Case Report: Possible C3 nephritic factor–driven complement-mediated severe hemolytic anemia and acute kidney injury in a child with Bordetella parapertussis infection

Overactivation of the complement system can cause life-threatening intravascular hemolysis, acute kidney injury (AKI), and multi-organ failure. Expanding the spectrum of rarer triggers of complement dysregulation that may cause severe hemolysis is essential for timely diagnosis and treatment. We report the case of a three-year-old boy admitted with macroscopic hematuria and jaundice. The patient tested positive for <i>Bordetella parapertussis</i>. Atypical hemolytic uremic syndrome (aHUS) was initially suspected due to decreasing hemoglobin, platelet count, and worsening of AKI, and empirical treatment with eculizumab (ECZ) was initiated. No red blood cell (RBC) autoantibodies were detected by standard serology methods or extended flow cytometry including antibody fixation at both room temperature and 4°C, no underlying hematological disorder was found, and genetic screening revealed no pathogenic variants associated with aHUS. However, the patient was strongly positive for C3 nephritic factor (C3NeF), an autoantibody stabilizing the C3 convertase (C3bBb) of the alternative complement pathway. C3NeF is typically linked to C3 glomerulopathy, but in this case appears to have triggered severe complement overdrive and extra- and intravascular hemolysis (bystander hemolysis) during an infection (two-hit immunopathology). Concomitantly, <i>B. parapertussis</i> is known to bind complement factor H, a key regulator of the alternative pathway, creating a "perfect storm" of dysregulation. Following infection control and complement blockade with ECZ, C3d deposition on RBCs declined, renal function recovered, and no clinical relapse has been observed 2 years and 6 months after discharge. To our knowledge, this is the first reported case of a possible C3NeF-driven complement-mediated severe hemolysis with associated AKI due to free hemoglobin toxicity during a severe infection.

Authors

Institutions

Publication Details

Journal
Frontiers in Immunology
Published
2026-01-02
DOI
https://doi.org/10.3389/fimmu.2025.1715464
Primary Topic
Complement system in diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Case Report: Possible C3 nephritic factor–driven complement-mediated severe hemolytic anemia and acute kidney injury in a child with Bordetella parapertussis infection

Anne Todsen Hansen, Alex Christian Yde Nielsen, Hans Jakob Hartling, Mira Marie Laustsen et al.
Frontiers in Immunology
Complement system in diseases
article

Case Report: Possible C3 nephritic factor–driven complement-mediated severe hemolytic anemia and acute kidney injury in a child with Bordetella parapertussis infection

Anne Todsen Hansen, Alex Christian Yde Nielsen, Hans Jakob Hartling, Mira Marie Laustsen, Morten Hanefeld Dziegiel, Lillemor Skattum, Line Thousig Sehested, Hanne Nørgaard, S. Thorsen, Ida Maria Schmidt, Hanne Vibeke Marquart, Line Borgwardt
article en

Abstract

Overactivation of the complement system can cause life-threatening intravascular hemolysis, acute kidney injury (AKI), and multi-organ failure. Expanding the spectrum of rarer triggers of complement dysregulation that may cause severe hemolysis is essential for timely diagnosis and treatment. We report the case of a three-year-old boy admitted with macroscopic hematuria and jaundice. The patient tested positive for <i>Bordetella parapertussis</i>. Atypical hemolytic uremic syndrome (aHUS) was initially suspected due to decreasing hemoglobin, platelet count, and worsening of AKI, and empirical treatment with eculizumab (ECZ) was initiated. No red blood cell (RBC) autoantibodies were detected by standard serology methods or extended flow cytometry including antibody fixation at both room temperature and 4°C, no underlying hematological disorder was found, and genetic screening revealed no pathogenic variants associated with aHUS. However, the patient was strongly positive for C3 nephritic factor (C3NeF), an autoantibody stabilizing the C3 convertase (C3bBb) of the alternative complement pathway. C3NeF is typically linked to C3 glomerulopathy, but in this case appears to have triggered severe complement overdrive and extra- and intravascular hemolysis (bystander hemolysis) during an infection (two-hit immunopathology). Concomitantly, <i>B. parapertussis</i> is known to bind complement factor H, a key regulator of the alternative pathway, creating a "perfect storm" of dysregulation. Following infection control and complement blockade with ECZ, C3d deposition on RBCs declined, renal function recovered, and no clinical relapse has been observed 2 years and 6 months after discharge. To our knowledge, this is the first reported case of a possible C3NeF-driven complement-mediated severe hemolysis with associated AKI due to free hemoglobin toxicity during a severe infection.

Frontiers in ImmunologyVol. 16
University of Copenhagen (DK), Lund University (SE), Copenhagen University Hospital (DK), Rigshospitalet (DK)
Good health and well-being
Openalex Percentile: Top 99%
Complement system in diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.