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The Role of JAK2 in Alveolar Macrophages (AM's) in Chronic Beryllium Disease (CBD)

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ClinicalTrials.gov Identifier: NCT02596347
Recruitment Status : Unknown
Verified September 2016 by Li Li, National Jewish Health.
Recruitment status was:  Recruiting
First Posted : November 4, 2015
Last Update Posted : September 22, 2016
Sponsor:
Information provided by (Responsible Party):
Li Li, National Jewish Health

Brief Summary:

Current studies suggest that alveolar macrophages (AM) act as silencers of most immune responses in the lung. However, in pathological conditions, such as asthma, hypersensitivity pneumonitis, and sarcoidosis, AMs become involved in the maintenance and further expansion of the immune response in the target organ. The Investigator has preliminary data demonstrating that CBD AMs at the site of disease involvement (bronchoalveolar lavage, BAL) display an activated cell surface phenotype compared to AMs from healthy controls. Furthermore, exciting data from our group demonstrates significant differences in gene expression profiles between CBD and Beryllium Sensitivity (BeS) bronchial alveolar lavage (BAL) cells, in pivotal immune response genes and networks. Specifically, the Investigator has found the JAK/STAT pathway and the JAK2 gene was dramatically overexpressed in CBD BAL cells. In addition, constitutively phosphorylated JAK2 (pJAK2) was found in AMs from Chronic Beryllium Disease (CBD) patients by Westernblot and was increased after beryllium (Be) stimulation for 30 min. Moreover, the JAK2 inhibitor TG101348 significantly inhibited Be-induced CBD AMs TNFa and IFNy production. Meanwhile, overexpression of the JAK2 inhibitor SOCS 1 (suppressors of cytokine signaling) protein decreased Be-induced TNFa production from AMs. Based on this information, the Investigator hypothesizes that CBD AMs overexpress JAK2, which augments the immune response to Be and development of CBD but not BeS.

The investigators believe that these studies are highly innovative since they will undoubtedly shed light on exposure-mediated immune dysregulation in Alveolar Macrophages (AMs) that lead to disease development and likely progression and with additional study of this pathway will reveal potential biomarkers for clinical prognosis and diagnosis. The results obtained from this study will improve the investigators understanding of factors involved in the development of Chronic Beryllium disease (CBD), as well as define targets for therapy, and will serve as a model of other exposure-related immune responses and environmentally-induced chronic diseases. Most importantly, these studies will provide the investigator with preliminary data to submit a high quality R01, allowing the Investigator to apply similar approaches to other genes, define a potential target for this and other similar immune-mediated diseases and continue research efforts at National Jewish Health (NJH.)


Condition or disease Intervention/treatment
Chronic Beryllium Disease (CBD) Beryllium Sensitization (BeS) Procedure: Blood draw Procedure: bronchoscopy

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Study Type : Observational
Estimated Enrollment : 12 participants
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: The Role of JAK2 in Alveolar Macrophages in Chronic Beryllium Disease
Study Start Date : April 2015
Estimated Primary Completion Date : July 2017

Resource links provided by the National Library of Medicine


Group/Cohort Intervention/treatment
Beryllium Sensitization (BeS)
Blood draw
Procedure: Blood draw
We will draw 4 heparin tubes for peripheral blood mononuclear cells (PBMC)

Chronic Beryllium Disease(CBD)
blood draw BAL
Procedure: Blood draw
We will draw 4 heparin tubes for peripheral blood mononuclear cells (PBMC)

Procedure: bronchoscopy
CBD subjects will undergo a bronchoscopy with lavage. This is the passage of a think flexible tube through the nose into the windpipe then into the bronchial tubes. Sterile saltwater solution is through the flexible tube then immediately removed.
Other Name: BAL




Primary Outcome Measures :
  1. The primary outcome for the aims is the downregulation of Th1 cytokine TNFalpha with the inhibition of the JAK2 using siRNA and the inhibitor INCB018424, CEP-701 and TG101348 in CBD or overexpression of the JAK2 gene. [ Time Frame: year 1 ]
    As the primary outcome is the downregulation of TNFalpha level with the inhibition of the JAK2 using the inhibitor TG101348 in CBD, we expect a 50% reduction with a standard deviation of 0.2 based on our preliminary data. We will have more than 95% power with n=6 CBD patients for these aims.

  2. The secondary outcomes for the aims are the changes in BeLPT and AMs phenotype from BeS, CBD and Healthy controls (HC). [ Time Frame: year 2 ]
    The investigator will use repeated measure Welch's ANOVA in SAS 9.4, which correctly accounts for the correlation between measurements and allows for comparisons within and between groups. Normalizing transformations will be performed when necessary to conform to model assumptions and Mauchly's sphericity test will be assessed and adjustments will be added to the analysis as necessary. Estimate and contrast statements will be developed to test hypotheses of interest.


Biospecimen Retention:   Samples With DNA
Bronchoalveolar lavage fluid 4 heparin tubes for PBMC


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Those diagnosed with Beryllium Sensitization. Those diagnosed with Chronic beryllium disease
Criteria

Inclusion Criteria:

  • Chronic Beryllium Disease - These individuals will meet the following inclusion criteria:

Inclusion Criteria:

  1. History of beryllium exposure;
  2. Positive blood and/or bronchoalveolar lavage (BAL) Beryllium Lymphocyte Proliferation Tests (BeLPT);
  3. Biopsy-proven pathologic changes consistent with CBD, specifically non-caseating granulomas and/or mononuclear cell interstitial infiltrates .

Beryllium Sensitization - These individuals will meet the following inclusion criteria:

Inclusion Criteria:

  1. History of beryllium exposure;
  2. Two or more positive blood beryllium lymphocyte proliferation tests (BeLPT) or positive bronchoalveolar lavage (BAL) BeLPT;
  3. Normal lung tissue (no histology suggestive of CBD).

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02596347


Contacts
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Contact: Gina M Atnes, BA 303-398-1679 mondellog@njhealth.org

Locations
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United States, Colorado
National Jewish Health Recruiting
Denver, Colorado, United States, 80206
Contact: Gina M Atnes, BA    303-398-1679    mondellog@njhealth.org   
Principal Investigator: Li Li, MD         
Sponsors and Collaborators
National Jewish Health
Investigators
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Principal Investigator: Li Li, MD National Jewish Health

Publications:

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Responsible Party: Li Li, Dr., National Jewish Health
ClinicalTrials.gov Identifier: NCT02596347     History of Changes
Other Study ID Numbers: 2877
First Posted: November 4, 2015    Key Record Dates
Last Update Posted: September 22, 2016
Last Verified: September 2016

Additional relevant MeSH terms:
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Berylliosis
Pneumoconiosis
Lung Diseases, Interstitial
Lung Diseases
Respiratory Tract Diseases
Lung Injury
Occupational Diseases