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UnknownNCT05954260

Immune Dysfunction in Critical Illness: Utility of a Panel of Genes and Molecules Involved in the Immunological Synapse

Cuantificación de la Disfunción Inmunitaria Inducida Por la Enfermedad Crítica Mediante el Estudio de un Panel de Genes y Moléculas Implicadas en la Sinapsis Inmunológica y su Utilidad Pronóstica

Status
Unknown
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
David Pérez Torres · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Critical illnesses represent a significant physiological assault that triggers changes in the patient's immune system, resulting in an immunopotentiating response (systemic inflammatory response syndrome, SIRS) and an immunosuppressive response (compensatory anti-inflammatory response syndrome, CARS). The balance between SIRS and CARS is essential for the patient to return to a state of immune homeostasis and accelerate the healing process. However, when CARS is disproportionately intense, it leads to a state of immunoparalysis, which predisposes the patient to vulnerability to opportunistic infections, associated with a peak in late mortality. The majority of patients admitted to the ICU are considered immunocompetent. However, the investigators suspect that a significant proportion of them exhibit predominance of CARS and a state of functional immunosuppression. There is currently no diagnostic test to determine whether a patient is functionally immunocompetent at a specific point in time. The goal of this observational study is to learn about the immune system dysfunction occurring in critical illness. The main questions it aims to answer are: * What is the prevalence of immune system dysfunction in critical illness? * Does immune system dysfunction affect multiple organ failure trajectory and mortality in critical illness? * Is immune system dysfunction related to an increased risk of opportunistic hospital-acquired infections in critical illness? * Is immune system dysfunction related to age, fragility, nutritional status or previous comorbidities in critical illness? To answer these questions, the investigators will prospectively study a population of critically ill patients, defined by the presence of organ failure. The investigators will analyse a panel of genes and molecules involved in immunological synapse, using peripheral blood samples at different moments of the evolution of critical illness. Based on the analysis, the investigators will classify the patients' functional immune status and correlate it with the outcomes.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTBlood samplingWe will collect blood samples from the patients included in the study on ICU days 1, 3 and 5. We will measure gene expression (mRNA) and plasma levels of various elements involved in the immunological synapse.

Timeline

Start date
2023-08-20
Primary completion
2024-12-31
Completion
2025-12-31
First posted
2023-07-20
Last updated
2023-08-23

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT05954260. Inclusion in this directory is not an endorsement.