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Robert S. Mittler - Department of Surgery - Emory University

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Completed:<br />

Project Number (Principal Investigator) Dates <strong>of</strong> Approved Project: 8/1/2000 – 7/31/02<br />

R21 AI 48471-01 (<strong>Robert</strong> S. <strong>Mittler</strong>)<br />

Source: DAIDS/NIAID<br />

Title <strong>of</strong> Project: The Effect <strong>of</strong> Anti-4-1BB on SIV-Specific Cellular Immunity. The goal <strong>of</strong> this<br />

proposal is to determine whether humanized rat anti-human 4-1BB mAbs enhance development<br />

<strong>of</strong> cell-mediated immunity in Rhesus macaques vaccinated with a DNA + MVA vaccine against<br />

SIV. It is also a study to determine if these antibodies can induce protective anti-viral CTL<br />

immunity in SIV infected macaques.<br />

Role: Principal Investigator<br />

Project Number (Principal Investigator) Dates <strong>of</strong> Approved Project: 03/01/02 – 02/29/06<br />

1 RO1 CA 85860-01A1 (<strong>Robert</strong> .S. <strong>Mittler</strong>)<br />

Source: NIH/NCI<br />

Title <strong>of</strong> Project: Functional Analysis <strong>of</strong> anti-4-1BB mediated tumor immunity. The goal <strong>of</strong> this<br />

project is to determine how best to utilize CD137 mediated signaling to achieve maximal antitumor<br />

efficacy and to elucidate the CD137 mediated molecular and biochemical signaling<br />

events that drive CD8 + T cells to eradicate tumors that they otherwise fail to respond to.<br />

Project Number (Principal Investigator) Dates <strong>of</strong> Approved Project: 04/01/01–03/31/06<br />

1RO1 AI RR49155 (Mark Feinberg)<br />

Source: NIH/NIAIDS<br />

Title <strong>of</strong> Project:<br />

Cellular Immune Responses and AIDS Pathogenesis. This study is designed to test the<br />

hypothesis that SIV pathology develops in monkeys <strong>of</strong> Asian descent because <strong>of</strong> a strong<br />

CD8+ T cell response to the infection whereas monkeys <strong>of</strong> African descent do not develop<br />

pathology as a consequence <strong>of</strong> infection because <strong>of</strong> an absence <strong>of</strong> a discernable CD8+ T cell<br />

response.<br />

Role: Co-Investigator<br />

Project Number (Principal Investigator) Dates <strong>of</strong> Approved Project: 09/30/98 – 02/28/07<br />

PO1 AI 044644-06 (Christian P. Larsen)<br />

Source: NIH/NIAID<br />

Title <strong>of</strong> Project: Transplant Tolerance: Costimulation, Cytokines & Chimerism. The objective <strong>of</strong><br />

this study is to understand the causes that give rise to rejection <strong>of</strong> transplanted organs and to<br />

block them.<br />

Role: Co-Principal Investigator<br />

Current:<br />

Project Number:<br />

1RO1 AI059290-01 (<strong>Robert</strong> S. <strong>Mittler</strong>) Dates <strong>of</strong> Approved Project: 5/01/05-<br />

1/31/10<br />

Source: NIH/NIAIDS<br />

Title <strong>of</strong> Project: CD137 signals in DC during antigen priming induce tolerance.<br />

This study explores the mechanisms through which CD137 signaling regulates antigen priming<br />

<strong>of</strong> T cells by dendritic cells.<br />

Project Number (Principal Investigator) Dates <strong>of</strong> Approved Project: 9/1/2000-8/31/08<br />

2000N-00065 (<strong>Robert</strong> S. <strong>Mittler</strong>)<br />

Source: Centers for Disease Control (CDC)<br />

6

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