Cutting Edge: Conditional MHC Class II Expression Reveals a Limited Role for B Cell Antigen Presentation in Primary and Secondary CD4 T Cell Responses
Author(s) -
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
Publication year - 2013
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1201598
Subject(s) - antigen presenting cell , mhc class ii , t cell , microbiology and biotechnology , antigen presentation , priming (agriculture) , experimental autoimmune encephalomyelitis , biology , immunology , immune system , botany , germination
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.
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