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Authors |
Hara, Sayuri
Division of Molecular Pathology, Department of Pathology, School of Medicine, Tottori University Faculty of Medicine
Nagata, Keiko
Division of Molecular Pathology, Department of Pathology, School of Medicine, Tottori University Faculty of Medicine
Researchers DB
KAKEN
Nakayama, Yuji
Division of Radioisotope Science, Research Initiative Center, Organization for Research Initiative and Promotion
Researchers DB
KAKEN
Higaki, Katsumi
Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University
Researchers DB
KAKEN
Matsushita, Michiko
Department of Pathobiological Science and Technology, School of Health Science, Tottori University Faculty of Medicine
Researchers DB
KAKEN
Kuwamoto, Satoshi
Division of Molecular Pathology, Department of Pathology, School of Medicine, Tottori University Faculty of Medicine
Researchers DB
KAKEN
Kato, Masako
Division of Molecular Pathology, Department of Pathology, School of Medicine, Tottori University Faculty of Medicine
Researchers DB
KAKEN
Hayashi, Kazuhiko
Division of Molecular Pathology, Department of Pathology, School of Medicine, Tottori University Faculty of Medicine
Researchers DB
KAKEN
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Keywords | anti-gp350/220 antibody (72A1)
Epstein-Barr virus, estradiol
Graves’ disease
reactivation
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Abstract | Graves’ disease occurs predominantly in women. Epstein-Barr virus (EBV) mainly persists in human B lymphocytes, and its reactivation stimulates antibody production. We previously suggested that the EBV reactivation-induced production of TRAb and IgM at 100 nM estradiol (pregnant level) was lower than that at 0 nM estradiol and that class switch recombination may be increased by estradiol. In this study, we examined the effect of estradiol on EBV reactivation. We identified the expression of EBV-glycoprotein 350/220 (gp350/220) in the late phase of reactivation and plasma cell differentiation of EBV-infected cells using 72A1 antibody and CD138 antibody, respectively. We found the mean ratio of gp 350/220(+) CD138(+) cells at 100 nM estradiol was higher than that at 0 nM estradiol. These results suggested that EBV-infected cells could survive with keeping the ability of antibody production in 100 nM estradiol, which is consistent with the improvement of Graves’ disease during maternity and exacerbation postpartum.
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Publisher | Tottori University Medical Press
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Content Type |
Journal Article
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ISSN | 0513-5710
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EISSN | 1346-8049
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NCID | AA00892882
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Journal Title | Yonago Acta Medica
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Current Journal Title |
Yonago Acta Medica
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Volume | 62
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Issue | 2
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Start Page | 240
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End Page | 243
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Published Date | 2019-6-20
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Text Version |
Publisher
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Rights | 注があるものを除き、この著作物は日本国著作権法により保護されています。 / This work is protected under Japanese Copyright Law unless otherwise noted.
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Citation | Sayuri Hara, Keiko Nagata, Yuji Nakayama, Katsumi Higaki, Michiko Matsushita, Satoshi Kuwamoto, Masako Kato, Kazuhiko Hayashi, High Level Estradiol Induces EBV Reactivation and EBV gp350/220(+)CD138(+) Double-positive B Cell Population in Graves’ Disease Patients and Healthy Controls, Yonago Acta Medica, 2019, Volume 62, Issue 2, Pages 240-243
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Department |
Faculty of Medicine/Graduate School of Medical Sciences/University Hospital
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Language |
English
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