Cell and tissue engineering in lymph nodes for cancer immunotherapy

被引:51
作者
Najibi, Alexander J. [1 ,2 ]
Mooney, David J. [1 ,2 ]
机构
[1] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[2] Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA
基金
美国国家科学基金会;
关键词
Cancer vaccines; Nanoparticles; Biomaterials; Immune checkpoint blockade; CAR-T therapy; Adoptive cell transfer; Tertiary lymphoid structures; Lymphoid organs; HUMAN DENDRITIC CELLS; CD8(+) T-CELLS; IN-VIVO; B-CELLS; MICROFLUIDIC PLATFORM; CHECKPOINT INHIBITORS; THERAPEUTIC-EFFICACY; INTRANODAL INJECTION; PROGNOSTIC RELEVANCE; CHRONIC INFLAMMATION;
D O I
10.1016/j.addr.2020.07.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In cancer, lymph nodes (LNs) coordinate tumor antigen presentation necessary for effective antitumor immunity, both at the levels of local cellular interactions and tissue-level organization. In this review, we examine how LNs may be engineered to improve the therapeutic outcomes of cancer immunotherapy. At the cellular scale, targeting the LNs impacts the potency of cancer vaccines, immune checkpoint blockade, and adoptive cell transfer. On a tissue level, macro-scale biomaterials mimicking LN features can function as immune niches for cell reprogramming or delivery in vivo, or be utilized in vitro to enable preclinical testing of drugs and vaccines. We additionally review strategies to induce ectopic lymphoid sites reminiscent of LNs that may improve antitumor T cell priming. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 62
页数:21
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