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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Improving the histologic detection of DSA-negative antibody-mediated rejection in kidney transplants</dc:title><dc:creator>Hidalgo,	Luis G.	(Avtor)
	</dc:creator><dc:creator>Arnol,	Miha	(Avtor)
	</dc:creator><dc:creator>Kojc,	Nika	(Avtor)
	</dc:creator><dc:creator>Večerić-Haler,	Željka	(Avtor)
	</dc:creator><dc:creator>Halloran,	Philip F	(Avtor)
	</dc:creator><dc:subject>donor-derived cell-free DNA</dc:subject><dc:subject>kidney biopsy</dc:subject><dc:subject>donor-specific antibody</dc:subject><dc:subject>microarrays antibody-mediated rejection</dc:subject><dc:subject>kidney transplant rejection</dc:subject><dc:description>Emerging treatments for antibody-mediated rejection (ABMR, NEJM391(2):122-132) have increased the importance of ABMR detection when donor-specific antibody (DSA) is negative. We addressed this issue in the Trifecta-Kidney study (ClinicalTrials.gov #NCT04239703) using three centralized tests in 690 kidney transplant biopsies: DSA (One Lambda Inc.), blood donor-derived cell-free DNA (dd-cfDNA, Prospera™ test, Natera, Inc.), and molecular biopsy assessment (MMDx). We used an “AutoBanff 2022” algorithm to model the impact of alternative DSA interpretations on the histologic diagnosis of “DSA-negative” ABMR following Banff guidelines, including agreement with dd-cfDNA and molecular ABMR. Lowering MFI cutoffs for DSA-positivity did not improve detection of DSA-negative ABMR. However, simply calling all DSA positive allowed Banff 2022 guidelines to identify 46% more ABMR cases with no measurable DSA, and per Net Reclassification Improvement increased agreement between histologic diagnoses and both dd-cfDNA (P=7.72E-7) and molecular ABMR (P=7.69E-7). New ABMR cases were as strongly positive for dd-cfDNA and molecular ABMR as those found using the conventional DSA interpretation. A validation set analysis using INTERCOMEX study data (ClinicalTrials.gov NCT#01299168) confirmed these findings, and found that the new DSA-negative ABMR cases identified by calling all DSA positive had the same risk for graft loss as those found with conventional DSA interpretation.</dc:description><dc:date>2026</dc:date><dc:date>2026-04-07 09:09:14</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>181417</dc:identifier><dc:identifier>UDK: 616.61</dc:identifier><dc:identifier>ISSN pri članku: 1600-6143</dc:identifier><dc:identifier>DOI: 10.1016/j.ajt.2025.08.029</dc:identifier><dc:identifier>COBISS_ID: 246735107</dc:identifier><dc:language>sl</dc:language></metadata>
