Stem Cell Transplantation Clinical Trial
— ALLOVIROOfficial title:
Inflammatory Response to Paramyxovirus Infection in an Ex-vivo Model of Bronchial Epithelial Cells in Allogeneic Hematopoietic Stem Cell Recipients
Verified date | December 2019 |
Source | Assistance Publique - Hôpitaux de Paris |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Introduction. Chronic graft-versus-host-disease (GVHD) is the main late noninfectious
complication after allogeneic hematopoietic stem cell transplantation (HSCT) that can affect
several organs. Bronchiolitis obliterans syndrome (BOS) is recognized as pulmonary chronic
GVHD. A diagnosis of a lower respiratory tract infection in the first 100 days following
transplant has been associated to the development of BOS. One hypothesis is that the first
stage driving to BOS is a previous aggression of bronchial epithelial cells by various
factors such as chemotherapy and radiotherapy. Thereafter, data suggest that viral
infections, in particular Parainfluenza viruses could be a trigger for BOS. The alloimmune
reaction activated by the respiratory virus could lead to the fibrosis process. Our
hypothesis is that the bronchial epithelium of allogeneic HSCT recipients has phenotypic
specificities that are associated with a specific response to the viral respiratory
infections (in particular paramyxovirus) leading to the development of BOS.
Main objective. To characterize and compare the inflammatory response after infection with
Parainfluenza 3 virus in an ex-vivo model of bronchial epithelial cells obtained from
allogeneic HSCT recipients and controls.
Objective secondary. To characterize the phenotypic specificities of allogeneic HSCT
recipients' bronchial epithelium.
Methodology, and experimental plan. Prospective, monocentric research. Bronchial biopsies
obtained from patients, will be completely differentiated after 21 days of culture.
Epithelial cells will be infected by the virus strain Parainfluenza 3. Transcriptome of the
cells from both allogeneic HSCT patients and controls, infected and non-infected will be
analyzed 48 hours after infection.
Status | Active, not recruiting |
Enrollment | 14 |
Est. completion date | July 2020 |
Est. primary completion date | October 1, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Allogeneic HSCT patients [case] - requirement of ng bronchial fibroscopy with bronchial biopsies for the exploration of FEV1 decline [case] - non Allogeneic HSCT patients [control] - .requirement of bronchial fibroscopy for exploration of a lung mass or of interstitial lung disease, requiring bronchial biopsies [control] Exclusion Criteria: - Minor or major patients protected - Radiotherapy or chemotherapy [control group] - Respiratory infection - History of smoking >= 15 packs/yr |
Country | Name | City | State |
---|---|---|---|
France | Saint Louis Hospital | Paris |
Lead Sponsor | Collaborator |
---|---|
Assistance Publique - Hôpitaux de Paris |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cells Transcriptome after infection by parainfluenza virus | inflammatory response after infection with Parainfluenza 3 virus in an ex-vivo model of bronchial epithelial cells assessed by cells transcriptome | 21 days |
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