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N-二氢半乳糖壳聚糖作为树突状细胞的强效免疫激活剂。

N-dihydrogalactochitosan as a potent immune activator for dendritic cells.

作者信息

El-Hussein Ahmed, Lam Samuel S K, Raker Joseph, Chen Wei R, Hamblin Michael R

机构信息

Massachusetts General Hospital, Wellman Center for Photomedicine, Boston, Massachusetts 02114.

Department of Dermatology, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Biomed Mater Res A. 2017 Apr;105(4):963-972. doi: 10.1002/jbm.a.35991. Epub 2017 Jan 10.

Abstract

Immunotherapy has become one of the fastest growing areas of cancer research. A promising in situ autologous cancer vaccine (inCVAX) uses a novel immune activator, N-dihydrogalactochitosan (GC), that possesses the ability to stimulate dendritic cells (DC). inCVAX is a combination treatment procedure involving treatment of the tumor with a thermal near-infrared laser to liberate whole cell tumor antigens, followed by injection of GC (a glucosamine polymer with galactose attached to the amino groups) into the treated tumor thereby inducing a systemic antitumor immune response. Regression of both the treated tumor and distant untreated metastases has been observed in both nonclinical and clinical settings following inCVAX. We studied the stimulatory action of GC on relatively immature DCs (DC2.4 cell line) in vitro. GC at 1 mg/mL was a potent stimulator for DC with limited toxicity, giving increased expression of major histocompatibility complex class 2, CD80, and CD11c. Confocal imaging also revealed qualitatively increased uptake of antigen (Texas red-labeled ovalbumin) by DCs after the introduction of GC. To visualize cellular uptake, GC was conjugated with FITC-fluorophore revealing its cellular internalization after 8 hours. In some cases GC was more effective than the toxic TLR4 agonist, lipopolysaccharide. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 963-972, 2017.

摘要

免疫疗法已成为癌症研究中发展最快的领域之一。一种有前景的原位自体癌症疫苗(inCVAX)使用了一种新型免疫激活剂N - 二氢半乳糖壳聚糖(GC),它具有刺激树突状细胞(DC)的能力。inCVAX是一种联合治疗程序,包括用热近红外激光治疗肿瘤以释放全细胞肿瘤抗原,随后将GC(一种氨基上连接有半乳糖的葡糖胺聚合物)注射到经治疗的肿瘤中,从而诱导全身性抗肿瘤免疫反应。在inCVAX治疗后的非临床和临床环境中,均观察到了经治疗肿瘤和远处未治疗转移灶的消退。我们在体外研究了GC对相对未成熟的DC(DC2.4细胞系)的刺激作用。1mg/mL的GC是DC的有效刺激剂,毒性有限,可使主要组织相容性复合体II类、CD80和CD11c的表达增加。共聚焦成像还定性地显示,引入GC后DC对抗原(德克萨斯红标记的卵清蛋白)的摄取增加。为了观察细胞摄取情况,将GC与FITC荧光团偶联,显示其在8小时后发生细胞内化。在某些情况下,GC比有毒的TLR4激动剂脂多糖更有效。©2017威利期刊公司。《生物医学材料研究杂志》A部分:105A:963 - 972,2017年。

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