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  • 1
    Online-Ressource
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    The American Association of Immunologists ; 2019
    In:  The Journal of Immunology Vol. 202, No. 1_Supplement ( 2019-05-01), p. 70.6-70.6
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 202, No. 1_Supplement ( 2019-05-01), p. 70.6-70.6
    Kurzfassung: In tumor immunotherapeutic vaccines, it is important to select tumor-associated antigen because of immunogenicity and oncogenic properties of tumor antigens. Many vaccination platforms were developed to enhance immunogenicity of antigens. In addition, many strategies are using tumor antigens in artificially mutated or truncated forms to eliminate oncogenic function of antigens. On the other hand, as the T cell immune responses depend on the recognition of epitopes that are loaded on the MHC class I molecules, it is important to maintain the original size as much as possible. In this study, we engineered HER2 antigens with four different forms, K684, K965, K1001, and K1117 and tested immunogenicity in B cell and monocyte based vaccine models. In murine models, we observed antigen specific T cell response in the antigen size dependent manner and antigen specific antibody response in the antigen expression dependent manner. We also tested tumor therapeutic models with full-length HER2 expressing CT26. All of four antigens showed tumor suppression in full-length HER2 expressing CT26 tumor models and K1117 showed highest therapeutic effect. In addition, the K1117 showed significant therapeutic effect in HER2 intracellular domain expressing CT26 tumor models compared to the K684. Moreover, in human PBMC studies, the K1117 showed better CD4 and CD8 T cell responses than the others did. These data suggested that antigens containing wide epitope repertoire could show better therapeutic effect.
    Materialart: Online-Ressource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: The American Association of Immunologists
    Publikationsdatum: 2019
    ZDB Id: 1475085-5
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
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    The American Association of Immunologists ; 2019
    In:  The Journal of Immunology Vol. 202, No. 1_Supplement ( 2019-05-01), p. 195.15-195.15
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 202, No. 1_Supplement ( 2019-05-01), p. 195.15-195.15
    Kurzfassung: Treatment with glucocorticoid-induced tumor necrosis factor receptor-related protein (GITR) agonistic antibody (DTA-1) elicits potent antitumor immune responses in various tumor models. In this study, we demonstrate the crucial role of interleukin (IL)-21–producing follicular helper T (Tfh) cells in DTA-1-induced tumor inhibition. Administration of DTA-1 increased IL-21 expression from CD4 T cells, which is mainly made up of Tfh cells, in an antigen specific manner. Furthermore, mice treated with a neutralizing antibody to IL-21 receptor and Bcl6fl/flCD4cre mice exhibited abrogated antitumor activity induced by DTA-1. Mechanistically, IL-4 plays critical roles for the induction of IL-21–expressing Th cells by GITR co-stimulation, which is mediated by Bcl6 and c-Maf. Thus, our findings identify GITR co-stimulation as an inducer of IL-21–expressing Tfh cells and provide a novel mechanism for its antitumor activity.
    Materialart: Online-Ressource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: The American Association of Immunologists
    Publikationsdatum: 2019
    ZDB Id: 1475085-5
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 67, No. 15 ( 2007-08-01), p. 7477-7486
    Kurzfassung: Her-2/neu is a well-characterized tumor-associated antigen overexpressed in human carcinomas such as breast cancer. Because Her-2/neu is a self-antigen with poor immunogenicity due to immunologic tolerance, active immunotherapy targeting Her-2/neu should incorporate methods to overcome immunologic tolerance to self-proteins. In this study, we developed a tolerogenic tumor model in mice using mouse Her-2/neu as self-antigen and investigated whether genetic vaccination with DNA plasmid and/or adenoviral vector expressing the extracellular and transmembrane domain of syngeneic mouse Her-2/neu or xenogenic human Her-2/neu could induce mouse Her-2/neu–specific CTL responses. Interestingly, adenoviral vectors expressing xenogenic human Her-2/neu (AdhHM) proved capable of breaking immune tolerance and of thereby inducing self-reactive CTL and antibodies, but not to the degree required to induce therapeutic antitumor immunity. In attempting to generate therapeutic antitumor immunity against established tumors, we adopted several approaches. Treatment with agonistic anti-glucocorticoid-induced TNFR family-related receptor (GITR) antibody plus AdhHM immunization significantly increased self-reactive CTL responses, and α-galactosylceramide (αGalCer)–loaded dendritic cells (DC) transduced with AdhHM were shown to break self-tolerance in a tolerogenic murine tumor model. Furthermore, gemcitabine treatment together with either AdhHM plus agonistic anti-GITR antibody administration or αGalCer-loaded DC transduced with AdhHM showed potent therapeutic antitumor immunity and perfect protection against preexisting tumors. Gemcitabine treatment attenuated the tumor-suppressive environment by eliminating CD11b+/Gr-1+ myeloid-derived suppressor cells. When combined with immunotherapies, gemcitabine offers a promising strategy for the Ag-specific treatment of human cancer. [Cancer Res 2007;67(15):7477–86]
    Materialart: Online-Ressource
    ISSN: 0008-5472 , 1538-7445
    RVK:
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    Sprache: Englisch
    Verlag: American Association for Cancer Research (AACR)
    Publikationsdatum: 2007
    ZDB Id: 2036785-5
    ZDB Id: 1432-1
    ZDB Id: 410466-3
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 80, No. 16_Supplement ( 2020-08-15), p. CT123-CT123
    Kurzfassung: BVAC-C is a B cell-based and monocyte-based immuno-therapeutic vaccine transfected with a recombinant human papillomavirus (HPV) 16/18 E6/E7 gene and loaded with alpha-galactosyl ceramide, which is a natural killer T cell ligand. This phase I study sought to determine the tolerability and immunogenicity of BVAC-C in platinum-resistant recurrent cervical cancer patients. Patients with HPV 16-positive or 18-positive recurrent or persistent cervical cancer who had received at least one prior platinum-based combination chemotherapy were enrolled. BVAC-C was injected intravenously three times every four weeks, and dose escalation was planned in a three-patient cohort design at doses of 1×107, 4×107, or 1×108 cells/dose. Eleven patients were enrolled, and six (55%) patients had received two or more lines of platinum-based chemotherapy prior to enrollment. Treatment-related adverse events (TRAEs) were observed in 21 cycles. Most TRAEs were mild fever (n = 6.55%) or myalgia (n = 4.36%). No dose-limiting toxicities occurred. The overall response rate was 11% among nine patients evaluable, and the duration of response was 10 months. Five patients (56%) achieved a stable disease for 4.2-11 months as their best overall response. The median progression-free survival in all patients was 6.8 months (95% CI, 3.2 to infinite months), and the overall survival rate at 6 and 12 months was 89% (95% CI, 71 to 100%) and 65% (95% CI, 39 to 100%), respectively. BVAC-C induced the activation of natural killer T cells, natural killer cells, and HPV 16/18 E6/E7-specific T cells upon vaccination in all patients evaluated. BVAC-C was well tolerated and demonstrated a durable anti-tumor activity with an immune response in HPV 16-positive or 18-positive recurrent cervical carcinoma patients. A Phase 2 efficacy trial is currently underway. Citation Format: Chel Hun Choi, Hyun Jin Choi, Jeong-Won Lee, Eun-Suk Kang, Duck Cho, Byung Kwan Park, Yong-Man Kim, Dae-Yeon Kim, Hyungseok Seo, Myunghwan Park, Wuhyun Kim, Ki-Young Choi, Taegwon Oh, Chang-Yuil Kang, Byoung-Gie Kim. Phase I study of a B cell-based and monocyte-based immunotherapeutic vaccine, BVAC-C, in human papillomavirus type 16- or 18-positive recurrent cervical cancer [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr CT123.
    Materialart: Online-Ressource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: American Association for Cancer Research (AACR)
    Publikationsdatum: 2020
    ZDB Id: 2036785-5
    ZDB Id: 1432-1
    ZDB Id: 410466-3
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
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    Wiley ; 2008
    In:  International Journal of Cancer Vol. 122, No. 12 ( 2008-06-15), p. 2774-2783
    In: International Journal of Cancer, Wiley, Vol. 122, No. 12 ( 2008-06-15), p. 2774-2783
    Materialart: Online-Ressource
    ISSN: 0020-7136 , 1097-0215
    URL: Issue
    RVK:
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2008
    ZDB Id: 218257-9
    ZDB Id: 1474822-8
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
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    The American Association of Immunologists ; 2009
    In:  The Journal of Immunology Vol. 182, No. 1_Supplement ( 2009-04-01), p. 132.11-132.11
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 182, No. 1_Supplement ( 2009-04-01), p. 132.11-132.11
    Kurzfassung: α-galactosylceramide (α-GalCer) can act as a safe and effective adjuvant for a nasal vaccine that induces protective immune responses against tumors and viral infections. In this study, α-GalCer analogues were designed to have branched acyl chain by modification of their fatty acyl chain based on the CD1d/glycolipid structures. Two α-GalCer analogues with various branched chain lengths; LDH-II-28 and LDH-II-30 were prepared and evaluated for their efficacy as a nasal influenza vaccine adjuvant. These analogues displayed improved solubility over α-GalCer and effectively stained NKT cells both in mouse and human. They also potently stimulated NKT cells to exhibit different cytokine release profiles from α-GalCer in vitro and in vivo. When profiling serum cytokines in vivo, LDH-II-30 provoked both Th1/Th2 cytokines, while LDH-II-28 induced more Th2-biased cytokine release with diminished IFN-γ production. We found that single immunization of inactivated influenza virus A/PR/8/34 (PR8) together with α-GalCer analogues enhanced PR8-specific humoral and cellular immune responses in both systemic and mucosal compartments. Notably, LDH-II-30 exhibited potent adjuvant effects with significantly higher systemic IgG, mucosal sIgA Ab titers and enhanced CTL generation compared to immunization with inactivated PR8 alone, while addition of LDH-II-28 to inactivated PR8 only marginally increased PR8-specific immune responses. These results suggest that α-GalCer analogues with branched acyl chain could be used as an effective mucosal adjuvant for the induction of influenza vaccine-specific humoral and cellular immune responses.
    Materialart: Online-Ressource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: The American Association of Immunologists
    Publikationsdatum: 2009
    ZDB Id: 1475085-5
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 7
    Online-Ressource
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    The American Association of Immunologists ; 2020
    In:  The Journal of Immunology Vol. 204, No. 1_Supplement ( 2020-05-01), p. 169.23-169.23
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 204, No. 1_Supplement ( 2020-05-01), p. 169.23-169.23
    Kurzfassung: Combination therapy is a cornerstone of anticancer therapy, suggesting potential therapeutic benefit to nonresponders to single-agent treatment. BVAC, a B-cell-and-monocyte-based vaccine loaded with alpha-galactosylceramide (α-GC) and tumor antigen as reported in our previous studies, can be successfully combined with other treatments. Here we found out a novel synergistic regimen in TC-1 tumor model which combines BVAC with topotecan, a chemotherapeutic agent as a topoisomerase I inhibitor. We demonstrated some significant alteration in the immunoprofiles of topotecan-treated mice. We observed increased tumor recruitment of monocytes and CD8+ T cells, and decreased frequencies in regulatory T cells in tumor. Accordingly, we are currently investigating how topotecan-induced changes in immune cell composition could lead to improvement of antitumor effect. These data indicate that topotecan not only has cytotoxicity to tumor but can contribute to modulating tumor immune microenvironment. We anticipate that this study could provide a rationale for combination of cancer vaccine and chemotherapy and define future optimal treatment regimens in cancer patients.
    Materialart: Online-Ressource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: The American Association of Immunologists
    Publikationsdatum: 2020
    ZDB Id: 1475085-5
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
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    Wiley ; 2004
    In:  European Journal of Immunology Vol. 34, No. 9 ( 2004-09), p. 2471-2479
    In: European Journal of Immunology, Wiley, Vol. 34, No. 9 ( 2004-09), p. 2471-2479
    Kurzfassung: NKT cells play contradictory roles in vivo , both regulating autoimmunity and activating immunity to intracellular pathogens and tumors. In this study, we studied the effect of NKT cell activation on the induction of systemic tolerance by oral administration of antigen. Administration of α‐galactosylceramide (αGC) at the time of oral ovalbumin (OVA) feeding completely blocked the OVA‐specific tolerance induced by both high‐ and low‐dose regimens in BALB/c mice. In the mesenteric lymph nodes (MLN) of αGC‐treated mice, the proliferation of OVA‐specific T cells was greater than that seen in the MLN of vehicle‐treated mice in vivo . The administration of αGC triggered the full maturation of mesenteric dendritic cells (DC), which were in turn responsible for the enhanced division of OVA‐specific T cells in vitro . To further determine whether the costimulation provided by DC in αGC‐treated mice was responsible for the reversal of oral tolerance in vivo , mice were given αGC together with anti‐CD80 and anti‐CD86 blocking Ab. OVA‐specific systemic tolerance was restored in mice given the blocking Ab, even when they simultaneously received αGC. Therefore, oral tolerance can be reversed via costimulation by DC that have been triggered to fully mature by the administration of αGC.
    Materialart: Online-Ressource
    ISSN: 0014-2980 , 1521-4141
    URL: Issue
    RVK:
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2004
    ZDB Id: 1491907-2
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 9
    In: Viral Immunology, Mary Ann Liebert Inc, Vol. 26, No. 4 ( 2013-08), p. 268-276
    Materialart: Online-Ressource
    ISSN: 0882-8245 , 1557-8976
    RVK:
    Sprache: Englisch
    Verlag: Mary Ann Liebert Inc
    Publikationsdatum: 2013
    ZDB Id: 2030616-7
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 10
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    The American Association of Immunologists ; 2018
    In:  The Journal of Immunology Vol. 201, No. 4 ( 2018-08-15), p. 1287-1294
    In: The Journal of Immunology, The American Association of Immunologists, Vol. 201, No. 4 ( 2018-08-15), p. 1287-1294
    Kurzfassung: Secretory IgA is a key host defense mechanism that controls the intestinal microbiota. We investigated the role of CD11c+CX3CR1+CD64+ macrophages in IgA production in the intestine. Intestinal CX3CR1+ macrophages directly induced IgA secretion by B cells. Ag delivery to lamina propria (LP) CX3CR1+ macrophages specifically induced intestinal IgA production. The induction of IgA by CX3CR1+ macrophages required BAFF, a proliferation-inducing ligand, and TNF-α, but was surprisingly independent of TLR-mediated microbial recognition and retinoic acid signaling. IgA secretion by CX3CR1+ macrophages was enhanced by LP CD8+ T cells through the secretion of IL-9 and IL-13. CX3CR1+ macrophages and CD8+ T cells induced IgA production by B cells independently of mesenteric lymph nodes and Peyer patches. Our data reveal a previously unrecognized cellular circuitry in which LP CX3CR1+ macrophages, B cells, and CD8+ T cells coordinate the protective Ig secretion in the small intestine upon peripheral Ag delivery.
    Materialart: Online-Ressource
    ISSN: 0022-1767 , 1550-6606
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: The American Association of Immunologists
    Publikationsdatum: 2018
    ZDB Id: 1475085-5
    Standort Signatur Einschränkungen Verfügbarkeit
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