i. IL-10 is considered to be a multifaceted anti-inflammatory cytokine  that helps to control inflammation. The up-regulation of IL-10 by methylxanthines such as PTX has previously been reported . Interestingly, other anti-inflammatory agents, such as steroids and allergen-specific immunotherapy, are also known to elevate endogenous IL-10 levels, which may account for their efficacy .
The high levels of IL-10, IL-4, and IL-13 in the Pb-infected-PTX-treated mice might explain the persistence of plasmocytes in this group.
RANTES/CCL5 is a potent chemokine for T cells, dendritic cells, eosinophils, NK cells, mast cells, and basophils  and is up-regulated at all times post-Pb infection in this and other Pb infection models . The reduced levels of RANTES observed in the Pb-infected-PTX-treated group might be another mechanism by which PTX exerted its immunomodulation in this experimental model.
Interestingly, the PTX treatment induced an eotaxin-rich pulmonary micro-environment. Eotaxin is an eosinophil chemoattractant ; however, the numbers of eosinophils did not increase in the lungs of the Pb-infected-PTX-treated mice during therapy. Eosinophils appeared after PTX release. One possible explanation is that PTX inhibits the recruitment of cells to the inflammatory sites as suggested by other studies [23–26]. Indeed, PTX has been considered to be a migration-inhibiting factor for human lymphocytes, monocytes, and neutrophils [23–26] and acts by inhibiting the adherence of these cells to the endothelium and their transendothelial migration .
It has been increasingly recognized that the inflammatory response and the deregulated cytokine production play key roles in the pathogenesis of many diseases, including certain infectious processes . This study reinforces the idea that, in addition to itraconazole, a second therapeutic avenue for the treatment of PCM might be host-directed therapy with PTX . Host-directed therapy is routinely used for the management of infectious diseases such as pediatric meningitis (corticosteroids and antibiotics) and hepatitis C (IFN-2b and antivirals). However, the concept of correcting the host responses that had been subverted by pathogen virulence strategies has not been fully exploited .
Host-directed therapy has been evaluated in experimental PCM. The immunosuppressor cyclophosphamide has been used to modulate immune responses to Pb in rats infected with Pb yeasts via the intracardiac route [30, 31]. This study reported that treated rats presented with the following: a) a decrease in granuloma size and granulomas with fewer fungal cells, b) a lack of specific antibodies, and c) a significant increase in the paracoccidioidin footpad swelling test (delayed-type hypersensitivity (DTH)). In another study , resistant (A/Sn) and susceptible (B10.A) mice were treated with either a low dose of cyclophosphamide or indomethacin, which is a potent inhibitor of prostaglandin synthesis. In the A/Sn mice, the cyclophosphamide induced a recovery of the IgE anti-ovalbumin antibody (OA) antibody response. In the B10.A mice, this effect was extended to IgG1, IgG2a, and total levels of anti-OA antibodies. In general, these studies suggested that “the suppressive stages” in PCM, such as the lack of specific antibodies and DTH, could be inhibited by some immunomodulators such as cyclophosphamide and indomethacin. Indeed, in the present study, we observed that PTX hindered the immune down-regulation induced by Pb during the infection’s natural course.
PTX has been studied in other fungal infections previously. Ostrosky-Zeichner et al.  reported on the effects of pentoxifylline or dexamethasone alone or in combination with amphotericin-B in experimental mouse cerebral cryptococcosis. The amphotericin-B plus pentoxifylline-treated mice exhibited survived for significantly longer and exhibited decreased fungal burdens in the brain than the mice in the other treated groups . However, in another study, PTX at 20 mg/kg every 8 h had no effect on experimental systemic Candida albicans infection, but higher doses of 30 and 60 mg/kg of pentoxifylline every 8 h increased fungal counts in kidneys when compared to the controls . In this last study, the authors used doses that were higher than we employed and administered PTX by intraperitoneal injection, which likely induced an immunosuppressive state.
Granulomas are a hallmark of PCM and tuberculosis and have traditionally been thought to restrict mycobacterial growth. However, analysis of Mycobacterium marinum in zebrafish has shown that early granulomas facilitate mycobacterial growth. Uninfected macrophages are recruited to the granuloma where they are productively infected by M. marinum to facilitate the disease progress . We believe that a similar situation might occur with Pb.
The antifibrogenic effect of PTX that was also observed in this study has been attributed to both the inhibition of extracellular matrix (ECM)-producing cell proliferation and the reduction in the deposition of ECM components, primarily collagen type I, by producer cells [4, 34–37].
The use of PTX apparently caused a paradoxical situation, i.e., simultaneous decreases in the inflammatory reaction and the number of fungi. If PTX induces inhibitions of peripheral blood mononuclear cells, endothelial production of IL-8 and monocyte chemotactic protein-1 (MCP-1), leucocyte chemotaxis and diapedesis, endothelial adhesion molecule expression, T/NK cell cytotoxicity and cytokine production and apoptosis pathways, and the Fas ligand (FasL or CD95L) [4, 34–37], it should be expected to increase the fungal load. However, the opposite was observed. This phenomenon is more puzzling if we consider the possible direct effect of PTX on the fungi; i.e., the inhibition of the Pb phosphodiesterase and the consequent increase in intracellular cyclical AMP, which has a role in the dimorphic transition from mycelium to yeast [4, 34–37].
This paradox raises the hypothesis of a possible effect of the inflammatory reaction and its products on fungal viability or a direct and unknown effect of PTX on P. brasiliensis; in the first sense and since IFN-γ plays an important role both on the immune response by the modulation of some activities of macrophages and T and B cells and on the host resistance against several pathogens including P. brasiliensis [16, 38, 39], it is possible that the increased IFN-γ levels observed in Pb-infected-PTX-treated mice could have triggered an effective immune response inducing the elimination of P. brasiliensis. In the second sense, some reports have shown that methylxanthines have antifungal properties related to the inhibition of fungal chitinases [40, 41]. More specifically, Cryptococcus neoformans and Aspergillus fumigatus treated with pentoxifylline exhibited abnormal cell morphology. In addition, pentoxifylline-treated C. neoformans showed increased susceptibility to calcofluor and a leaky melanin phenotype consistent with defective cell wall function . Unfortunately, no direct experiments in this sense have been made with P. brasiliensis.
Although we found a positive PTX effect on the course of pulmonary lesions in Pb-infected mice, our study has some limitations. We focused exclusively on the lungs and other organs which were not included in our study, the evaluation of fungal dissemination, the characterization of the IFN-γ-producing cells, and the treatment of infected IFN-γ knockout mice with PTX to determine whether PTX combats P. brasiliensis via the intermediacy of IFN-γ-mediated processes are worthy to be conducted in future studies.
In conclusion, this study showed that Pb infection can be positively modulated by anti-inflammatory therapy with PTX administered at the “early” stages of granulomatous inflammation.
All animals were handled according to the Colombian national (Law 84 of 1989, Res No. 8430 of 1993) and international (Council of European Communities and Canadian Council of Animal Care, 1998) guidelines for animal research. Additionally, the experimental protocols were approved by the research ethics committee of the Corporación para Investigaciones Biológicas (CIB).
Mice and experimental groups
BALB/c mice were originally obtained from Taconic Farms, Inc. Quality Laboratory Animals and Services for Research, New York, USA, and the breeding colony was later expanded at the CIB, Medellin, Colombia. The mice were divided into four groups: (A) non-infected or control (n = 50), (B) infected with 3 × 106 Pb conidia (n = 50), (C) non-infected-PTX-treated mice (n = 30), and (D) Pb-infected-PTX-treated mice (n = 30).
Fungus and experimental infection
Pb isolate ATCC-60855 from a Colombian patient registered at the American Type Culture (Rockville, MD, USA) and known to produce abundant conidia was used in all experiments . Pb conidia were produced and collected as previously described [42–44].
Seven-week-old male mice weighing approximately 20 g were anesthetized by intramuscular injection of a solution containing ketamine hydrochloride (Park, Davis & Company, Berlin, Germany; 100 mg/kg) and xylazine (Bayer, Brazil; 10 mg/kg) . When deep anesthesia was obtained, 3 × 106 Pb viable conidia (in 0.06 ml of the inoculum) were intranasally (i.n) instilled. Control mice received an intranasal inoculum of 0.06 ml of PBS.
Pentoxifylline (P1784 Sigma-Aldrich, St. Louis, MO, USA) was provided at a dose of 20 mg/kg in 10 μl of solution. This concentration had been previously used in a mouse model of cryptococcosis . Treatment began 4 weeks p.i when the granulomatous inflammation had begun and continued daily for 8 weeks.
PBS-inoculated and Pb-infected mice were evaluated at 0 (2 h), 4, 8, 12, and 16 weeks post-infection. The PTX-treated mice were analyzed during therapy (at 8 and 12 weeks p.i) and 4 weeks post-treatment (at 16 weeks p.i). The chests of ten mice from each group were scanned by HRCT at each period of observation (see section 2.6). Then, the mice were sacrificed by intraperitoneal injection of 1.0 ml of 2.5 % sodium pentothal (Sandoz Laboratories, Kundl, Austria), and their lungs were removed and assigned for further testing in histopathological (five mice) and immunological (five mice) studies.
The thoraxes of the mice were scanned as previously published by our group . Briefly, the mice were anesthetized with ketamine hydrochloride and xylazine and placed in the prone position inside polypropylene tubes (50 ml) that were arranged together in a wood box with parallel holes. All of the animals were placed with their noses in the same vertical plane. Each animal had a code for future identification. The box containing the mice was then placed in the CT gantry for thorax scanning.
CT images were taken in a multislice CT-scanner (General Electric, EU) with 16 canals by applying 140 kV at 165 mAs/s (Kernel U90). Thin-section slices, each 0.625 mm thick and spaced 1 mm apart, covered the complete mouse lung from the apex to the hemidiaphragm. Images were acquired in the axial plane, and the bone algorithm was applied to better visualize the lung. The field of view was 18 cm to simultaneously include all of the animals with a matrix of 512 × 512 and an acquisition time of one second per section. Approximately 20 to 22 slices covered the entire lung.
Following the scan, the mice were placed in their cages to recover from the anesthesia for 35 min. The animals were supplied with standard laboratory diet and water ad libitum.
The image analysis was performed independently and blindly by two radiologists from the Radiology Department of the University Hospital San Vicente de Paul (Medellín, Colombia). The images were visualized using an Advantage workstation version 4.3 (General Electric) via the lung and mediastinal windows.
The pulmonary densities were evaluated as described by Plathow et al.  with some modifications . Representative tomographic slides were used to calculate the HU. Briefly, eight ROIs were selected in the following areas of the right and left lungs: the upper or hilar region (approximately 5 slides below the apex, where the main bronchi enter the lungs), the anterior and posterior middle or central region (approximately 12 slides below the apex where the heart presents its largest diameter), and the lower lung region (approximately 18 slides bellow the apex, corresponding to the bases of the lungs). These circles were 2 mm2 for the upper and middle regions and 4 mm2 for the lower regions.
After scanning, five animals per group at each period of evaluation were killed by thiopental overdose (Sandoz GmbH., Kundl, Austria; 1 ml at 2.5 %, i.p.) in accordance with animal ethical practices. The lungs of the mice were intracardially perfused with 10 % neutral formalin in phosphate-buffered saline, removed, and fixed in the same solution for at least 48 h. The fixed lungs were embedded in paraffin, and coronal sections (4 μm) were stained with the following methods: hematoxylin-eosin (HE) for evaluation of the lung histology and inflammation, Grocott’s methenamine-silver nitrate technique (Grocott) for identification of the fungi, picrosirius with fast green (PIFG) for identification of I and III interstitial collagens , Lennert’s Giemsa for lymphocyte and plasma cell recognition , sirius red (pH 10.2) for cellular characterization and eosinophil identification [50, 51], and Masson’s trichrome for the collagen fibers and the recognition of the Mott cells that correspond to abnormal plasma cells, and are characterized by the presence of globular cytoplasmic inclusions that are composed of immunoglobulins.
The cellular compositions were evaluated blinded by a pathologist using a semi-quantitative approach. Scores of (−) to (+++) were given according to the degree of infiltration as follows: (+++) for intense, (++) for moderate, (+) for slight, (±) for very slight, and (−) for no reaction .
Quantitative image analysis
The H&E-, Grocott- and PIFG-stained slides were automatically scanned with a ScanScope® CS (Aperio, Vista, CA, USA) at 20X and also analyzed with an Axio Observer.Z1 (Zeiss) coupled with digital camera with AxioCam HRc and software AxioVision 4.7.2 (Zeiss).
The lung inflammatory areas were measured based on one panoramic image of both lungs per mouse. The images were analyzed with the free ImageScope software (http://www.aperio.com/download-imagescope-viewer.asp). The areas of interest (AOIs) corresponding to the inflammatory regions were manually drawn and measured. The percentage of pulmonary area exhibiting an inflammatory reaction was calculated by dividing the sum of the total of the AOIs by the total area occupied by the lung tissue (excluding the air space).
The Aperio positive pixel count algorithm was used to quantify the amount of a specific stain present in a scan slide image. Red pixels in the PIFG-stained slides were measured to quantify collagen, and brown/black pixels in the Grocott’s-stained slides were measured to quantify the glucans present in the fungal wall. The results are expressed as the sum of strong-, medium- and weak-positive pixels in the total area measured.
Cytokines, chemokines, and growth factor detection by multiplex micro-bead immunoassay
The lungs of five animals per group were individually homogenized in a tissue grinder (Tissue tearor, model 985–370, Biospec Products) with a cocktail solution of protease inhibitors (pepsin 0.1 μM, leupeptin 0.1 μM, phenylmethyl sulfonide fluoride 1 mM, N-tosyl-L-phenylalanine chloromethyl ketone 0.2 mM, (a)-p-methyl L-lysine chloromethyl ketone 0.1 mM from Sigma chemical, plus ethylene-diamine-tetraacetic acid (EDTA) 1 nM from Merck Germany). The homogenized lung supernatants were collected by centrifugation at 3000 rpm for 15 min at 4 °C, aliquoted, and stored at −70 °C until the day of analysis.
All homogenized lung supernatants were normalized to 1 mg/ml of protein. Then, a magnetic bead-based multiplex assay containing fluorescent-dyed microspheres conjugated with a monoclonal antibody specific for a target protein was used for cytokines, chemokines, and growth factor measurements according to the manufacturer’s instructions (Bio-Plex pro-mouse cytokine 21-plex assay; Bio-Rad Inc., Hercules, CA, USA). The following molecules were measured: IL1-α, IL-1β, IL-2, IL-3, IL-4, IL-5, IL-6, IL-9, IL-10, IL-12 (p40), IL-12 (p70), IL-13, IL-17, eotaxin, GM-CSF, IFN-γ, monocyte chemoattractive protein (MCP-1/CCL2), macrophage inflammatory protein alpha and beta (MIP-1α/CCL3 and MIP-1β/CCL4), RANTES (CCL5), and TNF-α.
The levels of each molecule were determined in duplicate with the multiplex array reader of the Luminex™ Instrumentation System (Bio-Plex Workstation from Bio-Rad Laboratories). The analyte concentrations were calculated using software provided by the manufacturer (Bio-Plex Manager Software) and are expressed as pg/ml.
The statistical analyses were performed with Prism 5.0 software (GraphPad, San Diego, CA, USA). Non-parametric Kruskal-Wallis tests with Dunn’s post tests were used to compare the selected groups. The values are expressed as medians with interquartile ranges. p values under 0.05 were considered statistically significant. The kappa (κ) coefficient was used as a statistical measure of agreement between the two radiologists.
granulocyte-monocyte colony-stimulating factor
high-resolution computed tomography
monocyte chemoattractive protein 1
macrophage inflammatory protein-1β
region of interest
tumor necrosis factor alpha
Windmeier C, Gressner AM. Pharmacological aspects of pentoxifylline with emphasis on its inhibitory actions on hepatic fibrogenesis. Gen Pharmacol. 1997;29(2):181–96.
Neuner P, Klosner G, Schauer E, Pourmojib M, Macheiner W, Grunwald C, et al. Pentoxifylline in vivo down-regulates the release of IL-1 beta, IL-6, IL-8 and tumour necrosis factor-alpha by human peripheral blood mononuclear cells. Immunology. 1994;83(2):262–7.
Mandell GL. Cytokines, phagocytes, and pentoxifylline. J Cardiovasc Pharmacol. 1995;25 Suppl 2:S20–2.
Berman B, Duncan MR. Pentoxifylline inhibits normal human dermal fibroblast in vitro proliferation, collagen, glycosaminoglycan, and fibronectin production, and increases collagenase activity. J Invest Dermatol. 1989;92(4):605–10.
Gilhar A, Grossman N, Kahanovicz S, Reuveni H, Cohen S, Eitan A. Antiproliferative effect of pentoxifylline on psoriatic and normal epidermis. In vitro and in vivo studies. Acta Derm Venereol. 1996;76(6):437–41.
Kremsner PG, Grundmann H, Neifer S, Sliwa K, Sahlmuller G, Hegenscheid B, et al. Pentoxifylline prevents murine cerebral malaria. J Infect Dis. 1991;164(3):605–8.
Das BK, Mishra S, Padhi PK, Manish R, Tripathy R, Sahoo PK, et al. Pentoxifylline adjunct improves prognosis of human cerebral malaria in adults. Trop Med Int Health. 2003;8(8):680–4.
Di Perri G, Di Perri IG, Monteiro GB, Bonora S, Hennig C, Cassatella M, et al. Pentoxifylline as a supportive agent in the treatment of cerebral malaria in children. J Infect Dis. 1995;171(5):1317–22.
Saez-Llorens X, Ramilo O, Mustafa MM, Mertsola J, de Alba C, Hansen E, et al. Pentoxifylline modulates meningeal inflammation in experimental bacterial meningitis. Antimicrob Agents Chemother. 1990;34(5):837–43.
Haque KN, Pammi M. Pentoxifylline for treatment of sepsis and necrotizing enterocolitis in neonates. Cochrane Database of Systematic Reviews 2003, Issue 2. Art. No.: CD004205.
Staubach KH, Schroder J, Stuber F, Gehrke K, Traumann E, Zabel P. Effect of pentoxifylline in severe sepsis: results of a randomized, double-blind, placebo-controlled study. Arch Surg. 1998;133(1):94–100.
Lundblad R, Ekstrom P, Giercksky KE. Pentoxifylline improves survival and reduces tumor necrosis factor, interleukin-6, and endothelin-1 in fulminant intra-abdominal sepsis in rats. Shock. 1995;3(3):210–5.
Ostrosky-Zeichner L, Soto-Hernandez JL, Angeles-Morales V, Teixeira F, Nava-Ruiz C, Rios C, et al. Effects of pentoxifylline or dexamethasone in combination with amphotericin B in experimental murine cerebral cryptococcosis: evidence of neuroexcitatory pathogenic mechanisms. Antimicrob Agents Chemother. 1996;40(5):1194–7.
Naranjo TW, Lopera DE, Diaz-Granados LR, Duque JJ, Restrepo MA, Cano LE. Combined itraconazole-pentoxifylline treatment promptly reduces lung fibrosis induced by chronic pulmonary paracoccidioidomycosis in mice. Pulm Pharmacol Ther. 2011;24:81–91.
Restrepo A, Benard G, de Castro CC, Agudelo CA, Tobon AM. Pulmonary paracoccidioidomycosis. Semin Respir Crit Care Med. 2008;29(2):182–97.
Kashino SS, Fazioli RA, Cafalli-Favati C, Meloni-Bruneri LH, Vaz CA, Burger E, et al. Resistance to Paracoccidioides brasiliensis infection is linked to a preferential Th1 immune response, whereas susceptibility is associated with absence of IFN-gamma production. J Interferon Cytokine Res. 2000;20(1):89–97.
Bazzoni F, Tamassia N, Rossato M, Cassatella MA. Understanding the molecular mechanisms of the multifaceted IL-10-mediated anti-inflammatory response: lessons from neutrophils. Eur J Immunol. 2010;40(9):2360–8.
Jilg S, Barsig J, Leist M, Kusters S, Volk HD, Wendel A. Enhanced release of interleukin-10 and soluble tumor necrosis factor receptors as novel principles of methylxanthine action in murine models of endotoxic shock. J Pharmacol Exp Ther. 1996;278(1):421–31.
Ogawa Y, Duru EA, Ameredes BT. Role of IL-10 in the resolution of airway inflammation. Curr Mol Med. 2008;8(5):437–45.
Levy JA. The unexpected pleiotropic activities of RANTES. J Immunol. 2009;182(7):3945–6.
Souto JT, Aliberti JC, Campanelli AP, Livonesi MC, Maffei CM, Ferreira BR, et al. Chemokine production and leukocyte recruitment to the lungs of Paracoccidioides brasiliensis-infected mice is modulated by interferon-gamma. Am J Pathol. 2003;163(2):583–90.
Conroy DM, Williams TJ. Eotaxin and the attraction of eosinophils to the asthmatic lung. Respir Res. 2001;2(3):150–6.
Dominguez-Jimenez C, Sancho D, Nieto M, Montoya MC, Barreiro O, Sanchez-Madrid F, et al. Effect of pentoxifylline on polarization and migration of human leukocytes. J Leukoc Biol. 2002;71(4):588–96.
Elferink JG, Huizinga TW, de Koster BM. The effect of pentoxifylline on human neutrophil migration: a possible role for cyclic nucleotides. Biochem Pharmacol. 1997;54(4):475–80.
Bruynzeel I, van der Raaij LM, Willemze R, Stoof TJ. Pentoxifylline inhibits human T-cell adhesion to dermal endothelial cells. Arch Dermatol Res. 1997;289(4):189–93.
Williams Jr JH, Heshmati S, Tamadon S, Guerra J. Inhibition of alveolar macrophages by pentoxifylline. Crit Care Med. 1991;19(8):1073–8.
Bahra PS, Rainger GE, Wautier JL, Nash GB. Effects of pentoxifylline on the different steps during adhesion and transendothelial migration of flowing neutrophils. Cell Biochem Funct. 2001;19(4):249–57.
Riedemann NC, Guo RF, Ward PA. The enigma of sepsis. J Clin Invest. 2003;112(4):460–7.
Agarwal N, Bishai WR. Microbiology: subversion from the sidelines. Science. 2010;327(5964):417–8.
Blejer JL, Godio CM, Negroni R, Nejamkis MR. Cyclophosphamide effect on paracoccidioidomycosis in the rat. Rev Inst Med Trop Sao Paulo. 1995;37(3):219–24.
Amarante-Mendes JG, Ferreira AP, Macedo MS. Suppression of antibody response to an unrelated antigen in experimental murine paracoccidioidomycosis: effect of cyclophosphamide and indomethacin. J Investig Allergol Clin Immunol. 1991;1(3):185–93.
Davis JM, Ramakrishnan L. The role of the granuloma in expansion and dissemination of early tuberculous infection. Cell. 2009;136(1):37–49.
Louie A, Baltch AL, Franke MA, Ritz WJ, Smith RP, Singh JK, et al. Effect of pentoxifylline on the course of systemic Candida albicans infection in mice. J Antimicrob Chemother. 1996;37(5):943–54.
Romanelli RG, Caligiuri A, Carloni V, DeFranco R, Montalto P, Ceni E, et al. Effect of pentoxifylline on the degradation of procollagen type I produced by human hepatic stellate cells in response to transforming growth factor-beta 1. Br J Pharmacol. 1997;122(6):1047–54.
Berman B, Duncan MR. Pentoxifylline inhibits the proliferation of human fibroblasts derived from keloid, scleroderma and morphoea skin and their production of collagen, glycosaminoglycans and fibronectin. Br J Dermatol. 1990;123(3):339–46.
Preaux AM, Mallat A, Rosenbaum J, Zafrani ES, Mavier P. Pentoxifylline inhibits growth and collagen synthesis of cultured human hepatic myofibroblast-like cells. Hepatology. 1997;26(2):315–22.
Fang CC, Lai MN, Chien CT, Hung KY, Tsai CC, Tsai TJ, et al. Effects of pentoxifylline on peritoneal fibroblasts and silica-induced peritoneal fibrosis. Perit Dial Int. 2003;23(3):228–36.
Cano LE, Kashino SS, Arruda C, Andre D, Xidieh CF, Singer-Vermes LM, et al. Protective role of gamma interferon in experimental pulmonary paracoccidioidomycosis. Infect Immun. 1998;66(2):800–6.
Souto JT, Figueiredo F, Furlanetto A, Pfeffer K, Rossi MA, Silva JS. Interferon-gamma and tumor necrosis factor-alpha determine resistance to Paracoccidioides brasiliensis infection in mice. Am J Pathol. 2000;156(5):1811–20.
Tsirilakis K, Kim C, Vicencio AG, Andrade C, Casadevall A, Goldman DL. Methylxanthine inhibit fungal chitinases and exhibit antifungal activity. Mycopathologia. 2012;173(2–3):83–91.
Rao FV, Andersen OA, Vora KA, Demartino JA, van Aalten DM. Methylxanthine drugs are chitinase inhibitors: investigation of inhibition and binding modes. Chem Biol. 2005;12(9):973–80.
Restrepo A, Salazar ME, Cano LE, Patino MM. A technique to collect and dislodge conidia produced by Paracoccidioides brasiliensis mycelial form. J Med Vet Mycol. 1986;24(3):247–50.
Restrepo A, Jimenez BE. Growth of Paracoccidioides brasiliensis yeast phase in a chemically defined culture medium. J Clin Microbiol. 1980;12(2):279–81.
Bustamante-Simon B, McEwen JG, Tabares AM, Arango M, Restrepo-Moreno A. Characteristics of the conidia produced by the mycelial form of Paracoccidioides brasiliensis. Sabouraudia. 1985;23(6):407–14.
Green CJ, Knight J, Precious S, Simpkin S. Ketamine alone and combined with diazepam or xylazine in laboratory animals: a 10 year experience. Lab Anim. 1981;15(2):163–70.
Lopera D, Naranjo T, Hidalgo JM, de Oliveira Pascarelli BM, Patino JH, Lenzi HL, et al. Pulmonary abnormalities in mice with paracoccidioidomycosis: a sequential study comparing high resolution computed tomography and pathologic findings. PLoS Negl Trop Dis. 2010;4(6):e726.
Plathow C, Li M, Gong P, Zieher H, Kiessling F, Peschke P, et al. Computed tomography monitoring of radiation-induced lung fibrosis in mice. Invest Radiol. 2004;39(10):600–9.
Junqueira LC, Bignolas G, Brentani RR. Picrosirius staining plus polarization microscopy, a specific method for collagen detection in tissue sections. Histochem J. 1979;11(4):447–55.
Lennert K. Malignant lymphomas other than Hodgkin’s disease. Berlin: Springer; 1978.
Bogolometz W. Avantages de la coloration par le rouge Sirius de amyloïde e des eosinophils. Arch Anat Cyt Pathol. 1980;28:252–3.
Luque EH, Montes GS. Progesterone promotes a massive infiltration of the rat uterine cervix by the eosinophilic polymorphonuclear leukocytes. Anat Rec. 1989;223(3):257–65.
Silva AA, Roffe E, Lannes-Vieira J. Expression of extracellular matrix components and their receptors in the central nervous system during experimental toxoplasma gondii and trypanosoma cruzi infection. Braz J Med Biol Res. 1999;32(5):593–600.
The authors thank Beatriz E. Finkel-Jimenez, Director, Immunology Core, Stanley S. Scott Cancer Center, LSU HSC, New Orleans, USA; Laura Catalina Echeverri COLCIENCIAS young researcher; Andres Zuluaga, MD, Director del Departamento de Farmacología de la Universidad de Antioquia, Colombia; The authors also thank the technical personnel of the Laboratório de Patología, Instituto Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil for their assistance with histologic methods and the technical personnel of the Radiology Department, Hospital Universitario San Vicente de Paúl, Medellín, Colombia for their assistance with the tomography of the mice. The National Doctoral Program of COLCIENCIAS supported the doctoral fellowship of Damaris Lopera.
The authors declare that they have no competing interests.
DL and TWN participated in the design of the study, carried out the animal and in vitro experiments, participated in the histopathological, immunological, and radiological analyses, and drafted the manuscript. JMH and JHP participated in the design of the study and in the radiological analyses. LE participated in the histomorphometry analyses. HLL participated in the histopathological, immunological, and radiological analyses. AR aided in drafting and editing the manuscript. LEC participated in the design of the study and in the histopathological, immunological, and radiological analyses, and drafted the manuscript. All authors read and approved the final manuscript.
Henrique Leonel Lenzi is deceased.
Damaris Elena Lopera and Tonny Williams Naranjo contributed equally to this work.
About this article
Cite this article
Lopera, D.E., Naranjo, T.W., Hidalgo, J.M. et al. Pentoxifylline immunomodulation in the treatment of experimental chronic pulmonary paracoccidioidomycosis. Fibrogenesis Tissue Repair 8, 10 (2015). https://doi.org/10.1186/s13069-015-0027-8
- Lung fibrosis