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

Archambault, A.S., Carrero, J.A., Barnett, L.G., McGee, N.G., Sim, J., Wright, J.O., Raabe, T., Chen, P., Ding, H., Allenspach, E.J., Dragatsis, I., Laufer, T.M., Wu, G.F.; Journal of Immunology Volume 191, Issue 2, 15 July 2013, Pages 545-550 Read More

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.

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Posted on July 25, 2013
Posted in: Axon Injury & Repair, Publications Authors: