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Updated: Apr 19, 2026

Generation of Induced Pluripotent Stem Cells from Human Melanoma Tumor-infiltrating Lymphocytes
Published on: November 11, 2016
Class II transactivator expression in melanoma cells facilitates T-cell engulfment
Mark C Lloyd1, Karoly Szekeres2, Joel S Brown3
1Analytic Microscopy Core, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, U.S.A. Biological Sciences Department, Ecology and Evolution division, University of Illinois at Chicago, Chicago, IL, U.S.A.
Background/Aim:
Melanoma cells express high levels of HLA class II, cell surface antigen-presenting proteins, which is an anomalous phenotype among solid tumors. There has never been a satisfying explanation for how this HLA class II-positive phenotype is related to tumor development. Lugini and colleagues demonstrated that melanoma cells have the capacity to engulf T-cells. We considered the possibility that this capacity could be dependent on HLA class II expression.
Materials And Methods:
We co-cultured melanoma and CD4-positive, labeled, Jurkat-C T-cells. The melanoma cells were transformed with an expression vector for CIITA, the obligate HLA class II gene transactivator. We then assayed for the transfer of label to the melanoma cells.
Results:
CIITA expression facilitated engulfment of the T-cell material but not material from B-cells.
Conclusion:
The results suggest a possible mechanism for HLA class II-positive melanoma cells in blunting an anti-tumor response and suggest a possible target for melanoma therapy.
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