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  <title><![CDATA[PhD Proposal by Elizabeth Campbell]]></title>
  <body><![CDATA[<p><strong>Elizabeth Campbell</strong></p>

<p><strong>PhD Proposal Presentation</strong></p>

<p>&nbsp;</p>

<p><strong>Date:</strong> November 6, 2017</p>

<p><strong>Time:</strong> 1-3pm</p>

<p><strong>Location:</strong> IBB 1128 (Georgia Institute of Technology)</p>

<p>&nbsp;</p>

<p><strong>Committee:</strong></p>

<p>Advisor: Todd A. Sulchek, PhD</p>

<p>Edmund K. Waller, MD, PhD</p>

<p>Krishnendu Roy, PhD</p>

<p>Edward A. Botchwey, PhD</p>

<p>Gabe A. Kwong, PhD</p>

<p>&nbsp;</p>

<p><strong>Title: </strong>Crosslinking activated immune cells with tumor cells using a novel Janus particle platform</p>

<p>&nbsp;</p>

<p><strong>Abstract: </strong>Although CD8+ T cells commonly migrate to solid tumors, cancer cells suppress and evade these cells through a variety of intrinsic and extrinsic mechanisms. As a result, recruited cytotoxic T cells are rendered anergic or apoptotic and are thus ineffective at killing cancer cells. Cancer is traditionally treated using chemotherapy, radiation, and surgery; however, these treatments are often unsuccessful alone and are usually used in some combination &ndash; resulting in numerous side effects. Antibody therapy, include PD-L1 blockade, has shown great promise but only a subset of cancer patients respond to treatment. We have developed a novel particle platform capable of two distinct biological functions. The overarching hypothesis of the proposed research is that physically crosslinking and activating CD8+ T cells with cancer cells will enhance cytotoxicity. We will optimize a particle to maximize T cell activation and subsequent cytotoxicity. This will inform the design of our engineered Janus particle capable of specifically targeting cancer cells and physically crosslinking T cells and selected cancer cells. Enhanced particle-mediated T cell cytotoxicity will be assessed for specificity and efficacy using in vitro co-cultures</p>
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