Abstract
Neutrophils are essential to control several fungal infections. These cells are commonly known for their pro-inflammatory activities. However, some studies have demonstrated the anti-inflammatory properties of neutrophils during certain infectious diseases, culminating in the inhibition of T cell proliferation. Chromoblastomycosis (CBM) is a deep and progressive mycosis that affects thousands of people worldwide. Although neutrophil infiltrates are observed in the lesion histopathology, the fungus can overtake the immune system response and destroy the host-infected tissue. The present study demonstrated that neutropenic animals had an increase in the IL-6 production in the spleen and liver, followed by a lower fungal burden in these organs up to 14 days of infection. Neutropenic animals also showed a lower F. pedrosoi-specific antibody production 14-days post infection and higher T-cell proliferation in the in vitro experiments after stimulation with F. pedrosoi-purified proteins. Taken together, our results suggest that the presence of regulatory neutrophils in the mouse model of F. pedrosoi infection could act favoring the spread of the fungus and the chronicity of the infection. These findings shed light on the CBM treatment, which might target neutrophil polarization as a new therapy approach to treat CBM lesions.
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Introduction
Fonsecaea pedrosoi is a dematiaceous fungus of the Herpotrichiellaceae family, known as the main agent of chromoblastomycosis (CBM) disease, a deep and chronic subcutaneous mycosis1,2. The CBM lesions are characterized by verrucous, erythematous papules, and atrophic lesions in the skin3. Similar to most fungal infections, the treatment of CBM is complex and usually demands multi-drug administration4 associated with heat/freezing therapy5,6 and, in some cases, surgery7. Moreover, costly and long-term treatments might result in high rates of disease relapse and treatment discontinuation. Therefore, understanding the host–pathogen interaction is crucial to develop new therapeutic tools for CBM treatment8. In the last decade, great effort was made to understand the host immune response in CBM infection (for a review in this topic see Ref.8). Skin biopsies from CBM patients show a characteristic external layer of fibrous tissue with an internal layer of thick granulomatous inflammatory tissue containing mainly macrophages and neutrophils9,10,11. Several studies have demonstrated that the macrophage is poorly activated in CBM and does not seem to play a crucial role in this disease12,13,14,15. However, the importance of neutrophils controlling fungal spread remains unclear. One of the leading studies demonstrating the neutrophil fungicidal activity against F. pedrosoi conidia was published in the 1990s by the Rozental group16. Recently, our group demonstrated that neutrophils eliminate F. pedrosoi conidia in vitro through TLR-2 and TLR-4-dependent phagocytosis and ROS production, whereas hyphal killing occurs through Neutrophil Extracellular Traps (NETs) released independently of ROS production and TLR-2/TLR-4 receptors17. Neutrophils—also named polymorphonuclear (PMN) cells—are granulocytes from the innate immune system, known to be essential in several fungal infections, including Candida albicans18, Aspergillus fumigatus19, Cryptococcus neoformans20, Paracoccidioides brasiliensis21, and Sporothrix schenckii22. Neutrophils are the first leukocytes to migrate from the bloodstream to the infection site to contain and eliminate foreign pathogens. Therefore, for a long time, they were considered highly pro-inflammatory cells with antimicrobial features such as phagocytosis, oxidative burst, degranulation, and NETs release. However, in 1987, Young and colleagues observed in mice bearing lung carcinoma a myeloid-lineage cell similar to neutrophils but with anti-inflammatory activities23. After 8 years, Pekarek and colleagues demonstrated that the elimination of granulocyte cells in vivo fostered the mice’s immune system by inhibiting tumor growth24. Over the past 15 years, the interest in these myeloid-lineage cells with suppressive features has increased, but the lack of a uniform nomenclature leads to misunderstandings by researchers. In 2007, the term PMN myeloid-derived suppressor cells (PMN-MDSCs) was suggested to designate these anti-inflammatory neutrophils25. Although this cell is usually studied in a cancer context, it is known to be related to other pathological conditions, such as autoimmune and infectious diseases. Recently, studies have demonstrated the PMN-MDSC accumulation in several fungal diseases such as Cryptococcus neoformans26, Aspergillus fumigatus26,27, and Candida albicans28,29.
Since CBM infection is a chronic fungal disease with chronic skin lesions characterized by severe neutrophils and macrophages infiltrated, we hypothesized whether these neutrophils were modulated by the fungus to a PMN-MDSC profile, favoring the fungal survival and the chronicity of the infection. So, we used a specific anti-granulocyte antibody (α-Gr1) to induce mouse transient neutropenia. We found that granulocyte-depleted animals had a lower fungal burden in the spleen and liver in the early and late phases of the infection. We also showed that neutropenic animals had higher T-cell proliferation and lower F. pedrosoi specific-antibody production. This pattern is usually observed in patients with mild disease, while lower T-cell response and greater antibody titers are associated with severe forms of the disease. Therefore, our results suggest that F. pedrosoi modulates neutrophils to an anti-inflammatory/PMN-MDSC profile with implications for host protection in the CBM infection.
Material and methods
Animals
The experimental protocols involving animals were previously approved by the Institutional Ethics Committee for Animal Care and Research at the School of Pharmaceutical Sciences (CEUA/FCF Protocol 474). The in vivo experiments were carried out following the recommendations of the ARRIVE Guidelines and the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. Briefly, male C57Bl/6 mice at 10–12 weeks of age were obtained from the Animal House Production and Experimentation Facility of the School of Pharmaceutical Sciences of the University of São Paulo. The animals were maintained in an SPF environment and housed in temperature-controlled rooms at 23–25 °C with food and water ad-libitum throughout the experiments. The euthanasia procedure was performed according to the American Veterinary Medical Association Guidelines for the Euthanasia of Animals (2020), using the overdose of ketamine and xylazine method. In this study, we used 4–5 animals per group and we performed the experiments in two independent days. These two experiments were compiled, unless otherwise stated. In this study, no strategies were used to blind or randomize our groups.
Fungal strain and growth conditions
This study was conducted using F. pedrosoi strain CBS 271.37, which was previously isolated from a Brazilian patient diagnosed with CBM. The genome of F. pedrosoi CBS 271.37 is completely sequenced and this strain is commonly used to study F. pedrosoi infection due to their large infection capacity30. The F. pedrosoi was cultivated on a Sabouraud agar at 30 °C until the inoculum preparation. To avoid attenuation or loss of the fungal virulence, we inoculated some animals once a month and recovered the fungus from the mouse spleen and liver after 15–20 days of infection. The sample was kept on a Sabouraud agar until use (maximum of three passages). The fungi were transferred to 150 mL of potato dextrose broth (Difco, BD) and grown for 5 days at 30 °C under shaking. After this period, the inoculum was filtered through a 40 μM cell strainer. The conidial particles were obtained from the flow-through solution and centrifuged for 5 min in 300×g to precipitate the small hyphae and large conidia. The supernatant with the small conidia was collected and centrifuged for 10 min at 9000×g and then resuspended in 1 × PBS. The conidia concentration was determined by the Neubauer chamber counting.
Peripheral blood neutrophil depletion
C57BL/6 animals at 8–12 weeks of age were treated with anti-Gr1 to deplete granulocytes (named depleted animals) or with isotype control anti-LTF2 (BioxCell®—named isotype control animals). Briefly, animals were intraperitoneally (i.p.) treated with different concentrations of anti-Gr1 (0–200 μg) on day − 1. After 24 h (day 0), peripheral blood was collected by tail snip, the red blood cells were lysed with a hypotonic solution, and a Cytospin slide was prepared. Leukocytes were stained using the Wright-Giemsa kit (InstantProv kit, New Prov®), and the differential leukocyte count was performed under conventional microscopy, in which 100 leukocytes were analyzed by their nuclear shape and morphology followed by the calculation of the neutrophil percentage.
The anti-Gr1 antibody was obtained from the supernatant of hybridoma culture (clone RB6-8C5). Approximately 1 × 107 hybridoma cells were cultured in bioreactor flasks (Cell-Line Bioreactor—Argos Technologies) containing RPMI and 10% ultra-low IgG fetal bovine serum (ThermoFisher®), according to the bioreactor manufacturer’s instructions. After 5 days of cell culture, the supernatant was collected and frozen with 0.01% sodium azide until the IgG purification. The IgG purification was performed using the protein G column (Hitrap Protein G—GE Healthcare®) according to the manufacturer’s instructions. The samples were then placed into a dialysis membrane and kept in PBS solution for 24 h. The antibody concentration was determined using the NanoDrop equipment (ThermoFisher®). The anti-Gr1 functionality was first assessed by staining mouse neutrophils with secondary antibody anti-rat labeled with FITC followed by flow cytometry analysis (data not shown). Later, we tested the anti-Gr1 activity by analyzing the neutrophil depletion in the peripheral blood of murine animals after treatment with different concentrations of anti-Gr1 (Fig. 1).
In vivo infection
The animals were i.p. infected with 5 × 107 of F. pedrosoi conidia after 24 h of anti-Gr1 administration (day 0). They were euthanized after 1 and 2 days of infection to investigate the early phase of infection. For the late phase, animals received two extra doses of the antibody, one on day 3 and the other on day 7. After 14 days of infection, they were euthanized, and the spleen and liver were harvested to analyze fungal burden, cell populations, and cytokines production since these are the most commonly affected organs in this mouse model infection by F. pedrosoi. Briefly, the organs were harvested and smashed using a cell strainer (70 μM). An aliquot of the organ macerated was collected and seeded into Sabouraud agar for further colony-forming unit (CFU) analysis, and the remainder was centrifuged. After centrifugation, the supernatants were collected and frozen at − 80 °C for later cytokine measurement, while the cells were resuspended in 1 mL of PBS and placed over 3 mL Ficoll (1119 density) to isolate the leukocytes (top of the Ficoll layer) from the other tissue cells (bottom of the Ficoll layer). The leukocytes were collected from the top of the Ficoll layer and stained with proper antibodies for flow cytometry analysis (Suppl. Table 1). Cytokines from the organ supernatant were measured by the ELISA technique, according to the manufacturer's instructions (R&D Systems).
Because this work aimed to verify the role of neutrophils in a murine model of F. pedrosoi infection, we first analyzed the animals after 1 and 2 days of infection (early phase), since it is well-established that during this period, the main response of the immune system relies on the migration and activation of the innate cells, especially neutrophils31,32. Later, we intended to understand the consequences of the neutropenia in the adaptive immune system; therefore, we performed this analysis after 14 days of infection, when the adaptive immune system was fully activated.
Lymphocyte proliferation assay
For the T cell proliferation evaluation, the spleen from the isotype control (α-LTF1) and neutropenic animals (α-Gr1) was harvested after 14 days of intraperitoneal infection with 5 × 107 of F. pedrosoi conidia. The spleen was removed and the total cells were collected and stained with 10 μM CFSE (carboxyfluorescein diacetate succinimidyl ester), according to the manufacturer’s instructions (Molecular Probes). Next, 1 × 105 cells/mL were plated and cultivated in supplemented R10 medium (RPMI containing 10% fetal bovine serum, 1% non-essential amino acids, and 1 mM sodium pyruvate) at 37 °C for 3 days. The non-stimulated cells were cultivated only with medium, whereas the stimulated cells were cultivated with medium containing 15 μg F. pedrosoi purified proteins (protein extraction protocol as described below). After this period, the cells were harvested and the T-cell proliferation was analyzed by flow cytometry (FACSCanto II—Becton Dickinson) by gating the CD3+ cells.
Humoral immune response to F. pedrosoi
The host-specific antibody production against F. pedrosoi was analyzed by the Western blot technique. First, proteins from F. pedrosoi were extracted according to Almeida and colleagues with modifications33. Briefly, F. pedrosoi conidial and hyphal were washed three times in ultrapure water by centrifugation at 5000×g for 5 min (4 °C). The pellet was macerated with liquid nitrogen and a pestle until we get a slim powder. The proteins were suspended and vortexed for 5 min. The conidial and hyphal debris were removed by centrifugation (8000×g, 4 °C, 10 min). Protein concentrations were determined by the Bradford assay and the samples were kept at − 80 °C until use. We loaded an SDS-PAGE with the ladder marker and 10 μg F. pedrosoi proteins under reducing conditions. The proteins were transferred to nitrocellulose membranes, and nonspecific binding sites were blocked using 10% (w/v) dried milk in PBS-Tween (0.05%) for 2 h at RT. The membrane was then cut, so that each strip would contain two wells, one with the ladder marker and the other with the F. pedrosoi purified proteins. To assess the F. pedrosoi-specific antibody production by previously infected animals, each strip was incubated for 2 h with sera (diluted 1:200) from a single animal (isotype control or neutropenic). After washing, the strips were incubated with peroxidase-conjugated secondary antibodies for 60 min. Positive signals were detected by enhanced chemiluminescence (SuperSignal West Pico, Pierce). All strips were developed simultaneously and within the same exposure time (using the ImageQuant LAS 500—GE Healthcare®), so the densitometry of the bands could be determined (by the ImageJ program) and compared between the different groups of animals.
Statistical analyses
Statistical analysis was performed using the GraphPad Prism® program. Student t-test was used for the analyses between two groups with one variable. Data are expressed as the mean ± SEM, and the differences observed were considered significant when p < 0.05 (5%).
Statement of ethics
The in vivo experiments were carried out following the recommendations of the ARRIVE Guidelines and the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The experimental protocols involving animals were previously approved by the Institutional Ethics Committee for Animal Care and Research at the School of Pharmaceutical Sciences (CEUA/FCF Protocol 474).
Results
Anti-Gr1 treatment led to early severe neutropenia
First, we aimed to determine the necessary amount of α-Gr1 to induce mouse severe neutropenia. Thus, different amounts of anti-Gr1 antibodies were administrated to adjust the suitable dose of our model. Blood samples collected by tail snip showed a 50% decrease in circulating neutrophils after 24 h of antibody administration, even in the lowest dose (50 μg) (Fig. 1a–c). When increasing the antibody amount up to 200 μg, we enhanced the neutrophil depletion to approximately 75%. We also observed that a single shot of α-Gr1 maintained the neutrophil depletion around 50% after 48 h, but this depletion level decreased to approximately 25% after 72 h (Fig. 1b). We decided to use the lowest dose in our future set of experiments because no greater depletion was observed in animals treated with 200 μg α-Gr1 comparing to those who received 150 μg (Fig. 1b).
Neutropenic animals showed a lower fungal burden in the early phase of F. pedrosoi infection
Once we defined the antibody dose to deplete the neutrophils, we treated the animals with 150 μg of α-Gr1 (or anti-LTF2, isotype control) on day − 1, followed by the infection with F. pedrosoi (day 0). We showed a great depletion of neutrophils in the spleen (Fig. 2a,b) and liver (Fig. 2c,d) of the animals after 1 and 2 days of infection. An increase number of macrophages (MO) and dendritic cells (DC) was also observed in the liver 2-days post infection (Fig. 2d); however, these changes were not present in the spleen nor liver of the 1 day-infected animals (Fig. 2a–c). Neutrophil-depleted animals showed a reduction in fungal burden in the spleen and liver after 1 and 2 days of infection (Fig. 2e,f), suggesting that the neutrophils have a PMN-MDSCs profile with an anti-inflammatory activity over the F. pedrosoi infection.
Neutrophil-depleted animals have higher levels of IL-6 during the early phase of infection
When we assessed the cytokines production in the spleen and liver of the animals, we observed higher levels of IL-6 in neutropenic animals 1- and 2-days post infection (Fig. 3a–d) together with an increased level of IL-10 in the liver of these animals 2-days post infection (Fig. 3d). However, IL-4 and TNF-α levels were decreased in the spleen of neutropenic animals 1-day post infection (Fig. 3a). No differences in the IL-12, IL-17 and IFN-γ production was observed comparing the isotype control and neutropenic animals during the early phase of the infection.
Neutropenic animals showed lower levels of B-cells
To better understand the influence of neutrophils over the adaptive immune response, a 14-day infection was induced in isotype control and neutropenic animals. Once we showed that a single shot of α-Gr1 kept the neutrophil depletion up to 72 h (Fig. 1), we included two extra doses to keep the neutrophil depletion for a longer period. Briefly, we performed the same protocol as described above and included one extra dose on day 3 and another on day 7. The neutrophil level was tracked by tail snip blood smear on days 2, 5, 8, and 12 after infection (Fig. 4a). Using the 14-day time-point, we aimed to analyze the lymphocytes population. We verified that neutropenic animals presented lower levels of B-lymphocytes with no difference in the T-lymphocyte populations (Fig. 4b,c).
Neutrophil-depleted animals showed higher T-cell proliferation and a lower humoral response
We next determined whether the presence of neutrophils was impairing the humoral and cellular immune response in F. pedrosoi infection. Besides the lower levels of B-cell (Fig. 4b,c), neutropenic animals also showed a decreased production of a specific antibody against F. pedrosoi, confirming the impairment of humoral response in these animals (Fig. 5a,b). However, assessing the T-cell function through the proliferation assay we verified a higher cellular immune response in neutropenic animals (Fig. 5c,d), suggesting the presence of PMN-MDSC in control animals impairing the T-cell proliferation.
Neutropenic animals showed a better outcome during the late phase of the F. pedrosoi infection
Having characterized the adaptive immune response in the neutropenic and control animals, we analyzed the cytokines production during the late phase of the infection. We verified lower concentrations of IL-6, IL-10, IL-12, and TNF-α in the spleen (Fig. 6a,b) but higher concentrations of IL-6, IL-12, and IL-17 in the liver of neutropenic animals (Fig. 6c,d). Moreover, in agreement with our previous findings of 1- and 2-days post infection, a lower fungal burden was also observed in the spleen and liver of neutropenic animals 14-days post infection, demonstrating a better clearance of F. pedrosoi in the absence of PMN-MDSC (Fig. 6e).
Discussion
Fungal infections are known for their high complexity treatment. Several fungus species can evade the host immune system, leading to the chronicity of the disease. Chronic CBM skin wounds show a high rate of neutrophil and macrophage infiltrates, suggesting that the cell migration is not impaired in this disease9,10,11. While macrophages have a low fungicidal capacity in in vitro studies, probably because F. pedrosoi can inhibit nitric oxide production in these cells14,15, neutrophils show an important in vitro fungicidal capacity over F. pedrosoi conidia and hyphae16,17. However, the importance of macrophages and neutrophils in in vivo CBM infection is poorly understood. Since neutrophils with suppressor features were recently observed in Cryptococcus neoformans26, Aspergillus fumigatus27, and Candida albicans28,29 infections, we wondered whether F. pedrosoi could also modulate the neutrophils activities in vivo, leading to the inhibition of the host immune response and the chronicity of the infection. To answer this question, we induced transient neutropenia in the mouse by the α-Gr1 administration approach. We verified a significant decrease of neutrophils in the peripheral blood, spleen, and liver of those animals after 24 and 48 h of F. pedrosoi infection. The absence of neutrophils leads to a better clearance of the fungal infection (Fig. 2e,f), followed by higher IL-6 production in the spleen and liver after the first 48 h of infection (Fig. 3). This cytokine is generated in the infectious lesion by different cell types from the innate immune cells to mesenchymal cells, endothelial cells, fibroblasts, and others34. First described in the 1980s, IL-6 presents a pleiotropic effect on inflammation, immune response, and hematopoiesis35. At present, the role of IL-6 over granulopoiesis36 and PMN-MDSCs differentiation37 is well defined. Therefore, our results suggest that the F. pedrosoi modulates neutrophils’ activity to a PMN-MDSCs profile in the early phase of the host immune response through the stimulation of IL-6 production. Once these cells are depleted, a higher accumulation of IL-6 is seen at the lesion site of α-Gr1 treated animals. Similar results were observed in Pneumococcus pneumoniae38 and Trypanosoma cruzi39 infections, in which neutropenic animals showed lower pathogen load and higher levels of IL-6. Although the PMN-MDSCs are usually related to T-cell inhibition40,41, recent studies have demonstrated that these cells can also modulate the innate immune cells such as MO42,43, DC44,45,46, and Natural Killer (NK) Cells27,47,48,49. The relevance of these cells in in vivo CBM infection remains unclear. We believe F. pedrosoi stimulates PMN-MDSCs accumulation as an immune evasion mechanism, resulting in the impairment of the innate immunity activation and progression of the infection. However, a detailed study of the innate immune response in in vivo CBM infection is necessary to confirm this hypothesis.
Although MDSCs exert an important suppressor activity on innate immunity, the primary inhibitory activity occurs on adaptive immunity50. Here, we demonstrated an increased T-cell proliferation (Fig. 5c,d) and a lower B-cell population (Fig. 4b,c) followed by impaired F. pedrosoi specific-antibody production (Fig. 5a) by neutrophil-depleted animals. These findings suggest that the neutrophils infiltrate on the spleen of F. pedrosoi infected animals shows an anti-inflammatory profile (MDSCs profile), inhibiting the T-cell proliferation ex-vivo. The antibodies analysis from sera of infected animals identified two major groups of F. pedrosoi antigens, one with lower immunogenicity weighing around 54 kDa and a higher immunogenic group around 48 kDa. At least two previous studies had similar results, showing antibodies from CBM patients’ serum reacting to an F. pedrosoi antigen weighing around 54 kDa51,52. In addition to the 54 kDa antigens, Vidal and colleagues also observed a strong immune reaction to 66 kDa antigens52. We believe this difference might be due to the different protocols used for F. pedrosoi-antigen extraction or the species-specific humoral response of CBM infection. Previous studies showed that the host humoral response is not protective in human CBM infection and the severity of the disease is directly proportional to humoral response activation and indirectly proportional to the T-cell response activation53,54,55,56. Therefore, our findings corroborate these previous studies, demonstrating that PMN-MDSCs-depleted animals developed a mild infection—with lower spleen and liver fungal load (Fig. 6e)—associated with higher T-cell proliferation and lower antibody levels (Fig. 5). Although the cytokine profile did not follow a clear pattern, we believe that lower levels of IL-10 (Fig. 6b) in the spleen of neutropenic animals favor a higher rate of splenic T-cell proliferation ex vivo (Fig. 5), once IL-10 is known to stimulate PMN-MDSCs activities such as inhibition of T-cell proliferation42,57,58. However, no cytokines were measured during the T-cell lymphoproliferative assay to confirm this hypothesis.
It is important to mention that like others experimental models, the murine model of F. pedrosoi infection has some limitations. This model does not mimic exactly the human disease. While the human disease is chronic and requires a long-lasting and complex treatment, the mouse can easily eliminate the infection after 25–30 days. Therefore, in order to assess the infectious/inflammatory process in our model we chose the 14-day time point after the infection (our late phase) to compare the fungal burden in the presence or absence of neutrophils.
Several studies have reported that the survival, differentiation, and immunosuppressive activity of MDSCs are affected by different Toll-like receptors (TLRs)59. Activation of TLR-4 by BCG60 and Immunomax® immunostimulant61 decreased MDSCs frequency, whereas stimulation of TLR-7/8 by Imiquimod switched the anti-inflammatory profile of MDSC to a pro-inflammatory and antitumoral profile62. Therefore, TLRs-agonists arise as potential drugs for cancer treatment, being the Imiquimod recently approved by the Food and Drug Administration (FDA) for basal cell carcinoma treatment63. Although this is the first study demonstrating the presence of MDSCs in CBM infection, previous studies have successfully used TLR-464 and TLR-7/8 agonists to treat murine CBM disease65,66. Several authors suggested that F. pedrosoi poorly activates the host immune system; therefore, the TLR-agonists are necessary to boost the host immune response and kill the infection. However, a high infiltration of neutrophils and macrophages is seen in patients’ wounds, suggesting that the host immune system is, at least, partially activated by the fungus. Thus, we believe that F. pedrosoi negatively regulates the host immune response stimulating the MDSCs differentiation and proliferation. The treatment with TLR-agonists would help the host immune system subverting these anti-inflammatory cells to a pro-inflammatory profile, favoring the resolution of the infection. Therefore, this work established a new field of study in CBM infection, demonstrating for the first time that F. pedrosoi stimulates PMN-MDSCs and inhibits host immune response leading to the chronicity of the infection. However, the main question still needs to be addressed: What is the mechanism used by F. pedrosoi to stimulate the proliferation and differentiation of PMN-MDSC?
Data availability
Data sharing do not apply to this article as no datasets were generated or analyzed during the current study.
References
Queiróz, A. J. R., Pereira Domingos, F. & Antônio, J. R. Chromoblastomycosis: Clinical experience and review of literature. Int. J. Dermatol. 57(11), 1351–1355 (2018).
Caligiorne, R. B. et al. Dematiaceous fungal pathogens: Analysis of ribosomal DNA gene polymorphism by polymerase chain reaction-restriction fragment length polymorphism. Mycoses 42(11–12), 609–614 (1999).
Queiroz-Telles, F. et al. Chromoblastomycosis: An overview of clinical manifestations, diagnosis and treatment. Med. Mycol. 47(1), 3–15 (2009).
Bonifaz, A., Paredes-Solís, V. & Saúl, A. Treating chromoblastomycosis with systemic antifungals. Expert Opin. Pharmacother. 5(2), 247–254 (2004).
Castro, L. G., Pimentel, E. R. & Lacaz, C. S. Treatment of chromomycosis by cryosurgery with liquid nitrogen: 15 years’ experience. Int. J. Dermatol. 42(5), 408–412 (2003).
Hira, K. et al. Successful treatment of chromomycosis using carbon dioxide laser associated with topical heat applications. J. Eur. Acad. Dermatol. Venereol. 16(3), 273–275 (2002).
Brito, A. C. & Bittencourt, M. J. S. Chromoblastomycosis: An etiological, epidemiological, clinical, diagnostic, and treatment update. An. Bras. Dermatol. 93(4), 495–506 (2018).
Breda, L. C. D. et al. Immune sensing and potential immunotherapeutic approaches to control chromoblastomycosis. J. Fungi (Basel) 7(1) (2020).
Uribe, F. et al. Histopathology of chromoblastomycosis. Mycopathologia 105(1), 1–6 (1989).
Siqueira, I. M. et al. Modulation of the immune response by Fonsecaea pedrosoi morphotypes in the course of experimental chromoblastomycosis and their role on inflammatory response chronicity. PLoS Negl. Trop. Dis. 11(3), e0005461 (2017).
Esterre, P. et al. Granulomatous reaction and tissue remodelling in the cutaneous lesion of chromomycosis. Virchows Arch. A Pathol. Anat. Histopathol. 422(4), 285–291 (1993).
Farbiarz, S. R. et al. Fine structure and cytochemistry of the interaction between Fonsecaea pedrosoi and mouse resident macrophages. J. Med. Vet. Mycol. 28(5), 373–383 (1990).
Rozental, S., Alviano, C. S. & de Souza, W. The in vitro susceptibility of Fonsecaea pedrosoi to activated macrophages. Mycopathologia 126(2), 85–91 (1994).
Hayakawa, M. et al. Phagocytosis, production of nitric oxide and pro-inflammatory cytokines by macrophages in the presence of dematiaceous [correction of dematiaceus] fungi that cause chromoblastomycosis. Scand. J. Immunol. 64(4), 382–387 (2006).
Bocca, A. L. et al. Inhibition of nitric oxide production by macrophages in chromoblastomycosis: A role for Fonsecaea pedrosoi melanin. Mycopathologia 161(4), 195–203 (2006).
Rozental, S., Alviano, C. S. & de Souza, W. Fine structure and cytochemical study of the interaction between Fonsecaea pedrosoi and rat polymorphonuclear leukocyte. J. Med. Vet. Mycol. 34(5), 323–330 (1996).
Breda, L. C. D. et al. Conidia and hyphae activate neutrophils distinctly: requirement of TLR-2 and TLR-4 in neutrophil effector functions. Front. Immunol. 11, 540064 (2020).
Gazendam, R. P. et al. How neutrophils kill fungi. Immunol. Rev. 273(1), 299–311 (2016).
Gazendam, R. P. et al. Human neutrophils use different mechanisms to kill Aspergillus fumigatus conidia and hyphae: Evidence from phagocyte defects. J. Immunol. 196(3), 1272–1283 (2016).
Rocha, J. D. et al. Capsular polysaccharides from Cryptococcus neoformans modulate production of neutrophil extracellular traps (NETs) by human neutrophils. Sci. Rep. 5, 8008 (2015).
Rodrigues, D. R. et al. Paracoccidioides brasiliensis killing by IFN-gamma, TNF-alpha and GM-CSF activated human neutrophils: Role for oxygen metabolites. Med. Mycol. 45(1), 27–33 (2007).
Rex, J. H. & Bennett, J. E. Administration of potassium iodide to normal volunteers does not increase killing of Sporothrix schenckii by their neutrophils or monocytes. J. Med. Vet. Mycol. 28(3), 185–189 (1990).
Young, M. R., Newby, M. & Wepsic, H. T. Hematopoiesis and suppressor bone marrow cells in mice bearing large metastatic Lewis lung carcinoma tumors. Cancer Res. 47(1), 100–105 (1987).
Pekarek, L. A. et al. Inhibition of tumor growth by elimination of granulocytes. J. Exp. Med. 181(1), 435–440 (1995).
Gabrilovich, D. I. et al. The terminology issue for myeloid-derived suppressor cells. Cancer Res. 67(1), 425 (2007) (author reply 426).
Mednick, A. J. et al. Neutropenia alters lung cytokine production in mice and reduces their susceptibility to pulmonary cryptococcosis. Eur. J. Immunol. 33(6), 1744–1753 (2003).
Mueller-Leisse, J. et al. Polymorphonuclear neutrophils and granulocytic myeloid-derived suppressor cells inhibit natural killer cell activity toward Aspergillus fumigatus. Med. Mycol. 53(6), 622–629 (2015).
Singh, A. et al. Differential regulation of myeloid-derived suppressor cells by Candida species. Front. Microbiol. 7, 1624 (2016).
Rieber, N. et al. Pathogenic fungi regulate immunity by inducing neutrophilic myeloid-derived suppressor cells. Cell Host Microbe 17(4), 507–514 (2015).
Teixeira, M. M. et al. Exploring the genomic diversity of black yeasts and relatives. Stud. Mycol. 86, 1–28 (2017).
Rosales, C. Neutrophil: A cell with many roles in inflammation or several cell types?. Front. Physiol. 9, 113 (2018).
Mayadas, T. N., Cullere, X. & Lowell, C. A. The multifaceted functions of neutrophils. Annu. Rev. Pathol. 9, 181–218 (2014).
de Almeida, J. R. F. et al. An immunoproteomic approach revealing peptides from Sporothrix brasiliensis that induce a cellular immune response in subcutaneous sporotrichosis. Sci. Rep. 8(1), 4192 (2018).
Akira, S., Taga, T. & Kishimoto, T. Interleukin-6 in biology and medicine. Adv. Immunol. 54, 1–78 (1993).
Tanaka, T., Narazaki, M. & Kishimoto, T. IL-6 in inflammation, immunity, and disease. Cold Spring. Harb. Perspect. Biol. 6(10), a016295 (2014).
Liu, F. et al. Interleukin-6 and the granulocyte colony-stimulating factor receptor are major independent regulators of granulopoiesis in vivo but are not required for lineage commitment or terminal differentiation. Blood 90(7), 2583–2590 (1997).
Bunt, S. K. et al. Reduced inflammation in the tumor microenvironment delays the accumulation of myeloid-derived suppressor cells and limits tumor progression. Cancer Res. 67(20), 10019–10026 (2007).
Marks, M. et al. Influence of neutropenia on the course of serotype 8 pneumococcal pneumonia in mice. Infect. Immun. 75(4), 1586–1597 (2007).
Arocena, A. R. et al. Myeloid-derived suppressor cells are key players in the resolution of inflammation during a model of acute infection. Eur. J. Immunol. 44(1), 184–194 (2014).
Fridlender, Z. G. et al. Polarization of tumor-associated neutrophil phenotype by TGF-beta: “N1” versus “N2” TAN. Cancer Cell 16(3), 183–194 (2009).
Ostrand-Rosenberg, S. & Fenselau, C. Myeloid-derived suppressor cells: Immune-suppressive cells that impair antitumor immunity and are sculpted by their environment. J. Immunol. 200(2), 422–431 (2018).
Sinha, P. et al. Cross-talk between myeloid-derived suppressor cells and macrophages subverts tumor immunity toward a type 2 response. J. Immunol. 179(2), 977–983 (2007).
Sinha, P., Clements, V. K. & Ostrand-Rosenberg, S. Reduction of myeloid-derived suppressor cells and induction of M1 macrophages facilitate the rejection of established metastatic disease. J. Immunol. 174(2), 636–645 (2005).
Greifenberg, V. et al. Myeloid-derived suppressor cell activation by combined LPS and IFN-gamma treatment impairs DC development. Eur. J. Immunol. 39(10), 2865–2876 (2009).
Poschke, I. et al. Myeloid-derived suppressor cells impair the quality of dendritic cell vaccines. Cancer Immunol. Immunother. 61(6), 827–838 (2012).
Ostrand-Rosenberg, S. et al. Cross-talk between myeloid-derived suppressor cells (MDSC), macrophages, and dendritic cells enhances tumor-induced immune suppression. Semin. Cancer Biol. 22(4), 275–281 (2012).
Suzuki, E. et al. Gemcitabine selectively eliminates splenic Gr-1+/CD11b+ myeloid suppressor cells in tumor-bearing animals and enhances antitumor immune activity. Clin. Cancer Res. 11(18), 6713–6721 (2005).
Li, H. et al. Cancer-expanded myeloid-derived suppressor cells induce anergy of NK cells through membrane-bound TGF-beta 1. J. Immunol. 182(1), 240–249 (2009).
Elkabets, M. et al. IL-1β regulates a novel myeloid-derived suppressor cell subset that impairs NK cell development and function. Eur. J. Immunol. 40(12), 3347–3357 (2010).
Aarts, C. E. M. et al. Neutrophils as suppressors of T cell proliferation: Does age matter?. Front. Immunol. 10, 2144 (2019).
Ibrahim-Granet, O., de Bièvre, C. & Jendoubi, M. Immunochemical characterisation of antigens and growth inhibition of Fonsecaea pedrosoi by species-specific IgG. J. Med. Microbiol. 26(3), 217–222 (1988).
Vidal, M. S. et al. Highly specific and sensitive, immunoblot-detected 54 kDa antigen from Fonsecaea pedrosoi. Med. Mycol. 42(6), 511–515 (2004).
Sousa, M. G. et al. Fonsecaea pedrosoi infection induces differential modulation of costimulatory molecules and cytokines in monocytes from patients with severe and mild forms of chromoblastomycosis. J. Leukoc. Biol. 84(3), 864–870 (2008).
Mazo Fávero Gimenes, V. et al. Cytokines and lymphocyte proliferation in patients with different clinical forms of chromoblastomycosis. Microbes Infect. 7(4), 708–713 (2005).
Esterre, P., Jahevitra, M. & Andriantsimahavandy, A. Humoral immune response in chromoblastomycosis during and after therapy. Clin. Diagn. Lab. Immunol. 7(3), 497–500 (2000).
d’Avila, S. C., Pagliari, C. & Duarte, M. I. The cell-mediated immune reaction in the cutaneous lesion of chromoblastomycosis and their correlation with different clinical forms of the disease. Mycopathologia 156(2), 51–60 (2003).
Heim, C. E., Vidlak, D. & Kielian, T. Interleukin-10 production by myeloid-derived suppressor cells contributes to bacterial persistence during Staphylococcus aureus orthopedic biofilm infection. J. Leukoc. Biol. 98(6), 1003–1013 (2015).
Hart, K. M. et al. IL-10 immunomodulation of myeloid cells regulates a murine model of ovarian cancer. Front. Immunol. 2, 29 (2011).
Zhou, H. et al. Dual roles of myeloid-derived suppressor cells induced by Toll-like receptor signaling in cancer. Oncol. Lett. 21(2), 149 (2021).
Wang, Y. et al. Bacillus Calmette–Guérin and anti-PD-L1 combination therapy boosts immune response against bladder cancer. Onco Targets Ther. 11, 2891–2899 (2018).
Ghochikyan, A. et al. Targeting TLR-4 with a novel pharmaceutical grade plant derived agonist, Immunomax®, as a therapeutic strategy for metastatic breast cancer. J. Transl. Med. 12, 322 (2014).
Wang, J. et al. Effect of TLR agonists on the differentiation and function of human monocytic myeloid-derived suppressor cells. J. Immunol. 194(9), 4215–4221 (2015).
Urban-Wojciuk, Z. et al. The role of TLRs in anti-cancer immunity and tumor rejection. Front. Immunol. 10, 2388 (2019).
Sousa, M. A. G. et al. Restoration of pattern recognition receptor costimulation to treat chromoblastomycosis, a chronic fungal infection of the skin. Cell Host Microbe 9(5), 436–443 (2011).
de Sousa, M. A. G. et al. Topical application of imiquimod as a treatment for chromoblastomycosis. Clin. Infect. Dis. 58(12), 1734–1737 (2014).
Belda, W., Criado, P. R. & Passero, L. F. D. Successful treatment of chromoblastomycosis caused by Fonsecaea pedrosoi using imiquimod. J. Dermatol. 47(4), 409–412 (2020).
Funding
This research was funded by the “Fundação de Amparo à Pesquisa do Estado de São Paulo” (FAPESP—grant number 2012/18598-7, 2014/11146-9, 2016/047293, 2019/14347-9, 21/02708-7), “Conselho Nacional de Desenvolvimento Científico e Tecnológico” (CNPQ), and “Coordenação de Aperfeiçoamento de Pessoal de Nível Superior” (CAPES).
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L.C.D.B. and S.R.A. designed the study. L.C.D.B., C.N.S.B., G.H.K., J.R.F.A., G.P.J., and L.G.F. performed experiments and analyzed the data. L.C.D.B. and S.R.A. interpreted the data. L.C.D.B. wrote the manuscript and all authors approved the final draft.
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Breda, L.C.D., de Souza Breda, C.N., Kaihami, G.H. et al. Neutrophil-suppressive activity over T-cell proliferation and fungal clearance in a murine model of Fonsecaea pedrosoi infection. Sci Rep 11, 20220 (2021). https://doi.org/10.1038/s41598-021-99847-z
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DOI: https://doi.org/10.1038/s41598-021-99847-z
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