{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,11]],"date-time":"2026-10-11T21:46:12Z","timestamp":1791755172224,"version":"4.3.4"},"reference-count":22,"publisher":"SAGE Publications","issue":"10","license":[{"start":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T00:00:00Z","timestamp":1790812800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T00:00:00Z","timestamp":1790812800000},"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":["J Int Med Res"],"published-print":{"date-parts":[[2026,10]]},"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>Glucocorticoids are used to treat nephrotic syndrome; however, some patients develop resistance. T-lymphocyte subsets are involved in immune regulation and may be associated with disease progression and treatment response. The current prospective pilot cohort study explored T-cell immune phenotypes associated with steroid responsiveness in patients with nephrotic syndrome.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Eleven patients newly diagnosed with nephrotic syndrome between 2023 and 2024, classified as steroid-sensitive or steroid-resistant based on treatment outcomes, and 14 healthy volunteers were enrolled. Peripheral blood samples were collected at diagnosis (baseline), at weeks 4 and 8 after hormone therapy, and during monthly follow-up visits. T-cell subsets and T-cell immunoglobulin and mucin domain\u2013containing protein 3 (TIM-3) expression were analyzed using flow cytometry. Differences were identified by performing variance analysis, and correlations were assessed by performing linear regression.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      CD3\n                      <jats:sup>+<\/jats:sup>\n                      \u2009CD8\n                      <jats:sup>+<\/jats:sup>\n                      T cells differed between steroid-resistant patients and both steroid-responsive patients and controls (\n                      <jats:italic toggle=\"yes\">p<\/jats:italic>\n                      \u2009&lt;\u20090.05). The proportion of CD3\n                      <jats:sup>+<\/jats:sup>\n                      TIM-3\n                      <jats:sup>+<\/jats:sup>\n                      \u2009T cells differed between controls and steroid-sensitive patients (\n                      <jats:italic toggle=\"yes\">p<\/jats:italic>\n                      \u2009&lt;\u20090.001). Steroid treatment was associated with an increase in CD3\n                      <jats:sup>+<\/jats:sup>\n                      \u2009TIM-3\n                      <jats:sup>+<\/jats:sup>\n                      T cells and a potential negative correlation with albumin levels in steroid-sensitive patients.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>T-cell immune phenotypes, particularly TIM-3-expressing T cells, may be associated with steroid responsiveness in nephrotic syndrome. The current findings provide preliminary evidence for potential laboratory markers related to immune regulation.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/03000605261493753","type":"journal-article","created":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T03:49:09Z","timestamp":1791517749000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["A pilot prospective cohort study: Changes in circulating T-lymphocyte subsets during steroid therapy in patients with nephrotic syndrome"],"prefix":"10.1177","volume":"54","author":[{"given":"Yu","family":"Shan","sequence":"first","affiliation":[{"name":"Department of Nephrology, First People's Hospital of Pingjiang County, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-7956-4354","authenticated-orcid":false,"given":"Zhifen","family":"Xie","sequence":"additional","affiliation":[{"name":"Department of Nephrology, First People's Hospital of Pingjiang County, China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2026,10,8]]},"reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(18)30536-1"},{"key":"e_1_3_2_3_2","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.39576.709711.80"},{"key":"e_1_3_2_4_2","article-title":"Identification of patients with minimal change nephrotic syndrome from initial response to prednisone","volume":"98","author":"The primary nephrotic syndrome in children","year":"1981","unstructured":"The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children. 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