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Reprogramming Autophagy to Strengthen Antitumour Immunity: Advances in Immunotherapeutic Strategies

Hamzeh J. Al AmeerFaculty of Allied Medical Sciences, Hourani Center for Applied Scientific Research Al‐Ahliyya Amman University Amman JordanRenuka Jyothi SDepartment of Biotechnology and Genetics, School of Sciences JAIN (Deemed to be University) Bangalore IndiaIsraa Abdulhameed AhmadDepartment of Anesthesia Techniques, Health and Medical Techniques College Alnoor University Mosul IraqPradeepta Sekhar PatroDepartment of Immunology IMS and SUM Hospital, Siksha 'O' Anusandhan Bhubaneswar Odisha IndiaVimal AroraUniversity Institute of Pharma Sciences Chandigarh University Mohali Punjab IndiaSiya SinglaCentre for Research Impact & Outcome Chitkara University Institute of Engineering and Technology, Chitkara University Rajpura IndiaTashpulatov TulkinDepartment of Natural Sciences Termez University of Economics and Service Termez UzbekistanAbdullayeva Fazilat ArslanbekovnaTeacher of Departmeny of Natural Sciences Mamun University Khiva UzbekistanManoj Kumar‐MishraSharda School of Bio‐Science & Technology Sharda University Greater Noida India
Immunologyjournal2026en
ABI

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Autophagy is a central cellular process that supports homeostasis, yet it also plays a critical part in tumour immune evasion and treatment resistance, creating substantial obstacles for contemporary cancer immunotherapy. Because of this dual nature, targeted modulation of autophagy in either tumour cells or immune cells holds considerable potential to enhance therapeutic outcomes. However, the successful integration of autophagy directed strategies requires a clearer understanding of the molecular pathways through which autophagy shapes immune activity and treatment response. A more refined view of autophagy within the tumour immune microenvironment may open new therapeutic opportunities. Selectively targeting specific autophagy pathways could help overcome immune resistance and strengthen the impact of immunotherapy. Progress in this field will likely depend on the development of delivery systems that allow precise control of tumour autophagy in a compartment specific manner, as well as combination approaches that complement emerging treatments. Incorporating insights from immuno oncology, metabolic regulation, and immune surveillance may accelerate the translation of novel autophagy modulators into clinical testing, although current progress remains shaped largely by preclinical and early translational evidence.

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