Sarcoidosis and Immune Cells in Lung, Lymph Nodes and Blood

Sponsor
Region Stockholm (Other)
Overall Status
Recruiting
CT.gov ID
NCT05751447
Collaborator
Karolinska Institutet (Other)
560
1
1
55
10.2

Study Details

Study Description

Brief Summary

Background:

Sarcoidosis is an inflammatory disease, most commonly affecting the lungs and intrathoracic lymph nodes but can affect virtually any organ, sometimes manifesting as life threatening cardiac arrythmias. Some patients resolve spontaneously, whereas others get a chronic disease leading to for instance impaired lung function and cardiac failure. The most severe cases might need a transplantation.

In the lungs, activated T cells are accumulated leading to release of cytokines, especially TNF-alpha is regarded as crucial for disease progression. Some segments of the T cell receptor and specific genes (HLA types) are connected to a resolving disease. More detailed knowledge about mechanisms why some experience a chronic disease course and others resolve spontaneously without treatment is to a large extent lacking. There is no cure, and despite treatment with immunosuppressants (often corticosteroids and cytotoxic agents), many patients experience a deteriorating disease.

Aim:
  1. Find biomarkers to be able to early predict which patients will develop a more severe/ chronic disease course and thereby enabeling early intervention before irreversible damage.

  2. Predict which treatment is best for a specific patient, i.e. individualize treatment.

  3. Find targets for new potential therapies.

Methods:

The majority of data is collected at investigations normally performed during diagnostic work-up for sarcoidosis. Most patients undergo a bronchoscopy with bronchoalveolar lavage (BAL) and some also lymph node punction through oesophagus with the help of ultrasound. The BAL fluid that remains after clinical analysis is used for research purpose. For patients undergoing lymph node punction, one extra punction is performed for research purpose. Extra blood samples are taken from all patients.

The samples will mostly be used for studying T cells with immunohistochemistry, flow cytometry including activity markers, subtypes and receptors, but also cytokines and other cells (for instance B cells, NK and NKT cells). The patients are followed longitudinally, minimum 2 years. Some patients will undergo a second bronchoscopy 6-12 months after the first. Results from the immunological investigations will be correlated to disease course, genetics and result of treatment.

Significance :

By comparing the inflammation in several compartments (lung, lymph node , blood) at a molecular level with clinical disease course, genotype, and treatment response we hope to find biomarkers that can predict disease course and response to therapy. Thereby, we hope to be able to tailor therapy for each individual patient. By studying several compartments, the results may also help to improve understanding of how a systemic inflammation is distributed within the body, and thus also contribute to understanding of other inflammatory diseases.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Lymph node puncture, bronchoscopy
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
560 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Studie av cellulära Uttryck i lymfkörtlar, lungsköljvätska Och Blod Vid Sarkoidos.
Actual Study Start Date :
Oct 1, 2019
Anticipated Primary Completion Date :
May 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Immune cells

Lymph node puncture and/ or bronchoscopy.

Diagnostic Test: Lymph node puncture, bronchoscopy
Included patients will undergo an extra lympn node punction through oesophagus and/ or an extra bronchoscopy.

Outcome Measures

Primary Outcome Measures

  1. Immune cell percentages in lung, lymph nodes and blood [2 years]

    Is there a difference in frequency of different immune cells (percentage) between different compartments in clinical disease phenotypes?

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Suspicion of sarcoidosis

  • Swedish speaking

  • Able to understand and approve of study protocol

  • No contraindications for planned interventions

Exclusion Criteria:
  • No suspicion of sarcoidosis

  • Not Swedish-speking

  • Not able to understand study protocol

  • Not approving of stydy protocol

  • Contraindications for planned interventions

Contacts and Locations

Locations

Site City State Country Postal Code
1 Karolinska University Hospital Stockholm Sweden

Sponsors and Collaborators

  • Region Stockholm
  • Karolinska Institutet

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Region Stockholm
ClinicalTrials.gov Identifier:
NCT05751447
Other Study ID Numbers:
  • K2019-6557
First Posted:
Mar 2, 2023
Last Update Posted:
Mar 2, 2023
Last Verified:
Feb 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2023