Drug intelligence / Profile preview

aldesleukin + zoledronic acid

Development stage
Unknown
Lead developer
Shanghai Pulmonary Hospital, Tongji University
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

aldesleukin + zoledronic acid is an investigational combination immunotherapy being evaluated for the treatment of multidrug-resistant tuberculosis (MDR-TB). Aldesleukin is a recombinant form of interleukin-2 (IL-2) that promotes the proliferation and activation of T cells and natural killer cells by binding to IL-2 receptors. Zoledronic acid, a nitrogen-containing bisphosphonate, is used in this context to stimulate the expansion of Vγ2Vδ2 T cells by inhibiting farnesyl pyrophosphate synthase, which leads to the accumulation of phosphoantigens like isopentenyl pyrophosphate (IPP). The combination aims to enhance the host's cellular immune response against *Mycobacterium tuberculosis* when used alongside standard chemotherapy. This specific regimen is being studied in an exploratory Phase 4 clinical trial led by the Shanghai Pulmonary Hospital in China.

Other names
Vγ2Vδ2 T lymphocyte-based immunotherapyzoledronic acid/interleukin 2zoledronic acid/interleukin-2
02

Targets

FDPS (Farnesyl pyrophosphate synthase)STAT3 (Signal Transducer and Activator of Transcription 3)IL-2 (Interleukin 2)IL2RB (IL-2 receptor beta chain)

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