
Molecular and Cellular Probes, Год журнала: 2024, Номер 79, С. 102004 - 102004
Опубликована: Дек. 21, 2024
Язык: Английский
Molecular and Cellular Probes, Год журнала: 2024, Номер 79, С. 102004 - 102004
Опубликована: Дек. 21, 2024
Язык: Английский
Trends in Pharmacological Sciences, Год журнала: 2025, Номер unknown
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0Vaccines, Год журнала: 2025, Номер 13(4), С. 344 - 344
Опубликована: Март 24, 2025
Breast cancer (BC) remains a significant global health challenge due to its complex biology, which complicates both diagnosis and treatment. Immunotherapy vaccines have emerged as promising alternatives, harnessing the body’s immune system precisely target eliminate cells. However, several key factors influence selection effectiveness of these therapies, including BC subtype, tumor mutational burden (TMB), tumor-infiltrating lymphocytes (TILs), PD-L1 expression, HER2 resistance, microenvironment (TME). subtypes play critical role in shaping treatment responses. Triple-negative breast (TNBC) exhibits highest sensitivity immunotherapy, while HER2-positive hormone receptor-positive (HR+) often require combination strategies for optimal outcomes. High TMB enhances responses by generating neoantigens, making tumors more susceptible checkpoint inhibitors (ICIs); whereas, low may indicate resistance. Similarly, elevated TIL levels are associated with better immunotherapy efficacy, expression serves predictor inhibitor success. Meanwhile, resistance an immunosuppressive TME contribute evasion, highlighting need multi-faceted approaches. Current immunotherapies encompass range targeted treatments. HER2-directed such trastuzumab pertuzumab, block dimerization enhance antibody-dependent cellular cytotoxicity (ADCC), small-molecule inhibitors, like lapatinib tucatinib, suppress signaling curb growth. Antibody–drug conjugates (ADCs) improve targeting coupling monoclonal antibodies cytotoxic agents, minimizing off-target effects. ICIs, pembrolizumab, restore T-cell function, CAR-macrophage (CAR-M) therapy leverages macrophages reshape overcome While particularly TNBC, has demonstrated promise eliciting durable responses, efficacy varies across subtypes. Challenges immune-related adverse events, mechanisms, high costs, delayed remain barriers widespread vaccines—including protein-based, whole-cell, mRNA, dendritic cell, epitope-based vaccines—aim stimulate tumor-specific immunity. Though clinical success been limited, ongoing research is refining vaccine formulations, integrating identifying biomarkers improved patient stratification. Future advancements will depend on optimizing through biomarker-driven approaches, addressing heterogeneity, developing innovative therapies By leveraging strategies, researchers aim ultimately
Язык: Английский
Процитировано
0Cancer Cell International, Год журнала: 2024, Номер 24(1)
Опубликована: Дек. 19, 2024
Язык: Английский
Процитировано
0Molecular and Cellular Probes, Год журнала: 2024, Номер 79, С. 102004 - 102004
Опубликована: Дек. 21, 2024
Язык: Английский
Процитировано
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