Tharmaraj Dhakshayini, Mulley William R, Dendle Claire
Department of Nephrology, Monash Health, Clayton, VIC, Australia.
Centre for Inflammatory Diseases, Department of Medicine, Monash University, Clayton, VIC, Australia.
Front Immunol. 2024 Nov 26;15:1490472. doi: 10.3389/fimmu.2024.1490472. eCollection 2024.
Infection and rejection are major complications that impact transplant longevity and recipient survival. Balancing their risks is a significant challenge for clinicians. Current strategies aimed at interrogating the degree of immune deficiency or activation and their attendant risks of infection and rejection are imprecise. These include immune (cell counts, function and subsets, immunoglobulin levels) and non-immune (drug levels, viral loads) markers. The shared risk factors between infection and rejection and the bidirectional and intricate relationship between both entities further complicate transplant recipient care and decision-making. Understanding the dynamic changes in the underlying net state of immunity and the overall risk of both complications in parallel is key to optimizing outcomes. The allograft biopsy is the current gold standard for the diagnosis of rejection but is associated with inherent risks that warrant careful consideration. Several biomarkers, in particular, donor derived cell-free-DNA and urinary chemokines (CXCL9 and CXCL10), show significant promise in improving subclinical and clinical rejection risk prediction, which may reduce the need for allograft biopsies in some situations. Integrating conventional and emerging risk assessment tools can help stratify the individual's short- and longer-term infection and rejection risks in parallel. Individuals identified as having a low risk of rejection may tolerate immunosuppression wean to reduce medication-related toxicity. Serial monitoring following immunosuppression reduction or escalation with minimally invasive tools can help mitigate infection and rejection risks and allow for timely diagnosis and treatment of these complications, ultimately improving allograft and patient outcomes.
感染和排斥反应是影响移植器官长期存活及受者生存的主要并发症。平衡它们的风险对临床医生而言是一项重大挑战。目前旨在探究免疫缺陷或激活程度及其伴随的感染和排斥反应风险的策略并不精确。这些策略包括免疫(细胞计数、功能和亚群、免疫球蛋白水平)和非免疫(药物水平、病毒载量)标志物。感染和排斥反应之间的共同风险因素以及这两种情况之间双向且复杂的关系,进一步使移植受者的护理和决策变得复杂。了解免疫基础净状态的动态变化以及两种并发症的总体风险,对于优化治疗结果至关重要。移植器官活检是目前诊断排斥反应的金标准,但存在一些固有风险,需要仔细考虑。特别是一些生物标志物,如供体来源的游离DNA和尿趋化因子(CXCL9和CXCL10),在改善亚临床和临床排斥反应风险预测方面显示出巨大潜力,这在某些情况下可能减少移植器官活检的必要性。整合传统和新兴的风险评估工具有助于同时对个体的短期和长期感染及排斥反应风险进行分层。被确定为排斥反应风险较低的个体可能耐受免疫抑制的减量,以降低药物相关毒性。在免疫抑制减少或增加后,使用微创工具进行连续监测有助于降低感染和排斥反应风险,并能及时诊断和治疗这些并发症,最终改善移植器官和患者的治疗结果。