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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2025.2
- 수록면
- 98 - 117 (20page)
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초록· 키워드
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Regulatory T (Treg) cells are essential for maintaining immune homeostasis by suppressing excessive immune responses. In the context of cancer, however, Tregs promote immune evasion and tumor progression, particularly through their unique adaptations within the tumor microenvironment (TME). Recent research has emphasized how metabolic characteristics shape Treg activation, migration, and immunosuppressive function, revealing the impact of metabolic pathways on Treg fitness in homeostasis and within the TME. In this review, we first provide an overview of Tregs in cancer immunology, discussing their immunosuppressive roles and properties specific to the TME. We then examine the metabolic requirements for Treg activation and migration under normal conditions, followed by a discussion of how hypoxia, lactate accumulation, nutrient limitation, oxidative stress, and other TME-specific factors alter Treg metabolism and contribute to cancer immune evasion. Finally, we explore therapeutic strategies that target Treg metabolism within the TME, including pharmacological modulation of specific metabolic pathways to diminish Treg-mediated immunosuppression. Thus, we could suggest future directions and clinical implications for Treg-targeted metabolic modulation as a complementary approach in cancer treatment, setting the stage for novel strategies in immunotherapy.
목차
ABSTRACT
INTRODUCTION
Treg METABOLISM IN HOMEOSTASIS
Treg MIGRATION AND METABOLISM
Treg SUPPRESSIVE FUNCTION
TUMOR MICROENVIRONMENT AND Treg METABOLIC ADAPTATIONS
THERAPEUTIC POTENTIAL: STRATEGIES TARGETING METABOLISM FOR THERAPY
CHALLENGES AND RISKS OF TARGETING Treg METABOLISM
CONCLUDING REMARKS
REFERENCES
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