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Toxocara Canis-Originated Recombinant C-Type Lectin Improves the Disability Scores of Experimental Autoimmune Encephalomyelitis in Murine in Vivo Models Publisher Pubmed



Shahbakhsh M1 ; Jalousian F1 ; Hosseini SH1 ; Naser Moghadasi A2 ; Shayan P1 ; Bonab SF3 ; Malekzade P1 ; Vojgani M3 ; Lalehpour M4
Authors
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Authors Affiliations
  1. 1. Department of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
  2. 2. Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Immunology and Biology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Pathology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

Source: Journal of Neuroimmunology Published:2025


Abstract

Background: The recombinant C-type lectin protein (r-CTL) derived from Toxocara canis larvae is thought to play a role in promoting regulatory T cell-dominant immune responses in toxocariasis. This study aimed to highlight the therapeutic potential of the r-CTL protein in improving the disability scores of EAE by enhancing the Foxp3+-CD25+ T cells population. Methods: The r-CTL was expressed in prokaryotic systems and purified using Ni-NTA spin columns. Balb/C57 mice were divided into six groups, with EAE induced in four of them, excluding the healthy control group and the group receiving only r-CTL treatment. Group I (n = 10) received r-CTL treatment post EAE induction, Group II (n = 10) underwent EAE induction only, Group III (n = 5) received treatment with E. coli lysate proteins containing E. coli BL21 and plasmid pET32a without r-CTL after EAE induction, Group IV (n = 5) received sterile PBS after EAE induction, Group V (n = 5) served as the healthy control group, and Group VI (n = 5) received only r-CTL treatment. Results: The study's findings revealed that r-CTL treatment significantly decreased disability scores in EAE-induced mice. There was a notable increase in the population of CD4+, CD25+, FOXP3+ regulatory T cells following r-CTL treatment. The gene expression levels of IL-10, FOXP3, and GATA3 were significantly elevated in the r-CTL treated group, while the expression of T-bet and RORγ genes was reduced. Treatment with r-CTL significantly mitigated cell infiltration and demyelination in both the spinal cord and brain. Conclusion: In conclusion, the observed improvements in disability scores in the EAE mouse model suggest that r-CTL protein could be a potential new treatment approach worth further investigation. © 2025