Technology ID
TAB-4839

Development and Characterization of Anti-Idiotypic Monoclonal Antibodies for PGT121 Anti-HIV Therapy Monitoring

E-Numbers
E-019-2021-0
Lead Inventor
Mascola, John
Lead IC
NIAID
Co-Inventors
Pegu, Amarendra ("Amar")
Shi, Wei
ICs
NIAID
Applications
Vaccines­­­
Therapeutics
Research Materials
Diagnostics
Therapeutic Areas
Infectious Disease
Immunology
Development Stages
Pre-clinical (in vivo)
Research Products
Plasmids/Vectors
Antibodies
Animal Models

The document details the creation of an anti-idiotypic monoclonal antibody specifically targeting the PGT121 monoclonal antibody (mAb) used in HIV treatment, highlighting its potential in both therapeutic and preventative applications. To ensure the consistent quality and effectiveness of the PGT121 mAb, these anti-idiotypic antibodies are developed for monitoring purposes during clinical applications. The research involved immunizing female BALB/cJ mice with a fragment of the PGT121 antibody, followed by cell fusion, screening for antibody production, and subsequent cloning to establish stable hybridomas. These procedures culminated in the isolation of monoclonal antibodies with desired specificities. The antibodies were then subjected to isotyping, reverse transcription, PCR amplification, and expression in Expi-293 cells, ensuring a consistent supply of high-fidelity reagents for the assessment of PGT121 mAb in various settings.

 

Commercial Applications
The anti-idiotypic monoclonal antibodies against PGT121 mAb are promising for fine-tuning HIV treatment dosages, conducting detailed pharmacological research, improving diagnostic tests, and potentially aiding in the development of novel HIV therapies and vaccines.

Competitive Advantages
The anti-idiotypic monoclonal antibodies targeting PGT121 offer distinct competitive advantages in HIV therapy: enhanced assay specificity for accurate mAb monitoring, consistent production for reliable supply, and optimized dosing for improved patient outcomes. These attributes strengthen their position in therapeutic protocols, ensuring superior efficacy and safety in clinical use.
Licensing Contact:
Rainwater, Charles
crainwater@mail.nih.gov