Compositions and Methods for Increased Circulation Half-Life

Background:

While strategies such as PEGylation (PEG, polyethylene glycol), albumin binding, and Fc-fusion have been employed to extend the half-life of biological and pharmaceutical agents, there remains a need for additional strategies that not only serve as alternative approaches but ones that may enable further improvements or benefits, especially given that certain existing approaches (e.g. PEGylation) may increase immunogenicity and lead to neutralizing antibodies or hypersensitivity reactions.

Technology Overview:

This University at Buffalo invention provides a series of single domain antibodies (sdAbs) that bind to a specific target on red blood cells (RBCs).  These erythrocyte-binding sdAbs enable exploitation of RBCs' 110-day half-life.  Selection of the sdAb based on its affinity for the target domain allows for tunable half-life extension of up to 110 days, thereby limiting the dosing interval and mass of therapeutic protein required to be administered.  Further, others have shown that erythrocyte binding may decrease immunogenicity and/or lead to immune tolerance.  These sdAb compositions are intended to be used as a component of a multicomponent composition wherein the other component is the therapeutic agent for which increased half-life is desired.

Advantages:

• Improved and tunable circulation half-life
• Increased blood:tissue ratios
• Potential for reduced immunogenicity and/or tolerance induction

Applications:

• Therapeutic proteins across a variety of clinical indications

Intellectual Property Summary:

PCT/US2024/043288 filed August 21, 2024.

Stage of Development:

In vivo.

Licensing Status:

Available for licensing or collaboration.

Additional Information:

Publication link(s): Int. J Mol Sci. 2023 Jan; 24(1):475 (doi:10.3390/ijms2401475)