An Injectable Hydrogel to Modulate T Cells for Cancer Immunotherapy. Issue 32 (17th July 2022)
- Record Type:
- Journal Article
- Title:
- An Injectable Hydrogel to Modulate T Cells for Cancer Immunotherapy. Issue 32 (17th July 2022)
- Main Title:
- An Injectable Hydrogel to Modulate T Cells for Cancer Immunotherapy
- Authors:
- Zhang, Di
Li, Qian
Chen, Xiangwu
Nie, Xinxin
Xue, Fumin
Xu, Wei
Luan, Yuxia - Abstract:
- Abstract: T cell exhaustion caused by mitochondrial dysfunction is the major obstacle of T cells‐based cancer immunotherapy. Besides exhausted T cells, the insufficient major histocompatibility complex class I (MHC I) on tumor cells leads to inefficient T cell recognition of tumor cells, compromising therapeutic efficacy. Therapeutic platform to regulate T cell exhaustion and MHC I expression for boosting T cells‐based cancer immunotherapy has not been realized up to date. Herein, an injectable hydrogel is designed to simultaneously tune T cell exhaustion and MHC I expression for amplified cancer immunotherapy. The hydrogel is in situ constructed in tumor site by utilizing oxidized sodium alginate‐modified tumor cell membrane vesicle (O‐TMV) as a gelator, where axitinib is encapsulated in the lipid bilayer of O‐TMV while 4‐1BB antibody and proprotein convertase subtilisin/kexin type 9 inhibitor PF‐06446846 nanoparticles are present in the cavities of hydrogel. After immune response trigged by O‐TMV antigen, the 4‐1BB antibody‐promoted T cell mitochondrial biogenesis and the axitinib‐lowered hypoxia synergistically reverse T cell exhaustion while the PF‐06446846‐amplified MHC I expression facilitates T cell recognition of tumor cells, demonstrating a powerful immunotherapeutic efficacy. This strategy on reprograming T cell exhaustion and improving T cell potency offers new concept for T cells‐based cancer immunotherapy. Abstract : An injectable hydrogel is designed toAbstract: T cell exhaustion caused by mitochondrial dysfunction is the major obstacle of T cells‐based cancer immunotherapy. Besides exhausted T cells, the insufficient major histocompatibility complex class I (MHC I) on tumor cells leads to inefficient T cell recognition of tumor cells, compromising therapeutic efficacy. Therapeutic platform to regulate T cell exhaustion and MHC I expression for boosting T cells‐based cancer immunotherapy has not been realized up to date. Herein, an injectable hydrogel is designed to simultaneously tune T cell exhaustion and MHC I expression for amplified cancer immunotherapy. The hydrogel is in situ constructed in tumor site by utilizing oxidized sodium alginate‐modified tumor cell membrane vesicle (O‐TMV) as a gelator, where axitinib is encapsulated in the lipid bilayer of O‐TMV while 4‐1BB antibody and proprotein convertase subtilisin/kexin type 9 inhibitor PF‐06446846 nanoparticles are present in the cavities of hydrogel. After immune response trigged by O‐TMV antigen, the 4‐1BB antibody‐promoted T cell mitochondrial biogenesis and the axitinib‐lowered hypoxia synergistically reverse T cell exhaustion while the PF‐06446846‐amplified MHC I expression facilitates T cell recognition of tumor cells, demonstrating a powerful immunotherapeutic efficacy. This strategy on reprograming T cell exhaustion and improving T cell potency offers new concept for T cells‐based cancer immunotherapy. Abstract : An injectable hydrogel is designed to reprogram T cell exhaustion and amplify specific T cell recognition of tumor cells for boosting T cells‐based cancer immunotherapy, demonstrating powerful suppression of tumor growth, metastasis, and recurrence via the induced strong systemic and long‐term memory immune response. This study offers new concept for T cells‐based cancer immunotherapy. … (more)
- Is Part Of:
- Small. Volume 18:Issue 32(2022)
- Journal:
- Small
- Issue:
- Volume 18:Issue 32(2022)
- Issue Display:
- Volume 18, Issue 32 (2022)
- Year:
- 2022
- Volume:
- 18
- Issue:
- 32
- Issue Sort Value:
- 2022-0018-0032-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-07-17
- Subjects:
- hydrogels -- immunotherapy -- mitochondria -- T cell exhaustion -- T cell recognition
Nanotechnology -- Periodicals
Nanoparticles -- Periodicals
Microtechnology -- Periodicals
620.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1613-6829 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/smll.202202663 ↗
- Languages:
- English
- ISSNs:
- 1613-6810
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8309.952000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23855.xml