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Structure <strong>of</strong> <strong>the</strong> Group<br />

Group Leader<br />

Pr<strong>of</strong>. Dr. Wolfgang Uckert<br />

Scientists<br />

Dr. Boris Engels*<br />

Dr. Haike Gelfort<br />

Dr. Lilian Stärk*<br />

Graduate and<br />

Undergraduate Students<br />

Petra Biese*<br />

Florian Helm*<br />

Elisa Kieback<br />

Matthias Leisegang<br />

Kristina Mahnken*<br />

Simone Reuß<br />

Nicole Scheumann*<br />

Daniel Sommermeyer<br />

Technical Assistants<br />

Uta Fischer<br />

Martina Grabbert<br />

Kordelia Hummel<br />

Janina Kunze*<br />

Irmgard Küttner<br />

Secretariat<br />

Romana Worm<br />

* part <strong>of</strong> <strong>the</strong> period reported<br />

A<br />

B<br />

Figure 2. Prevention <strong>of</strong> autoimmune diabetic<br />

disease mediated by myc-antibody depletion. (A)<br />

B6 splenocytes were transduced with ei<strong>the</strong>r OT-<br />

I/TCRwt (n=5) or OT-I/TCRmyc (n=10) and 2x10 7<br />

TCR-positive cells were injected i.v. into sublethally<br />

irradiated RIP-mOVA mice. Mice which were irradiated<br />

but received no cells served as a negative control<br />

(n=3). Two days after adoptive transfer 500 µg <strong>of</strong><br />

an anti-myc antibody was administered i.p. into all<br />

mice which had received T cells harboring <strong>the</strong> TCRwt<br />

and half <strong>of</strong> <strong>the</strong> mice (n=5) which had received T<br />

cells carrying <strong>the</strong> TCRmyc (arrow). The o<strong>the</strong>r half<br />

(n=5) which had received OT-I/TCRmyc-transduced<br />

cells was not treated with antibody. Mice with blood<br />

glucose levels higher than 14 mM are considered<br />

diabetic. Depicted are mean values <strong>of</strong> all animals in<br />

one group, error bars show <strong>the</strong> standard deviation.<br />

If measurement exceeded <strong>the</strong> upper detection limit<br />

<strong>of</strong> 33.3 mM, values were set as 35 mM to allow <strong>the</strong><br />

calculation <strong>of</strong> mean blood glucose levels. (B) Ten<br />

days after adoptive transfer pancreases <strong>of</strong> mice from<br />

each group were analyzed by immunohistochemistry<br />

with a CD8-specific antibody. In antibody-treated<br />

mice no remaining CD8-positive T cells were found in<br />

β-islets.<br />

Selected Publications<br />

Engels, B, Nößner, E, Frankenberger, B, Blankenstein, T,<br />

Schendel, D, Uckert, W. (2005). Redirecting human T lymphocytes<br />

towards renal cell carcinoma-specificity by retroviral transfer<br />

<strong>of</strong> T cell receptor genes. Hum. Gene Ther. 16, 799-810.<br />

Xue, S-A. Gao, L, Hart, D, Gillmore, R, Qasim, W, Thrasher, A,<br />

Apperley, J, Engels, B, Uckert, W, Morris, E, Stauss, H. (2005).<br />

Elimination <strong>of</strong> human leukemia cells in NOD/SCID mice by<br />

WT1-TCR gene-transduced human T cells. Blood 106, 3062-3067.<br />

Sommermeyer, D, Neudorfer, J, Weinhold, M, Leisegang, M,<br />

Charo, J, Engels, B, Nößner, E. Heemskerk, M, Schendel, DJ,<br />

Blankenstein, T, Bernhard, H, Uckert, W. (2006). Designer T<br />

cells by T cell receptor replacement. Eur. J. Immunol. 36,<br />

3052-3059.<br />

Reuss, S, Biese, P, Cosset, FL, Takeuchi, Y, Uckert, W. (2007).<br />

Suspension packaging cell lines for <strong>the</strong> simplified generation <strong>of</strong><br />

T cell receptor encoding retrovirus vector particles. Gene Therapy<br />

14, 595-603.<br />

Engels, B, Uckert, W. (2007). Redirecting T lymphocyte specificity<br />

by T cell receptor gene transfer – A new era for immuno<strong>the</strong>rapy.<br />

Mol. Aspects Med. 28, 115-142.<br />

Cancer Research 139

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