Vonbrunn Eva, Serikova Sofya, Daniel Christoph, Amann Kerstin, Schödel Johannes, Buchholz Björn, Ferrazzi Fulvia, Heller Katharina, Apel Hendrik, Büttner-Herold Maike
Department of Nephropathology, Institute of Pathology, Friedrich-Alexander-University Erlangen-Nuremberg and University Hospital, Erlangen, Germany.
Department of Nephrology and Hypertension, Friedrich-Alexander-University Erlangen-Nuremberg and University Hospital, Erlangen, Germany.
Front Med (Lausanne). 2021 Apr 6;8:656840. doi: 10.3389/fmed.2021.656840. eCollection 2021.
The quality of a renal transplant can influence the clinical course after transplantation. Glomerular immune reactivity in renal transplants has previously been described, focusing particularly on IgA, and has been shown to disappear in most cases without affecting the outcome. Here, we describe a cohort of time zero biopsies with regard to glomerular immune reactivity and implications for histomorphology and follow-up. 204 Time zero biopsies were analyzed by immunohistochemistry for glomerular immune reactivity. Time zero and 1-year biopsies were evaluated for histomorphological changes, which, together with clinical and follow-up data, were assessed for associations with glomerular immune profiles. Nearly half of the analyzed time zero biopsies showed glomerular immune reactivity with mesangial C3 being the most common (32.9%), followed by IgA (13.7%) and fullhouse patterns (6.9%). Strong C3 deposits (C3high) were only observed in deceased transplants. In the majority of cases immune reactivity was undetectable in follow-up biopsies and had no adverse effect on transplant function in follow-up of 5 years. In kidney pairs transplanted to different recipients a strong concordance of immune profiles in both kidneys was observed. Moreover, an association of male donor sex and deceased donor transplantation with the presence of immune reactivity was observed. In conclusion, glomerular immune reactivity is a very frequent finding in time zero biopsies, which seems to be determined by donor parameters including male sex and deceased donor transplants. It had no adverse impact on transplant function in 5-year follow-up. Glomerular immune reactivity in time zero biopsies, therefore, does not appear to indicate an inferior quality of the transplant.
肾移植的质量会影响移植后的临床进程。此前已有关于肾移植中肾小球免疫反应性的描述,尤其侧重于免疫球蛋白A(IgA),并且已表明在大多数情况下其会消失而不影响预后。在此,我们描述了一组关于肾小球免疫反应性的零时间点活检病例及其对组织形态学和随访的影响。通过免疫组织化学分析了204份零时间点活检标本的肾小球免疫反应性。对零时间点和1年时的活检标本进行了组织形态学变化评估,并将其与临床和随访数据一起评估与肾小球免疫谱的相关性。近一半的分析零时间点活检标本显示肾小球免疫反应性,其中系膜区C3最常见(32.9%),其次是IgA(13.7%)和满堂亮模式(6.9%)。仅在死亡供者肾移植中观察到强C3沉积(C3高)。在大多数病例中,随访活检标本中未检测到免疫反应性,且在5年随访中对移植肾功能无不良影响。在移植给不同受者的肾对中,观察到两个肾脏的免疫谱有很强的一致性。此外,观察到男性供者性别和死亡供者肾移植与免疫反应性的存在有关。总之,肾小球免疫反应性在零时间点活检中是非常常见的发现,似乎由包括男性性别和死亡供者肾移植在内的供者参数决定。在5年随访中对移植肾功能没有不良影响。因此,零时间点活检中的肾小球免疫反应性似乎并不表明移植质量较差。