Infection-Associated Immune Reconstitution Inflammatory Syndrome in Hematopoietic Cell Transplantation

被引:1
作者
Chaturvedi, Mansi [1 ,2 ]
Epling, Brian P. [3 ]
Pei, Luxin [3 ]
Sullivan, Brigit [4 ]
Kuehn, Hye Sun [5 ]
Hammoud, Dima A. [6 ]
Rosenzweig, Sergio [5 ]
Pai, Sung-Yun [7 ]
Sereti, Irini [3 ]
Freeman, Alexandra F. [3 ]
Cuellar-Rodriguez, Jennifer [3 ]
Gonzalez, Corina E. [7 ]
Manion, Maura [8 ]
机构
[1] NHLBI, Crit Care Med & Pulm Branch, NIH, Bethesda, MD 20892 USA
[2] Univ Maryland, Sch Med, Div Pulm Crit Care & Sleep Med, Baltimore, MD 21201 USA
[3] NIAID, Div Intramural Res, NIH, Bethesda, MD USA
[4] NIH, Natl Inst Hlth Lib, Off Res Serv, Bethesda, MD USA
[5] NIH, Dept Lab Med, Bethesda, MD USA
[6] NIH, Ctr Infect Dis Imaging, Clin Ctr, Bethesda, MD USA
[7] NCI, Immune Deficiency Cellular Therapy Program, NIH, Bethesda, MD USA
[8] NIAID, Div Clin Res, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Bacillus Calmette-Gu & eacute; rin; hematopoietic cell transplantation; immune reconstitution inflammatory syndrome; inborn errors of immunity; severe combined immunodeficiency syndrome; SEVERE COMBINED IMMUNODEFICIENCY; REGULATORY T-CELLS; SYNDROME IRIS; STEM-CELLS; COMPLICATIONS; CYCLOPHOSPHAMIDE; TUBERCULOSIS; CHILDREN; DISEASE;
D O I
10.1111/tid.70000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immune reconstitution inflammatory syndrome (IRIS) is a well-recognized complication in people with HIV (PWH) starting antiretroviral therapy (ART), but data on IRIS in hematopoietic cell transplantation (HCT) recipients are limited. To address this gap, we conducted a narrative review of the literature on IRIS in HCT recipients, including 21 studies encompassing 53 patients. The majority of reported patients had inborn errors of immunity (IEI) and developed IRIS associated with Bacillus Calmette-Gu & eacute;rin (BCG)-infection from prior vaccination ("BCG-IRIS"). The remainder had IRIS linked to other infections, most commonly Aspergillus and Non-tuberculous mycobacteria ("non-BCG-IRIS"). The median time between transplant and IRIS was 3 months; however, some patients developed IRIS multiple years posttransplant. BCG-IRIS was predominantly unmasking, while non-BCG-IRIS was mostly associated with a new infection acquired after HCT alongside immune recovery and/or changes in immunosuppression ("post-HCT infection IRIS"). Inflammatory biomarkers and tissue pathology were helpful in distinguishing IRIS from uncontrolled infection. Initiation or continuation of appropriate antimicrobial therapy in the peri-transplant period was foremost in the prevention and treatment of IRIS. Use of steroidal and nonsteroidal immunosuppression was common, while surgery was used as an adjunctive measure to infection control. Recrudescence of IRIS symptoms was common with discontinuation or decrease in immunosuppression. About one-third of the patients were reported to have graft-versus-host disease, and the rate of graft failure was 8%. The mortality rate was 15%, with most deaths attributed to superimposed infections. Through this review, we aim to highlight that IRIS is an under-recognized entity in HCT recipients and future research is needed to explore its pathogenesis, risk factors, and management in this complex patient population.
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页数:17
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