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Immunopathology of Autoimmune Hemolytic Anemia

Immunopathology of Autoimmune Hemolytic Anemia: an Open, Prospective and Multicenter Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02158195
Acronym
IAHAI
Enrollment
27
Registered
2014-06-06
Start date
2013-07-03
Completion date
2018-12-27
Last updated
2026-02-09

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

Conditions

Autoimmune Hemolytic Anemia

Brief summary

Autoimmune hemolytic anemia (AIHA) is an auto-immune disease mediated by specific antibodies targeting red blood cells. Its pathogenesis is not completely understood, and the role of T cells have been rarely studied. The aim of this study is to compare the frequency of circulating T cells, T cell polarization and functions, notably regulatory T cells, during warm AIHA by comparison to healthy controls. The role of treatments, such as steroids, will also be determined in patients with warm AIHA.

Interventions

BIOLOGICALblood samples

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients diagnosed with primary warm Autoimmune Hemolytic Anemia (wAIHA) * Secondary AHAI (infections, hematological diseases, systemic diseases) * Naive of treatment for hemolytic anemia or in relapse * Older than 16 * Able to understand written and spoken French * who have provided written informed consent * INCLUSION CRITERIA for CONTROLS * Persons without auto-immune disease, cancer or active infection. * Older than 16 * Able to understand written and spoken French * who have provided written informed consent

Exclusion criteria

* Cold agglutinin disease * Pregnancy * Persons without national health insurance

Design outcomes

Primary

MeasureTime frame
physiological parameter : blood level of regulatory T cells (Treg, CD4+CD25HighFoxp3+)Change from baseline to 3 months
physiological parameter : percentage of inhibiting LT proliferation inhibitionChange from baseline to 3 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026