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CpG ODN D35 improves the response to abbreviated low-dose pentavalent antimonial treatment in non-human primate model of cutaneous leishmaniasis.

Authors :
Thacker SG
McWilliams IL
Bonnet B
Halie L
Beaucage S
Rachuri S
Dey R
Duncan R
Modabber F
Robinson S
Bilbe G
Arana B
Verthelyi D
Source :
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2020 Feb 28; Vol. 14 (2), pp. e0008050. Date of Electronic Publication: 2020 Feb 28 (Print Publication: 2020).
Publication Year :
2020

Abstract

Cutaneous leishmaniasis (CL) affects the lives of 0.7-1 million people every year causing lesions that take months to heal. These lesions can result in disfiguring scars with psychological, social and economic consequences. Antimonials are the first line of therapy for CL, however the treatment is lengthy and linked to significant toxicities; further, its efficacy is variable and resistant parasites are emerging. Shorter or lower dose antimonial treatment regimens, which would decrease the risk of adverse events and improve patient compliance, have shown reduced efficacy and further increase the risk emergence of antimonial-resistant strains. The progression of lesions in CL is partly determined by the immune response it elicits, and previous studies showed that administration of immunomodulatory type D CpG ODNs, magnifies the immune response to Leishmania and reduces lesion severity in nonhuman primates (NHP) challenged with Leishmania major or Leishmania amazonensis. Here we explored whether the addition of a single dose of immunomodulating CpG ODN D35 augments the efficacy of a short-course, low-dose pentavalent antimonial treatment regimen. Results show that macaques treated with D35 plus 5mg/kg sodium stibogluconate (SbV) for 10 days had smaller lesions and reduced time to re-epithelization after infection with Leishmania major. No toxicities were evident during the studies, even at doses of D35 10 times higher than those used in treatment. Critically, pentavalent antimonial treatment did not modify the ability of D35 to induce type I IFNs. The findings support the efficacy of D35 as adjuvant therapy for shorter, low dose pentavalent antimonial treatment.<br />Competing Interests: Daniela Verthelyi is named as an inventor on a patent covering D35 filed on April, 1999, US 7,960,356 B2 under the Serial number 60/128,898. WO2000/061151. The patent is owned by the US government and licensed to DNDi.

Details

Language :
English
ISSN :
1935-2735
Volume :
14
Issue :
2
Database :
MEDLINE
Journal :
PLoS neglected tropical diseases
Publication Type :
Academic Journal
Accession number :
32109251
Full Text :
https://doi.org/10.1371/journal.pntd.0008050