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Current Understanding of Cytotoxic T Lymphocyte Antigen-4 (CTLA-4) Signaling in T-Cell Biology and Disease Therapy

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dc.contributor.authorKim, Gil-Ran-
dc.contributor.authorChoi, Je-Min-
dc.date.accessioned2023-05-03T14:19:51Z-
dc.date.available2023-05-03T14:19:51Z-
dc.date.issued2022-08-
dc.identifier.issn1016-8478-
dc.identifier.issn0219-1032-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/185394-
dc.description.abstractCytotoxic T lymphocyte antigen-4 (CTLA-4) is an immune checkpoint molecule that is mainly expressed on activated T cells and regulatory T (Treg) cells that inhibits T-cell activation and regulates immune homeostasis. Due to the crucial functions of CTLA-4 in T-cell biology, CTLA-4-targeted immunotherapies have been developed for autoimmune disease as well as cancers. CTLA-4 is known to compete with CD28 to interact with B7, but some studies have revealed that its downstream signaling is independent of its ligand interaction. As a signaling domain of CTLA-4, the tyrosine motif plays a role in inhibiting T-cell activation. Recently, the lysine motif has been shown to be required for the function of Treg cells, emphasizing the importance of CTLA-4 signaling. In this review, we summarize the current understanding of CTLA-4 biology and molecular signaling events and discuss strategies to target CTLA-4 signaling for immune modulation and disease therapy.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisher한국분자세포생물학회-
dc.titleCurrent Understanding of Cytotoxic T Lymphocyte Antigen-4 (CTLA-4) Signaling in T-Cell Biology and Disease Therapy-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.14348/molcells.2022.2056-
dc.identifier.scopusid2-s2.0-85136200318-
dc.identifier.wosid000888494800001-
dc.identifier.bibliographicCitationMolecules and Cells, v.45, no.8, pp 513 - 521-
dc.citation.titleMolecules and Cells-
dc.citation.volume45-
dc.citation.number8-
dc.citation.startPage513-
dc.citation.endPage521-
dc.type.docTypeShort Survey-
dc.identifier.kciidART002872553-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusCLATHRIN-ASSOCIATED PROTEIN-
dc.subject.keywordPlusREGULATORY T-
dc.subject.keywordPlusPOSTTRANSLATIONAL MODIFICATIONS-
dc.subject.keywordPlusCOSTIMULATION BLOCKADE-
dc.subject.keywordPlusAUTOIMMUNE-DISEASE-
dc.subject.keywordPlusCYTOPLASMIC DOMAIN-
dc.subject.keywordPlusFOLLICULAR HELPER-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusCD28-
dc.subject.keywordPlusABATACEPT-
dc.subject.keywordAuthorcytotoxic T lymphocyte antigen-4 (CTLA-4)-
dc.subject.keywordAuthorimmunotherapy-
dc.subject.keywordAuthorsignaling motif-
dc.subject.keywordAuthorT cell-
dc.subject.keywordAuthorTreg cell-
dc.subject.keywordAuthor--
dc.identifier.urlhttps://www.molcells.org/journal/view.html?doi=10.14348/molcells.2022.2056-
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