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. 2020 Dec 22;7(1):3. doi: 10.3390/jof7010003

Table 1.

Features of the reported chromoblastomycosis immunotherapeutic approaches.

Immunotherapy Class Immunotherapy Agent Mechanisms Dose Study Protocol Antifungal Association Treatment Outcome
Immunostimulants Imiquimod Toll receptor 7 agonist 5% of imiquimod Human Five times a week (topical) for 6 to 19 months Monotherapy Lesions healed after 6 to 7 months [120]
Five times a week (topical) for 6 to 17 months Monotherapy or ITZ and/or TERB Improvement in clinical aspects [117]
β1,3 glucan T cell proliferation and IFN-γ production 5 mg Human Once a week (IM) for 2 years ITZ Resolution of the majority of lesions [121]
DNA Vaccine DNA-hsp65 vaccine Reduction in NO production 9 mg Mice Once each 15 days (IM) during 15 or 30 days Monotherapy or ITZ and/or AMB Healed injuries and eliminated F. pedrosoi from lesions [127]
Monoclonal antibody (Mab) therapy Mab anti-GlcCer Fungistatic and fungicidal activities NA In vitro NA NA Inhibition of F. pedrosoi growth in vitro and enhanced antifungal activity of murine macrophages [37]
Purified antibodies Purified antibodies anti-Melanin Fungicidal activities NA in vitro NA NA Inhibition of F. pedrosoi growth in vitro [86]

Abbreviations: AMB, amphotericin B; CBM, chromoblastomycosis; IM, intramuscular; ITZ, itraconazole; Mab, monoclonal antibodies; NA, not applied; TERB, terbinafine; GlcCer, glucosylceramides.