TY - JOUR
T1 - Tumor lymphangiogenesis promotes T cell infiltration and potentiates immunotherapy in melanoma
AU - Fankhauser, Manuel
AU - Broggi, Maria A.S.
AU - Potin, Lambert
AU - Bordry, Natacha
AU - Jeanbart, Laura
AU - Lund, Amanda W.
AU - Da Costa, Elodie
AU - Hauert, Sylvie
AU - Rincon-Restrepo, Marcela
AU - Tremblay, Christopher
AU - Cabello, Elena
AU - Homicsko, Krisztian
AU - Michielin, Olivier
AU - Hanahan, Douglas
AU - Speiser, Daniel E.
AU - Swartz, Melody A.
N1 - Publisher Copyright:
Copyright © 2017. The Authors, some rights reserved.
PY - 2017/9/13
Y1 - 2017/9/13
N2 - In melanoma, vascular endothelial growth factor-C (VEGF-C) expression and consequent lymphangiogenesis correlate with metastasis and poor prognosis. VEGF-C also promotes tumor immunosuppression, suggesting that lymphangiogenesis inhibitors may be clinically useful in combination with immunotherapy. We addressed this concept in mouse melanoma models with VEGF receptor-3 (VEGFR-3)-blocking antibodies and unexpectedly found that VEGF-C signaling enhanced rather than suppressed the response to immunotherapy. We further found that this effect was mediated by VEGF-C-induced CCL21 and tumor infiltration of naïve T cells before immunotherapy because CCR7 blockade reversed the potentiating effects of VEGF-C. In human metastatic melanoma, gene expression of VEGF-C strongly correlated with CCL21 and T cell inflammation, and serum VEGF-C concentrations associated with both T cell activation and expansion after peptide vaccination and clinical response to checkpoint blockade. We propose that VEGF-C potentiates immunotherapy by attracting naïve T cells, which are locally activated upon immunotherapy-induced tumor cell killing, and that serum VEGF-C may serve as a predictive biomarker for immunotherapy response.
AB - In melanoma, vascular endothelial growth factor-C (VEGF-C) expression and consequent lymphangiogenesis correlate with metastasis and poor prognosis. VEGF-C also promotes tumor immunosuppression, suggesting that lymphangiogenesis inhibitors may be clinically useful in combination with immunotherapy. We addressed this concept in mouse melanoma models with VEGF receptor-3 (VEGFR-3)-blocking antibodies and unexpectedly found that VEGF-C signaling enhanced rather than suppressed the response to immunotherapy. We further found that this effect was mediated by VEGF-C-induced CCL21 and tumor infiltration of naïve T cells before immunotherapy because CCR7 blockade reversed the potentiating effects of VEGF-C. In human metastatic melanoma, gene expression of VEGF-C strongly correlated with CCL21 and T cell inflammation, and serum VEGF-C concentrations associated with both T cell activation and expansion after peptide vaccination and clinical response to checkpoint blockade. We propose that VEGF-C potentiates immunotherapy by attracting naïve T cells, which are locally activated upon immunotherapy-induced tumor cell killing, and that serum VEGF-C may serve as a predictive biomarker for immunotherapy response.
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U2 - 10.1126/scitranslmed.aal4712
DO - 10.1126/scitranslmed.aal4712
M3 - Article
C2 - 28904226
AN - SCOPUS:85029456338
SN - 1946-6234
VL - 9
JO - Science Translational Medicine
JF - Science Translational Medicine
IS - 407
M1 - eaal4712
ER -