Bacillus Calmette-Guerin immunotherapy of bladder cancer induces selection of human leukocyte antigen class I-deficient tumor cells
Metadatos
Mostrar el registro completo del ítemAutor
Carretero Coca, Rafael; Cabrera Castillo, María Teresa; Gil, Hernani; Sáenz-López, Pablo; Maleno, Isabel; Aptsiauri, Natalia; Cózar Olmo, José Manuel; Garrido Torres-Puchol, FedericoEditorial
Wiley
Materia
Cancer Immunotherapy BCG Bladder HLA
Fecha
2011-08-15Referencia bibliográfica
Carretero Coca, Rafael. Int J Cancer. 2011 Aug 15;129(4):839-46. doi: 10.1002/ijc.25733. Epub 2011 Jun 10. https://doi.org/10.1002/ijc.25733
Patrocinador
Virgen de las Nieves University Hospital, Granada; University of Granada, SpainResumen
Bacillus Calmette-Guerin (BCG) immunotherapy is a standard treatment for high-risk non-muscle-infiltrating bladder cancer patients. Although the outcomes are good, cancer relapse is observed in around 40% of patients. We present the comparative analysis of human leukocyte antigen (HLA) class I expression in recurrent bladder tumors in patients treated with mitomycin or BCG. HLA class I expression was analyzed by RT-Q-PCR and immunohistochemical techniques. Loss of heterozygosity (LOH) was determined by microsatellite amplification of markers in chromosome 6 and 15. More profound alterations in HLA class I expression were found in post-BCG recurrent tumors than in pre-BCG lesions, whereas mitomycin treatment did not change the HLA class I expression pattern. Post-BCG recurrent tumors also showed a higher incidence of structural defects underlying altered HLA class I expression. We hypothesize that the immunotherapy-activated immune system recognizes and eliminates tumor cells with reversible ("soft") HLA class I changes but not transformed cells with additional, irreversible ("hard") alterations. To our knowledge, this is the first clinical evidence of immunotherapy-induced immunoselection of HLA class I loss tumor variants in bladder cancer, although the study involved a small number of patients.





