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Study on Antigen-presenting Function of Gamma Delta T Cells in Sepsis and Its Molecular Mechanisms

Conditions
Sepsis
Antigen-presenting Function
γδ T Cells
Interventions
Other: Collect peripheral blood sample
Registration Number
NCT03379896
Lead Sponsor
West China Hospital
Brief Summary

Study on antigen-presenting function of gamma delta T cells in sepsis and its molecular mechanisms

Detailed Description

The latest definition of sepsis highlights the role of dysregulated host response to infection in organ dysfunction aggravation. Maintenance of immune homeostasis of septic patients through immunotherapy is the key breakthrough to improve success rate. Antigen-presenting cell (APC) is the bridge that connects the innate and adaptive immunity. Decrease of count and function of APC has been shown to be associated with worsened clinical outcomes in patients with sepsis. Gamma-delta T cells (γδ T cells) are the newly identified population of T lymphocytes. Recent studies have found that γδ T cells possess unique and powerful antigen-presenting function, making them the hot topic in infection and cancer research. Based on the results, the investigator plan to evaluate the antigen-presenting function changes of γδ T cells in septic status by analyzing the antigen-presenting related molecules on γδ T cells, antigen protein uptake ability, and their function on the proliferation and activation of CD8+ T lymphocytes. Furthermore, the investigator will explore the mechanism and signal pathways for the APC function changes of γδ T cells. Findings from this research could help explain the mechanism of sepsis induced immune dysfunction, enrich our understanding of the important role of γδ T cells, and build a good foundation for immunotherapy in sepsis.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
Inclusion Criteria
  1. ≥18 year old;
  2. a known or suspected infection based on clinical data at the time of admission and sepsis-induced dysfunction of at least one organ.
Exclusion Criteria
  1. autoimmune disease,
  2. history of transplantation,
  3. acute tuberculosis,
  4. chronic hepatitis B or C infection,
  5. HIV infection,
  6. active malignancy, and
  7. long-term use of cortical steroids.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
SepsisCollect peripheral blood samplePatient diagnosed with sepsis according to the new sepsis definition (infection+SOFA≥2).
ControlCollect peripheral blood sampleAge-matched healthy control
Primary Outcome Measures
NameTimeMethod
28-day clinical outcome28-day after ICU admission

death

Secondary Outcome Measures
NameTimeMethod
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