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In vivo accumulation of the same anti-melanoma T cell clone in two different metastatic sites

By Makoto Hishii, David Andrews, Lenora A. Boyle, Johnson T. Wong, Franco Pandolfi, Peter J. van den Elsen and James T. Kurnick

Abstract

In a patient with progressing metastatic melanoma, we showed that the same autologous tumor-cytolytic CD8(+) tumor infiltrating lymphocyte (TIL) clone accumulated in two separate metastatic sites. This clone, which represented three of eight independently derived clones from a tumor deposit on the skin of the abdomen, also represented two of eight clones derived from a skin lesion on the shoulder. This clone could be identified by its use of a unique TCRBV2-nD1n-J1S6 sequence, and could also be detected by single-stranded conformational polymorphism (SSCP) as the dominant TCRBV2-expressing clone among CD8(+) TILs propagated from both shoulder and abdominal lesions. Using SSCP analysis, we also demonstrated that this clone was dominant in the fresh tumor tissue and in all TILs in which CD8(+) were strongly represented, including several separate but parallel cultures. The SSCP pattern for this clone was not apparent among CD4(+) TILs or CD8(+) peripheral blood mononuclear cells. The SSCP analysis of the tumor tissue prior to in vitro culture is an indication that the selection for this anti-tumor cytotoxic T cell clone was a reflection of its in vivo accumulation. Thus, we provide evidence that melanomas are immunogenic and able to select for cytotoxic anti-tumor-specific TIL clones that are expanded in vivo and can circulate to accumulate in different tumor sites. However, because these clones were isolated from progressing tumor metastases, the accumulation of these specific cytotoxic T cells was not sufficient to contain tumor growth

Topics: Biological Sciences
Publisher: The National Academy of Sciences of the USA
Year: 1997
DOI identifier: 10.1073/pnas.94.4.1378
OAI identifier: oai:pubmedcentral.nih.gov:19799
Provided by: PubMed Central
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