Evidence map›Paper›PMID 41486473›Full record

ArticleThe Journal of infectious diseases2026

Corticosteroid Therapy and Long-Term Outcomes of Post-Infectious Inflammatory Syndrome in Non-HIV Immunosuppressed Cryptococcal Meningitis: A Multicenter Case Series.

Yuya Ito, Tracey-Ann Hoeltermann, Seher Anjum, Londyn Robinson, Jessica S Little, Michael Kiritsy, Julie M Steinbrink, Andrea Finocchi, Lorne W Walker, Robin K Avery and 7 more

Abstract readMulticenter Study
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Yuya ItoLaboratory of Clinical Immunology and Microbiology (LCIM), Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, Maryland, USA.ORCID 0000-0003-1295-4357
Tracey-Ann HoeltermannLaboratory of Clinical Immunology and Microbiology (LCIM), Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, Maryland, USA.ORCID 0000-0001-6922-6786
Seher AnjumLaboratory of Clinical Immunology and Microbiology (LCIM), Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Londyn RobinsonDepartment of Medicine, Division of Rheumatology, University of Washington School of Medicine, Seattle, Washington, USA.ORCID 0000-0002-0961-4020
Jessica S LittleHarvard Medical School, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.ORCID 0000-0001-8093-5647
Michael KiritsyDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.
Julie M SteinbrinkDepartment of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0003-0771-3647
Andrea FinocchiAcademic Department of Pediatrics, Bambino Gesù Children's Hospital, Unit of Immunoinfectivology, IRCCS, Rome, Italy.
Lorne W WalkerDivision of Pediatric Infectious Diseases, Oregon Health and Science University, Portland, Oregon, USA.ORCID 0000-0002-2500-0504
Robin K AveryDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0001-7692-3619
Shmuel ShohamDepartment of Medicine, Division of Infectious Diseases, Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0001-7276-7786
Omer E BeairdDepartment of Medicine, Division of Infectious Diseases, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Song C OngDepartment of Medicine, Division of Nephrology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Cornelius N Van DamRegional Center for Infectious Diseases, Cone Health, Greensboro, North Carolina, USA.
Ina StephensDepartment of Infectious Diseases, University of Virginia Children's Hospital, Charlottesville, Virginia, USA.
Ambar HaleemDepartment of Medicine, Division of Infectious Disease, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.ORCID 0000-0001-9026-7128
Peter R WilliamsonLaboratory of Clinical Immunology and Microbiology (LCIM), Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, Maryland, USA.ORCID 0000-0002-7953-2178

Funding

Novel Host-Response Biomarker Diagnostics for Invasive AspergillosisK23AI187748 · NIAID · DUKE UNIVERSITY · PI Julie Marie Steinbrink · 2025 to 2026
$363k
National Institute of Allergy and Infectious DiseasesNIAID NIH HHS K23 AI187748NIH HHS AI001123NIH HHS AI001124
6 · The paper itself

Abstract

backgroundPost-infectious inflammatory response syndrome (PIIRS) is recognized as a cause of neurologic deterioration in previously healthy patients with cryptococcal meningoencephalitis (CM). However, data on non-human immunodeficiency virus (HIV), immunosuppressed patients remain limited.

methodsBetween July 2018 and April 2025, 13 non-HIV immunosuppressed patients with CM who subsequently developed PIIRS were included. Clinical features, Karnofsky performance scores, cerebrospinal fluid (CSF) parameters, and magnetic resonance imaging (MRI) findings were compared at PIIRS diagnosis and during follow-up after corticosteroid therapy.

resultsAll patients showed evidence of CNS inflammation, including abnormal CSF, MRI findings, and neurological symptoms such as altered mental status or visual/hearing loss. Corticosteroid therapy was associated with significant improvements in Karnofsky scores at 1 month (P = .001), with sustained benefit at 6 and twelve months (P = .002); all 10 surviving patients demonstrated resolution of neurological symptoms. CSF inflammatory parameters including white blood cell (WBC) count, protein, and CSF/serum glucose ratio also significantly improved at 1 month. Brain MRI findings also showed a trend toward improvement. All patients remained culture-negative post-PIIRS diagnosis. Three patients died: 1 from complications of alcoholic cirrhosis, the second from liver failure in the setting of systemic lupus erythematosus and immunosuppression, and the third from sepsis after initiation of corticosteroids.

conclusionsCorticosteroids were associated with improvement in neurological status and neuroinflammation in non-HIV, immunosuppressed patients with PIIRS following CM. These findings support its potential role as salvage therapy in this population and highlight the need for systematic data collection or randomized trials to better guide corticosteroid use.

Indexed as

Adrenal Cortex HormonesImmunocompromised HostMeningitis, CryptococcalAdultAgedFemaleHumansMagnetic Resonance ImagingMaleMeningoencephalitisMiddle AgedTreatment OutcomeAdrenal Cortex HormonescorticosteroidsCryptococcusimmunosuppressed patientsmeningoencephalitispost-infectious inflammatory response syndrome (PIIRS)

Identifiers

PMID41486473
PMCPMC12861043

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.