厌氧抗生素与异基因造血干细胞移植后移植物抗宿主病的风险

IF 4.3 Q1 Medicine
John S. Tanaka , Rebecca R. Young , Sarah M. Heston , Kirsten Jenkins , Lisa P. Spees , Anthony D. Sung , Kelly Corbet , Jillian C. Thompson , Lauren Bohannon , Paul L. Martin , Andre Stokhuyzen , Richard Vinesett , Doyle V. Ward , Shakti K. Bhattarai , Vanni Bucci , Mehreen Arshad , Patrick C. Seed , Matthew S. Kelly
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引用次数: 0

摘要

某些厌氧菌对维持肠道屏障完整性和免疫耐受很重要,并可能影响同种异体造血干细胞移植(HSCT)后移植物抗宿主病(GVHD)的风险。我们对异基因造血干细胞移植受者进行了一项单中心回顾性队列研究,以评估抗生素治疗与厌氧活性谱与GVHD结果之间的关系。我们确定了1214名在移植前7天至移植后28天发生发热性中性粒细胞减少症的儿童和成人,并比较了使用厌氧抗生素(哌哌西林-他唑巴坦或碳青霉烯类;N = 491)到仅接受抗厌氧菌活性最低的抗生素(唑曲南、头孢吡肟或头孢他啶)的患者;n = 723)。我们对来自36名儿科患者的一系列粪便样本进行宏基因组测序,以比较特定抗生素对肠道宏基因组的影响。接受厌氧抗生素与急性肠/肝GVHD的高风险相关(风险比[HR], 1.26;95%可信区间[CI], 1.03 ~ 1.54)和急性GVHD死亡率(HR, 1.63;95% CI, 1.08 - 2.46),但没有慢性GVHD诊断(HR, 1.04;95% CI: 0.84 ~ 1.28)或慢性GVHD死亡率(HR, 0.88;95% CI, 0.53 ~ 1.45)。厌氧抗生素导致肠道细菌多样性降低,双歧杆菌和梭菌的丰度降低,肠道宏基因组中编码丁酸生物合成酶的细菌基因丢失。在急性肠/肝GVHD之前,抗生素治疗会导致细菌丁酸盐生物合成基因急剧下降。我们的研究结果表明,暴露于厌氧抗生素与异基因造血干细胞移植后急性肠道/肝脏GVHD和急性GVHD死亡率的风险增加有关。哌拉西林-他唑巴坦或碳青霉烯类药物应保留用于怀疑有厌氧或多重耐药感染的发热性中性粒细胞减少病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anaerobic Antibiotics and the Risk of Graft-versus-Host Disease after Allogeneic Hematopoietic Stem Cell Transplantation

Certain anaerobic bacteria are important for maintenance of gut barrier integrity and immune tolerance and may influence the risk of graft-versus-host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (HSCT). We conducted a single-center retrospective cohort study of allogeneic HSCT recipients to evaluate associations between receipt of antibiotics with an anaerobic spectrum of activity and GVHD outcomes. We identified 1214 children and adults who developed febrile neutropenia between 7 days before and 28 days after HSCT and compared GVHD risk and mortality among patients who received anaerobic antibiotics (piperacillin-tazobactam or carbapenems; n = 491) to patients who received only antibiotics with minimal activity against anaerobes (aztreonam, cefepime, or ceftazidime; n = 723). We performed metagenomic sequencing of serial fecal samples from 36 pediatric patients to compare the effects of specific antibiotics on the gut metagenome. Receipt of anaerobic antibiotics was associated with higher hazards of acute gut/liver GVHD (hazard ratio [HR], 1.26; 95% confidence interval [CI], 1.03 to 1.54) and acute GVHD mortality (HR, 1.63; 95% CI, 1.08 to 2.46), but not chronic GVHD diagnosis (HR, 1.04; 95% CI: .84 to 1.28) or chronic GVHD mortality (HR, .88; 95% CI, .53 to 1.45). Anaerobic antibiotics resulted in decreased gut bacterial diversity, reduced abundances of Bifidobacteriales and Clostridiales, and loss of bacterial genes encoding butyrate biosynthesis enzymes from the gut metagenome. Acute gut/liver GVHD was preceded by a sharp decline in bacterial butyrate biosynthesis genes with antibiotic treatment. Our findings demonstrate that exposure to anaerobic antibiotics is associated with increased risks of acute gut/liver GVHD and acute GVHD mortality after allogeneic HSCT. Use of piperacillin-tazobactam or carbapenems should be reserved for febrile neutropenia cases in which anaerobic or multidrug-resistant infections are suspected.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
1061
审稿时长
3-6 weeks
期刊介绍: Biology of Blood and Marrow Transplantation publishes original research reports, reviews, editorials, commentaries, letters to the editor, and hypotheses and is the official publication of the American Society for Transplantation and Cellular Therapy. The journal focuses on current technology and knowledge in the interdisciplinary field of hematopoetic stem cell transplantation.
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