Induction of tolerogenic properties by Anisakis larval antigens on murine dendritic cells

• Published in: Parasite immunology 2019-04, Vol.41 (4), p.e12616-n/a
• Main Authors: Zamora, Vega, Rodero, Marta, Andreu‐Ballester, Juan Carlos, Mendez, Susana, Cuéllar, Carmen
• Format: Article
• Language: English
• Subjects: Animals; Anisakis; Anisakis - embryology; Anisakis - immunology; Anthelmintic agents; Antigens; Antigens, Helminth - immunology; B7-1 Antigen; BALB/c mice; Bone marrow; C57BL/6J mice; CD80 antigen; CD86 antigen; CpG islands; Dendritic cells; Dendritic Cells - immunology; Immunomodulation; Inflammation; Interleukin-10 - metabolism; Interleukin-12 - metabolism; interleukin‐10; interleukin‐12; Larva - immunology; Larva - metabolism; Lipopolysaccharides; Lipopolysaccharides - pharmacology; Lymphocytes T; Major histocompatibility complex; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Oligodeoxyribonucleotides - pharmacology; Rodents; Signal Transduction - immunology; T-Lymphocytes, Regulatory - immunology; Th2 Cells - immunology; TLR4 protein; TLR9 protein; Toll-Like Receptor 4 - agonists; Toll-Like Receptor 9 - agonists; Toll-like receptors
• ISSN: 0141-9838; 1365-3024
• DOI: 10.1111/pim.12616

Summary Aims The objective of this work is to investigate whether Anisakis simplex larval antigens present immunomodulatory properties by the induction of tolerogenic dendritic cells (DCs) from two strains of mice (BALB/c and C57BL/6J). Methods and Results We used mouse bone marrow‐derived DCs. We determined their antigen‐presenting ability by expression of membrane markers (MHC I and MHC II, CD80, CD86) and intracellular expression levels of IL‐10 and IL‐12 cytokines. We also analysed whether stimulation with A simplex larval antigens is enhanced by the co‐administration of the TLR4 and TLR9 agonists [LPS E coli 026B6 and CpG (ODN1826), respectively]. Two differential types of responses were found in the two mouse strains studied: the BALB/c strain showed an acute and inflammatory response, whereas the C57BL/6J mice developed a more discrete and resistant response. This suggests the coexistence of two opposing responses generated by A simplex larval antigens and confirms that the host genetic basis plays a role in the development of a Th2 or Treg response. Conclusion The study of the mechanisms by which Anisakis manipulates the immune response through anti‐inflammatory molecules is of interest not only for the direct application on the development of anthelmintic strategies, but also for the development of new anti‐inflammatory products.