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Alteration of the Immune Response in Bacterial Infection

Alteration of the Immune Response in Bacterial Infection

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03948308
Acronym
ARIIBACT
Enrollment
15
Registered
2019-05-13
Start date
2019-05-01
Completion date
2020-09-01
Last updated
2019-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infection

Brief summary

The pilot study ARIIBO was conducted to analyze changes in immune parameters reported in obese subjects, which had never been the subject of a global study outside of an infectious context, and studied in period septic only sporadically. This study was intended to contribute to a better understanding of the probably adverse impact of obesity on the immune response to bacterial infections, and to describe a specific immunological profile of an infectious excess risk in obese subjects. In terms of infection, obesity is a risk factor due to mechanical and pharmacodynamic variations, but also to the immune system. One of the best studied immunological parameters in obese patients, leptin resistance, is associated with a decrease in innate and adaptive immunity through a modification of the lymphocyte and cytokine profile. It is important to compare the data collected in obese patients infected (first study called ARIIBO), with those of non-obese subjects presenting the same type of infection, which will be included in the study ARIIBACT

Interventions

BIOLOGICALblood sample

blood sample before, during and after infection treatment

Sponsors

Versailles Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* age between 18 and 80 years * BMI 18 to 25 * presence of a bacterial infection * pneumopathy (documented or probable) * acute pyelonephritis / prostatitis * skin and soft tissue infection (erysipelas, fasciitis, excluding pressure ulcers) * cholecystitis / cholangitis, * surgical site infection * signed informed consent

Exclusion criteria

* patients with documented viral, parasitic or mycotic infections * patients with bacterial infection\> 4 weeks (eg endocarditis, osteoarticular infections) * patients followed in intensive unit care * patients with progressive cancerous pathology or malignant hemopathy diagnosed in the previous five years * patients with systemic diseases (connective tissue diseases, vasculitis) * known immunodepression syndrome (CVID, HIV ...) * immunosuppressive therapy in progress until less than one month before inclusion (corticosteroids, DMARDs, biotherapies, hydroxychloroquine)

Design outcomes

Primary

MeasureTime frameDescription
cytokin analysis (IL-6, IL-10, IL-17, TNFα, IFNγ)1 monthDescription of an immunological profile of inflammation using current inflammatory cytokines during sepsis in non-obese subjects in comparison with this same profile in obese subjects
adipokin analysis (leptine, adiponectine)1 monthDescription of the kinetics of 2 cytokines more speficically involved in obesity (leptine, adipokinine) during sepsis in non-obese subjects in comparison with this same profile in obese subjects
leptin polymorphism analysis1 monthDescription of the genetic polymorphism of leptine and leptine receptor in non-obese subjects in comparison with this same profile in obese subjects

Countries

France

Contacts

Primary ContactMeckenstock
rmeckenstock@ch-versailles.fr+331 39 63 93 19
Backup ContactLaure Morisset
lmorisset@ch-versailles.fr+33139239785

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026