Recent Advances of Mesoporous Silica as a Platform for Cancer Immunotherapy
Immunotherapy is a promising modality of treatment for cancer. Immunotherapy is comprised of systemic and local treatments that induce an immune response, allowing the body to fight back against cancer. Systemic treatments such as cancer vaccines harness antigen presenting cells (APCs) to activate T...
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Published in | Biosensors (Basel) Vol. 12; no. 2; p. 109 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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10.02.2022
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Abstract | Immunotherapy is a promising modality of treatment for cancer. Immunotherapy is comprised of systemic and local treatments that induce an immune response, allowing the body to fight back against cancer. Systemic treatments such as cancer vaccines harness antigen presenting cells (APCs) to activate T cells with tumor-associated antigens. Small molecule inhibitors can be employed to inhibit immune checkpoints, disrupting tumor immunosuppression and immune evasion. Despite the current efficacy of immunotherapy, improvements to delivery can be made. Nanomaterials such as mesoporous silica can facilitate the advancement of immunotherapy. Mesoporous silica has high porosity, decent biocompatibility, and simple surface functionalization. Mesoporous silica can be utilized as a versatile carrier of various immunotherapeutic agents. This review gives an introduction on mesoporous silica as a nanomaterial, briefly covering synthesis and biocompatibility, and then an overview of the recent progress made in the application of mesoporous silica to cancer immunotherapy. |
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AbstractList | Immunotherapy is a promising modality of treatment for cancer. Immunotherapy is comprised of systemic and local treatments that induce an immune response, allowing the body to fight back against cancer. Systemic treatments such as cancer vaccines harness antigen presenting cells (APCs) to activate T cells with tumor-associated antigens. Small molecule inhibitors can be employed to inhibit immune checkpoints, disrupting tumor immunosuppression and immune evasion. Despite the current efficacy of immunotherapy, improvements to delivery can be made. Nanomaterials such as mesoporous silica can facilitate the advancement of immunotherapy. Mesoporous silica has high porosity, decent biocompatibility, and simple surface functionalization. Mesoporous silica can be utilized as a versatile carrier of various immunotherapeutic agents. This review gives an introduction on mesoporous silica as a nanomaterial, briefly covering synthesis and biocompatibility, and then an overview of the recent progress made in the application of mesoporous silica to cancer immunotherapy. Immunotherapy is a promising modality of treatment for cancer. Immunotherapy is comprised of systemic and local treatments that induce an immune response, allowing the body to fight back against cancer. Systemic treatments such as cancer vaccines harness antigen presenting cells (APCs) to activate T cells with tumor-associated antigens. Small molecule inhibitors can be employed to inhibit immune checkpoints, disrupting tumor immunosuppression and immune evasion. Despite the current efficacy of immunotherapy, improvements to delivery can be made. Nanomaterials such as mesoporous silica can facilitate the advancement of immunotherapy. Mesoporous silica has high porosity, decent biocompatibility, and simple surface functionalization. Mesoporous silica can be utilized as a versatile carrier of various immunotherapeutic agents. This review gives an introduction on mesoporous silica as a nanomaterial, briefly covering synthesis and biocompatibility, and then an overview of the recent progress made in the application of mesoporous silica to cancer immunotherapy.Immunotherapy is a promising modality of treatment for cancer. Immunotherapy is comprised of systemic and local treatments that induce an immune response, allowing the body to fight back against cancer. Systemic treatments such as cancer vaccines harness antigen presenting cells (APCs) to activate T cells with tumor-associated antigens. Small molecule inhibitors can be employed to inhibit immune checkpoints, disrupting tumor immunosuppression and immune evasion. Despite the current efficacy of immunotherapy, improvements to delivery can be made. Nanomaterials such as mesoporous silica can facilitate the advancement of immunotherapy. Mesoporous silica has high porosity, decent biocompatibility, and simple surface functionalization. Mesoporous silica can be utilized as a versatile carrier of various immunotherapeutic agents. This review gives an introduction on mesoporous silica as a nanomaterial, briefly covering synthesis and biocompatibility, and then an overview of the recent progress made in the application of mesoporous silica to cancer immunotherapy. |
Author | Chen, Huaqing Wang, Zixian Guo, Bing Yu, Albert Huang, Laiqiang Dai, Xiaoyong |
AuthorAffiliation | 3 School of Science and Shenzhen Key Laboratory of Flexible Printed Electronics Technology, Harbin Institute of Technology, Shenzhen 518055, China; guobing2020@hit.edu.cn 2 Shenzhen Key Laboratory of Gene and Antibody Therapy, State Key Laboratory of Chemical Oncogenomics, State Key Laboratory of Health Sciences and Technology, Tsinghua University, Shenzhen 518055, China 1 Precision Medicine and Healthcare Research Center, Tsinghua-Berkeley Shenzhen Institute (TBSI), Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China; yxz20@mails.tsinghua.edu.cn (A.Y.); dai-xy18@mails.tsinghua.edu.cn (X.D.); wzx21@mails.tsinghua.edu.cn (Z.W.); chq20@mails.tsinghua.edu.cn (H.C.) |
AuthorAffiliation_xml | – name: 2 Shenzhen Key Laboratory of Gene and Antibody Therapy, State Key Laboratory of Chemical Oncogenomics, State Key Laboratory of Health Sciences and Technology, Tsinghua University, Shenzhen 518055, China – name: 1 Precision Medicine and Healthcare Research Center, Tsinghua-Berkeley Shenzhen Institute (TBSI), Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China; yxz20@mails.tsinghua.edu.cn (A.Y.); dai-xy18@mails.tsinghua.edu.cn (X.D.); wzx21@mails.tsinghua.edu.cn (Z.W.); chq20@mails.tsinghua.edu.cn (H.C.) – name: 3 School of Science and Shenzhen Key Laboratory of Flexible Printed Electronics Technology, Harbin Institute of Technology, Shenzhen 518055, China; guobing2020@hit.edu.cn |
Author_xml | – sequence: 1 givenname: Albert surname: Yu fullname: Yu, Albert organization: Shenzhen Key Laboratory of Gene and Antibody Therapy, State Key Laboratory of Chemical Oncogenomics, State Key Laboratory of Health Sciences and Technology, Tsinghua University, Shenzhen 518055, China – sequence: 2 givenname: Xiaoyong surname: Dai fullname: Dai, Xiaoyong organization: Shenzhen Key Laboratory of Gene and Antibody Therapy, State Key Laboratory of Chemical Oncogenomics, State Key Laboratory of Health Sciences and Technology, Tsinghua University, Shenzhen 518055, China – sequence: 3 givenname: Zixian surname: Wang fullname: Wang, Zixian organization: Shenzhen Key Laboratory of Gene and Antibody Therapy, State Key Laboratory of Chemical Oncogenomics, State Key Laboratory of Health Sciences and Technology, Tsinghua University, Shenzhen 518055, China – sequence: 4 givenname: Huaqing surname: Chen fullname: Chen, Huaqing organization: Shenzhen Key Laboratory of Gene and Antibody Therapy, State Key Laboratory of Chemical Oncogenomics, State Key Laboratory of Health Sciences and Technology, Tsinghua University, Shenzhen 518055, China – sequence: 5 givenname: Bing orcidid: 0000-0001-7981-0644 surname: Guo fullname: Guo, Bing organization: School of Science and Shenzhen Key Laboratory of Flexible Printed Electronics Technology, Harbin Institute of Technology, Shenzhen 518055, China – sequence: 6 givenname: Laiqiang orcidid: 0000-0002-2237-5300 surname: Huang fullname: Huang, Laiqiang organization: Shenzhen Key Laboratory of Gene and Antibody Therapy, State Key Laboratory of Chemical Oncogenomics, State Key Laboratory of Health Sciences and Technology, Tsinghua University, Shenzhen 518055, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35200369$$D View this record in MEDLINE/PubMed |
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Copyright | 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2022 by the authors. 2022 |
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Keywords | mesoporous silica nanoparticles nanomaterial cancer drug delivery immunotherapy |
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SubjectTerms | Antigen (tumor-associated) Antigen-presenting cells Antigens Biocompatibility Biodistribution Cancer Cancer immunotherapy Cancer vaccines Cancer Vaccines - immunology Cancer Vaccines - therapeutic use Chemotherapy drug delivery Drug delivery systems Humans Immune checkpoint Immune response Immune system Immunosuppression Immunotherapy Laboratories Lymphocytes Lymphocytes T mesoporous silica nanoparticles Morphology nanomaterial Nanomaterials Nanoparticles Nanotechnology Neoplasms - drug therapy Particle size Pore size Porosity Review Silica Silicon Dioxide Surfactants Tumors Vaccines |
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Title | Recent Advances of Mesoporous Silica as a Platform for Cancer Immunotherapy |
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