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Role of CD28null NKG2Dpos T Cells on Human Alloimmune Reactivity T Cell Population

Role of CD28null NKG2Dpos T Cells on Human Alloimmune Reactivity: An Untargeted T Cell Population (# 859869783).

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01914354
Acronym
NKG2D
Enrollment
90
Registered
2013-08-02
Start date
2012-02-29
Completion date
2014-06-30
Last updated
2016-10-28

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

Conditions

Kidney Transplant

Keywords

T cells, Human Alloimmune Reactivity, immunosuppression

Brief summary

This is an observational multi-center study to determine whether any single immune monitoring test or a combination of tests obtained in the first 6 months after renal transplantation correlates with acute rejection or graft loss in renal allograft recipients receiving commonly used immunosuppressive.

Interventions

None listed

Sponsors

The Cleveland Clinic
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* human kidney transplant recipients * ATG or basiliximab induction therapy

Exclusion criteria

* induction therapy other than ATG or basiliximab

Design outcomes

Primary

MeasureTime frame
To document the prevalence and frequencies of CD4+ and CD8+ CD28null/NKG2Dpos T cells at the time of transplantation.6 months
To test whether CD28null/NKG2Dpos T cells have unique rapid activation properties to allogeneic HLA antigens in vitro6 months

Secondary

MeasureTime frame
To study the clinical correlations between the frequencies of alloreactive CD28null/NKG2Dpos T cells with kidney graft function and histopathology.6 months
To test the effects of induction therapy with rabbit anti-thymocyte globulin (ATG) vs. IL-2 receptor blocker antibodies on circulating CD28null/NKG2Dpos T cells.6 months

Outcome results

None listed

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