{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,24]],"date-time":"2026-03-24T11:26:32Z","timestamp":1774351592838,"version":"3.50.1"},"reference-count":28,"publisher":"S. Karger AG","issue":"6","license":[{"start":{"date-parts":[[2017,1,1]],"date-time":"2017-01-01T00:00:00Z","timestamp":1483228800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"},{"start":{"date-parts":[[2017,1,1]],"date-time":"2017-01-01T00:00:00Z","timestamp":1483228800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am J Nephrol"],"published-print":{"date-parts":[[2017]]},"abstract":"<jats:p>&lt;b&gt;&lt;i&gt;Background:&lt;\/i&gt;&lt;\/b&gt; This analysis compared efficacy, renal function, and histology in kidney transplant recipients receiving tacrolimus (TAC) combined with everolimus (EVR) or mycophenolate (MPS). &lt;b&gt;&lt;i&gt;Methods:&lt;\/i&gt;&lt;\/b&gt; This was a retrospective analysis from a randomized trial in kidney transplant recipients who received a single 3 mg\/kg dose of rabbit antithymocyte globulin (r-ATG), TAC, EVR, and prednisone (PRED; r-ATG\/EVR, &lt;i&gt;n&lt;\/i&gt; = 85), basiliximab (BAS), TAC, EVR, and PRED (BAS\/EVR, &lt;i&gt;n&lt;\/i&gt; = 102) or BAS, TAC, MPS, and PRED (BAS\/MPS, &lt;i&gt;n&lt;\/i&gt; = 101). We evaluated the incidence of de novo donor-specific anti-human leukocyte antigens antibodies (DSA) and histology on protocol biopsies at 12 months, and the incidence of acute rejection, estimated glomerular filtration rate (eGFR) and proteinuria at 36 months. &lt;b&gt;&lt;i&gt;Results:&lt;\/i&gt;&lt;\/b&gt; At 12 months, there were no differences in de novo DSA (6.4 vs. 3.4 vs. 5.5%) or in subclinical inflammation (2.0 vs. 4.8 vs. 10.2%), interstitial fibrosis\/tubular atrophy (57.1 vs. 58.5 vs. 53.8%) and C4d deposition (2.0 vs. 7.3 vs. 2.6%). At 36 months, there were no differences in the incidence of treatment failure (19.0 vs. 27.7 vs. 27.7%, &lt;i&gt;p&lt;\/i&gt; = 0.186), first biopsy-proven acute rejection (9.5 vs. 21.8 vs. 16.8%, &lt;i&gt;p&lt;\/i&gt; = 0.073), and urine protein\/creatinine ratios (0.53 \u00b1 1.05 vs. 0.62 \u00b1 0.75 vs. 0.71 \u00b1 1.24). eGFR was lower in the BAS\/EVR compared to that in the BAS\/MPS group (53.4 \u00b1 20.9 vs. 50.8 \u00b1 19.5 vs. 60.7 \u00b1 21.2 mL\/min\/1.73 m&lt;sup&gt;2&lt;\/sup&gt;, &lt;i&gt;p&lt;\/i&gt; = 0.017) but comparable using a sensitive analysis (49.5 \u00b1 23 vs. 47.5 \u00b1 22.6 vs. 53.6 \u00b1 27.8 mL\/min\/1.73 m&lt;sup&gt;2&lt;\/sup&gt;, &lt;i&gt;p&lt;\/i&gt; = 0.207). &lt;b&gt;&lt;i&gt;Conclusion:&lt;\/i&gt;&lt;\/b&gt; In this cohort, the use of EVR and reduced TAC concentrations were associated with comparable efficacy, renal function, and histological parameters compared to the standard-of-care immunosuppressive regimen.<\/jats:p>","DOI":"10.1159\/000475888","type":"journal-article","created":{"date-parts":[[2017,5,16]],"date-time":"2017-05-16T21:01:53Z","timestamp":1494968513000},"page":"497-508","source":"Crossref","is-referenced-by-count":18,"title":["Donor-Specific Anti-Human Leukocyte Antigens Antibodies, Acute Rejection, Renal Function, and Histology in Kidney Transplant Recipients Receiving Tacrolimus and 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