4.5 Article

Contribution of the TIM-3/Gal-9 immune checkpoint to tropical parasitic diseases

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ACTA TROPICA
卷 238, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.actatropica.2022.106792

关键词

Neglected tropical diseases; Immune checkpoint; TIM-3; Antiparasitic drugs; Galectin-9; T cell exhaustion

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Neglected tropical parasitic diseases (NTD) are prevalent and require cost-effective treatments. The TIM-3/galectin-9 checkpoint has been shown to play a key role in antiparasitic immunity. This review discusses the role of this checkpoint in seven major NTD and evaluates the potential use of anti-TIM-3 antibodies as a therapeutic approach. The use of anti-TIM-3 antibodies has shown promising results in cases of leishmaniasis, malaria, and schistosomiasis, but has been less effective in echinococcosis and Chagas disease.
Neglected tropical parasitic diseases (NTD) are prevalent in many countries and cost-effective treatments remain urgently needed. Novel approaches have been proposed to address these diseases through an action on immune co-inhibitory checkpoints which are exploited by parasites to evade the immune system. Among these check -points, TIM-3 has been shown to play a key role in antiparasitic immunity via a repression and functional attenuation of CD4+ and/or CD8+ T-cells. The present review discusses the role of the TIM-3/galectin-9 checkpoint in seven major NTD: Chagas disease, leishmaniasis and malaria (3 trypanosomatid infections), schistosomiasis, toxoplasmosis, echinococcosis and filariasis (4 helminth infections). In each case, the role of the checkpoint has been analyzed and the use of anti-TIM-3 antibodies evaluated as a potential therapeutic approach. In general, the parasitic infection is coupled with an upregulation of TIM-3 expressed on T cells, but not necessarily with an exhaustion of those T cells. In several cases, the use of anti-TIM-3 antibodies represent a possible strategy to reinforce the clearance and to reduce the parasite load. Promising data have been reported in cases of leishmaniasis, malaria and schistosomiasis, whereas a similar approach proved much less efficient (if not deleterious) in cases of echinococcosis and the Chagas disease. Nevertheless, the TIM-3 checkpoint warrants further consideration as a potential immune target to combat these pathologies, using antibodies or drugs capable of reducing directly or indirectly the expression and function of the checkpoint, to restore an immune control.

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