首页> 外文期刊>Transplant international : >Viral load, CMV-specific T-cell immune response and cytomegalovirus disease in solid organ transplant recipients at higher risk for cytomegalovirus infection during preemptive therapy.
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Viral load, CMV-specific T-cell immune response and cytomegalovirus disease in solid organ transplant recipients at higher risk for cytomegalovirus infection during preemptive therapy.

机译:实体器官移植接受者的病毒载量,CMV特异性T细胞免疫应答和巨细胞病毒病在先发制人治疗期间发生巨细胞病毒感染的风险较高。

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摘要

Despite advances in prevention, cytomegalovirus (CMV) recurrence is an important challenge in high-risk organ recipients. The present study prospectively evaluates the impact of CMV-specific T-cell immune response and secondary prophylaxis on the risk of recurrence in a cohort of CMV high-risk organ recipients and whether it is possible to determine a safe standardized viral load value below which CMV disease is unlikely. Thirty-nine recipients were included. Thirty-six had primary infections, and 88.9% recurred. Rate and duration of recurrent CMV infection was similar in patients with and without secondary prophylaxis: 57.9% vs. 53.6%, P?=?0.770 and 16 vs. 15?days, P?=?0.786, respectively. The only factor independently associated with no episodes of CMV recurrence was the acquisition of CMV-specific T-cell immune response (OR: 0.151, 95% CI: 0.028-0.815; P?=?0.028). Cytomegalovirus diseases (N?=?5) occurred in patients with CMV viral load above 1500?IU/ml who did not follow the planned monitorization schedule. Our observations suggest that episodes of recurrent CMV infection are common after preemptive therapy despite secondary prophylaxis and that CMV-specific T-cell immune response is associated with a decreased risk of recurrent infections. Preemptive therapy may be safe in patients at high risk for CMV infection with strict close monitoring of the CMV viral load.
机译:尽管在预防方面取得了进步,但巨细胞病毒(CMV)的复发仍是高危器官接受者的重要挑战。本研究前瞻性评估了CMV高风险器官接受者队列中CMV特异性T细胞免疫应答和二级预防对复发风险的影响,以及是否有可能确定低于该CMV的安全标准病毒载量疾病不太可能。包括三十九名收件人。三十六例原发感染,复发88.9%。在有和没有进行二级预防的患者中,CMV的复发率和持续时间相似:分别为57.9%vs. 53.6%,P <= 0.770和16 vs. 15-day,P <= 0.786。独立于无CMV复发发作的唯一因素是CMV特异性T细胞免疫应答的获得(OR:0.151,95%CI:0.028-0.815; P == 0.028)。巨细胞病毒疾病(N≥5)发生在CMV病毒载量高于1500?IU / ml的患者中,但未遵循计划的监测时间表。我们的观察结果表明,尽管进行了二级预防,但先发制人疗法后复发性CMV感染仍很常见,而CMV特异的T细胞免疫反应与复发性感染的风险降低相关。对CMV病毒载量进行严格的密切监测,对于有巨细胞病毒感染高风险的患者,抢先治疗可能是安全的。

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