Abstract:
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Leishmania spp. promastigotes preferentially infect host macrophages, where parasite internalization is
facilitated by several host and parasite surface molecules. This study aimed to demonstrate the role of
humoral immunity in Leishmania parasite internalization into host macrophages. First, informed
consent sera were obtained from 67 parasitologically confirmed visceral leishmaniasis patients
reporting to our field treatment centre, Eastern Sudan. Then following titre determination, sera that had
a titre of >102,400 were selected for parasite coating. An in vitro parasite internalization system was
developed to enhance the Leishmania/ macrophage interactions. The mean parasite number per
monocytes was 626 ± 91 for antibody-coated Leishmania donovani, compared to 412 ± 70 uncoated
isolates (p= 0.01). On the other hand, the percentage of infected cells was significantly higher for all
antibody-coated isolates (100%) compared to uncoated ones (40%). This evidence of high infectivity
probably points to the fact that anti-Leishmania antibodies facilitated the parasite uptake by host
macrophages and monocytes-derived macrophages (MDM). Moreover, the rate of parasite uptake by
MDM was significantly higher compared to monocytes (p= 0.00). This could be explained by the fact that
the functional capabilities of fully differentiated macrophages differ from monocytes. In conclusion,
host humoral immunity probably plays a pivotal role in Leishmania parasites internalization into host
macrophages. |