Natural Killer Cell Presence in Antibody-Mediated Rejection

被引:2
|
作者
Diebold, Matthias [1 ,2 ]
Farkash, Evan A. [3 ]
Barnes, Jenna [3 ]
Regele, Heinz [4 ]
Kozakowski, Nicolas [4 ]
Schatzl, Martina [1 ]
Mayer, Katharina A. [1 ]
Haindl, Susanne [1 ]
Vietzen, Hannes [5 ]
Hidalgo, Luis G. [6 ]
Halloran, Philip F. [7 ]
Eskandary, Farsad [1 ]
Boehmig, Georg A. [1 ]
机构
[1] Med Univ Vienna, Div Nephrol & Dialysis, Dept Clin Pharmacol, Vienna, Austria
[2] Univ Hosp Basel, Clin Transplantat Immunol & Nephrol, Basel, Switzerland
[3] Univ Michigan, Dept Pathol, Ann Arbor, MI USA
[4] Med Univ Vienna, Dept Pathol, Vienna, Austria
[5] Med Univ Vienna, Ctr Virol, Vienna, Austria
[6] Univ Wisconsin, Dept Surg, Madison, WI USA
[7] Univ Alberta, Alberta Transplant Appl Genom Ctr, Edmonton, AB, Canada
基金
瑞士国家科学基金会;
关键词
natural killer cell; antibody-mediated rejection; microvascular inflammation; immunohistochemistry; genetics; NK CELLS; EXPRESSION; TRANSPLANTATION; INVOLVEMENT; BIOPSIES;
D O I
10.3389/ti.2024.13209
中图分类号
R61 [外科手术学];
学科分类号
摘要
Transcript analyses highlight an important contribution of natural killer (NK) cells to microvascular inflammation (MVI) in antibody-mediated rejection (ABMR), but only few immunohistologic studies have quantified their spatial distribution within graft tissue. This study included 86 kidney transplant recipients who underwent allograft biopsies for a positive donor-specific antibody (DSA) result. NK cells were visualized and quantified within glomeruli and peritubular capillaries (PTC), using immunohistochemistry for CD34 alongside CD16/T-bet double-staining. Staining results were analyzed in relation to histomorphology, microarray analysis utilizing the Molecular Microscope Diagnostic System, functional NK cell genetics, and clinical outcomes. The number of NK cells in glomeruli per mm(2) glomerular area (NKglom) and PTC per mm(2) cortical area (NKPTC) was substantially higher in biopsies with ABMR compared to those without rejection, and correlated with MVI scores (NKglom Spearman's correlation coefficient [SCC] = 0.55, p < 0.001, NKPTC 0.69, p < 0.001). In parallel, NK cell counts correlated with molecular classifiers reflecting ABMR activity (ABMR(prob): NKglom 0.59, NKPTC 0.75) and showed a trend towards higher levels in association with high functional FCGR3A and KLRC2 gene variants. Only NKPTC showed a marginally significant association with allograft function and survival. Our immunohistochemical results support the abundance of NK cells in DSA-positive ABMR.
引用
收藏
页数:12
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