Evidence map›Paper›PMID 41778809›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2026

Immunomodulation in the Treatment of Disseminated Coccidioidomycosis.

Alexis V Stephens, Timothy J Thauland, Gregory D Whitehill, Maria I Garcia-Lloret, Manish J Butte

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
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

5 authors.

Alexis V StephensDepartment of Human Genetics, UCLA, Los Angeles, California, USA.ORCID 0000-0002-5979-6838
Timothy J ThaulandDepartment of Pediatrics, Division of Immunology, Allergy, and Rheumatology, Department of Pediatrics, UCLA, Los Angeles, California, USA.ORCID 0000-0003-4121-0453
Gregory D WhitehillDepartment of Medicine, Division of Infectious Diseases, Department of Medicine, UCLA, Los Angeles, California, USA.ORCID 0000-0002-7920-1686
Maria I Garcia-LloretDepartment of Pediatrics, Division of Immunology, Allergy, and Rheumatology, Department of Pediatrics, UCLA, Los Angeles, California, USA.ORCID 0000-0003-3763-7702
Manish J ButteDepartment of Human Genetics, UCLA, Los Angeles, California, USA.ORCID 0000-0002-4490-5595

Funding

Innate immune mechanisms of the host response to CoccidioidesU19AI166059 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Joshua Fierer · 2022 to 2026
$10.0M
NIAID NIH HHS U19 AI166059NIH HHS U19 AI166059
6 · The paper itself

Abstract

backgroundMortality rates for disseminated coccidioidomycosis remain high despite modern antifungal therapies, resulting in substantial costs to society. We propose that immunomodulation as an adjunctive therapy with antifungals can improve clinical outcomes. Previous work suggested that treatment with interferon gamma or by blocking the IL-4/IL-13 receptor with dupilumab could improve clinical outcomes.

methodsWe present a case series of 18 patients at UCLA with severe or persistent coccidioidomycosis receiving maximal antifungal treatment who received immunomodulatory therapy. Treatment selection based on the clinical context and intracellular cytokine staining that measured T helper cells producing interferon gamma or IL-4. Patients with severe disease received recombinant interferon gamma, while those showing Type-2 immune dysregulation were treated with dupilumab.

resultsPatients receiving dupilumab showed a reduction in Type-2 T-cell responses. Importantly, 16 of the 18 patients survived (88%), with clinical outcomes improving relative to baseline in the majority.

conclusionsThis case series provides evidence that patients with severe and/or disseminated coccidioidomycosis may benefit from immunomodulation. These positive outcomes support the consideration of off-label use of these medications. Clinical trials are warranted for interferon gamma in severe disease and dupilumab for disseminated disease when Type-2 immune dysregulation is present. Further research is needed to identify the specific patient populations that may benefit most from the addition of immunomodulatory medications.

Indexed as

Antifungal AgentsCoccidioidomycosisImmunomodulationAdultAgedAntibodies, Monoclonal, HumanizedFemaleHumansInterferon-gammaMaleMiddle AgedTh2 CellsTreatment OutcomeAntibodies, Monoclonal, HumanizedAntifungal AgentsdupilumabInterferon-gammacoccidioidomycosisdupilumabimmunomodulationinterferon gammaTh2

Identifiers

PMID41778809
PMCPMC13242165

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.