Targeting the IL-15 Receptor with an Antagonist IL-15 Mutant/Fc gamma 2a Protein Blocks Delayed-Type Hypersensitivity

• Published in: The Journal of immunology (1950) Vol. 160; no. 12; pp. 5742 - 5748
• Main Authors: Kim, Yon Su, Maslinski, W, Zheng, Xin Xiao, Stevens, A C, Li, Xian Chang, Tesch, G H, Kelley, V R, Strom, T B
• Format: Journal Article
• Language: English
• Published: 15.06.1998
• ISSN: 0022-1767

Owing to shared receptor components, the biologic activities of IL-15 are similar to those of IL-2. However, the patterns of tissue expression of IL-2/IL-2R alpha and IL-15/IL-15R alpha differ. The development of agents targeting the receptor and signaling elements of IL-15 may provide a new perspective for treatment of diseases associated with expression of IL-15/IL-15R. We designed, genetically constructed, and expressed a receptor site-specific IL-15 antagonist by mutating glutamine residues within the C terminus of IL-15 to aspartic acid and genetically linked this mutant IL-15 to murine Fc gamma 2a. These mutant IL-15 proteins specifically bind to the IL-15R, competitively inhibit IL-15-triggered cell proliferation, and do not activate the STAT-signaling pathway. Because the receptor site-specific antagonist IL-15 mutant/Fc gamma 2a fusion proteins had a prolonged t one half in vivo and the potential for destruction of IL-15R super(+) leukocytes, we examined the immunosuppressive activity of this agent. An IL-15 mutant//Fc gamma 2a fusion protein markedly attenuated Ag-specific delayed-type hypersensitivity responses and decreased leukocyte infiltration within the delayed-type hypersensitivity sites. These findings suggest that 1) IL-15/IL-15R super(+) cells are crucial to these T cell-dependent immune responses, and 2) treatment with IL-15 mutant/Fc gamma 2a protein may ameliorate T cell-dependent immune/inflammatory diseases.