Ex Vivo Analysis of the Association of GFP-Expressing <i>L. aethiopica</i> and <i>L. mexicana</i> with Human Peripheral Blood-Derived (PBD) Leukocytes over 24 Hours
2024
Medhavi Ranatunga | Andrew Deacon | Laurence S. Harbige | Paul Dyer | Joshua Boateng | Giulia T. M. Getti
Leishmania parasites are transmitted to mammalian hosts through the bite of sandflies. These parasites can infect phagocytic cells (macrophages, dendritic cells, and neutrophils) and non-phagocytic cells (B cells and fibroblasts). In mice models, the disease development or resolution is linked to T cell responses involving inflammatory cytokines and the activation of macrophages with the M1/M2 phenotype. However, this mechanism does not apply to human infection where a more complex immunological response occurs. The understanding of interactions between immune cells during Leishmania infection in humans is still limited, as current infection models focus on individual cell types or late infection using controlled human infection models (CHIMs). This study investigated the early parasite infection in freshly isolated peripheral blood-derived (PBD) leukocytes over 24 h. Flow cytometer analysis is used in immunophenotyping to identify different subpopulations. The study found that among the <i>L. aethiopica<sup>GFP</sup></i>-associated leukocytes, most cells were neutrophils (55.87% ± 0.09 at 4 h) and monocytes (23.50% ± 0.05% at 24 h). B cells were 12.43% ± 0.10% at 24 h. Additionally, 10–20% of GFP<sup>+</sup> leukocytes did not belong to the aforementioned cell types, and further investigation revealed their identity as CD4<sup>+</sup> T cells. Data not only confirm previous findings of Leishmania infection with PBD leukocytes and association with B cells but also suggest that CD4<sup>+</sup> T cells might influence the early-stage of infection.
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