E3 ligase RNF128 restricts A. alternata-induced ILC2 activation and type 2 immune response in the murine lung

Sci Rep. 2025 Jan 7;15(1):1193. doi: 10.1038/s41598-025-85227-4.

Abstract

Allergic airway inflammation is a universal airway disease induced by inhaling allergens. Published data show that RNF128, an E3 ligase, promotes Th2 activation in the OVA-induced asthma model. Recent advances have shown that group 2 innate lymphoid cells (ILC2s) produce the cytokines IL-5 and IL-13 to mediate type 2 immune response. However, whether RNF128 regulates ILC2-dependent allergic lung inflammation remains unclear. In this study, we observed greater expression of the E3 ligase RNF128 in ILC2s than in other immune cells. RNF128 deficiency caused a selective increase in the number of peripheral mature ILC2s, and mice with RNF128 deficiency were more susceptible to Alternaria alternata (A. alternata) -induced allergic lung inflammation. Furthermore, RNF128 deficiency increased recruitment of eosinophils and levels of IL-5 and IL-13 in the bronchoalveolar lavage fluid. RNF128 effectively inhibited the expansion of ILC2s and the number of IL-5- and IL-13-producing ILC2s. Specially, RNF128 deficiency promoted the expression of the interleukin-33 (IL-33) receptor ST2 in A. alternata-induced allergic lung inflammation. Above all, our study demonstrated that RNF128 played a key role in A. alternata-induced ILC2 activation and type 2 immune response, suggesting that RNF128 may be an effective therapeutic target for allergic lung inflammation initiated by ILC2s.

Keywords: Allergic lung inflammation; E3 ligase RNF128; Group 2 innate lymphoid cells.

MeSH terms

  • Alternaria* / immunology
  • Animals
  • Bronchoalveolar Lavage Fluid / immunology
  • Disease Models, Animal
  • Female
  • Immunity, Innate
  • Interleukin-1 Receptor-Like 1 Protein / genetics
  • Interleukin-1 Receptor-Like 1 Protein / metabolism
  • Interleukin-13 / metabolism
  • Interleukin-33 / genetics
  • Interleukin-33 / metabolism
  • Interleukin-5 / metabolism
  • Lung* / immunology
  • Lung* / metabolism
  • Lung* / pathology
  • Lymphocytes* / immunology
  • Lymphocytes* / metabolism
  • Mice
  • Mice, Knockout
  • Pneumonia / immunology
  • Th2 Cells / immunology
  • Ubiquitin-Protein Ligases* / genetics
  • Ubiquitin-Protein Ligases* / metabolism

Substances

  • Ubiquitin-Protein Ligases
  • Interleukin-33
  • Interleukin-13
  • Interleukin-5
  • Interleukin-1 Receptor-Like 1 Protein
  • Il1rl1 protein, mouse

Supplementary concepts

  • Alternaria alternata