SNU CBE

A stealth-body Fc engineering platform enables complete effector silencing in antibody and ADC therapeutics

2026 · Journal of Biological Engineering

저자

Suyeon Kim, Migyeong Jo, Munsu Kyung, Woo Hyung Ko, Wonju Lee, Kihwan Chang, Pedro Lee, Sungkuk Cho, Seongin Seomun, Byoung Joon Ko, tae-erk kim, Jungmin Choi, 정상택 (Sang Taek Jung)

연구주제

Monoclonal and Polyclonal Antibodies Research · Protein purification and stability · Viral Infectious Diseases and Gene Expression in Insects

NTIS 과학기술표준분류

가장 가까운 분류(보건의료 > 신약·의약품개발 > 치료용항체)가 화학·화공 범위 밖이다. 배정 근거: AI 키워드가 잡은 NTIS 과제의 분류.

AI 연구 키워드·방법

antibody drug conjugate 항체 Fc 엔지니어링 complement c1q binding effector function silencing

키워드 (OpenAlex)

Fc engineering Fc gamma receptor C1q binding antibody-drug conjugates CD47 blockade antibody-dependent cellular cytotoxicity CDC FcRn binding

초록

The development of next-generation antibody therapeutics requires Fc scaffolds that suppress unwanted effector functions while preserving core developability attributes. Existing effector-attenuated Fc backbones, however, retain residual interactions with Fcγ receptors (FcγRs) and C1q, highlighting a persistent design limitation in achieving complete effector silencing without compromising glycosylation, FcRn-mediated persistence, and manufacturability. This is particularly relevant for formats in which Fc effector function is undesirable, including immune-engaging antibodies, CD47 blockers, and antibody–drug conjugates (ADCs). Accordingly, a robust Fc engineering framework enabling complete and transferable effector silencing across antibody modalities is required. We developed Stealth-Body (SB) Fc variants, a fully effector-silenced Fc platform that abolishes Fc-mediated immune engagem…

이 논문을 지원한 국가R&D 과제 (NTIS 성과)

NTIS 성과DB(2020–24)에서 DOI 매칭 없음

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교수 1

정상택

연구주제 1

Monoclonal and Polyclonal Antibodies Research

키워드 1

항체 Fc 엔지니어링