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| ID | Type | Description | Link |
|---|---|---|---|
| 2018-A01719-46 | Other Identifier | ID-RCB |
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Better understanding of the specificities of the vaccine response in patients with COPD
Chronic obstructive pulmonary disease (COPD) will become the third leading cause of death worldwide in 2020 (3.5 million patients, 16500 deaths in France). Its socio-economic cost is related to the handicap induced by the decline of the respiratory function, as well as to the occurrence of exacerbations, main causes of hospitalization and mortality. Since exacerbations are mostly infectious, a preventive strategy involves routine influenza vaccination. Although it is highly recommended in this population, there is no formal evidence of its effectiveness during COPD. While correlates of influenza vaccine efficacy exist, cellular and humoral responses to this vaccine have been poorly evaluated in these patients. This alteration of the vaccine response could also be integrated into an overall deficit of the response to a vaccine in these patients.
As influenza virus infection is one of the most important causes of death in patients with COPD, and vaccination is the best way to prevent it, it is essential to better understand the immune response in the context of vaccination in this population. The investigator's hypothesis is that there would be a global alteration of the immunological immune response in the COPD patient involving abnormalities of lymphocyte B differentiation and the effector capacity of T lymphocytes, notably through the activation of the PD1 / PDL1 axis.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patient | patient with COPD |
| |
| control group | patient without COPD |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Anti-influenza and DTp pertussis vaccinations | Other | Anti-influenza and DTp pertussis vaccinations will be performed during the visit by the clinical research nurse. The vaccine has been prescribed as part of the care either by the patient's physician (pulmonologist or general practitioner). |
| Measure | Description | Time Frame |
|---|---|---|
| Rate and evolution of specific antibodies and Cellular B vaccine response | Rate and evolution of J30-specific antibodies according to WHO criteria Tetanus: before vaccination a rate> 0.1 IU / ml is considered protective, that is usually at a rate> 1 IU / ml after booster vaccination Influenza: antibody concentrations exceeding 0.15 μg / ml are considered protective Pertussis: anti-pertussis toxin IgG (PT) Cellular B vaccine response (plasmablast on D7) | 30 days |
| Measure | Description | Time Frame |
|---|---|---|
| Type of Cellular T cell response | Cellular T cell response (Tfh, Treg, TCD4 / TCD8 specific) | 15 days |
| Transcriptomic analysis | Transcriptomic analysis in the pre- and post-vaccination period (vaccine signature) and comparison with matched subjects |
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Inclusion Criteria:
Exclusion Criteria:
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The study will be offered to patients for whom there is a prescription for influenza vaccination and DTp, COPD or non-COPD
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| Name | Affiliation | Role |
|---|---|---|
| Laurent Boyer, MD | CHU Henri-Mondor | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHI Créteil | Créteil | 94000 | France | |||
| CHU Henri-Mondor |
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| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
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| 30 days |
| Number of Lymphocyte populations | Analysis of lymphocyte populations B and T | 7 days |
| Number of exacerbations | Number of minimal, moderate and severe exacerbations within 6 months of vaccination | 6 months |
| Créteil |
| 94000 |
| France |
| D020969 |
| Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |