Oral-nasopharyngeal dendritic cells mediate T cell-independent IgA class switching on B-1 B cells

PLoS One. 2011;6(9):e25396. doi: 10.1371/journal.pone.0025396. Epub 2011 Sep 29.

Abstract

Native cholera toxin (nCT) as a nasal adjuvant was shown to elicit increased levels of T-independent S-IgA antibody (Ab) responses through IL-5- IL-5 receptor interactions between CD4+ T cells and IgA+ B-1 B cells in murine submandibular glands (SMGs) and nasal passages (NPs). Here, we further investigate whether oral-nasopharyngeal dendritic cells (DCs) play a central role in the induction of B-1 B cell IgA class switch recombination (CSR) for the enhancement of T cell-independent (TI) mucosal S-IgA Ab responses. High expression levels of activation-induced cytidine deaminase, Iα-Cμ circulation transcripts and Iμ-Cα transcripts were seen on B-1 B cells purified from SMGs and NPs of both TCRβ⁻/⁻ mice and wild-type mice given nasal trinitrophenyl (TNP)-LPS plus nCT, than in the same tissues of mice given nCT or TNP-LPS alone. Further, DCs from SMGs, NPs and NALT of mice given nasal TNP-LPS plus nCT expressed significantly higher levels of a proliferation-inducing ligand (APRIL) than those in mice given TNP-LPS or nCT alone, whereas the B-1 B cells in SMGs and NPs showed elevated levels of transmembrane activator and calcium modulator cyclophilin ligand interactor (TACI) expression. Interestingly, high frequencies of IgA+ B-1 B cells were induced when peritoneal IgA⁻ IgM+ B cells were stimulated with mucosal DCs from mice given nasal TNP-LPS plus nCT. Taken together, these findings show that nasal nCT plays a key role in the enhancement of mucosal DC-mediated TI IgA CSR by B-1 B cells through their interactions with APRIL and TACI.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Animals
  • B-Cell Activation Factor Receptor / genetics
  • B-Cell Maturation Antigen / genetics
  • B-Lymphocytes / immunology*
  • Cholera Toxin / immunology
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Female
  • Gene Expression Regulation / immunology
  • Immunoglobulin A / chemistry
  • Immunoglobulin A / immunology*
  • Immunoglobulin Class Switching / immunology*
  • Lipopolysaccharides / immunology
  • Mice
  • Mouth Mucosa / immunology*
  • Nasopharynx / immunology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Submandibular Gland / immunology
  • T-Lymphocytes
  • Tumor Necrosis Factor Ligand Superfamily Member 13 / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • B-Cell Activation Factor Receptor
  • B-Cell Maturation Antigen
  • Caml protein, mouse
  • Immunoglobulin A
  • Lipopolysaccharides
  • RNA, Messenger
  • Tumor Necrosis Factor Ligand Superfamily Member 13
  • trinitrophenyl-lipopolysaccharide
  • Cholera Toxin