AI Article Synopsis

  • CM-HUS is a type of thrombotic microangiopathy linked to genetic variants or acquired antibodies affecting complement proteins.
  • Researchers developed biosensors using HEK293 cells with modified complement regulation to improve the diagnosis and treatment monitoring of CM-HUS.
  • The study reveals that about 50% of CM-HUS patients may have an immune response driven by IgM antibodies, providing insight into why some patients do not show specific genetic variants.

Article Abstract

Unlabelled: Complement-mediated hemolytic uremic syndrome (CM-HUS) is a thrombotic microangiopathy characterized by germline variants or acquired antibodies to complement proteins and regulators. Building upon our prior experience with the modified Ham (mHam) assay for ex vivo diagnosis of complementopathies, we have developed an array of cell-based complement "biosensors'' by selective removal of complement regulatory proteins (CD55 and CD59, CD46, or a combination thereof) in an autonomously bioluminescent HEK293 cell line. These biosensors can be used as a sensitive method for diagnosing CM-HUS and monitoring therapeutic complement blockade. Using specific complement pathway inhibitors, this model identifies IgM-driven classical pathway stimulus during both acute disease and in many patients during clinical remission. This provides a potential explanation for ~50% of CM-HUS patients who lack an alternative pathway "driving" variant and suggests at least a subset of CM-HUS is characterized by a breakdown of IgM immunologic tolerance.

Key Points: CM-HUS has a CP stimulus driven by polyreactive IgM, addressing the mystery of why 40% of CM-HUS lack complement specific variantsComplement biosensors and the bioluminescent mHam can be used to aid in diagnosis of CM-HUS and monitor complement inhibitor therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11160691PMC
http://dx.doi.org/10.1101/2024.05.29.596475DOI Listing

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