Human IL-2 (Interleukin-2) is a central T cell–derived cytokine that regulates lymphocyte proliferation, differentiation, and immune homeostasis. IL-2 is produced primarily by activated CD4⁺ T helper cells and, to a lesser extent, by CD8⁺ T cells following antigen recognition and costimulatory signaling. It functions through the IL-2 receptor complex (IL-2Rα/CD25, IL-2Rβ/CD122, and the common γ chain/CD132) to promote clonal expansion of antigen-specific T cells, enhance cytotoxic T lymphocyte and natural killer (NK) cell activity, and support the development and maintenance of regulatory T cells (Tregs), which are essential for immune tolerance. In healthy individuals, circulating IL-2 levels are typically low but rise transiently during infection or immune activation. Dysregulated IL-2 signaling has been implicated in autoimmune diseases such as type 1 diabetes, multiple sclerosis, and systemic lupus erythematosus, as well as in immunodeficiency and chronic viral infections. Recombinant IL-2 has been used clinically as an immunotherapy for certain cancers (e.g., metastatic melanoma and renal cell carcinoma) and is being investigated at low doses to selectively expand Tregs in autoimmune and inflammatory disorders. In clinical and translational research, human IL-2 is a key biomarker and therapeutic target for modulating T cell–mediated immunity and immune tolerance.