CXCL10 rs8878 identifies a genotype-associated immune phenotype linked to T-lymphocyte preservation and survival in sepsis - Report - MDSpire

CXCL10 rs8878 as a Genetic Marker for Immune Phenotypes Associated with T-Lymphocyte Maintenance and Survival in Sepsis

  • By

  • Birte Dyck

  • Andrea Witowski

  • Thilo Bracht

  • Malte Bayer

  • Patrick Thon

  • Dominik Ziehe

  • Tim Rahmel

  • Matthias Unterberg

  • Britta Westhus

  • Lars Palmowski

  • Hartmuth Nowak

  • Stefan Felix Ehrentraut

  • Jennifer Orlowski

  • Alexander von Busch

  • Alexander Zarbock

  • Nina Babel

  • Moritz Anft

  • Dietrich Henzler

  • Michael Adamzik

  • Lars Bergmann

  • Barbara Sitek

  • Björn Koos

  • Katharina Rump

  • July 17, 2026

Share

CXCL10 rs8878 as a Genetic Marker for Immune Phenotypes in Sepsis

Overview

The study identifies the CXCL10 rs8878 genotype as a significant factor influencing T cell dynamics and 30-day survival in septic patients. Carriers of the AA genotype demonstrated higher T cell counts compared to G-allele carriers.

Background

Sepsis is a critical condition characterized by a dysregulated immune response to infection, leading to high morbidity and mortality. T lymphocytes play a crucial role in immune response, and their dysregulation during sepsis is linked to poor clinical outcomes. Understanding genetic factors influencing T cell behavior may provide insights into patient stratification and therapeutic targets.

Data Highlights

GenotypeT Cell Counts30-Day Survival
AAHigherImproved
G-alleleLowerWorse

Key Findings

  • Variants in the CXCL10 gene are associated with T cell dysregulation in sepsis.
  • AA genotype carriers exhibited higher circulating T cell counts compared to G-allele carriers.
  • Higher total and CD8+ T cell counts correlated with improved survival rates.
  • Increased CXCL10 mRNA expression was observed in AA-genotype carriers among non-survivors.
  • CXCL10 concentrations on day 1 were positively correlated with inflammatory cytokines and inversely correlated with total T cell counts.

Clinical Implications

Understanding the genetic influences on T cell dynamics could provide insights into patient stratification.

Conclusion

The CXCL10 rs8878 genotype is linked to T cell maintenance and survival outcomes in sepsis.

Related Resources & Content

  1. Blood Cancer Journal, 2022 -- Functional Assessment and Validation of GWAS-Identified Genetic Variants Linked to Chronic Lymphocytic Leukemia: Insights from the CRuCIAL Study
  2. Intensive Care Medicine, 2022 -- EASIX Levels Prior to Transplantation and Subsequent Sepsis Following Allogeneic Stem Cell Transplantation
  3. Clinical Rheumatology, 2020 -- Reduced IKBKE Expression in Patients with Systemic Lupus Erythematosus
  4. Intensive Care Medicine, 2025 -- Subphenotypes of Sepsis, Theragnostic Approaches, and Tailored Management Strategies
  5. Intensive Care Medicine, 2026 -- Surviving Sepsis Campaign: international guidelines for management of sepsis and septic shock 2026
  6. Annals of Intensive Care, 2023 -- Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial
  7. Critical Care: Sepsis and Severe Infection, 2026 -- Beyond the sepsis label: heterogeneity, subphenotypes, and the path to precision therapy
  8. Surviving Sepsis Campaign: international guidelines for management of sepsis and septic shock 2026 | Intensive Care Medicine | Springer Nature Link
  9. Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial | Annals of Intensive Care | Springer Nature Link
  10. Beyond the sepsis label: heterogeneity, subphenotypes, and the path to precision therapy | Critical Care: Sepsis and Severe Infection | Springer Nature Link

Original Source(s)

Related Content