材料科学
体内
淋巴结
基质(化学分析)
刺激
抗原
细胞生物学
生物物理学
纳米技术
生物医学工程
免疫学
生物
医学
神经科学
复合材料
生物技术
作者
Natalie K. Livingston,John W. Hickey,Hajin Sim,Sebastian F. Salathe,Joseph Choy,Jiayuan Kong,Aliyah B. Silver,Jessica L. Stelzel,Mary O. Omotoso,Shuyi Li,Worarat Chaisawangwong,Suheeta Roy,Emily Ariail,Mara Lanis,P. S. Pradeep,Joan Glick Bieler,Savannah Est-Witte,Elissa K. Leonard,Joshua C. Doloff,Jamie B. Spangler,Hai‐Quan Mao,Jonathan P. Schneck
标识
DOI:10.1002/adma.202310043
摘要
Abstract T cells are critical mediators of antigen‐specific immune responses and are common targets for immunotherapy. Biomaterial scaffolds have previously been used to stimulate antigen‐presenting cells to elicit antigen‐specific immune responses; however, structural and molecular features that directly stimulate and expand naïve, endogenous, tumor‐specific T cells in vivo have not been defined. Here, an artificial lymph node (aLN) matrix is created, which consists of an extracellular matrix hydrogel conjugated with peptide‐loaded‐MHC complex (Signal 1), the co‐stimulatory signal anti‐CD28 (Signal 2), and a tethered IL‐2 (Signal 3), that can bypass challenges faced by other approaches to activate T cells in situ such as vaccines. This dynamic immune‐stimulating platform enables direct, in vivo antigen‐specific CD8+ T cell stimulation, as well as recruitment and coordination of host immune cells, providing an immuno‐stimulatory microenvironment for antigen‐specific T cell activation and expansion. Co‐injecting the aLN with naïve, wild‐type CD8+ T cells results in robust activation and expansion of tumor‐targeted T cells that kill target cells and slow tumor growth in several distal tumor models. The aLN platform induces potent in vivo antigen‐specific CD8+ T cell stimulation without the need for ex vivo priming or expansion and enables in situ manipulation of antigen‐specific responses for immunotherapies.
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