Biomaterial‐Based Therapeutic Delivery of Immune Cells

Author:

Dravid Ameya A.1,Singh Ankur123,García Andrés J.13ORCID

Affiliation:

1. Woodruff School of Mechanical Engineering Georgia Institute of Technology Atlanta GA 30332 USA

2. Coulter Department of Biomedical Engineering Georgia Institute of Technology and Emory University Atlanta GA 30332 USA

3. Petit Institute for Bioengineering and Bioscience Georgia Institute of Technology Atlanta GA 30332 USA

Abstract

AbstractImmune cell therapy (ICT) is a transformative approach used to treat a wide range of diseases including type 1 diabetes, sickle cell disease, disorders of the hematopoietic system, and certain forms of cancers. Despite excellent clinical successes, the scope of adoptively transferred immune cells is limited because of toxicities like cytokine release syndrome and immune effector cell‐associated neurotoxicity in patients. Furthermore, reports suggest that such treatment can impact major organ systems including cardiac, renal, pulmonary, and hepatic systems in the long term. Additionally, adoptively transferred immune cells cannot achieve significant penetration into solid tissues, thus limiting their therapeutic potential. Recent studies suggest that biomaterial‐assisted delivery of immune cells can address these challenges by reducing toxicity, improving localization, and maintaining desired phenotypes to eventually regain tissue function. In this review, recent efforts in the field of biomaterial‐based immune cell delivery for the treatment of diseases, their pros and cons, and where these approaches stand in terms of clinical treatment are highlighted.

Funder

National Cancer Institute

Wellcome Leap

Publisher

Wiley

Reference129 articles.

1. What's New for Biologics Latest News from the Center for Biologics Evaluation and Research at FDA U.S. Food and Drug Administration [Available from https://www.fda.gov/vaccines‐blood‐biologics/news‐events‐biologics/whats‐new‐biologics.

2. Translational pharmacokinetics and pharmacodynamics of monoclonal antibodies

3. Pharmacokinetic and pharmacodynamic considerations for the next generation protein therapeutics

4. A multifunctional AAV–CRISPR–Cas9 and its host response

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3