{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T08:53:01Z","timestamp":1791276781994,"version":"4.1.0"},"reference-count":28,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2017,3,27]],"date-time":"2017-03-27T00:00:00Z","timestamp":1490572800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2017,3,27]],"date-time":"2017-03-27T00:00:00Z","timestamp":1490572800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clin Exp Pharma Physio"],"published-print":{"date-parts":[[2017,4]]},"abstract":"<jats:title>Summary<\/jats:title>\n                  <jats:p>\n                    Bone fractures may result in delayed union (\n                    <jats:styled-content style=\"fixed-case\">DU<\/jats:styled-content>\n                    ) or non\u2010union (\n                    <jats:styled-content style=\"fixed-case\">NU<\/jats:styled-content>\n                    ) in some patients. Evidence suggests that the skewing of the immune system toward the proinflammatory type is a contributing factor. Because B cells were previously found to infiltrate the fracture healing site at abundant levels, we examined the regulatory B cells (Bregs) in\n                    <jats:styled-content style=\"fixed-case\">DU<\/jats:styled-content>\n                    \/\n                    <jats:styled-content style=\"fixed-case\">NU<\/jats:styled-content>\n                    patients. In bone fracture patients with normal healing, the frequency of interleukin (\n                    <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                    )\u201010\u2010expressing B cells was significantly upregulated in the early healing process (6\u00a0weeks post\u2010surgery) and was downregulated later on (18\u00a0weeks post\u2010surgery), whereas in\n                    <jats:styled-content style=\"fixed-case\">DU<\/jats:styled-content>\n                    \/\n                    <jats:styled-content style=\"fixed-case\">NU<\/jats:styled-content>\n                    patients, the early upregulation of\n                    <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                    \u201010\u2010expressing B cells was missing. The majority of\n                    <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                    \u201010\u2010expressing B cells were concentrated in the IgM\n                    <jats:sup>+<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    27\n                    <jats:sup>+<\/jats:sup>\n                    fraction in both controls and patients. IgM\n                    <jats:sup>+<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    27\n                    <jats:sup>+<\/jats:sup>\n                    B cells effectively suppressed interferon gamma (\n                    <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                    \u2010\u03b3), tumor necrosis factor alpha (\n                    <jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\n                    \u2010\u03b1), and\n                    <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                    \u20102 expression from\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    4\n                    <jats:sup>+<\/jats:sup>\n                    T cells, as well as\n                    <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\n                    \u2010\u03b3 and\n                    <jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\n                    \u2010\u03b1 expression from\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    8\n                    <jats:sup>+<\/jats:sup>\n                    T cells. The IgM\n                    <jats:sup>+<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    27\n                    <jats:sup>+<\/jats:sup>\n                    B cell\u2010mediated suppression was restricted to the sample from the early healing time point in controls, as the IgM\n                    <jats:sup>+<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    27\n                    <jats:sup>+<\/jats:sup>\n                    B cells from normal healing patients later on or from\n                    <jats:styled-content style=\"fixed-case\">DU<\/jats:styled-content>\n                    \/\n                    <jats:styled-content style=\"fixed-case\">NU<\/jats:styled-content>\n                    patients did not present significant regulatory function. In addition, culturing of\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    4\n                    <jats:sup>+<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    25\n                    <jats:sup>+<\/jats:sup>\n                    Tregs with IgM\n                    <jats:sup>+<\/jats:sup>\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    27\n                    <jats:sup>+<\/jats:sup>\n                    B cells from controls at early healing time point resulted in higher Foxp3 expression, a function absent in controls at later time point, or in\n                    <jats:styled-content style=\"fixed-case\">DU<\/jats:styled-content>\n                    \/\n                    <jats:styled-content style=\"fixed-case\">NU<\/jats:styled-content>\n                    patients. In conclusion, our results support a role of B cell\u2010mediated regulation early during the bone healing process.\n                  <\/jats:p>","DOI":"10.1111\/1440-1681.12719","type":"journal-article","created":{"date-parts":[[2016,12,24]],"date-time":"2016-12-24T11:49:08Z","timestamp":1482580148000},"page":"455-462","source":"Crossref","is-referenced-by-count":67,"title":["Regulatory B cell is critical in bone union process through suppressing proinflammatory cytokines and stimulating Foxp3 in Treg cells"],"prefix":"10.1111","volume":"44","author":[{"given":"Guojing","family":"Sun","sequence":"first","affiliation":[{"name":"Department of Orthopedics Jinling Hospital Nanjing University School of Medicine  Nanjing Jiangsu Province China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yicun","family":"Wang","sequence":"additional","affiliation":[{"name":"Department of Orthopedics Jinling Hospital Nanjing University School of Medicine  Nanjing Jiangsu Province 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