Abstract:SYNOPSIS. Intracardial inoculation of 1–10 million L. donovani in 0.1 ml. of ground spleen suspension from an infected animal (hamster) results in a uniform rise of parasite numbers in the untreated animal over the first 8 days after the inoculation. This rise is highly consistent from experiment to experiment.
Treatment is accomplished by parenteral injection of a compound for 6 successive days in this time interval, starting 24 hours after inoculation.
No known active compound in proper dosage (sodium stibo… Show more
“…The parasite load was expressed in Leishman Donovan units, calculated by the following formula: number of amastigotes per 1,000 cell nuclei ϫ organ weight (milligram) (32).…”
“…The parasite load was expressed in Leishman Donovan units, calculated by the following formula: number of amastigotes per 1,000 cell nuclei ϫ organ weight (milligram) (32).…”
“…(through the tail vein) with freshly purified amastigotes of L. donovani (1 ϫ 10 7 / mouse). Splenic and liver parasite burdens were determined from impression smears after Giemsa staining and are reported as the total parasite load per organ using the formula: organ weight (milligrams) ϫ number of amastigotes per cell nucleus ϫ (2 ϫ 10 5 ) (17). To further evaluate whether these organs contained live parasites, in selected experiments homogenates of these organs were cultured for 2 wk after serial dilution (18).…”
Section: Parasites and Infection Of Micementioning
Dendritic cells (DCs) have been proposed to play a critical role as adjuvants in vaccination and immunotherapy. In this study we evaluated the combined effect of soluble Leishmania donovani Ag (SLDA)-pulsed syngeneic bone marrow-derived DC-based immunotherapy and antimony-based chemotherapy for the treatment of established murine visceral leishmaniasis. Three weekly injections of SLDA-pulsed DCs into L. donovani-infected mice reduced liver and splenic parasite burden significantly, but could not clear parasite load from these organs completely. Strikingly, the conventional antileishmanial chemotherapy (sodium antimony gluconate) along with injections of SLDA-pulsed DCs resulted in complete clearance of parasites from both these organs. Repetitive in vitro stimulation of splenocytes from uninfected or L. donovani-infected mice with SLDA-pulsed DCs led to the emergence of CD4+ T cells with characteristics of Th1 cells. Our data indicate that DC-based immunotherapy enhances the in vivo antileishmanial potential of antimony or vice versa.
“…After Giemsa staining of the smears, the liver parasite burden (I) was calculated from the number of amastigotes/500 hepatocytes and related to the liver weight (P in mg), following the Stauber formula (Stauber L.A. et al, 1958).…”
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