نتایج جستجو برای: eso

تعداد نتایج: 3679  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Sacha Gnjatic Djordje Atanackovic Elke Jäger Mitsutoshi Matsuo Annamalai Selvakumar Nasser K Altorki Robert G Maki Bo Dupont Gerd Ritter Yao-Tseng Chen Alexander Knuth Lloyd J Old

NY-ESO-1 is one of the most immunogenic proteins described in human cancers, based on its capacity to elicit simultaneous antibody and CD8+ T cell responses in vivo. Although HLA class II restricted epitopes from NY-ESO-1 have been identified, no broad survey has yet established the status of natural CD4+ T cell responses in cancer patients in relation to CD8+ and antibody responses. We used a ...

Journal: :Journal of immunology 2005
Maja Mandic Florence Castelli Bratislav Janjic Christine Almunia Pedro Andrade Daniel Gillet Vladimir Brusic John M Kirkwood Bernard Maillere Hassane M Zarour

NY-ESO-1 is expressed by a broad range of human tumors and is often recognized by Abs in the sera of cancer patients with NY-ESO-1-expressing tumors. The NY-ESO-1 gene also encodes several MHC class I- and class II-restricted tumor epitopes recognized by T lymphocytes. In this study we report one novel pan-MHC class II-restricted peptide sequence, NY-ESO-1 87-111, that is capable of binding to ...

Journal: :International journal of molecular medicine 2013
Yuqing Chen Aimin Huang Meiqin Gao Yongqin Yan Wenmin Zhang

NY‑ESO‑1 is one of the most immunogenic cancer-testis (CT) antigens. Cancer vaccine trials based on NY‑ESO‑1 are currently ongoing. Dendritic cells (DCs) are the most potent antigen-presenting cells. The immune functions of DCs in a number of tumors have been identified; however, the potential therapeutic value of DCs pulsed with NY‑ESO‑1 in hepatocellular carcinoma (HCC) has not been extensive...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Xiao-Ying Shang Hong-Song Chen Hua-Gang Zhang Xue-Wen Pang Huan Qiao Ji-Run Peng Li-Ling Qin Ran Fei Ming-Hui Mei Xi-Sheng Leng Sacha Gnjatic Gerd Ritter Andrew J G Simpson Lloyd J Old Wei-Feng Chen

PURPOSE Hepatocellular carcinoma (HCC) can express various cancer-testis antigens including NY-ESO-1, members of the SSX family, members of the MAGE family, SCP-1, and CTP11. Immunotherapy directed against these antigens is a potential alternative treatment for HCC. To date, it remains unclear whether HCC patients have spontaneous immune responses to these tumor antigens. The objectives of this...

2010
Julien Fourcade Zhaojun Sun Mourad Benallaoua Philippe Guillaume Immanuel F. Luescher Cindy Sander John M. Kirkwood Vijay Kuchroo Hassane M. Zarour

The paradoxical coexistence of spontaneous tumor antigen-specific immune responses with progressive disease in cancer patients furthers the need to dissect the molecular pathways involved in tumor-induced T cell dysfunction. In patients with advanced melanoma, we have previously shown that the cancer-germline antigen NY-ESO-1 stimulates spontaneous NY-ESO-1-specific CD8(+) T cells that up-regul...

Journal: :Cancer research 2003
Kunle Odunsi Achim A Jungbluth Elisabeth Stockert Feng Qian Sacha Gnjatic Jonathan Tammela Marilyn Intengan Amy Beck Bernadette Keitz Darren Santiago Barbara Williamson Matthew J Scanlan Gerd Ritter Yao-Tseng Chen Deborah Driscoll Ashwani Sood Shashikant Lele Lloyd J Old

Cancer-testis (CT) antigens are expressed in a variety of cancers, but not in normal adult tissues, except for germ cells of the testis, and hence appear to be ideal targets for immunotherapy. In an effort to examine the potential of NY-ESO-1 and LAGE-1 CT antigens for immunotherapy in epithelial ovarian cancer (EOC), we examined the expression of these antigens by reverse transcription-PCR (RT...

2016
Elizabeth Shurell Maria E. Vergara-Lluri Yunfeng Li Joseph G. Crompton Arun Singh Nicholas Bernthal Hong Wu Fritz C. Eilber Sarah M. Dry

BACKGROUND Immunotherapy targeting cancer-testis antigen NY-ESO-1 shows promise for tumors with poor response to chemoradiation. Malignant peripheral nerve sheath tumors (MPNSTs) and liposarcomas (LPS) are chemoresistant and have few effective treatment options. Materials Methods: Using a comprehensive tissue microarray (TMA) of both benign and malignant tumors in primary, recurrent, and metast...

2003
Kunle Odunsi Achim A. Jungbluth Elisabeth Stockert Feng Qian Sacha Gnjatic Jonathan Tammela Marilyn Intengan Amy Beck Bernadette Keitz Darren Santiago Barbara Williamson Matthew J. Scanlan Gerd Ritter Yao-Tseng Chen Deborah Driscoll Ashwani Sood Shashikant Lele Lloyd J. Old

Cancer-testis (CT) antigens are expressed in a variety of cancers, but not in normal adult tissues, except for germ cells of the testis, and hence appear to be ideal targets for immunotherapy. In an effort to examine the potential of NY-ESO-1 and LAGE-1 CT antigens for immunotherapy in epithelial ovarian cancer (EOC), we examined the expression of these antigens by reverse transcription-PCR (RT...

Journal: :Cancer research 2000
H M Zarour W J Storkus V Brusic E Williams J M Kirkwood

The NY-ESO-1 gene is expressed by a range of human tumors and encodes HLA-A2-restricted melanoma peptides recognized by CD8+ CTLs. Here we report that the NY-ESO-1 gene also encodes two overlapping, but non-cross-reactive, HLA-DRB1*0401-presented peptides that are recognized by CD4+ T cells. The NY-ESO-1(119-143) peptide was able to induce specific CD4+ T cells in vitro from both an HLA-DRB1*04...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Junko Matsuzaki Sacha Gnjatic Paulette Mhawech-Fauceglia Amy Beck Austin Miller Takemasa Tsuji Cheryl Eppolito Feng Qian Shashikant Lele Protul Shrikant Lloyd J Old Kunle Odunsi

NY-ESO-1 is a "cancer-testis" antigen frequently expressed in epithelial ovarian cancer (EOC) and is among the most immunogenic tumor antigens defined to date. In an effort to understand in vivo tolerance mechanisms, we assessed the phenotype and function of NY-ESO-1-specific CD8(+) T cells derived from peripheral blood lymphocytes (PBLs), tumor-infiltrating lymphocytes (TILs), and tumor-associ...

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