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T Cell Dysfunction in ESRD

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Fudan University

Status

Unknown

Conditions

ESRD
T-Cell Dysfunction

Treatments

Other: no specific interventions

Study type

Observational

Funder types

Other

Identifiers

NCT04658069
TcdiESRD

Details and patient eligibility

About

Patients with end-stage renal disease (ESRD) suffer from high morbidity and mortality of cardiovascular and infectious disease and increased risk of all-cause mortality which is mainly attributed to the disturbed immune response. More and more evident indicated that T cell dysfunction was universal in ESRD. However, few studies clarified the association of T cell dysfunction and clinical outcomes. This study is aim to explore valuable markers of T cell dysfunction predicting bad clinical outcomes including death, cardiovascular disease, infection and tumor. Hopefully, these finding will provide foundation for further mechanism research and better therapeutic options for ESRD patients in the future.

Full description

Patients with end-stage renal disease (ESRD) suffer from high morbidity and mortality of cardiovascular and infectious disease and increased risk of all-cause mortality which is mainly attributed to the disturbed immune response. More and more evident indicated that T cell dysfunction was universal in ESRD. Recent evidence suggests uremia-related immune changes resemble to aging immune system, increasing immunological age of T cells by 20-30 years. As compared to an age-matched healthy control, ESRD patients present a lower thymic output of naïve T cells, a decline in the T-cell telomere length and an increase in the differentiation status towards the terminal differentiated memory phenotype with a large number of CD28-negative T cells. More importantly, these changes are strongly associated with a history of cardiovascular diseases and the occurrence of severe infectious episodes in this population, supporting the idea that T cell dysfunction is a critical feature in this population and will impact clinical outcomes profoundly. This study prospectively researched the predictive value of T cell dysfunction for all-cause mortality and clinical complication in hemodialysis (HD) patients.

Enrollment

400 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • had been on hemodialysis treatment for at least 6 months in Blood Purification Center,Zhongshan Hospital, Fudan University

Exclusion criteria

  • underwent any kind of cardiovascular or infection event in three months
  • with hematological diseases, rheumatic diseases, active malignancies
  • with history of human immunodeficiency virus infection
  • currently use of any immunosuppressants
  • not followed-up at Zhongshan Hospital, Fudan University

Trial design

400 participants in 1 patient group

One Cohort receiving routine hemodialysis therapy without any specific interventions
Description:
all HD patients enrolled in this study
Treatment:
Other: no specific interventions

Trial contacts and locations

0

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Central trial contact

Bo Shen, MD; Fangfang Xiang, MD

Data sourced from clinicaltrials.gov

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