{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,9]],"date-time":"2026-09-09T04:54:43Z","timestamp":1788929683680,"version":"build-2803163510"},"reference-count":61,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2026,1,1]],"date-time":"2026-01-01T00:00:00Z","timestamp":1767225600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Multiple Sclerosis Journal \u2013 Experimental, Translational and Clinical"],"published-print":{"date-parts":[[2026,1]]},"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>B cell depleting therapy has become a cornerstone in disease-modifying treatments for relapsing-remitting multiple sclerosis (RRMS). Given that the maximum blood concentration of ofatumumab (OFA) is two orders of magnitude lower than that of ocrelizumab, it was anticipated that OFA would result in fewer adverse events.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      The study included 38 RRMS patients had received at least 5 months of standard OFA administration. CD3\u2009\n                      <jats:sup>+<\/jats:sup>\n                      \u2009CD20\n                      <jats:sup>+<\/jats:sup>\n                      cell counts were assessed prior to OFA administration.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The number of CD3\u2009\n                      <jats:sup>+<\/jats:sup>\n                      \u2009CD20\n                      <jats:sup>+<\/jats:sup>\n                      cells reached up to 75\/\u03bcL in the treatment groups other than NTZ, and up to 200\/\u03bcL in the NTZ-treated group, where B cell levels increased. Lymphopenia classifies as Grade 2 (800\/\u03bcL or less) was observed in 7\/33 cases. Beyond the depletion of CD3\u2009\n                      <jats:sup>+<\/jats:sup>\n                      \u2009CD20\n                      <jats:sup>+<\/jats:sup>\n                      cells, a reduction in CD3\n                      <jats:sup>+<\/jats:sup>\n                      cells was noted in 29 of 33 cases (88%), and with seven cases showing progressive T cell decline for up to 5 months after OFA initiation.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>In addition to the expected depletion of B cells, there was a greater-than-anticipated reduction in T cells lacking CD20 expression. Long-term continuous BCDT appears to have a profound impact on the immune system. Adjustments to administration intervals should be considered to mitigate the risk of over-treatment.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/20552173251409954","type":"journal-article","created":{"date-parts":[[2026,1,2]],"date-time":"2026-01-02T17:45:43Z","timestamp":1767375943000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":2,"title":["T lymphopenia in multiple sclerosis patients treated with ofatumumab: Even with consideration for CD3\u2009\n                    <sup>+<\/sup>\n                    \u2009CD20\n                    <sup>+<\/sup>\n                    cells"],"prefix":"10.1177","volume":"12","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1274-8337","authenticated-orcid":false,"given":"Masami","family":"Tanaka","sequence":"first","affiliation":[{"name":"Kyoto MS Center, Kyoto Min-Iren Chuo Hospital, Kyoto, Japan"},{"name":"Department of Neurology, Kaikokai Josai Hospital, 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