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IL-40 and IL-41 Levels in Sepsis, Septic Shock, and Healthy Individuals

Comparison of IL-40 and IL-41 Levels in Patients With Sepsis and Septic Shock to Healthy Individuals

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06963541
Enrollment
80
Registered
2025-05-09
Start date
2025-05-15
Completion date
2025-12-31
Last updated
2025-05-09

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

Conditions

Biomarkers, Inflammation, Sepsis, Septic Shock

Keywords

IL-40, IL-41, Cytokines, Critical Illness, Septic Shock, Sepsis

Brief summary

This study aims to investigate the blood levels of two recently identified immune-related proteins, Interleukin-40 (IL-40) and Interleukin-41 (IL-41), in patients with sepsis and its more severe form, septic shock. Sepsis is a serious condition caused by an abnormal immune response to infection, which can lead to organ dysfunction. Septic shock represents an advanced stage of sepsis, characterized by significantly higher mortality risk. IL-40 and IL-41 are newly discovered molecules that are thought to play important roles in the immune system. In this study, the blood concentrations of IL-40 and IL-41 in patients diagnosed with sepsis or septic shock will be measured and compared with those in healthy individuals. The findings may contribute to understanding whether these proteins can be used as biomarkers in the diagnosis or monitoring of treatment in sepsis-related conditions.

Detailed description

Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection and is evaluated by an increase of two or more points in the Sequential Organ Failure Assessment (SOFA) score. Septic shock is characterized by hypotension that persists despite adequate fluid resuscitation (mean arterial pressure ≤65 mmHg) and a serum lactate level greater than 2 mmol/L. Septic shock represents a more severe clinical condition, with mortality rates reaching up to 60%. Interleukin-40 (IL-40) is a recently discovered pro-inflammatory cytokine encoded by the chromosome 17 open reading frame 99 (C17orf99) gene. It is primarily produced by bone marrow, fetal liver, and activated peripheral B cells. IL-40 plays an essential role in immunoglobulin A production, humoral immune regulation, and B cell development. It has also been implicated in the pathogenesis of inflammatory diseases such as rheumatoid arthritis. Interleukin-41 (IL-41), also known as meteorin-like protein (Metrnl), was identified in 2004 and is encoded by the meteorin-like (METRNL) gene located on chromosome 17q25.3. IL-41 is an anti-inflammatory cytokine expressed in tissues such as the intestines, skin, respiratory tract, and central nervous system. It is secreted primarily by alternatively activated macrophages and M2-like macrophages and has roles in both innate and adaptive immune responses. The roles of IL-40 and IL-41 in sepsis and septic shock have not yet been fully elucidated. Understanding the involvement of these novel cytokines in inflammatory processes may provide new insights into the diagnosis and treatment of critical conditions such as sepsis and septic shock. The aim of this study is to compare IL-40 and IL-41 levels in patients diagnosed with sepsis or septic shock to those of healthy individuals.

Interventions

No interventions are associated with either group. This is an observational study without experimental procedures.

Sponsors

Melahat Yalcin Solak
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patient Group: Clinical diagnosis of sepsis or septic shock, based on validated diagnostic criteria (e.g., Sepsis-3) Age 18 years or older Ability and willingness to provide a blood sample prior to initiation of antibiotic treatment Healthy Control Group: Determined to be in good general health based on physical examination and medical history Age 18 years or older Willingness to provide written informed consent

Exclusion criteria

* Patient Group: History of chronic inflammatory diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus) Active cancer or current use of immunosuppressive therapy Pregnant or breastfeeding Presence of other serious conditions that may interfere with diagnosis or treatment (e.g., liver failure, chronic kidney disease) Healthy Control Group: Recent infection within the past month or use of antibiotics in the last 6 weeks History of chronic inflammatory diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus) Underwent surgery within the past 6 months Conditions that may affect blood parameters, such as recent blood donation or intense physical activity Pregnant or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Comparison of Serum IL-40 Levels Between Patients With Sepsis or Septic Shock and Healthy ControlsAt time of enrollment (single time point)IL-40 concentration will be measured in serum samples from both groups using an ELISA-based method. The mean IL-40 levels will be compared between sepsis/septic shock patients and healthy individuals.
Comparison of Serum IL-41 Levels Between Patients With Sepsis or Septic Shock and Healthy ControlsAt time of enrollment (single time point)IL-41 concentration will be measured in serum samples from both groups using an ELISA-based method. The mean IL-41 levels will be compared between sepsis/septic shock patients and healthy individuals.

Secondary

MeasureTime frameDescription
Correlation Between IL-40 and IL-41 Levels in All ParticipantsAt time of enrollment (single time point)The study will assess the correlation between serum IL-40 and IL-41 levels among all participants, including both patient and control groups.

Countries

Turkey (Türkiye)

Contacts

Primary ContactMELAHAT YALÇIN SOLAK, Medical Doctor
melosyalcin@gmail.com+905326479195

Outcome results

None listed

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