Publication:
Circulating IgA/IgG memory B cells against Mycobacterium tuberculosis dormancy-associated antigens Rv2659c and Rv3128c in active and latent tuberculosis

dc.contributor.authorPhyu Thwe Soeen_US
dc.contributor.authorJariya Hanthamrongwiten_US
dc.contributor.authorChutiphon Saeleeen_US
dc.contributor.authorSoe Paing Kyawen_US
dc.contributor.authorPrasong Khaenamen_US
dc.contributor.authorSaradee Wariten_US
dc.contributor.authorNusara Satproedpraien_US
dc.contributor.authorSurakameth Mahasirimongkolen_US
dc.contributor.authorHideki Yanaien_US
dc.contributor.authorPatchanee Chootongen_US
dc.contributor.authorChaniya Leepiyasakulchaien_US
dc.contributor.otherJapan Anti-Tuberculosis Associationen_US
dc.contributor.otherThailand Ministry of Public Healthen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.other(1000) Bedded General Hospitalen_US
dc.contributor.otherUniversity of Medical Technologyen_US
dc.date.accessioned2022-08-04T09:14:22Z
dc.date.available2022-08-04T09:14:22Z
dc.date.issued2021-09-01en_US
dc.description.abstractObjective: To elucidate the antigenic potential of dormancy-associated antigens Rv2659c and Rv3128c of Mycobacterium tuberculosis by examining the persistence of specific IgG and IgA memory B cells (MBCs) among patients with active tuberculosis (TB), household contacts with latent tuberculosis (LTBI), and an endemic healthy control group. Methods: Fresh peripheral blood mononuclear cells from the three study groups were used to enumerate the numbers of IgG and IgA MBCs specific to recombinant protein Rv2659c and Rv3128c by ELISpot assay. The composition of MBC subsets IgA+ and IgG + was analyzed by flow cytometry. Results: The number of IgA MBCs specific to antigen Rv2659c was significantly higher in the LTBI group than the TB group. In contrast, no significant difference was found in IgA or IgG MBCs against antigen Rv3128c. The number of IgA+ MBCs was significantly higher than that of IgG+ MBCs in the classical MBC subset of the LTBI group. Conclusion: The results indicated that the dormancy-associated antigen Rv2659c induced an IgA MBCs response in individuals with latent TB, and IgA+ classical MBCs formed a major portion of the MBCs subset. This new knowledge will be beneficial for the development of novel TB vaccines and their control of latent TB.en_US
dc.identifier.citationInternational Journal of Infectious Diseases. Vol.110, (2021), 75-82en_US
dc.identifier.doi10.1016/j.ijid.2021.07.033en_US
dc.identifier.issn18783511en_US
dc.identifier.issn12019712en_US
dc.identifier.other2-s2.0-85111822762en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/77915
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85111822762&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleCirculating IgA/IgG memory B cells against Mycobacterium tuberculosis dormancy-associated antigens Rv2659c and Rv3128c in active and latent tuberculosisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85111822762&origin=inwarden_US

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