File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.tripleo.2008.08.012
- Scopus: eid_2-s2.0-53249113207
- PMID: 18929994
- WOS: WOS:000259973000019
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Transgenic B7-H3 therapy induces tumor-specific immune response in human oral squamous cell cancer: an in vitro study
Title | Transgenic B7-H3 therapy induces tumor-specific immune response in human oral squamous cell cancer: an in vitro study | ||||||||
---|---|---|---|---|---|---|---|---|---|
Authors | |||||||||
Keywords | Chemicals And Cas Registry Numbers | ||||||||
Issue Date | 2008 | ||||||||
Publisher | Mosby, Inc. The Journal's web site is located at http://www.elsevier.com/locate/tripleo | ||||||||
Citation | Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology And Endodontology, 2008, v. 106 n. 5, p. 721-728 How to Cite? | ||||||||
Abstract | Objective: Tumors may present antigens to T cells but lack costimulatory signals which are necessary to initialize an effective immunologic response. This study aimed to develop a tumor cell-based cancer vaccine by genetically modifying oral squamous cell cancer (OSCC) cell line Tca8113 with human B7-H3 immunoglobulin, and to evaluate its efficacy in enhancing the tumor-specific immune response. Study design: Human B7-H3 gene was extracted from isolated T lymphocytes of healthy volunteers. Tumor cell vaccine TCV-hB7-H3 and mock control were prepared by transfecting Tca8113 cells with B7-H3 or mock vector. After being stimulated with TCV-hB7-H3 or mock control, the proliferation, IFN-μ expression, and cytotoxicity of the T cells were assessed. Results: The Tca8113 cells transfected with human B7-H3 significantly enhanced the proliferation, IFN-μ expression, and cytotoxicity of the T cells. Conclusions: Genetically modified OSCC cells encoding B7-H3 enhance the induction of tumor specific immune response. © 2008 Mosby, Inc. All rights reserved. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/90590 | ||||||||
ISSN | 2011 Impact Factor: 1.457 | ||||||||
ISI Accession Number ID |
Funding Information: Supported by National Nature Science Foundation (30672335), Guangdong Provincial Nature Science Foundation (06027977), and Shenzhen Science and Technology Program (200601008). Tca8113 cell line kindly provided by Shanghai Jiaotong University. | ||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yang, HY | en_HK |
dc.contributor.author | Chu, M | en_HK |
dc.contributor.author | Zheng, L | en_HK |
dc.contributor.author | Zwahlen, RA | en_HK |
dc.contributor.author | Luo, J | en_HK |
dc.contributor.author | Zou, DH | en_HK |
dc.contributor.author | Sun, ST | en_HK |
dc.date.accessioned | 2010-09-17T10:05:21Z | - |
dc.date.available | 2010-09-17T10:05:21Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology And Endodontology, 2008, v. 106 n. 5, p. 721-728 | en_HK |
dc.identifier.issn | 1079-2104 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/90590 | - |
dc.description.abstract | Objective: Tumors may present antigens to T cells but lack costimulatory signals which are necessary to initialize an effective immunologic response. This study aimed to develop a tumor cell-based cancer vaccine by genetically modifying oral squamous cell cancer (OSCC) cell line Tca8113 with human B7-H3 immunoglobulin, and to evaluate its efficacy in enhancing the tumor-specific immune response. Study design: Human B7-H3 gene was extracted from isolated T lymphocytes of healthy volunteers. Tumor cell vaccine TCV-hB7-H3 and mock control were prepared by transfecting Tca8113 cells with B7-H3 or mock vector. After being stimulated with TCV-hB7-H3 or mock control, the proliferation, IFN-μ expression, and cytotoxicity of the T cells were assessed. Results: The Tca8113 cells transfected with human B7-H3 significantly enhanced the proliferation, IFN-μ expression, and cytotoxicity of the T cells. Conclusions: Genetically modified OSCC cells encoding B7-H3 enhance the induction of tumor specific immune response. © 2008 Mosby, Inc. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Mosby, Inc. The Journal's web site is located at http://www.elsevier.com/locate/tripleo | en_HK |
dc.relation.ispartof | Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology | en_HK |
dc.subject | Chemicals And Cas Registry Numbers | en_HK |
dc.subject.mesh | Antigens, CD - genetics - therapeutic use | en_HK |
dc.subject.mesh | B7 Antigens | en_HK |
dc.subject.mesh | Cancer Vaccines - genetics - therapeutic use | en_HK |
dc.subject.mesh | Carcinoma, Squamous Cell - drug therapy - immunology | en_HK |
dc.subject.mesh | Cell Line, Tumor | en_HK |
dc.subject.mesh | Cell Proliferation | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Interferons - biosynthesis | en_HK |
dc.subject.mesh | Mouth Neoplasms - drug therapy - immunology | en_HK |
dc.subject.mesh | Receptors, Immunologic - genetics - therapeutic use | en_HK |
dc.subject.mesh | T-Lymphocytes, Cytotoxic - immunology - metabolism | en_HK |
dc.subject.mesh | Transgenes | en_HK |
dc.title | Transgenic B7-H3 therapy induces tumor-specific immune response in human oral squamous cell cancer: an in vitro study | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Zheng, L:lwzheng@hku.hk | en_HK |
dc.identifier.email | Zwahlen, RA:zwahlen@hku.hk | en_HK |
dc.identifier.authority | Zheng, L=rp01411 | en_HK |
dc.identifier.authority | Zwahlen, RA=rp00055 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.tripleo.2008.08.012 | en_HK |
dc.identifier.pmid | 18929994 | - |
dc.identifier.scopus | eid_2-s2.0-53249113207 | en_HK |
dc.identifier.hkuros | 156024 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-53249113207&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 106 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 721 | en_HK |
dc.identifier.epage | 728 | en_HK |
dc.identifier.isi | WOS:000259973000019 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Yang, HY=7406556789 | en_HK |
dc.identifier.scopusauthorid | Chu, M=37017042500 | en_HK |
dc.identifier.scopusauthorid | Zheng, LW=11241247300 | en_HK |
dc.identifier.scopusauthorid | Zwahlen, RA=7004217269 | en_HK |
dc.identifier.scopusauthorid | Luo, J=35272549800 | en_HK |
dc.identifier.scopusauthorid | Zou, DH=25222293600 | en_HK |
dc.identifier.scopusauthorid | Sun, ST=25222309000 | en_HK |
dc.identifier.issnl | 1079-2104 | - |