Cargando…

Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients

Patients who receive a hematopoietic stem cell transplantation (HSCT) exhibit an immune defect after recovering from neutropenia. The current guidelines do not recommend fungal prophylaxis in these patients, except for grades III to IV GVHD in HSCT. Thus, the timing for the initiation and cessation...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Jiexian, Hu, Yingwei, Wu, Min, Wang, Xiaoqin, Xie, Yanhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840169/
https://www.ncbi.nlm.nih.gov/pubmed/29552004
http://dx.doi.org/10.3389/fmicb.2018.00370
_version_ 1783304520537735168
author Ma, Jiexian
Hu, Yingwei
Wu, Min
Wang, Xiaoqin
Xie, Yanhui
author_facet Ma, Jiexian
Hu, Yingwei
Wu, Min
Wang, Xiaoqin
Xie, Yanhui
author_sort Ma, Jiexian
collection PubMed
description Patients who receive a hematopoietic stem cell transplantation (HSCT) exhibit an immune defect after recovering from neutropenia. The current guidelines do not recommend fungal prophylaxis in these patients, except for grades III to IV GVHD in HSCT. Thus, the timing for the initiation and cessation of IFI prophylaxis in immune-compromised patients remains a challenging endeavor. We retrospectively analyzed patients who received auto or allo-HSCT and monitored their immune function after recovering from neutropenia by measuring the levels of IgG, IgA, IgM, as well as the number of T, B, NK cells. We found that the level of IgG and NK cell count exhibited a significant difference with the incidence of IFI by logistic regression (p = 0.000 vs. 0.000, respectively) and conditional logistic regression (p = 0.009 vs. p = 0.002). The initiation of IFI prophylaxis was determined to be IgG < 7 mg/mL and NK cell count < 6.5 × 104/mL by an receiver operating characteristic curve separately. Tests in parallel increased the test sensitivity and specificity. Thus, the optimal timing for initiating prophylaxis in patients after HSCT could be IgG < 7 mg/mL or NK cell count < 6.5 × 104/mL. Future large-scale prospective clinical trials are required to verify these findings. Patients who are immuno-compromised after auto or allo-HSCT may benefit from a lower fungi infection incidence with immune surveillance and proper fungal prophylaxis.
format Online
Article
Text
id pubmed-5840169
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-58401692018-03-16 Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients Ma, Jiexian Hu, Yingwei Wu, Min Wang, Xiaoqin Xie, Yanhui Front Microbiol Microbiology Patients who receive a hematopoietic stem cell transplantation (HSCT) exhibit an immune defect after recovering from neutropenia. The current guidelines do not recommend fungal prophylaxis in these patients, except for grades III to IV GVHD in HSCT. Thus, the timing for the initiation and cessation of IFI prophylaxis in immune-compromised patients remains a challenging endeavor. We retrospectively analyzed patients who received auto or allo-HSCT and monitored their immune function after recovering from neutropenia by measuring the levels of IgG, IgA, IgM, as well as the number of T, B, NK cells. We found that the level of IgG and NK cell count exhibited a significant difference with the incidence of IFI by logistic regression (p = 0.000 vs. 0.000, respectively) and conditional logistic regression (p = 0.009 vs. p = 0.002). The initiation of IFI prophylaxis was determined to be IgG < 7 mg/mL and NK cell count < 6.5 × 104/mL by an receiver operating characteristic curve separately. Tests in parallel increased the test sensitivity and specificity. Thus, the optimal timing for initiating prophylaxis in patients after HSCT could be IgG < 7 mg/mL or NK cell count < 6.5 × 104/mL. Future large-scale prospective clinical trials are required to verify these findings. Patients who are immuno-compromised after auto or allo-HSCT may benefit from a lower fungi infection incidence with immune surveillance and proper fungal prophylaxis. Frontiers Media S.A. 2018-03-02 /pmc/articles/PMC5840169/ /pubmed/29552004 http://dx.doi.org/10.3389/fmicb.2018.00370 Text en Copyright © 2018 Ma, Hu, Wu, Wang and Xie. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Ma, Jiexian
Hu, Yingwei
Wu, Min
Wang, Xiaoqin
Xie, Yanhui
Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients
title Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients
title_full Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients
title_fullStr Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients
title_full_unstemmed Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients
title_short Timing Determination of Invasive Fungal Infection Prophylaxis According to Immune Function in HSCT Patients
title_sort timing determination of invasive fungal infection prophylaxis according to immune function in hsct patients
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840169/
https://www.ncbi.nlm.nih.gov/pubmed/29552004
http://dx.doi.org/10.3389/fmicb.2018.00370
work_keys_str_mv AT majiexian timingdeterminationofinvasivefungalinfectionprophylaxisaccordingtoimmunefunctioninhsctpatients
AT huyingwei timingdeterminationofinvasivefungalinfectionprophylaxisaccordingtoimmunefunctioninhsctpatients
AT wumin timingdeterminationofinvasivefungalinfectionprophylaxisaccordingtoimmunefunctioninhsctpatients
AT wangxiaoqin timingdeterminationofinvasivefungalinfectionprophylaxisaccordingtoimmunefunctioninhsctpatients
AT xieyanhui timingdeterminationofinvasivefungalinfectionprophylaxisaccordingtoimmunefunctioninhsctpatients