Chitinase-3-like 1 regulates TH2 cells, TFH cells and IgE following helminth infection

Abstract

Data from patient cohorts and mouse models of atopic dermatitis, food allergy and asthma strongly support a role for the chitinase-like protein ChI3L1 in allergic disease. To address whether CHI3L1 also contributes to TH2 responses following nematode infection, we infected Chi3l1-/- mice with Heligmosomoides polygyrus (Hp) and analyzed T cell responses. Not surprisingly, we observed impaired TH2 responses in Hp-infected Chi3l1-/- mice. However, we also found that T cell intrinsic expression of Chi3l1 was required for ICOS upregulation following activation of naive CD4 T cells and was necessary for the development of the IL-4+ TFH subset, which supports germinal center (GC) B cell reactions and IgE responses. The requirement for Chi3l1 in TFH and IgE responses was also seen following alum-adjuvanted vaccination. While Chi3l1 was critical for IgE humoral responses it was not required for vaccine or infection induced IgG1 responses. These results suggest that Chi3l1 specifically modulates IgE responses that are highly dependent on help from IL-4-producing TFH cells.