Clinical Cancer Research · 2009 · 184 citations · 42 references
Life SciencesImmunologyOncologyCancer ImmunologyInnate ImmunityTumor ImmunologyCancer ImmunosurveillanceImmuno-oncology BiomarkersImmunohistochemistryTumor AntigensTumor MarkersTumor-associated AntigensImmunosurveillance BiomarkersMelanocytic Tumor PrognosisMelanoma BiomarkersMelanoma-associated AntigensNkg2d-mediated RecognitionS100b ProteinSkin MetastasesSoluble Pattern Recognition Molecules
PURPOSE: Cytotoxic lymphocytes interact with human tumor cells via the activating immunoreceptor NKG2D, recognizing a variety of stress-associated MIC and ULBP surface molecules. However, tumors can escape from this immunosurveillance by shedding NKG2D ligands (NKG2DL), rendering the soluble products detectable in patients' sera. EXPERIMENTAL DESIGN: To elucidate the clinical significance of NKG2DL diversity, we studied their expression on melanoma tissues and their presence as soluble molecules in sera from >200 melanoma patients and compared the latter with the well-established serum marker S100B. RESULTS: Immunohistochemistry revealed a heterogeneous expression of MIC and ULBP2 molecules between and within melanoma metastases. Compared with MIC, ULBP2 was less frequently expressed. Accordingly, elevated levels of soluble ULBP2 (sULBP2) were detected in sera of melanoma patients less frequently than elevated levels of soluble MICA (sMICA), although both soluble NKG2DL (sNKG2DL) were significantly increased compared with sera of healthy controls (P < 0.0001). Strikingly, elevated concentrations of sULBP2, but not of sMICA, were strongly associated with disease progression (P < 0.0001) and tumor load (P = 0.0003). Elevated serum levels of either sNKG2DL correlated with reduced overall survival, albeit considerably stronger for sULBP2 (P < 0.0001) than for sMICA (P = 0.011). In early-stage (I-III) melanoma patients, only sULBP2 (P < 0.0001) but neither sMICA nor S100B revealed prognostic significance. Multivariate analysis identified sULBP2 (P = 0.0015) and S100B (P = 0.013) but not sMICA as independent predictors of prognosis. CONCLUSION: Our data reveal marked differences in the clinical significance of individual sNKG2DL. Only sULBP2 is an independent predictor of prognosis, the significance of which is superior to the well-established and widely used melanoma serum marker S100B.
42
Tumour-derived soluble MIC ligands impair expression of NKG2D and T-cell activation
Veronika Groh, Jennifer D. Wu, Cassian Yee et al. · Nature · 2002 · 1.6K citations
Life Sciences, Immunology, Oncology +15
The DNA damage pathway regulates innate immune system ligands of the NKG2D receptor
Stephan Gasser, Sandra Oršulić, Eric J. Brown et al. · Nature · 2005 · 1.3K citations · Full text
Rae1 and H60 ligands of the NKG2D receptor stimulate tumour immunity
Andreas Diefenbach, Eric R. Jensen, A. M. Jamieson et al. · Nature · 2001 · 1.1K citations · Full text
Life Sciences, Immunology, Oncology +14