2025
Role of B cells in intratumoral MBTA immunotherapy of murine pheochromocytoma model
UHER, Ondrej; Katerina HADRAVA VANOVA; Kateřina PETRLÁKOVÁ; Rachael LABITT; Radka LENCOVA et. al.Basic information
Original name
Role of B cells in intratumoral MBTA immunotherapy of murine pheochromocytoma model
Authors
UHER, Ondrej (203 Czech Republic); Katerina HADRAVA VANOVA (203 Czech Republic); Kateřina PETRLÁKOVÁ (203 Czech Republic, belonging to the institution); Rachael LABITT; Radka LENCOVA (203 Czech Republic); Andrea FREJLACHOVA (203 Czech Republic); Juan YE; Herui WANG; Michal MASAŘÍK (203 Czech Republic, belonging to the institution); Jan ZENKA (203 Czech Republic); Zhengping ZHUANG and Karel PACAK (203 Czech Republic)
Edition
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, London, ELSEVIER SCI LTD, 2025, 1521-690X
Other information
Language
English
Type of outcome
Article in a journal
Field of Study
30202 Endocrinology and metabolism
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
is not subject to a state or trade secret
References:
Impact factor
Impact factor: 6.100 in 2023
Organization unit
Faculty of Medicine
UT WoS
001420745200001
EID Scopus
2-s2.0-85203831067
Keywords in English
pheochromocytoma; B cells; intratumoral immunotherapy; cytokine storm; melanoma
Tags
International impact, Reviewed
Changed: 3/3/2025 14:21, Mgr. Tereza Miškechová
Abstract
V originále
Immunotherapy represents a revolutionary advancement in cancer treatment, which has traditionally focused on T cells; however, the role of B cells in cancer immunotherapy has gained interest because of their role in antigen presentation, antibody production, and cytokine release. In this study, we examined the role of B cells in previously developed intratumoral MBTA therapy (mannan-BAM, TLR ligands, and anti-CD40 antibody) in murine models of MTT pheochromocytoma. The results indicated that B cells significantly enhance the success of MBTA therapy, with wild-type mice exhibiting a lower tumor incidence and smaller tumors compared with B cell-deficient mice. Increased IL-6 and TNF-alpha levels indicated severe inflammation and a potential cytokine storm in B cell-deficient mice. Neutralization of TNF-alpha ameliorated these complications but resulted in increased tumor recurrence. The results highlight the important role of B cells in enhancing the immune response and maintaining immune homeostasis during MBTA therapy. Our findings offer new insights into improving therapeutic outcomes.
Links
LUAUS24120, research and development project |
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