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dc.contributor.author홍소희*
dc.date.accessioned2023-04-14T16:31:12Z-
dc.date.available2023-04-14T16:31:12Z-
dc.date.issued2023*
dc.identifier.issn0741-5400*
dc.identifier.issn1938-3673*
dc.identifier.otherOAK-33132*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/264877-
dc.description.abstractGal-4 enhances the immunostimulatory activity of M2 macrophages upon viral infection, leading to the reinforced antiviral functionality of CD4(+) T cells. Galectin-4 (Gal-4) is a beta-galactoside-binding protein belonging to the galectin family. Although Gal-4 is known to be involved in several physiologic processes of the gastrointestinal tract, its immunomodulatory roles remain unclear. In this study, we investigated whether Gal-4 influences the function of M1 and M2 macrophages. Gal-4 treatment drove more robust changes in the gene expression of M2 macrophages compared to M1 macrophages. Antiviral immune response-related genes were significantly upregulated in Gal-4-treated M2 macrophages. Gal-4 significantly enhanced the immunostimulatory activity of M2 macrophages upon Toll-like receptor 7 stimulation or infection with lymphocytic choriomeningitis virus (LCMV). Moreover, the antibody production against LCMV infection and the antiviral CD4(+) T-cell responses, but not the antiviral CD8(+) T-cell responses, were greatly increased by Gal-4-treated M2 macrophages in vivo. The present results indicate that Gal-4 enhances the ability of M2 macrophages to promote antiviral CD4(+) T-cell responses. Thus, Gal-4 could be used to boost antiviral immune responses.*
dc.languageEnglish*
dc.publisherWILEY*
dc.subjectgalectin-4*
dc.subjectM1 macrophage*
dc.subjectM2 macrophage*
dc.subjectCD4(+) T cell*
dc.subjectlymphocytic choriomeningitis virus*
dc.titleGalectin-4 increases the ability of M2 macrophages to enhance antiviral CD4(+) T-cell responses*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume113*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage71*
dc.relation.lastpage83*
dc.relation.journaltitleJOURNAL OF LEUKOCYTE BIOLOGY*
dc.identifier.doi10.1093/jleuko/qiac008*
dc.identifier.wosidWOS:000911647700007*
dc.identifier.scopusid2-s2.0-85148682575*
dc.author.googleLee, In-Gu*
dc.author.googleJoo, Yong-Hyun*
dc.author.googleJeon, Hoyeon*
dc.author.googleJeong, Raehyuk*
dc.author.googleKim, Eui Ho*
dc.author.googleChung, Hyunwoo*
dc.author.googleEyun, Seong-il*
dc.author.googleKim, Jeongkyu*
dc.author.googleSeo, Young-Jin*
dc.author.googleHong, So-Hee*
dc.contributor.scopusid홍소희(57197470752)*
dc.date.modifydate20240315135631*
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의과대학 > 의학과 > Journal papers
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