Use of enhanced interleukin-2 formulations for improved immunotherapy against cancer

RA Rosalia, N Arenas-Ramirez, G Bouchaud… - Current opinion in …, 2014 - Elsevier
RA Rosalia, N Arenas-Ramirez, G Bouchaud, ME Raeber, O Boyman
Current opinion in chemical biology, 2014Elsevier
Highlights•IL-2 immunotherapy can induce durable tumor regression of metastatic cancer.•IL-
2 can lead to toxic adverse effects and stimulate regulatory CD4+ T cells.•Compared to IL-2,
CD122-directed IL-2 formulations show a better therapeutic profile.•CD122-directed
formulations include IL-2/anti-IL-2 mAb complexes and IL-2 muteins.The use of interleukin-2
(IL-2) for the stimulation of an effector immune response against metastatic cancer dates
back to the early 1980s. Administration of unmodified IL-2, either alone or together with …
Highlights
  • IL-2 immunotherapy can induce durable tumor regression of metastatic cancer.
  • IL-2 can lead to toxic adverse effects and stimulate regulatory CD4+ T cells.
  • Compared to IL-2, CD122-directed IL-2 formulations show a better therapeutic profile.
  • CD122-directed formulations include IL-2/anti-IL-2 mAb complexes and IL-2 muteins.
The use of interleukin-2 (IL-2) for the stimulation of an effector immune response against metastatic cancer dates back to the early 1980s. Administration of unmodified IL-2, either alone or together with antigen-specific approaches, has resulted in remarkably long-term survival of some patients suffering from metastatic melanoma. However, such treatment is usually hampered by the appearance of toxic adverse effects, which has motivated the engineering of modified IL-2 formulations showing reduced toxicity while being more potent at stimulating anti-tumor effector immune cells. In this review we summarize and discuss the features and biological relevance of several enhanced IL-2 formulations, compare these to IL-15-based therapeutics, and try to foreshadow their potential in immunological research and immunotherapy.
Elsevier