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Scientific Presentations Summer 2009 - Dana-Farber/Harvard ...

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The Effect of PolyIC on Cultured Lymph Node Fibroblastic Reticular Cells<br />

Pamela Cote<br />

Mentor: Shannon J. Turley, PhD<br />

<strong>Dana</strong>-<strong>Farber</strong> Cancer Institute<br />

Fibroblastic reticular cells (FRCs) in the lymph nodes (LNs) have been characterized<br />

as a subset of lymph node stromal cells (LNSCs) with a CD45-, gp38+, CD140a+,<br />

CD31- surface phenotype. These cells have also been found to express MHC Class I<br />

and II, costimulatory molecules (PD-L1, CD80) and adhesion molecules (VCAM-1,<br />

ICAM-1). Expression of these molecules may allow LNSCs to regulate T cell responses<br />

in the LNs and shape immunological tolerance. FRCs are important cells<br />

because they also secrete survival factors for memory and resting T cells in the LNs<br />

and they secrete chemokines which are necessary for the recruitment of Dendritic<br />

cells (DCs) and naïve T cells to the LNs. It has been established that certain viruses<br />

such as the Ebola virus and persistent lymphocytic choriomeningitis (LCMV) infect<br />

FRCs in the LNs which may result in immunological dysfunction and chronic infection.<br />

The purpose of this study is to ascertain whether exposure to PolyIC causes<br />

LNSCs to acquire immunostimulatory potential using flow cytometery. This study<br />

will allow us to determine if viral pathogens or viral products can cause FRCs to<br />

undergo phenotypic changes. Therefore this will allow us to establish whether FRCs<br />

continue to promote self tolerance induction or auto- reactivity of T cells during a<br />

viral infection and to ultimately recognize what important implications these cells<br />

have on immunological disorders.

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