| Literature DB >> 1324789 |
L Ferradini1, S Roman-Roman, J Azocar, M F Avril, S Viel, F Triebel, T Hercend.
Abstract
Multiple experimental and clinical studies have suggested that the immune system may, to some extent, control the development of melanomas. The presence of tumor-infiltrating lymphocytes could reflect an in situ immune reaction directed to the malignant cells. The characterization of T-cell receptor (TCR) expressed by tumor-infiltrating lymphocytes is one way to precisely analyze these local T-cell responses. In this study, we have assessed the TCR alpha/beta variability in tumor-infiltrating lymphocytes from a subcutaneous metastasis of a melanoma patient. Using the anchored-polymerase chain reaction 268 TCR alpha and 266 TCR beta chain transcripts have been cloned and sequenced. Their analysis shows that the T-cell infiltrate is extremely diverse, with no preferential TCR gene segment usage.Entities:
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Year: 1992 PMID: 1324789
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701