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Published on: February 15, 2011
Pharmacological management of paracoccidioidomycosis
Maria Aparecida Shikanai Yasuda1
1Universidade de São Paulo, Department of Infectious and Parasitic Diseases, Faculdade de Medicina, Brazil. dmip.secr@hcnet.usp.br
Abstract:
A systemic and endemic emerging mycosis in Latin America, paracoccidioidomycosis, is characterised by its chronicity and by the severity of the disseminated form in healthy individuals, as well as in immunocompromised individuals co-infected with HIV, resulting, in the latter, in a mortality rate in the range of 30 - 45%. The long (several years) duration of treatment results from the immunosuppression induced by the disease or from the survival capacity of the fungus in tissue. A few controlled studies and case reports have shown that fast-acting azolic and sulfa derivatives are useful treatment alternatives for patients presenting milder forms of the disease. However, when using such drugs, treatment regimens of longer duration are required for the maintenance of patients with more severe forms. The search for new alternatives for treating the most severe forms is an ongoing challenge. Novel treatments may be found among new classes of drugs, drug combinations, or agents capable of modulating the immune response, such as a peptide derived from the 43-kDa Paracoccidioides brasiliensis glycoprotein.
Insights
Paracoccidioidomycosis is a severe fungal infection in Latin America, often requiring long treatment. New therapeutic strategies are needed for severe cases, potentially involving immune response modulation.
Area of Science:
- Mycology
- Infectious Diseases
- Immunology
Background:
- Paracoccidioidomycosis is a systemic mycosis endemic to Latin America.
- It is characterized by chronicity and severe disseminated forms in both healthy and immunocompromised individuals, particularly those with HIV co-infection, leading to high mortality rates (30-45%).
- Current treatments, including azoles and sulfa derivatives, require long durations, especially for severe forms, and novel alternatives are sought.
Purpose of the Study:
- To address the challenge of finding new treatment alternatives for severe forms of paracoccidioidomycosis.
- To explore novel therapeutic strategies beyond existing drug classes.
Main Methods:
- Review of existing controlled studies and case reports on azolic and sulfa derivative treatments.
- Identification of potential new therapeutic avenues, including new drug classes, combinations, and immunomodulatory agents.
Main Results:
- Fast-acting azolic and sulfa derivatives show utility for milder forms of paracoccidioidomycosis.
- Longer treatment durations are necessary for severe forms using current therapies.
- The study highlights the ongoing challenge in treating severe paracoccidioidomycosis.
Conclusions:
- Novel treatments for severe paracoccidioidomycosis are urgently needed.
- Potential new treatments may involve new drug classes, drug combinations, or immune response modulators.
- A peptide derived from the 43-kDa Paracoccidioides brasiliensis glycoprotein is identified as a potential immunomodulatory agent.
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