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

被引:37
|
作者
Haldar, Arun Kumar [1 ]
Banerjee, Subha [1 ]
Naskar, Kshudiram [1 ]
Kalita, Diganta [2 ]
Islam, Nashreen S. [2 ]
Roy, Syamal [1 ]
机构
[1] Indian Inst Chem Biol, Dept Infect Dis & Immunol, Kolkata 700032, W Bengal, India
[2] Tezpur Univ, Dept Chem Sci, Tezpur 784028, India
关键词
Leishmania; Peroxovanadate (PV); Sodium Antimony Gluconate (SAG); Antileishmanial T cell; PHOSPHOTYROSINE PHOSPHATASE INHIBITORS; IN-VITRO; MURINE LEISHMANIASIS; ASCOPHYLLUM-NODOSUM; VANADIUM COMPOUNDS; P-GLYCOPROTEIN; NITRIC-OXIDE; KALA-AZAR; ACTIVATION; VANADATE;
D O I
10.1016/j.exppara.2009.02.001
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
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.
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页码:145 / 154
页数:10
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