Frontiers in Cellular and Infection Microbiology (Sep 2023)

Diagnostic efficiency of metagenomic next-generation sequencing for suspected infection in allogeneic hematopoietic stem cell transplantation recipients

  • Jiayu Huang,
  • Jiayu Huang,
  • Yeqian Zhao,
  • Chuanhe Jiang,
  • Chuanhe Jiang,
  • Dongsheng Han,
  • Zengkai Pan,
  • Zengkai Pan,
  • Zilu Zhang,
  • Zilu Zhang,
  • Luxiang Wang,
  • Luxiang Wang,
  • Wei Chen,
  • Wei Chen,
  • Su Li,
  • Yanmin Zhao,
  • Xiaoxia Hu,
  • Xiaoxia Hu

DOI
https://doi.org/10.3389/fcimb.2023.1251509
Journal volume & issue
Vol. 13

Abstract

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IntroductionImmunosuppression predisposes allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients to infection. Prompt and accurate identification of pathogens is crucial to optimize treatment strategies. This multi-center retrospective study aimed to assess the ability of metagenomic next-generation sequencing (mNGS) to detect causative pathogens in febrile allo-HSCT recipients and examined its concordance with conventional microbiological tests (CMT).MethodsWe performed mNGS and CMT on samples obtained from 153 patients with suspected infection during allo-HSCT. Patients were grouped based on their neutropenic status at the time of sampling.ResultsThe mNGS test was more sensitive than CMT (81.1% vs. 53.6%, P<0.001) for diagnosing clinically suspected infection, especially in the non-neutropenia cohort. mNGS could detect fungi and viruses better than bacteria, with a higher sensitivity than CMT. Immune events were diagnosed in 57.4% (35/61) of the febrile events with negative mNGS results, and 33.5% (48/143) with negative CMT results (P=0.002). The treatment success rate of the targeted anti-infection strategy was significantly higher when based on mNGS than on empirical antibiotics (85% vs. 56.5%, P=0.004).ConclusionThe mNGS test is superior to CMT for identifying clinically relevant pathogens, and provides valuable information for anti-infection strategies in allo-HSCT recipients. Additionally, attention should be paid to immune events in patients with negative mNGS results.

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