CD1d expression by dendritic cells and CD40L or ICOS expression by NKT cells is dispensable for NKT-enhanced humoral immunity (61.16)
Mark L. Lang, Hemangi B. Shah, Sunil K. Joshi, Susan Kovats, Gillian A. Lang, T. Scott Devera
Abstract
Mark L. Lang, Hemangi B. Shah, Sunil K. Joshi, Susan Kovats, Gillian A. Lang, T. Scott Devera
Abstract
Abstract CD1d-binding glycolipids have potent adjuvant effects on T-dependent humoral immune responses to co-administered protein antigen. We reported previously that cognate interactions between CD1d expressed on B cells and the T cell antigen receptor of natural Killer T (NKT)was critical for the adjuvant effect of the CD1d ligand α-galactosyl ceramide (α-GC). We have therefore tested the hypothesis that CD1d-expressing dendritic cells contribute to NKT-enhanced antibody production and that NKT cells provide co-receptor-mediated B cell help. Using bone marrow chimera approaches, we demonstrate that CD1d-expression by dendritic cells as well as CD40L and ICOS expression by NKT cells are dispensable for the adjuvant effects of α-GC. This reinforces the concept that the primary mode of NKT activation is through CD1d-expressing B cells and indicates that NKT cells utilize mechanisms distinct from that of helper T cells to provide specific B cell help.
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Abstract CD1d-binding glycolipids have potent adjuvant effects on T-dependent humoral immune responses to co-administered protein antigen. We reported previously that cognate interactions between CD1d expressed on B cells and the T cell antigen receptor of natural Killer T (NKT)was critical for the adjuvant effect of the CD1d ligand α-galactosyl ceramide (α-GC). We have therefore tested the hypothesis that CD1d-expressing dendritic cells contribute to NKT-enhanced antibody production and that NKT cells provide co-receptor-mediated B cell help. Using bone marrow chimera approaches, we demonstrate that CD1d-expression by dendritic cells as well as CD40L and ICOS expression by NKT cells are dispensable for the adjuvant effects of α-GC. This reinforces the concept that the primary mode of NKT activation is through CD1d-expressing B cells and indicates that NKT cells utilize mechanisms distinct from that of helper T cells to provide specific B cell help.
Key concepts: CD1D, Natural killer T cell, CD40, Biology, Immune system, Cell biology, CD1, Antigen