Immunomodulatory in vitro effects of Trichinella cystatin-like protein on mouse splenocytes

Exp Parasitol. 2023 Sep:252:108585. doi: 10.1016/j.exppara.2023.108585. Epub 2023 Jul 10.

Abstract

Trichinella parasites have developed specific mechanisms allowing successful completion of their life cycle. These mechanisms are in a great part involved in immunomodulation and studying them may provide a valuable insight into the functioning of the immune system. Trichinella products may be also used as potential therapeutic agents to treat immune diseases. This study investigates the immunomodulatory potential of recombinant multi cystatin-like protein (CLP) derived from T. britovi to determine whether CLP has anti-inflammatory properties in vitro. CLP is a highly antigenic glycoprotein present in Trichinella excetory-secretory (ES) products. AlphaFold structure prediction confirms that it consists of three type-two cystatin-like domains. Mouse splenocytes were stimulated in vitro with lipopolysaccharide (LPS) and co-stimulated with recombinant CLP. The culture supernatants were collected and tested for secreted cytokine levels using ELISA. CLP was found to reduce LPS-induced secretion of inflammatory cytokines TNFα and IL-6. On the contrary, in some experimental groups, co-stimulation with CLP resulted in increased secretion of the regulatory cytokine IL-10. The obtained results indicate that CLP has anti-inflammatory properties and future research on its function is advisable, specifically in the context of the therapy of inflammatory disorders.

Keywords: AlphaFold; CD11b; Cystatin-like protein; Cytokines; Immunomodulation; Trichinella.

MeSH terms

  • Animals
  • Cystatins* / metabolism
  • Cystatins* / pharmacology
  • Cytokines / metabolism
  • Immunomodulation
  • Lipopolysaccharides / pharmacology
  • Mice
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Spleen / metabolism
  • Trichinella spiralis*
  • Trichinella*

Substances

  • Lipopolysaccharides
  • Cytokines
  • Cystatins
  • Recombinant Proteins