Abstract
Reduced expression of CD62L can identify tumor-specific T cells in lymph nodes draining murine tumors. Here, we examined whether this strategy could isolate tumor-specific T cells from vaccinated patients. Tumor vaccine-draining lymph node (TVDLN) T cells of seven patients were separated into populations with reduced (CD62LLow) or high levels of CD62L (CD62LHigh). Effector T cells generated from CD62LLow cells maintained or enriched the autologous tumor-specific type 1 cytokine response compared to unseparated TVDLN T cells in four of four patients showing tumor-specific cytokine secretion. Interestingly, effector T cells generated from CD62LLow or CD62LHigh TVDLN were polarized towards a dominant type 1 or type 2 cytokine profile, respectively. For CD62LLow T cells the type 1 cytokine profile appeared determined prior to culture. Since a tumor-specific type 1 cytokine profile appears critical for mediating anti-tumor activity in vivo, this approach might be used to isolate T cells for adoptive immunotherapy.
| Original language | English |
|---|---|
| Pages (from-to) | 93-102 |
| Number of pages | 10 |
| Journal | Cellular Immunology |
| Volume | 227 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Feb 2004 |
| Externally published | Yes |
Keywords
- Cancer Vaccines/immunology
- Carcinoma, Renal Cell/immunology
- Humans
- Immunotherapy, Adoptive
- Interferon-gamma/biosynthesis
- Interleukin-5/biosynthesis
- Kidney Neoplasms/immunology
- L-Selectin/analysis
- Lymph Nodes/immunology
- Melanoma/immunology
- T-Lymphocytes/immunology
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