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Advances in Leishmaniasis and Chagas Disease: Biology, Epidemiology, Treatment and...
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Advances in Leishmaniasis and Chagas Disease: Biology, Epidemiology, Treatment and Control

A special issue of Biology (ISSN 2079-7737). This special issue belongs to the section "Microbiology".

Deadline for manuscript submissions: 15 August 2024 | Viewed by 4665

Special Issue Editors

Prof. Dr. Fernando Almeida-Souza

E-Mail Website
Guest Editor
Postgraduate Program in Animal Science, State University of Maranhão, Sao Luis 65055-310, Brazil
Interests: immunology; pharmacology; pathology; inflammation; immunomodulators; Leishmaniasis; tumor; cellular biology; molecular biology; biochemistry
Dr. Flávia De Oliveira Cardoso

E-Mail Website
Guest Editor
Laboratory of Immunomodulation and Protozoology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil
Interests: Leishmaniasis; Chagas disease; immunopathology; diagnosis; treatment; epidemiology; molecular biology
Dr. Kátia Da Silva Calabrese

E-Mail Website
Guest Editor
Laboratory of Immunomodulation and Protozoology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil
Interests: Leishmaniasis; Chagas disease; inflammation; host-pathogen interaction; extracellular matrix; immunopathology; toxoplasmosis; vaccine; treatment, murine model

Special Issue Information

Dear Colleagues,

Leishmaniasis and Chagas disease are neglected tropical diseases, prevalent in tropical regions, especially developing countries. Leishmaniases are a group of diseases that affects around 700,000 to 1 million people worldwide annually. Chagas disease is caused by Trypanosoma cruzi, and it is estimated that there are about 6 to 7 million people infected with it worldwide. In Brazil, visceral leishmaniasis is considered one of the top parasitic diseases with outbreak and mortality potential, while Chagas disease is the fourth cause of death resulting from infectious and parasitic diseases. Clinical outcomes of both diseases depend on the complexity of the factors involved, related both to the parasite (genetic variability, inoculum, infectivity, pathogenicity, virulence, and inoculation pathways) and to the host (age, sex, nutrition, immune profile, and species). Few effective therapeutic options are available for both diseases, with considerable side effects and long treatment periods, in addition to an increasing development of parasite resistance to the drugs in current use. The complexity of the factors involved in the immunopathology of both Leishmaniasis and Chagas disease influences the disease pathogenesis, chemotherapy outcome, and control, highlighting the need for further studies to improve our understanding of these relationships.

This Special Issue aims to report new insights into interdisciplinary approaches covering host–parasite and vector interaction, immune response of hosts, new molecular pathways for parasite survival and persistence, new drug development and mechanisms of antiparasitic drugs, as well as control, epidemiology, and vaccine development. Studies focusing on immunopathogeny and diagnosis, host defense, survival–resistance mechanisms, host–pathogen interactions, immune response, virulence factors, molecular diagnosis, immunological diagnosis, drug and vaccine development, pharmacological resistance, phytotherapy, synthetic compounds, drug repurposing, mechanisms of action, toxicology, preclinical trials, vaccine adjuvant, vaccine antigen, antibody, clinical and epidemiological insights, clinical manifestations, risk factors, distribution, ecology transmission, life cycle, wild cycle, reservoirs, and species taxonomy are welcome. We envision that this Special Issue will introduce valuable insights regarding Leishmaniasis and Chagas disease management.

Prof. Dr. Fernando Almeida-Souza
Dr. Flávia De Oliveira Cardoso
Dr. Kátia Da Silva Calabrese
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Biology is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

 

Keywords

  • Leishmaniasis
  • Chagas disease
  • immunopathogeny
  • diagnosis
  • epidemiology
  • control
  • clinical studies
  • treatment
  • vaccine
 

Published Papers (4 papers)

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Research

15 pages, 3461 KiB  
Article
Vascular Growth Factor Inhibition with Bevacizumab Improves Cardiac Electrical Alterations and Fibrosis in Experimental Acute Chagas Disease
by Lindice Mitie Nisimura, Roberto Rodrigues Ferreira, Laura Lacerda Coelho, Gabriel Melo de Oliveira, Beatriz Matheus Gonzaga, Marcelo Meuser-Batista, Joseli Lannes-Vieira, Tania Araujo-Jorge and Luciana Ribeiro Garzoni
Biology 2023, 12(11), 1414; https://doi.org/10.3390/biology12111414 - 10 Nov 2023
Viewed by 1033
Abstract
Chagas disease (CD) caused by Trypanosoma cruzi is a neglected illness and a major reason for cardiomyopathy in endemic areas. The existing therapy generally involves trypanocidal agents and therapies that control cardiac alterations. However, there is no treatment for the progressive cardiac remodeling [...] Read more.
Chagas disease (CD) caused by Trypanosoma cruzi is a neglected illness and a major reason for cardiomyopathy in endemic areas. The existing therapy generally involves trypanocidal agents and therapies that control cardiac alterations. However, there is no treatment for the progressive cardiac remodeling that is characterized by inflammation, microvasculopathy and extensive fibrosis. Thus, the search for new therapeutic strategies aiming to inhibit the progression of cardiac injury and failure is necessary. Vascular Endothelial Growth Factor A (VEGF-A) is the most potent regulator of vasculogenesis and angiogenesis and has been implicated in inducing exacerbated angiogenesis and fibrosis in chronic inflammatory diseases. Since cardiac microvasculopathy in CD is also characterized by exacerbated angiogenesis, we investigated the effect of inhibition of the VEGF signaling pathway using a monoclonal antibody (bevacizumab) on cardiac remodeling and function. Swiss Webster mice were infected with Y strain, and cardiac morphological and molecular analyses were performed. We found that bevacizumab significantly increased survival, reduced inflammation, improved cardiac electrical function, diminished angiogenesis, decreased myofibroblasts in cardiac tissue and restored collagen levels. This work shows that VEGF is involved in cardiac microvasculopathy and fibrosis in CD and the inhibition of this factor could be a potential therapeutic strategy for CD. Full article
(This article belongs to the Special Issue Advances in Leishmaniasis and Chagas Disease: Biology, Epidemiology, Treatment and Control)
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16 pages, 4616 KiB  
Article
Effectiveness of Systemic Insecticide Dog Treatment for the Control of Chagas Disease in the Tropics
by Edem Fiatsonu, Aniruddha Deka and Martial L. Ndeffo-Mbah
Biology 2023, 12(9), 1235; https://doi.org/10.3390/biology12091235 - 13 Sep 2023
Viewed by 941
Abstract
Chagas disease, caused by Trypanosoma cruzi and transmitted by triatomines, can lead to severe cardiac issues and mortality in many mammals. Recent studies have shown that systemic insecticide treatment of dogs is highly effective in killing triatomines. Here, we assessed the impact of [...] Read more.
Chagas disease, caused by Trypanosoma cruzi and transmitted by triatomines, can lead to severe cardiac issues and mortality in many mammals. Recent studies have shown that systemic insecticide treatment of dogs is highly effective in killing triatomines. Here, we assessed the impact of dog treatment on T. cruzi transmission. We developed a mathematical model of T. cruzi transmission among triatomines, dogs, humans, and rodents. We used the model to evaluate the impact of dog treatment regimens on T. cruzi transmission dynamics to determine their effectiveness in reducing T. cruzi infection among hosts. We show that a 3-month treatment regimen may reduce T. cruzi incidence among humans by 59–80% in a high transmission setting, and 26–82% in a low transmission setting. An annual treatment may reduce incidence among humans by 49–74% in a high transmission setting, and by 11–76% in a low transmission setting. However, dog treatment may substantially increase T. cruzi prevalence among dogs if dog consumption of dead triatomines increases. Our model indicates that dog treatment may reduce T. cruzi infections among humans, but it may increase infections in dogs. Therefore, a holistic approach targeting different hosts is necessary for Chagas elimination. Full article
(This article belongs to the Special Issue Advances in Leishmaniasis and Chagas Disease: Biology, Epidemiology, Treatment and Control)
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18 pages, 5167 KiB  
Article
Antitrypanosomal Activity of 1,2,3-Triazole-Based Hybrids Evaluated Using In Vitro Preclinical Translational Models
by Lorraine Martins Rocha Orlando, Leonardo da Silva Lara, Guilherme Curty Lechuga, Giseli Capaci Rodrigues, Omar Ginoble Pandoli, Druval Santos de Sá and Mirian Claudia de Souza Pereira
Biology 2023, 12(9), 1222; https://doi.org/10.3390/biology12091222 - 08 Sep 2023
Viewed by 906
Abstract
Chagas disease therapy still relies on two nitroderivatives, nifurtimox and benznidazole (Bz), which have important limitations and serious adverse effects. New therapeutic alternatives for this silent disease, which has become a worldwide public health problem, are essential for its control and elimination. In [...] Read more.
Chagas disease therapy still relies on two nitroderivatives, nifurtimox and benznidazole (Bz), which have important limitations and serious adverse effects. New therapeutic alternatives for this silent disease, which has become a worldwide public health problem, are essential for its control and elimination. In this study, 1,2,3-triazole analogues were evaluated for efficacy against T. cruzi. Three triazole derivatives, 1d (0.21 µM), 1f (1.23 µM), and 1g (2.28 µM), showed potent activity against trypomastigotes, reaching IC50 values 10 to 100 times greater than Bz (22.79 µM). Promising candidates are active against intracellular amastigotes (IC50 ≤ 6.20 µM). Treatment of 3D cardiac spheroids, a translational in vitro model, significantly reduced parasite load, indicating good drug diffusion and efficacy. Oral bioavailability was predicted for triazole derivatives. Although infection was significantly reduced without drug pressure in a washout assay, the triazole derivatives did not inhibit parasite resurgence. An isobologram analysis revealed an additive interaction when 1,2,3-triazole analogs and Bz were combined in vitro. These data indicate a strengthened potential of the triazole scaffold and encourage optimization based on an analysis of the structure–activity relationship aimed at identifying new compounds potentially active against T. cruzi. Full article
(This article belongs to the Special Issue Advances in Leishmaniasis and Chagas Disease: Biology, Epidemiology, Treatment and Control)
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14 pages, 1718 KiB  
Article
In Vitro Antioxidant and Antitrypanosomal Activities of Extract and Fractions of Terminalia catappa
by Sandra Alves de Araújo, Aldilene da Silva Lima, Cláudia Quintino da Rocha, Henrique Previtalli-Silva, Daiana de Jesus Hardoim, Noemi Nosomi Taniwaki, Kátia da Silva Calabrese, Fernando Almeida-Souza and Ana Lucia Abreu-Silva
Biology 2023, 12(7), 895; https://doi.org/10.3390/biology12070895 - 22 Jun 2023
Cited by 1 | Viewed by 1243
Abstract
Chagas disease is a severe infectious and parasitic disease caused by the protozoan Trypanosoma cruzi and considered a public health problem. Chemotherapeutics are still the main means of control and treatment of the disease, however with some limitations. As an alternative treatment, plants [...] Read more.
Chagas disease is a severe infectious and parasitic disease caused by the protozoan Trypanosoma cruzi and considered a public health problem. Chemotherapeutics are still the main means of control and treatment of the disease, however with some limitations. As an alternative treatment, plants have been pointed out due to their proven pharmacological properties. Many studies carried out with Terminalia catappa have shown several biological activities, but its effect against T. cruzi is still unknown. The objective of this work is to evaluate the therapeutic potential of extracts and fractions obtained from T. catappa on the parasite T. cruzi, in addition to analyzing its antioxidant activity. T. catappa ethyl acetate fraction were produced and submitted the chemical characterization by Liquid Chromatography Coupled to Mass Spectrometry (LC-MS). From all T. catappa extracts and fractions evaluated, the ethyl acetate and the aqueous fraction displayed the best antioxidant activity by the 2,2-diphenyl-1-picryl-hydrazyl (DPPH) radical scavenging method (IC50 of 7.77 ± 1.61 and 5.26 ± 1.26 µg/mL respectively), and by ferric ion reducing (FRAP) method (687.61 ± 0.26 and 1009.32 ± 0.13 µM of Trolox equivalent/mg extract, respectively). The ethyl acetate fraction showed remarkable T. cruzi inhibitory activity with IC50 of 8.86 ± 1.13, 24.91 ± 1.15 and 85.01 ± 1.21 µg/mL against epimastigotes, trypomastigotes and intracellular amastigotes, respectively, and showed no cytotoxicity for Vero cells (CC50 > 1000 µg/mL). The treatment of epimastigotes with the ethyl acetate fraction led to drastic ultrastructural changes such as the loss of cytoplasm organelles, cell disorganization, nucleus damage and the loss of integrity of the parasite. This effect could be due to secondary compounds present in this extract, such as luteolin, kaempferol, quercetin, ellagic acid and derivatives. The ethyl acetate fraction obtained from T. catappa leaves can be an effective alternative in the treatment and control of Chagas disease, and material for further investigations. Full article
(This article belongs to the Special Issue Advances in Leishmaniasis and Chagas Disease: Biology, Epidemiology, Treatment and Control)
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