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[Preprint]. 2024 Oct 17:2024.10.14.618178. [Version 1] doi: 10.1101/2024.10.14.618178

A comprehensive engineering strategy improves potency and manufacturability of a near pan-neutralizing antibody against HIV

Mohammad M Sajadi, Abdolrahim Abbasi, Zahra Rikhtegaran Tehrani, Christine Siska, Rutilio Clark, Woo Chi, Michael S Seaman, Dieter Mielke, Kshitij Wagh, Qingbo Liu, Taylor Jumpa, Randal R Ketchem, Dung N Nguyen, Willaim D Tolbert, Brian G Pierce, Ben Atkinson, Derrick Deming, Megan Sprague, Andrew Asakawa, David Ferrer, Yasmin Dunn, Sarah Calvillo, Rui Yin, Johnathan D Guest, Bette Korber, Bryan T Mayer, Alicia H Sato, Xin Ouyang, Scott Foulke, Parham Habibzadeh, Maryam Karimi, Arash Aslanabadi, Mahsa Hojabri, Saman Saadat, Roza Zareidoodeji, Mateusz Kędzior, Edwin Pozharski, Alonso Heredia, David Montefiori, Guido Ferrari, Marzena Pazgier, George K Lewis, Joseph G Jardine, Paolo Lusso, Anthony DeVico
PMCID: PMC11507801  PMID: 39464103

Abstract

Anti-HIV envelope broadly neutralizing antibodies (bnAbs) are alternatives to conventional antiretrovirals with the potential to prevent and treat infection, reduce latent reservoirs, and/or mediate a functional cure. Clinical trials with “first generation” bnAbs used alone or in combination show promising antiviral effects but also highlight that additional engineering of “enhanced” antibodies will be required for optimal clinical utility, while preserving or enhancing cGMP manufacturing capability. Here we report the engineering of an anti-CD4 binding-site (CD4bs) bnAb, N49P9.3, purified from the plasma of an HIV elite-neutralizer. Through a series of rational modifications we produced a variant that demonstrates: enhanced potency; superior antiviral activity in combination with other bnAbs; low polyreactivity; and longer circulating half-life. Additional engineering for manufacturing produced a final variant, eN49P9, with properties conducive to cGMP production. Overall, these efforts demonstrate the feasibility of developing enhanced anti-CD4bs bnAbs with greatly improved antiviral properties as well as potential translational value.

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