| Literature DB >> 26419961 |
Matteo Menotti1,2, Cristina Mastini1,2, Claudia Voena1,2, Filomena Di Giacomo1,2, Dario Livio Longo1,3, Barbara Castella1,2, Maria Elena Boggio Merlo1,2, Chiara Ambrogio4, Qi Wang5, Valerio Giacomo Minero1,2, Teresa Poggio1,2, Cinzia Martinengo1,2, Lucia D'Amico1,2, Elena Panizza1,2, Luca Mologni6, Federica Cavallo1,7, Fiorella Altruda1,7, Mohit Butaney8,9, Marzia Capelletti8,9, Giorgio Inghirami1,2, Pasi A Jänne8,9,10, Roberto Chiarle1,2,5.
Abstract
Non-small cell lung cancer (NSCLC) harboring chromosomal rearrangements of the anaplastic lymphoma kinase (ALK) gene is treated with ALK tyrosine kinase inhibitors (TKI), but the treatment is successful for only a limited amount of time; most patients experience a relapse due to the development of drug resistance. Here, we show that a vaccine against ALK induced a strong and specific immune response that both prophylactically and therapeutically impaired the growth of ALK-positive lung tumors in mouse models. The ALK vaccine was efficacious also in combination with ALK TKI treatment and significantly delayed tumor relapses after TKI suspension. We found that lung tumors containing ALK rearrangements induced an immunosuppressive microenvironment, regulating the expression of PD-L1 on the surface of lung tumor cells. High PD-L1 expression reduced ALK vaccine efficacy, which could be restored by administration of anti-PD-1 immunotherapy. Thus, combinations of ALK vaccine with TKIs and immune checkpoint blockade therapies might represent a powerful strategy for the treatment of ALK-driven NSCLC. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26419961 PMCID: PMC4674335 DOI: 10.1158/2326-6066.CIR-15-0089
Source DB: PubMed Journal: Cancer Immunol Res ISSN: 2326-6066 Impact factor: 11.151