Sub-optimal dose of Sodium Antimony Gluconate (SAG)-diperoxovanadate combination clears organ parasites from BALB/c mice infected with antimony resistant Leishmania donovani by expanding antileishmanial T-cell repertoire and increasing IFN-γ to IL-10 ratio
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Haldar, Arun Kumar
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Indian Inst Chem Biol, Dept Infect Dis & Immunol, Kolkata 700032, W Bengal, IndiaIndian Inst Chem Biol, Dept Infect Dis & Immunol, Kolkata 700032, W Bengal, India
Haldar, Arun Kumar
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Banerjee, Subha
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Indian Inst Chem Biol, Dept Infect Dis & Immunol, Kolkata 700032, W Bengal, IndiaIndian Inst Chem Biol, Dept Infect Dis & Immunol, Kolkata 700032, W Bengal, India
Banerjee, Subha
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Naskar, Kshudiram
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Indian Inst Chem Biol, Dept Infect Dis & Immunol, Kolkata 700032, W Bengal, IndiaIndian Inst Chem Biol, Dept Infect Dis & Immunol, Kolkata 700032, W Bengal, India
We demonstrate that the combination of sub-optimal doses of Sodium Antimony Gluconate (SAG) and the diperoxovanadate compound K[VO(O-2)(2)(H2O)], also designated as PV6, is highly effective in combating experimental infection of BALB/c mice with antimony resistant (Sb-R) Leishmania donovani (LD) as evident from the significant reduction in organ parasite burden where SAG is essentially ineffective. Interestingly, such treatment also allowed clonal expansion of antileishmanial T-cells coupled with robust Surge of IFN-gamma and concomitant decrease in IL-10 production. The splenocytes from the treated animals generated significantly higher amounts of IFN-gamma inducible parasiticidal effector molecules like superoxide and nitric oxide as compared to the infected group. Our study indicates that the combination of sub-optimal doses of SAG and PV6 may be beneficial for the treatment of SAG resistant visceral leishmaniasis patients. (c) 2009 Published by Elsevier Inc.