FĚDOROVÁ, Lenka, Peter MÚDRY, Kateřina PILÁTOVÁ, Iveta SELINGEROVA, Jana MERHAUTOVÁ, Zdenek REHAK, Dalibor VALÍK, Eva HLAVÁČKOVÁ, Dáša ČERNÁ, Lucie FABEROVÁ, Pavel MAZÁNEK, Zdeněk PAVELKA, Regina DEMLOVÁ, Jaroslav ŠTĚRBA and Lenka ZDRAŽILOVÁ DUBSKÁ. Assessment of Immune Response Following Dendritic Cell-Based Immunotherapy in Pediatric Patients With Relapsing Sarcoma. Frontiers in Oncology. Lausanne: Frontiers Media S.A., 2019, vol. 9, NOV 14 2019, p. 1-12. ISSN 2234-943X. Available from: https://dx.doi.org/10.3389/fonc.2019.01169.
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Basic information
Original name Assessment of Immune Response Following Dendritic Cell-Based Immunotherapy in Pediatric Patients With Relapsing Sarcoma
Authors FĚDOROVÁ, Lenka (203 Czech Republic, belonging to the institution), Peter MÚDRY (203 Czech Republic, belonging to the institution), Kateřina PILÁTOVÁ (203 Czech Republic, belonging to the institution), Iveta SELINGEROVA (203 Czech Republic), Jana MERHAUTOVÁ (203 Czech Republic, belonging to the institution), Zdenek REHAK (203 Czech Republic), Dalibor VALÍK (203 Czech Republic, belonging to the institution), Eva HLAVÁČKOVÁ (203 Czech Republic, belonging to the institution), Dáša ČERNÁ (703 Slovakia, belonging to the institution), Lucie FABEROVÁ (203 Czech Republic, belonging to the institution), Pavel MAZÁNEK (203 Czech Republic, belonging to the institution), Zdeněk PAVELKA (203 Czech Republic, belonging to the institution), Regina DEMLOVÁ (203 Czech Republic, belonging to the institution), Jaroslav ŠTĚRBA (203 Czech Republic, belonging to the institution) and Lenka ZDRAŽILOVÁ DUBSKÁ (203 Czech Republic, guarantor, belonging to the institution).
Edition Frontiers in Oncology, Lausanne, Frontiers Media S.A. 2019, 2234-943X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.848
RIV identification code RIV/00216224:14110/19:00111754
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3389/fonc.2019.01169
UT WoS 000501248600001
Keywords in English dendritic cells; anticancer immunotherapy; dendritic-cell (DC)-based vaccine; pediatric sarcoma; academic clinical trials; immunomonitoring; personalized medicine
Tags 14110321, 14110516, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 4/3/2020 12:10.
Abstract
Monocyte-derived dendritic cell (DC)-based vaccines loaded with tumor self-antigens represent a novel approach in anticancer therapy. We evaluated DC-based anticancer immunotherapy (ITx) in an academic Phase I/II clinical trial for children, adolescent, and young adults with progressive, recurrent, or primarily metastatic high-risk tumors. The primary endpoint was safety of intradermal administration of manufactured DCs. Here, we focused on relapsing high-risk sarcoma subgroup representing a major diagnosis in DC clinical trial. As a part of peripheral blood immunomonitoring, we evaluated quantitative association between basic cell-based immune parameters. Furthermore, we describe the pattern of these parameters and their time-dependent variations during the DC vaccination in the peripheral blood immunograms. The peripheral blood immunograms revealed distinct patterns in particular patients in the study group. As a functional testing, we evaluated immune response of patient T-cells to the tumor antigens presented by DCs in the autoMLR proliferation assay. This analysis was performed with T-cells obtained prior to DC ITx initiation and with T-cells collected after the fifth dose of DCs, demonstrating that the anticancer DC-based vaccine stimulates a preexisting immune response against self-tumor antigens. Finally, we present clinical and immunological findings in a Ewing's sarcoma patient with an interesting clinical course. Prior to DC therapy, we observed prevailing CD8+ T-cell stimulation and low immunosuppressive monocytic myeloid-derived suppressor cells (M-MDSC) and regulatory T-cells (Tregs). This patient was subsequently treated with 19 doses of DCs and experienced substantial regression of metastatic lesions after second disease relapse and was further rechallenged with DCs. In this patient, functional ex vivo testing of autologous T-cell activation by manufactured DC medicinal product during the course of DC ITx revealed that personalized anticancer DC-based vaccine stimulates a preexisting immune response against self-tumor antigens and that the T-cell reactivity persisted for the period without DC treatment and was further boosted by DC rechallenge.
Links
LM2015090, research and development projectName: Český národní uzel Evropské sítě infrastruktur klinického výzkumu (Acronym: CZECRIN)
Investor: Ministry of Education, Youth and Sports of the CR
MUNI/A/1586/2018, interní kód MUName: Personalizovaná léčba v dětské onkologii: na cestě k "liquid dynamic medecine" a "N-of-1 clinical trials" (Acronym: Personalizovaná léčba v dětské onkologii)
Investor: Masaryk University, Category A
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