T Lymphocyte-Captured DNA Network for Localized Immunotherapy.

Abstract

The efficient isolation of immune cells with high purity and low cell damage is important for immunotherapy and remains highly challenging. We herein report a cell capture DNA network containing polyvalent multimodules for the specific isolation and in situ incubation of T lymphocytes (T-cells). Two ultralong DNA chains synthesized by an enzymatic amplification process were rationally designed to include functional multimodules as cell anchors and immune adjuvants. Mutually complementary sequences facilitated the formation of a DNA network and encapsulation of T-cells, as well as offering cutting sites of a restriction enzyme for the responsive release of T-cells and immune adjuvants. The purity of captured tumor-infiltrating T-cells reached 98%, and the viability of T-cells maintained ∼90%. The T-cells-containing DNA network was further administrated to a tumor lesion for localized immunotherapy. Our work provides a robust nanobiotechnology for efficient isolation of immune cells and other biological particles.

• Authors: Chi Yao, Chenxu Zhu, Jianpu Tang, Junhan Ou, Rui Zhang, Dayong Yang
• Journal: Journal of the American Chemical Society (J Am Chem Soc) Vol. 143 Issue 46 Pg. 19330-19340 (11 24 2021) ISSN: 1520-5126 [Electronic] United States
• PMID: 34780151 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA

Topics

• Animals
• DNA (immunology)
• Immunotherapy
• Melanoma (immunology)
• Mice
• Mice, Inbred C57BL
• T-Lymphocytes (immunology)