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NY-ESO-1 protein formulated in ISCOMATRIX adjuvant is a potent anticancer vaccine inducing both humoral and CD8+ t-cell-mediated immunity and protection against NY-ESO-1+ tumors.

作者信息

Maraskovsky Eugene, Sjölander Sigrid, Drane Debbie P, Schnurr Max, Le Thuy T T, Mateo Luis, Luft Thomas, Masterman Kelly-Anne, Tai Tsin-Yee, Chen Qiyuan, Green Simon, Sjölander Anders, Pearse Martin J, Lemonnier Francois A, Chen Weisan, Cebon Jonathan, Suhrbier Andreas

机构信息

Ludwig Institute for Cancer Research, Austin and Repatriation Medical Centre, Melbourne, Victoria, Australia.

出版信息

Clin Cancer Res. 2004 Apr 15;10(8):2879-90. doi: 10.1158/1078-0432.ccr-03-0245.


DOI:10.1158/1078-0432.ccr-03-0245
PMID:15102697
Abstract

NY-ESO-1 is a 180 amino-acid human tumor antigen expressed by many different tumor types and belongs to the family of "cancer-testis" antigens. In humans, NY-ESO-1 is one of the most immunogenic tumor antigens and NY-ESO-1 peptides have been shown to induce NY-ESO-1-specific CD8(+) CTLs capable of altering the natural course of NY-ESO-1-expressing tumors in cancer patients. Here we describe the preclinical immunogenicity and efficacy of NY-ESO-1 protein formulated with the ISCOMATRIX adjuvant (NY-ESO-1 vaccine). In vitro, the NY-ESO-1 vaccine was readily taken up by human monocyte-derived dendritic cells, and on maturation, these human monocyte-derived dendritic cells efficiently cross-presented HLA-A2-restricted epitopes to NY-ESO-1-specific CD8(+) T cells. In addition, epitopes of NY-ESO-1 protein were also presented on MHC class II molecules to NY-ESO-1-specific CD4(+) T cells. The NY-ESO-1 vaccine induced strong NY-ESO-1-specific IFN-gamma and IgG2a responses in C57BL/6 mice. Furthermore, the NY-ESO-1 vaccine induced NY-ESO-1-specific CD8(+) CTLs in HLA-A2 transgenic mice that were capable of lysing human HLA-A2(+) NY-ESO-1(+) tumor cells. Finally, C57BL/6 mice, immunized with the NY-ESO-1 vaccine, were protected against challenge with a B16 melanoma cell line expressing NY-ESO-1. These data illustrate that the NY-ESO-1 vaccine represents a potent therapeutic anticancer vaccine.

摘要

相似文献

[1]
NY-ESO-1 protein formulated in ISCOMATRIX adjuvant is a potent anticancer vaccine inducing both humoral and CD8+ t-cell-mediated immunity and protection against NY-ESO-1+ tumors.

Clin Cancer Res. 2004-4-15

[2]
Identification of HLA-A24-restricted CTL epitope from cancer-testis antigen, NY-ESO-1, and induction of a specific antitumor immune response.

Clin Cancer Res. 2004-2-1

[3]
In vitro stimulation of CD8 and CD4 T cells by dendritic cells loaded with a complex of cholesterol-bearing hydrophobized pullulan and NY-ESO-1 protein: Identification of a new HLA-DR15-binding CD4 T-cell epitope.

Clin Cancer Res. 2006-3-15

[4]
Processing and cross-presentation of individual HLA-A, -B, or -C epitopes from NY-ESO-1 or an HLA-A epitope for Melan-A differ according to the mode of antigen delivery.

Blood. 2010-4-29

[5]
Antigen-specific immunity in neuroblastoma patients: antibody and T-cell recognition of NY-ESO-1 tumor antigen.

Cancer Res. 2003-10-15

[6]
Identification of a naturally processed NY-ESO-1 peptide recognized by CD8+ T cells in the context of HLA-B51.

Cancer Immun. 2002-9-19

[7]
Identification of NY-ESO-1 epitopes presented by human histocompatibility antigen (HLA)-DRB4*0101-0103 and recognized by CD4(+) T lymphocytes of patients with NY-ESO-1-expressing melanoma.

J Exp Med. 2000-2-21

[8]
[Estimation of an NY-ESO-1 expressing HCC cell line by NY-ESO-1b specific CD8+T cells in vitro induced by HLA-A2 restricted NY-ESO-1b peptide].

Beijing Da Xue Xue Bao Yi Xue Ban. 2005-12-18

[9]
Generation and characterization of HLA-A2 transgenic mice expressing the human TCR 1G4 specific for the HLA-A2 restricted NY-ESO-1 tumor-specific peptide.

J Immunother Cancer. 2021-6

[10]
Definition of key variables for the induction of optimal NY-ESO-1-specific T cells in HLA transgene mice.

J Immunol. 2010-8-23

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Methods Mol Biol. 2022

[2]
Cancer nanotechnology: current status and perspectives.

Nano Converg. 2021-11-2

[3]
Using Adjuvants to Drive T Cell Responses for Next-Generation Infectious Disease Vaccines.

Vaccines (Basel). 2021-7-24

[4]
Ropporin-1 and 1B Are Widely Expressed in Human Melanoma and Evoke Strong Humoral Immune Responses.

Cancers (Basel). 2021-4-9

[5]
A Phase 1b Study Evaluating the Safety, Tolerability, and Immunogenicity of CMB305, a Lentiviral-Based Prime-Boost Vaccine Regimen, in Patients with Locally Advanced, Relapsed, or Metastatic Cancer Expressing NY-ESO-1.

Oncoimmunology. 2020-11-19

[6]
Tumor ablation plus co-administration of CpG and saponin adjuvants affects IL-1 production and multifunctional T cell numbers in tumor draining lymph nodes.

J Immunother Cancer. 2020-5

[7]
Therapeutic ISCOMATRIX™ adjuvant vaccine elicits effective anti-tumor immunity in the TRAMP-C1 mouse model of prostate cancer.

Cancer Immunol Immunother. 2020-5-9

[8]
Co-delivery of human cancer-testis antigens with adjuvant in protein nanoparticles induces higher cell-mediated immune responses.

Biomaterials. 2017-11-20

[9]
Melanoma: tumor microenvironment and new treatments.

An Bras Dermatol. 2017

[10]
Saponin-based adjuvants induce cross-presentation in dendritic cells by intracellular lipid body formation.

Nat Commun. 2016-11-7

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