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ABBV-319: a CD19-targeting glucocorticoid receptor modulator antibody-drug conjugate therapy for B-cell malignancies.


ABSTRACT:

Abstract

Glucocorticoids are key components of the standard-of-care treatment regimens for B-cell malignancy. However, systemic glucocorticoid treatment is associated with several adverse events. ABBV-319 is a CD19-targeting antibody-drug conjugate engineered to reduce glucocorticoid-associated toxicities while possessing 3 distinct mechanisms of action (MOA) to increase therapeutic efficacy: (1) antibody-mediated delivery of a glucocorticoid receptor modulator (GRM) payload to activate apoptosis, (2) inhibition of CD19 signaling, and (3) enhanced fragment crystallizable (Fc)-mediated effector function via afucosylation of the antibody backbone. ABBV-319 elicited potent GRM-driven antitumor activity against multiple malignant B-cell lines in vitro, as well as in cell line-derived xenografts and patient-derived xenografts (PDXs) in vivo. Remarkably, a single dose of ABBV-319 induced sustained tumor regression and enhanced antitumor activity compared with repeated dosing of systemic prednisolone at the maximum tolerated dose in mice. The unconjugated CD19 monoclonal antibody (mAb) also displayed antiproliferative activity in a subset of B-cell lymphoma cell lines through the inhibition of phosphoinositide 3-kinase signaling. Moreover, afucosylation of CD19 mAb enhanced Fc-mediated antibody-dependent cellular cytotoxicity. Notably, ABBV-319 displayed superior efficacy compared with afucosylated CD19 mAb in human CD34+ peripheral blood mononuclear cell-engrafted NSG-Tg(Hu-IL15) transgenic mice, demonstrating enhanced antitumor activity when multiple MOAs are enabled. ABBV-319 also showed durable antitumor activity across multiple B-cell lymphoma PDX models, including nongerminal center B-cell diffuse large B-cell lymphoma and relapsed lymphoma after R-CHOP treatment. Collectively, these data support the ongoing evaluation of ABBV-319 in a phase 1 clinical trial.

SUBMITTER: Chang CA 

PROVIDER: S-EPMC11375461 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature

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ABBV-319: a CD19-targeting glucocorticoid receptor modulator antibody-drug conjugate therapy for B-cell malignancies.

Chang Chewei Anderson CA   Emberley Ethan E   D'Souza Aloma L AL   Zhao Weilong W   Cosgrove Cormac C   Parrish Karen K   Mitra Diya D   Payson Elmer E   Oleksijew Anatol A   Ellis Paul P   Rodriguez Luis L   Duggan Ryan R   Hrusch Cara C   Lasko Loren L   Assaily Wissam W   Zheng Pingping P   Liu Wei W   Hernandez Axel A   McCarthy Kimberley K   Zhang Zhaomei Z   Rha Geunbae G   Cao Zhensheng Z   Li Yingchun Y   Perng Olivia O   Campbell Jos J   Zhang Gloria G   Curran Tyler T   Bruncko Milan M   Marvin Christopher C CC   Hobson Adrian A   McPherson Michael M   Uziel Tamar T   Pysz Marybeth A MA   Zhao Xi X   Bankovich Alex A   Hayflick Joel J   McDevitt Michael M   Freise Kevin J KJ   Morgan-Lappe Susan S   Purcell James W JW  

Blood 20240801 7


<h4>Abstract</h4>Glucocorticoids are key components of the standard-of-care treatment regimens for B-cell malignancy. However, systemic glucocorticoid treatment is associated with several adverse events. ABBV-319 is a CD19-targeting antibody-drug conjugate engineered to reduce glucocorticoid-associated toxicities while possessing 3 distinct mechanisms of action (MOA) to increase therapeutic efficacy: (1) antibody-mediated delivery of a glucocorticoid receptor modulator (GRM) payload to activate  ...[more]

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