We established gastric cancer-specific CD8 1 T-cell (T CD8 1) lines derived from different lymphocyte sources in the same patients by repeated stimulation with mitomycin-C-treated autologous tumor cells with low-dose interleukin-2, and we compared recognition patterns among the T CD8 1 derived from
Analysis of tumor antigen-specific T cells and antibodies in cancer patients treated with radiofrequency ablation
✍ Scribed by Melanie Widenmeyer; Yuriy Shebzukhov; Sebastian P. Haen; Diethard Schmidt; Stephan Clasen; Andreas Boss; Dmitri V. Kuprash; Sergei A. Nedospasov; Arnulf Stenzl; Hermann Aebert; Dorothee Wernet; Stefan Stevanović; Philippe L. Pereira; Hans-Georg Rammensee; Cécile Gouttefangeas
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- French
- Weight
- 445 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Radiofrequency (RF) ablation is a minimally invasive technique routinely applied for the treatment of primary and secondary liver tumors. It induces cell death by thermal coagulative necrosis of tumor tissues, whereas cellular metabolism can still take place in a transition zone surrounding the necrotic area. An increase in heat shock protein expression occurs shortly after treatment, suggesting that the induction of activating signals may stimulate the host immune system. In addition, various effects on immune effectors have also been observed, including stimulation of tumor‐directed T lymphocytes. Here, we prospectively assessed the activation of tumor antigen‐specific antibodies, as well as antigen‐specific CD4^+^ and CD8^+^ T cells in patients suffering from primary or secondary malignancies and treated by RF ablation with or without concomitant chemotherapy. An increase of antibodies (in 4 patients of 49), CD4^+^ T cells or CD8^+^ T cells (in 2 patients of 49) could be detected several weeks to months following intervention. These findings suggest that in addition to the local control of tumor growth, RF ablation can provide the appropriate conditions for activating tumor‐antigen specific immune responses.
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