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HLA-G Immuno-Inhibitor Checkpoint Study in Patients With COVID-19 Infection: Molecular and Cellular Assessment

HLA-G Immuno-Inhibitor Checkpoint Study in Patients With COVID-19 Infection: Molecular and Cellular Assessment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04613297
Acronym
HLA-G-COVID
Enrollment
91
Registered
2020-11-03
Start date
2020-10-19
Completion date
2022-07-19
Last updated
2022-08-03

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

Conditions

Covid19

Keywords

HLA-G

Brief summary

The aim of the research is to study the immune checkpoint linked to the HLA-G molecule in the dysregulation of the control of COVID-19 infection.

Detailed description

Single-center, prospective, open-ended, interventional study with minimal risks and constraints. Patients will be divided into 3 groups: patients not infected with COVID-19, patients infected with COVID-19 not hospitalized, patients infected with COVID-19 hospitalized.

Interventions

OTHERBaseline and during hospitalization blood samples

Blood sample will be performed at the inclusion visit for all patient and for the hospitalized COVID-19 infected patients, extra-blood samples will be performed : * at day 3 * day 5 and * In case of aggravation * At the discharge from hospital

Blood sample will be performed at the inclusion visit only

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Patient with possible or confirmed infection by COVID-19

Exclusion criteria

* Patient without liberty or guardianship

Design outcomes

Primary

MeasureTime frameDescription
Comparison of the percentage of T cells expressing the HLA-G receptor ILT2 (CD3+CD4+ILT2+ T cells, and CD3+CD8+ILT2+ T cells) between the 3 groups of patients.1 monthThe CD3 + T lymphocyte cell populations (CD4 + ILT2 + and CD8 + ILT2 +) will be compared between the groups of patients
Comparison of the expression of circulating soluble HLA-G, between the groups of patients.1 dayBlood levels of soluble HLA-G and plasma microvesicles with expression of HLA-G will be compared between the groups of patients.

Secondary

MeasureTime frameDescription
1 month survival1 monthVital status collected 1 month post inclusion for all the patients
Assessment of the severity of the disease according to the isoform of HLA-G1 monthComparison of the isoforms (alleles) of HLA-G regarding the severity of the disease for the infected patients.
Comparison of the expression of one of the cell receptors of the SARS-CoV-2 virus, called BSG (Basigin), whose expression is modified by the interaction between HLA-G.1 dayThe expression of the BSG cell receptor induced by HLA-G will be compared between COVID19 patients and uninfected patients.

Countries

France

Outcome results

None listed

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