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Sylvie Fournier

Associate Professor; Immunology

Role of the B7/CD28/CTLA-4 costimulatory system in the maintenance of lymphocyte homeostasis and the development of autoimmunity


Lyman Duff Medical Buildingcostimulatory system in the maintenance of lymphocyte homeostasis and the development of autoimmunity
3775 University St., Room 603
Montreal, QC H3A 2B4
Tel: (514) 398-7273
Fax: (514) 398-7052
sylvie [dot] fournier [at] mcgill [dot] ca (Email)

Research Orientations

T lymphocytes require two signals for optimal proliferation and induction of effector functions. Signal one is delivered by the engagement of the T cell antigen receptor (TCR) with the peptide/MHC complex. Signal two is antigen-independent and provided by the ligation of accessory molecules called costimulatory receptors. The requirement for costimulatory signals to induce primary T cell responses suggest that the absence of costimulatory ligands may be a normal mechanism for the maintenance of peripheral T cell tolerance. The corollary of this is that aberrant expression of antigenic peptide/MHC complexes in conjunction with costimulatory ligands would lead to destructive autoimmune processes.

The best-characterized costimulatory receptor expressed on resting T cells is CD28. CD28 is highly homologous to CTLA-4, an inducible protein expressed on T cells. In contrast to CD28, CTLA-4 is a negative regulator of T cell activation. Although these two receptors have opposing functions, they share common ligands. The B7 molecules, B7.1 (CD80) and B7.2 (CD86), are the counter-receptors for both CD28 and CTLA-4.

To gain a better understanding of the influence and importance of the CD28/CTLA-4 system in vivo, we have generated 3 independent transgenic mouse lines that constitutively express the ligand B7.2. This transgenic model has revealed previously unexpected function for the B7.2/CD28 system in the regulation of B cell and CD8+ T cell homeostasis and the development of autoimmune demyelinating disease in the nervous system. Using tools of both cellular and molecular biology, we study this transgenic model to understand the mechanisms that lead to disruption of lymphocyte homeostasis and the development of autoimunity.

Selected Recent Publications

Estrada Guadarrama, JA., N'Diaye, MM., Wolak, K. and Fournier, S. Neither perforin nor Fas deficiency prevents the development of a CD8+ T cell-mediated demyelinating disease (submitted, 2010).

Johnson, TA., Jirik, FR. and Fournier, S. Exploring the roles of CD8(+) T lymphocytes in the pathogenesis of autoimmune demyelination. Semin. Immunopathol. 2010 Mar 18. [Epub ahead of print]

Berard, JL., Wolak, K., Fournier, S. and David, S. Characterization of relapsing-remitting and chronic forms of experimental autoimmune encephalomyelitis in C57BL/6 mice. Glia. 58:434-45.

Yam, KK., Pouliot, P., N'Diaye, MM., Fournier, S., Olivier, M. and Cousineau, B. Innate inflammatory responses to the Gram-positive bacterium Lactococcus lactis. Vaccine, 26:2689-99.

Brisebois, M., Zehntner, S.P., Estrada, J., Owens, T. and Fournier, S. (2006) A pathogenic role for CD8+ T cells in a spontaneous model of demyelinating disease. 177(4):2403-11.

Cadieux, C., Fournier, S., Peterson, A. and Nepveu, A. (2006) Transgenic Mice Expressing the p75 CCAAT-Displacement Protein/Cut Homeobox Isoform Develop a Myeloproliferative Disease–Like Myeloid Leukemia. 66(19):9492-501.