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Galectins in Protozoan Parasitic Diseases: Potential Applications in Diagnostics and Therapeutics

Overview
Journal Cells
Publisher MDPI
Date 2023 Dec 9
PMID 38067100
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Abstract

Neglected tropical diseases (NTDs) constitute a group of diseases that generally develop in tropical or subtropical climatic conditions and are related to poverty. Within the spectrum of NTDs, diseases caused by protozoa such as malaria, Chagas disease, and leishmaniasis exhibit elevated mortality rates, thereby constituting a substantial public health concern. Beyond their protozoan etiology, these NTDs share other similarities, such as the challenge of control and the lack of affordable, safe, and effective drugs. In view of the above, the need to explore novel diagnostic predictors and therapeutic targets for the treatment of these parasitic diseases is evident. In this context, galectins are attractive because they are a set of lectins bound to β-galactosides that play key roles in a variety of cellular processes, including host-parasite interaction such as adhesion and entry of parasites into the host cells, and participate in antiparasitic immunity in either a stimulatory or inhibitory manner, especially the galectins-1, -2, -3, and -9. These functions bestow upon galectins significant therapeutic prospects in the context of managing and diagnosing NTDs. Thus, the present review aims to elucidate the potential role of galectins in the diagnosis and treatment of malaria, leishmaniasis, and Chagas disease.

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References
1.
Chao C, Leone J, Vigliano C . Chagas disease: Historic perspective. Biochim Biophys Acta Mol Basis Dis. 2020; 1866(5):165689. DOI: 10.1016/j.bbadis.2020.165689. View

2.
Zhang Y, Jiang N, Zhang T, Chen R, Feng Y, Sang X . Tim-3 signaling blockade with α-lactose induces compensatory TIGIT expression in Plasmodium berghei ANKA-infected mice. Parasit Vectors. 2019; 12(1):534. PMC: 6849286. DOI: 10.1186/s13071-019-3788-x. View

3.
Si Y, Yao Y, Ayala G, Li X, Han Q, Zhang W . Human galectin-16 has a pseudo ligand binding site and plays a role in regulating c-Rel-mediated lymphocyte activity. Biochim Biophys Acta Gen Subj. 2020; 1865(1):129755. DOI: 10.1016/j.bbagen.2020.129755. View

4.
van den Berg T, Honing H, Franke N, van Remoortere A, Schiphorst W, Liu F . LacdiNAc-glycans constitute a parasite pattern for galectin-3-mediated immune recognition. J Immunol. 2004; 173(3):1902-7. DOI: 10.4049/jimmunol.173.3.1902. View

5.
Moxon C, Gibbins M, McGuinness D, Milner Jr D, Marti M . New Insights into Malaria Pathogenesis. Annu Rev Pathol. 2019; 15:315-343. DOI: 10.1146/annurev-pathmechdis-012419-032640. View