Study of Phenotypic and Functional Characteristics of Regulatory T Lymphocytes in Horton's Disease

NCT ID: NCT02857192

Last Updated: 2026-02-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

41 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-10-05

Study Completion Date

2019-03-25

Brief Summary

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Giant cell arteritis (GCA) is the most frequent vascularitis after 50 years of age The investigators recently showed that GCA was accompanied by an elevation in Th1 and Th17 response \[1\]. Even though a quantitative deficit in regulatory TL (Treg) was shown, there are to date no data concerning their precise phenotypic and functional characteristics and notably their ability to inhibit Th1 and Th17 polarisation. The hypothesis of the investigator is that, in GCA, there is quantitative and above all functional deficit of Treg. Recently, progress has been made in the identification of Treg with new markers (CD39), which will make it possible to better identify and to study their specific functions. In this study the phenotypic and functional characteristics of Treg in GCA will be analysed. Better understanding of the role des Treg in GCA should lead to better-targeted treatments for patients with GCA, notably via the blockage of cytokines that inhibit the differentiation and/or function of Treg.

The study is classified interventional because a lot of blood samples are taken.

Detailed Description

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Conditions

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Horton's Disease

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Horton

Group Type EXPERIMENTAL

Blood samples

Intervention Type BIOLOGICAL

control

Group Type PLACEBO_COMPARATOR

Blood samples

Intervention Type BIOLOGICAL

Interventions

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Blood samples

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

Patients

* Patients who have provided written consent
* Patients with national health insurance cover
* Age \> 50 years
* Patients with a diagnosis of Horton's disease, before any treatment

Horton's disease is defined by the American College Rheumatology ACR criteria \[2\], as the association of 3 of the following 5 criteria:

* age at disease onset 50 years or older
* recent onset localized headache
* indurated temporal artery or diminished/abolition of temporal pulse
* erythrocyte sedimentation rate (ESR) greater than 50 mm during the first hour (or C Reactive protein (CRP)\>20 mg/L)
* Positive temporal artery biopsy (TAB) showing vascularitis with infiltration by mononuclear cells or granulomatous inflammation with or without giant cells.

Control subjects

Control subjects will be healthy volunteers recruited among blood donors at Dijon University Hospital, voluntary hospital personnel (nurses, doctors, laboratory technicians and secretaries) and patients without infectious, inflammatory or auto-immune diseases or cancer (CRP\<5mg/L) recruited in the investigating departments of Dijon Hospital. They will be matched for age and sex and must meet the following criteria:

* Age \> 50 years
* Patients with national health insurance cover
* Signed written informed consent form
* Absence of an inflammatory syndrome (CRP\<5 mg /L)

Exclusion Criteria

* Adult under guardianship
* Persons without national health insurance cover
* Pregnant or breast-feeding women
* Patients treated with corticoids or immunosuppressants in the month preceding inclusion
* Patients treated with chemotherapy
Minimum Eligible Age

51 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire Dijon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre Hospitalier Universitaire

Dijon, , France

Site Status

Countries

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France

References

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Samson M, Greigert H, Ciudad M, Gerard C, Ghesquiere T, Trad M, Corbera-Bellalta M, Genet C, Ouandji S, Cladiere C, Thebault M, Ly KH, Liozon E, Maurier F, Bienvenu B, Terrier B, Guillevin L, Charles P, Quipourt V, Devilliers H, Gabrielle PH, Creuzot-Garcher C, Tarris G, Martin L, Saas P, Audia S, Cid MC, Bonnotte B. Improvement of Treg immune response after treatment with tocilizumab in giant cell arteritis. Clin Transl Immunology. 2021 Sep 12;10(9):e1332. doi: 10.1002/cti2.1332. eCollection 2021.

Reference Type RESULT
PMID: 34532040 (View on PubMed)

Maldiney T, Greigert H, Martin L, Benoit E, Creuzot-Garcher C, Gabrielle PH, Chassot JM, Boccara C, Balvay D, Tavitian B, Clement O, Audia S, Bonnotte B, Samson M. Full-field optical coherence tomography for the diagnosis of giant cell arteritis. PLoS One. 2020 Aug 31;15(8):e0234165. doi: 10.1371/journal.pone.0234165. eCollection 2020.

Reference Type DERIVED
PMID: 32866179 (View on PubMed)

Other Identifiers

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SAMSON APJ 2014

Identifier Type: -

Identifier Source: org_study_id

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