用真人实验验证大模型生成有害生物序列的危险性
An Early Warning of Emerging Biosecurity Risks in Frontier LLMs

- 构建专用红队模型与实验框架,测试大模型生成危险生物指令的能力
- 多款主流大模型攻击成功率接近100%,能诱导生成致病病毒序列
- 生成序列可被合成并表达出功能蛋白,实证威胁真实存在
前沿大语言模型日益融入科研流程,但其不断增强的生物学能力已超出现有安全防护范围。为评估风险,我们开发了Intern-BioBreaker——一种专门用于生物红队测试的模型,并建立从计算到物理的全流程验证框架。该框架通过生成针对性越狱提示,测试对齐模型是否会被诱导提供高风险生物操作指导或生成具有潜在危害的序列。筛选出的序列经基因合成、宿主表达和正交蛋白验证,确认其可实现预期生物功能。评估发现:(i)Intern-BioBreaker显著优于基线攻击模型,在开源与闭源前沿LLM中广泛暴露生物越狱漏洞,部分模型任务级攻击成功率(ASR)达近饱和或100%;(ii)GPT-5.5可被诱导生成具致病潜力的改造病毒序列,其翻译蛋白可能具备更强受体结合力,提升感染风险;(iii)端到端验证表明,部分模型生成的设计并非文本幻觉,可在受控实验条件下被物理实现。研究强调亟需加强生物红队测试、核酸合成筛查及与模型能力同步的安全机制。
原文摘要 · Abstract (English)
Frontier large language models (LLMs) are increasingly integrated into scientific workflows, yet their growing biological capabilities may outpace current safeguards. To assess the biological risks of frontier models, we develop Intern-BioBreaker, a specialized bio-red-teaming model, together with an integrated computational-to-physical framework that couples model-level stress testing with wet-lab validation. Within this framework, Intern-BioBreaker generates targeted jailbreak prompts to test whether aligned models can be induced to provide operational guidance for safety-sensitive biological tasks or produce sequence-level outputs with potentially harmful properties. Selected sequence outputs are then carried forward for DNA synthesis, host expression, and orthogonal protein verification to assess whether model-generated designs can yield the intended biological products. Our evaluation reveals a concerning gap between text-level safeguards and the risks posed by capable scientific models: (i) Intern-BioBreaker outperforms baseline attack models and reveals widespread bio-risk jailbreak vulnerabilities across both open-weight and proprietary frontier LLMs, with several targets reaching near-saturated or 100% task-level attack success rate (ASR); (ii) in sequence-level case studies, GPT-5.5 can be induced to generate modified viral candidate sequences with pathogenic potential; the corresponding translated proteins may exhibit even stronger receptor-binding affinity and thus enhanced infection potential; and (iii) end-to-end verification shows that selected model-generated biological designs are not merely textual artifacts, but can be physically realized under controlled experimental settings. These findings underscore the need for stronger biological red-teaming, nucleic acid synthesis screening, and safety mechanisms that keep pace with model capabilities.
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