Evidence map›Paper›PMID 42089302›Full record

ArticleAmerican journal of respiratory cell and molecular biology2026

Immune regulation by CD55 in chronic beryllium disease.

Li Li, Sucai Liu, Zhe Lei, Joshua Macaluso, Shujin Guo, Kristyn MacPhail, Margaret M Mroz, Clara I Restrepo, Ivana Y Yang, Lisa A Maier

Abstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Li LiDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.ORCID 0000-0002-0692-6889
Sucai LiuDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.
Zhe LeiDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.
Joshua MacalusoDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.
Shujin GuoDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.
Kristyn MacPhailDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.
Margaret M MrozDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.
Clara I RestrepoDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.
Ivana Y YangDivision of Pulmonary and Critical Care Sciences, Department of Medicine, School of Medicine, University of Colorado-Anschutz Medical Campus, Aurora, CO, United States.
Lisa A MaierDivision of Environmental and Occupational Health Sciences, Department of Medicine, National Jewish Health, Denver, Denver, CO, United States.

Funding

Predictive Models of Beryllium Sensitization and Chronic Beryllium DiseaseR01ES034767 · NIEHS · NATIONAL JEWISH HEALTH · PI Maneesh Bhargava, Li Li · 2023 to 2026
$3.2M
Using Multi-Omics to Define Regulators and Drivers of Granulomatous Inflammation and Chronic Beryllium DiseaseR01ES033678 · NIEHS · NATIONAL JEWISH HEALTH · PI LISA A MAIER, Ivana V Yang · 2022 to 2026
$3.1M
The immunoregulatory role of Alveolar Macrophages in Chronic Beryllium DiseaseR01ES025722 · NIEHS · NATIONAL JEWISH HEALTH · PI LI, LI · 2016 to 2020
$1.8M
The Role of Airway Epithelial Complement in Chronic Beryllium DiseaseR21ES036375 · NIEHS · NATIONAL JEWISH HEALTH · PI CHU, HONG W, LI, LI · 2024 to 2024
$471k
Anne Theodore Foundation Breakthrough Sarcoidosis InitiativeNIEHS NIH HHS R01 ES025722NIEHS NIH HHS R01 ES033678NIEHS NIH HHS R01 ES034767NIEHS NIH HHS R21 ES036375NIH HHS R01ES033678NIH HHS R01ES034767NIH HHS R21ES03637
6 · The paper itself

Abstract

CD55 is an immune regulator that inhibits T-cell activation and also binds to CD97, a molecule involved in immune cell migration and signaling. While CD55 expression is reduced in chronic beryllium disease (CBD), its functional role in disease pathogenesis remains unclear. We hypothesized that CD55 downregulation in peripheral blood mononuclear cells (PBMCs) contributes to heightened beryllium (Be)-specific immune responses in CBD. To test this, we characterized CD55 expression and function in PBMCs from patients with CBD and individuals with beryllium sensitization (BeS), as well as in a human Be-specific T-cell model. CD55, soluble CD55 (sCD55), and CD97 mRNA expression was quantified by qRT-PCR in PBMCs from CBD (n = 25), BeS (n = 36), and control (n = 7) participants. BeSO4 (beryllium sulfate) stimulation was used to assess CD55, STAT1, JAK2, and TNF-α expression over time in CBD PBMCs (n = 8). Serum sCD55 was measured by ELISA in an independent cohort. Functional studies using anti-CD55 neutralizing antibodies and the JAK2 inhibitor TG101348 evaluated effects on TNF-α production and lymphocyte proliferation (beryllium lymphocyte proliferation test [BeLPT]) in PBMCs, and IL-2 production in a Jurkat-Be cell model. CD55, sCD55, and CD97 were significantly downregulated in CBD PBMCs compared to BeS (P < .001). Serum sCD55 was also reduced in CBD (P < .05). BeSO4 stimulation further downregulated CD55 and upregulated STAT1. CD55 blockade increased TNF-α production and BeLPT responses in CBD (P < .001) and BeS (P < .05); these effects were reversed by JAK2 inhibition. In the Be-cell model, CD55 inhibition enhanced IL-2 production (P < .01), attenuated by JAK2 blockade. These findings suggest that CD55 downregulation amplifies Be-induced immune responses in CBD via JAK2/STAT1 signaling.

Indexed as

BerylliosisCD55 AntigensAdultBerylliumCell ProliferationChronic DiseaseFemaleHumansJanus Kinase 2Leukocytes, MononuclearLymphocyte ActivationMaleMiddle AgedSignal TransductionSTAT1 Transcription FactorT-LymphocytesBerylliumCD55 AntigensJAK2 protein, humanJanus Kinase 2STAT1 protein, humanSTAT1 Transcription FactorTumor Necrosis Factor-alphaBe: berylliumBeLPT: Be lymphocyte proliferation testBeS: beryllium sensitizationCBD: chronic beryllium diseaseDAF: decay-accelerating factorPBMC: peripheral blood mononuclear cellssCD55: soluble form CD55

Identifiers

PMID42089302
PMCPMC13479807

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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.