Cutting edge: Conditional MHC class II expression reveals a limited role for B cell antigen presentation in primary and secondary CD4 T cell responses

  • Angela S. Archambault
  • , Javier A. Carrero
  • , Lisa G. Barnett
  • , Nigel G. McGee
  • , Julia Sim
  • , Jonathan O. Wright
  • , Tobias Raabe
  • , Peiquin Chen
  • , Hua Ding
  • , Eric J. Allenspach
  • , Ioannis Dragatsis
  • , Terri M. Laufer
  • , Gregory F. Wu

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

The activation, differentiation, and subsequent effector functions of CD4 T cells depend on interactions with a multitude of MHC class II (MHCII)-expressing APCs. To evaluate the individual contribution of various APCs to CD4 T cell function, we have designed a new murine tool for selective in vivo expression of MHCII in subsets of APCs. Conditional expression of MHCII in B cells was achieved using a cre-loxP approach. After i.v. or s.c. priming, partial proliferation and activation of CD4 T cells was observed in mice expressing MHCII only by B cells. Restricting MHCII expression to B cells constrained secondary CD4 T cell responses in vivo, as demonstrated in a CD4 T cell-dependent model of autoimmunity, experimental autoimmune encephalomyelitis. These results highlight the limitations of B cell Ag presentation during initiation and propagation of CD4 T cell function in vivo using a novel system to study individual APCs by the conditional expression of MHCII.

Original languageEnglish
Pages (from-to)545-550
Number of pages6
JournalJournal of Immunology
Volume191
Issue number2
DOIs
StatePublished - Jul 15 2013

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