(Q41079157)

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Genetically modified bone marrow-derived dendritic cells expressing tumor-associated viral or "self" antigens induce antitumor immunity in vivo

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Europe PubMed Central

PubMed publication ID

26 September 2017

Genetically modified bone marrow-derived dendritic cells expressing tumor-associated viral or "self" antigens induce antitumor immunity in vivo (English)

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Europe PubMed Central

PubMed publication ID

26 September 2017

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Michael T Lotze

3

object named as

Lotze MT

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Europe PubMed Central

PubMed publication ID

26 September 2017

author name string

Tüting T

1

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Europe PubMed Central

PubMed publication ID

26 September 2017

DeLeo AB

2

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Europe PubMed Central

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26 September 2017

Storkus WJ

4

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26 September 2017

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publication date

1 October 1997

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Europe PubMed Central

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26 September 2017

European Journal of Immunology

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Europe PubMed Central

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26 September 2017

27

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Europe PubMed Central

PubMed publication ID

26 September 2017

10

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Europe PubMed Central

PubMed publication ID

26 September 2017

2702-2707

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Europe PubMed Central

PubMed publication ID

26 September 2017

Eradication of adenovirus E1-induced tumors by E1A-specific cytotoxic T lymphocytes.

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Use of tumor-infiltrating lymphocytes and interleukin-2 in the immunotherapy of patients with metastatic melanoma. A preliminary report

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New tumor antigens recognized by T cells

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Human tumor antigens recognized by T lymphocytes

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The dendritic cell system and its role in immunogenicity

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Dendritic cells: a major story unfolds

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Bone marrow-derived dendritic cells pulsed with synthetic tumour peptides elicit protective and therapeutic antitumour immunity

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Dendritic Cells as Carriers for a Cytotoxic T-Lymphocyte Epitope-Based Peptide Vaccine in Protection Against a Human Papillomavirus Type 16-Induced Tumor

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Murine dendritic cells loaded in vitro with soluble protein prime cytotoxic T lymphocytes against tumor antigen in vivo

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Therapy of murine tumors with p53 wild-type and mutant sequence peptide-based vaccines

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Therapy of murine tumors with tumor peptide-pulsed dendritic cells: dependence on T cells, B7 costimulation, and T helper cell 1-associated cytokines

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Peptide-pulsed dendritic cells induce tumoricidal cytotoxic T lymphocytes from healthy donors against stably HLA-A*0201-binding peptides from the Melan-A/MART-1 self antigen

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In vivo and in vitro gene transfer to mammalian somatic cells by particle bombardment

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Influenza virus nucleoprotein-specific immunoglobulin G subclass and cytokine responses elicited by DNA vaccination are dependent on the route of vector DNA delivery

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Vaccination with cytotoxic T lymphocyte epitope-containing peptide protects against a tumor induced by human papillomavirus type 16-transformed cells

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Role of bone marrow-derived cells in presenting MHC class I-restricted tumor antigens

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Identification of proliferating dendritic cell precursors in mouse blood

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Generation of large numbers of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony-stimulating factor

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Proliferating dendritic cell progenitors in human blood

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Flow-cytometric determination of peptide-class I complex formation. Identification of p53 peptides that bind to HLA-A2.

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In vitro induction of human cytotoxic T lymphocyte responses against peptides of mutant and wild-type p53.

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Targeting p53 as a general tumor antigen

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Spontaneous human squamous cell carcinomas are killed by a human cytotoxic T lymphocyte clone recognizing a wild-type p53-derived peptide

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DNA-based immunization by in vivo transfection of dendritic cells

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Generation of MHC class I-restricted cytotoxic T lymphocytes by expression of a viral protein in muscle cells: antigen presentation by non-muscle cells

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Gene vaccination with naked plasmid DNA: mechanism of CTL priming

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Dendritic cells in antitumor immune responses. II. Dendritic cells grown from bone marrow precursors, but not mature DC from tumor-bearing mice, are effective antigen carriers in the therapy of established tumors.

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Identifiers

10.1002/EJI.1830271033

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 September 2017

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