of the Max - MDC
of the Max - MDC
of the Max - MDC
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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