The role of anti-complement factor H antibodies in the development of atypical haemolytic uremic syndrome: a possible contribution to abnormality of platelet function

Br J Haematol. 2020 Apr;189(1):182-186. doi: 10.1111/bjh.16297. Epub 2019 Dec 26.

Abstract

Atypical haemolytic uremic syndrome (aHUS) is associated with complement system abnormality, such as production of complement factor H (CFH) autoantibodies. The growing evidence indicates complement overactivation on platelets is intimately involved in aHUS pathogenesis, besides endothelial injury. We here showed plasma from patients with anti-CFH antibodies induced aggregation of washed platelets, while purified anti-CFH antibodies suppressed aggregation. This suggested anti-CFH antibody itself suppressed thrombosis, while other plasma factor including complement factors could overactivate the platelets, leading to aggregation, which augmented the notion the state of complement activation influenced by anti-CFH antibodies is important in the aggregation of platelets in aHUS.

Keywords: anti-CFH antibodies; atypical haemolytic uremic syndrome; complement; complement factor H; platelet.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Atypical Hemolytic Uremic Syndrome* / blood
  • Atypical Hemolytic Uremic Syndrome* / immunology
  • Atypical Hemolytic Uremic Syndrome* / pathology
  • Autoantibodies* / blood
  • Autoantibodies* / immunology
  • Blood Platelets* / immunology
  • Blood Platelets* / metabolism
  • Blood Platelets* / pathology
  • Child
  • Child, Preschool
  • Complement Factor H / immunology*
  • Female
  • Humans
  • Male
  • Platelet Aggregation / immunology*

Substances

  • Autoantibodies
  • Complement Factor H