## Abstract To identify tumor‐associated antigens as putative targets for developing immunotherapies against prostate cancer, we investigated the ability of T cells derived from the peripheral blood lymphocytes of prostate cancer patients to recognize autologous tumor cells. The technical challenge
Spontaneous apoptosis of tumor-specific tetramer+ CD8+ T lymphocytes in the peripheral circulation of patients with head and neck cancer
✍ Scribed by Andreas E. Albers; Carsten Schaefer; Carmen Visus; William Gooding; Albert B. DeLeo; Theresa L. Whiteside
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 205 KB
- Volume
- 31
- Category
- Article
- ISSN
- 1043-3074
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✦ Synopsis
Abstract
Background
In cancer, tumor escape from the host immune system includes apoptosis of circulating CD3^+^CD8^+^ effector T lymphocytes. Here, we compare sensitivity to apoptosis of virus‐ with tumor‐specific circulating CD8^+^ T cells in patients with head and neck cancer.
Methods
Wild‐type p53 peptide‐specific (p53~264‐272~ and p53~149‐157~) and viral peptide‐specific (EBV BMLF~259‐267~ and CMVpp65~495‐503~) tetramers were used to measure the frequency of reactive T cells by flow cytometry. Annexin V (ANX) binding to circulating 7‐amino‐actinomycin D‐negative but tetramer^+^CD8^+^ T cells in PBMC obtained from 21 patients with head and neck cancer and 11 normal controls (NC) was evaluated.
Results
In patients with head and neck cancer, a higher percentage of tetramer^+^CD8^+^ than tetramer^−^CD8^+^ T cells bound ANX (p < .023–.005). Although most tumor‐epitope^+^CD8^+^ T cells bound ANX, lower percentages of virus‐specific CD8^+^ T cells were ANX^+^ in the same patients.
Conclusions
Preferential demise of circulating tumor‐specific CD8^+^ T cells and their paucity in head and neck cancer contribute to tumor escape. © 2009 Wiley Periodicals, Inc. Head Neck, 2009
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