Reduced L-selectin (CD62LLow) expression identifies tumor-specific type 1 T cells from lymph nodes draining an autologous tumor cell vaccine

Sybren L Meijer, Annemiek Dols, Hong-Ming Hu, Yiwei Chu, Pedro Romero, Walter J Urba, Bernard A Fox

Research output: Contribution to journalArticleAcademicpeer-review

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 languageEnglish
Pages (from-to)93-102
Number of pages10
JournalCellular Immunology
Volume227
Issue number2
DOIs
Publication statusPublished - Feb 2004
Externally publishedYes

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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