Cargando…

Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection

High titers of anti-interferon-γ autoantibodies (AIGAs) are an important factor leading to persistent, relapsed, and refractory infections in HIV-negative hosts infected with Talaromyces marneffei (TM). We report 5 patients treated with pulses of high-dose intravenous cyclophosphamide (IVCY) who wer...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Wen, Tang, Mengxin, Yang, Meiling, Fang, Gaoneng, Tang, Shudan, Zhang, Jianquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745774/
https://www.ncbi.nlm.nih.gov/pubmed/36519123
http://dx.doi.org/10.1093/ofid/ofac612
_version_ 1784849220890525696
author Zeng, Wen
Tang, Mengxin
Yang, Meiling
Fang, Gaoneng
Tang, Shudan
Zhang, Jianquan
author_facet Zeng, Wen
Tang, Mengxin
Yang, Meiling
Fang, Gaoneng
Tang, Shudan
Zhang, Jianquan
author_sort Zeng, Wen
collection PubMed
description High titers of anti-interferon-γ autoantibodies (AIGAs) are an important factor leading to persistent, relapsed, and refractory infections in HIV-negative hosts infected with Talaromyces marneffei (TM). We report 5 patients treated with pulses of high-dose intravenous cyclophosphamide (IVCY) who were followed for 2 years. Before IVCY therapy, all patients had multiple relapses, with a median (interquartile range [IQR]) of 2 (1–3) instances of relapse. The median serum AIGA titers (IQR) were 58 753 (41 203–89 605) ng/mL at diagnosis, 48 189.4 (15 537–83 375) ng/mL before IVCY therapy, and 10 721.2 (5637–13 245) ng/mL at the end of IVCY therapy (P < .05). After 3 months of follow-up, the median AIGA titers (IQR) rose gradually to 21 232.6 (9896–45 626) ng/mL, and to 37 464.2 (19 872–58 321) ng/mL at 24 months (P < .05). Five patients discontinued antimicrobial therapy within 3–12 months after completion of IVCY therapy, but only 1 patient had a relapse. In conclusion, pulses of short-term and high-dose IVCY can effectively reduce AIGA titers.
format Online
Article
Text
id pubmed-9745774
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-97457742022-12-13 Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection Zeng, Wen Tang, Mengxin Yang, Meiling Fang, Gaoneng Tang, Shudan Zhang, Jianquan Open Forum Infect Dis Major Article High titers of anti-interferon-γ autoantibodies (AIGAs) are an important factor leading to persistent, relapsed, and refractory infections in HIV-negative hosts infected with Talaromyces marneffei (TM). We report 5 patients treated with pulses of high-dose intravenous cyclophosphamide (IVCY) who were followed for 2 years. Before IVCY therapy, all patients had multiple relapses, with a median (interquartile range [IQR]) of 2 (1–3) instances of relapse. The median serum AIGA titers (IQR) were 58 753 (41 203–89 605) ng/mL at diagnosis, 48 189.4 (15 537–83 375) ng/mL before IVCY therapy, and 10 721.2 (5637–13 245) ng/mL at the end of IVCY therapy (P < .05). After 3 months of follow-up, the median AIGA titers (IQR) rose gradually to 21 232.6 (9896–45 626) ng/mL, and to 37 464.2 (19 872–58 321) ng/mL at 24 months (P < .05). Five patients discontinued antimicrobial therapy within 3–12 months after completion of IVCY therapy, but only 1 patient had a relapse. In conclusion, pulses of short-term and high-dose IVCY can effectively reduce AIGA titers. Oxford University Press 2022-11-11 /pmc/articles/PMC9745774/ /pubmed/36519123 http://dx.doi.org/10.1093/ofid/ofac612 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Zeng, Wen
Tang, Mengxin
Yang, Meiling
Fang, Gaoneng
Tang, Shudan
Zhang, Jianquan
Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection
title Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection
title_full Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection
title_fullStr Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection
title_full_unstemmed Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection
title_short Intravenous Cyclophosphamide Therapy for Anti-IFN-γ Autoantibody-Associated Talaromyces marneffei Infection
title_sort intravenous cyclophosphamide therapy for anti-ifn-γ autoantibody-associated talaromyces marneffei infection
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745774/
https://www.ncbi.nlm.nih.gov/pubmed/36519123
http://dx.doi.org/10.1093/ofid/ofac612
work_keys_str_mv AT zengwen intravenouscyclophosphamidetherapyforantiifngautoantibodyassociatedtalaromycesmarneffeiinfection
AT tangmengxin intravenouscyclophosphamidetherapyforantiifngautoantibodyassociatedtalaromycesmarneffeiinfection
AT yangmeiling intravenouscyclophosphamidetherapyforantiifngautoantibodyassociatedtalaromycesmarneffeiinfection
AT fanggaoneng intravenouscyclophosphamidetherapyforantiifngautoantibodyassociatedtalaromycesmarneffeiinfection
AT tangshudan intravenouscyclophosphamidetherapyforantiifngautoantibodyassociatedtalaromycesmarneffeiinfection
AT zhangjianquan intravenouscyclophosphamidetherapyforantiifngautoantibodyassociatedtalaromycesmarneffeiinfection