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Tumor-Specific CD8+ T Cell Reactivity in the Sentinel Lymph Node of GM-CSF–Treated Stage I Melanoma Patients is Associated with High Myeloid Dendritic Cell Content
Purpose: Impaired immune functions in the sentinel lymph node (SLN) may facilitate early metastatic events during melanoma development. Local potentiation of tumor-specific T cell reactivity may be a valuable adjuvant treatment option. Experimental Design: We examined the effect of locally administe...
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Published in: | Clinical cancer research 2006-05, Vol.12 (9), p.2826-2833 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Purpose: Impaired immune functions in the sentinel lymph node (SLN) may facilitate early metastatic events during melanoma development.
Local potentiation of tumor-specific T cell reactivity may be a valuable adjuvant treatment option.
Experimental Design: We examined the effect of locally administered granulocyte/macrophage-colony stimulating factor (GM-CSF) on the frequency
of tumor-specific CD8+ T cells in the SLN and blood of patients with stage I melanoma. Twelve patients were randomly assigned
to preoperative local administration of either recombinant human GM-CSF or NaCl 0.9%. CD8+ T cells from SLN and peripheral
blood were tested for reactivity in an IFNγ ELISPOT assay against the full-length MART-1 antigen and a number of HLA-A1, HLA-A2,
and HLA-A3–restricted epitopes derived from a range of melanoma-associated antigens.
Results: Melanoma-specific CD8+ T cell response rates in the SLN were one of six for the control group and four of six for the GM-CSF-administered
group. Only one patient had detectable tumor-specific CD8+ T cells in the blood, but at lower frequencies than in the SLN.
All patients with detectable tumor-specific CD8+ T cells had a percentage of CD1a+ SLN-dendritic cells (DC) above the median
(i.e., 0.33%). This association between above median CD1a+ SLN-DC frequencies and tumor antigen–specific CD8+ T cell reactivity
was significant in a two-sided Fisher's exact test ( P = 0.015).
Conclusions: Locally primed antitumor T cell responses in the SLN are detectable as early as stage I of melanoma development and may be
enhanced by GM-CSF-induced increases in SLN-DC frequencies. |
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ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.CCR-05-2431 |