Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing
Abstract Objectives Complete deficiency of alternative pathway (AP) complement factors, explained by homozygous mutations, is a well‐known risk factor for invasive bacterial infections; however, this is less obvious for heterozygous mutations. We describe two siblings with a heterozygous NM_001928.3...
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doaj-3310744fb55d431cbbd81ef7e5c999782021-04-29T11:54:30ZengWileyClinical & Translational Immunology2050-00682021-01-01104n/an/a10.1002/cti2.1256Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killingJeroen D Langereis0Renate G van derMolen1Corrie deKat Angelino2Stefanie S Henriet3Marien I deJonge4Irma Joosten5Annet Simons6Janneke HM Schuurs‐Hoeijmakers7Marcel vanDeuren8Koen vanAerde9Michiel van derFlier10Department of Laboratory Medicine Laboratory of Medical Immunology Radboud Institute for Molecular Life Sciences Radboudumc Nijmegen The NetherlandsDepartment of Laboratory Medicine Laboratory of Medical Immunology Radboud Institute for Molecular Life Sciences Radboudumc Nijmegen The NetherlandsDepartment of Laboratory Medicine Laboratory of Medical Immunology Radboud Institute for Molecular Life Sciences Radboudumc Nijmegen The NetherlandsPediatric Infectious Diseases and Immunology Amalia Children's Hospital Nijmegen The NetherlandsDepartment of Laboratory Medicine Laboratory of Medical Immunology Radboud Institute for Molecular Life Sciences Radboudumc Nijmegen The NetherlandsDepartment of Laboratory Medicine Laboratory of Medical Immunology Radboud Institute for Molecular Life Sciences Radboudumc Nijmegen The NetherlandsDepartment of Human Genetics Radboudumc Nijmegen The NetherlandsDepartment of Human Genetics Radboudumc Nijmegen The NetherlandsExpertise Center for Immunodeficiency and Autoinflammation (REIA) Radboudumc Nijmegen The NetherlandsPediatric Infectious Diseases and Immunology Amalia Children's Hospital Nijmegen The NetherlandsPediatric Infectious Diseases and Immunology Amalia Children's Hospital Nijmegen The NetherlandsAbstract Objectives Complete deficiency of alternative pathway (AP) complement factors, explained by homozygous mutations, is a well‐known risk factor for invasive bacterial infections; however, this is less obvious for heterozygous mutations. We describe two siblings with a heterozygous NM_001928.3(CFD):c.125C>A p.(Ser42*) mutation in the complement factor D (fD) gene having a history of recurrent bacterial infections. We determined the effect of heterozygous fD deficiency on AP complement activity. Methods We determined the effect of fD levels on complement activation as measured by AP activity, complement C3 binding to the bacterial surface of Neisseria meningitidis (Nm), Streptococcus pneumoniae (Sp) and non‐typeable Haemophilus influenzae (NTHi), and complement‐mediated killing of Nm and NTHi. In addition, we measured the effect of vaccination of complement C3 binding to the bacterial surface and killing of Nm. Results Reconstitution of fD‐deficient serum with fD increased AP activity in a dose‐ and time‐dependent way. Reconstitution of patient serum with fD to normal levels increased complement C3 binding to Sp, Nm and NTHi, as well as complement‐mediated killing of Nm and NTHi. Vaccination increased complement C3 binding and resulted in complete killing of Nm without fD reconstitution. Conclusion We conclude that low fD serum levels (< 0.5 μg mL−1) lead to a reduced speed of complement activation, which results in diminished bacterial killing, consistent with recurrent bacterial infections observed in our index patients. Specific antibodies induced by vaccination are able to overcome the diminished bacterial killing capacity in patients with low fD levels.https://doi.org/10.1002/cti2.1256complementfactor Dhaplodeficiencyimmunodeficiencyinfectionvaccination |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jeroen D Langereis Renate G van derMolen Corrie deKat Angelino Stefanie S Henriet Marien I deJonge Irma Joosten Annet Simons Janneke HM Schuurs‐Hoeijmakers Marcel vanDeuren Koen vanAerde Michiel van derFlier |
spellingShingle |
Jeroen D Langereis Renate G van derMolen Corrie deKat Angelino Stefanie S Henriet Marien I deJonge Irma Joosten Annet Simons Janneke HM Schuurs‐Hoeijmakers Marcel vanDeuren Koen vanAerde Michiel van derFlier Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing Clinical & Translational Immunology complement factor D haplodeficiency immunodeficiency infection vaccination |
author_facet |
Jeroen D Langereis Renate G van derMolen Corrie deKat Angelino Stefanie S Henriet Marien I deJonge Irma Joosten Annet Simons Janneke HM Schuurs‐Hoeijmakers Marcel vanDeuren Koen vanAerde Michiel van derFlier |
author_sort |
Jeroen D Langereis |
title |
Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing |
title_short |
Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing |
title_full |
Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing |
title_fullStr |
Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing |
title_full_unstemmed |
Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing |
title_sort |
complement factor d haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing |
publisher |
Wiley |
series |
Clinical & Translational Immunology |
issn |
2050-0068 |
publishDate |
2021-01-01 |
description |
Abstract Objectives Complete deficiency of alternative pathway (AP) complement factors, explained by homozygous mutations, is a well‐known risk factor for invasive bacterial infections; however, this is less obvious for heterozygous mutations. We describe two siblings with a heterozygous NM_001928.3(CFD):c.125C>A p.(Ser42*) mutation in the complement factor D (fD) gene having a history of recurrent bacterial infections. We determined the effect of heterozygous fD deficiency on AP complement activity. Methods We determined the effect of fD levels on complement activation as measured by AP activity, complement C3 binding to the bacterial surface of Neisseria meningitidis (Nm), Streptococcus pneumoniae (Sp) and non‐typeable Haemophilus influenzae (NTHi), and complement‐mediated killing of Nm and NTHi. In addition, we measured the effect of vaccination of complement C3 binding to the bacterial surface and killing of Nm. Results Reconstitution of fD‐deficient serum with fD increased AP activity in a dose‐ and time‐dependent way. Reconstitution of patient serum with fD to normal levels increased complement C3 binding to Sp, Nm and NTHi, as well as complement‐mediated killing of Nm and NTHi. Vaccination increased complement C3 binding and resulted in complete killing of Nm without fD reconstitution. Conclusion We conclude that low fD serum levels (< 0.5 μg mL−1) lead to a reduced speed of complement activation, which results in diminished bacterial killing, consistent with recurrent bacterial infections observed in our index patients. Specific antibodies induced by vaccination are able to overcome the diminished bacterial killing capacity in patients with low fD levels. |
topic |
complement factor D haplodeficiency immunodeficiency infection vaccination |
url |
https://doi.org/10.1002/cti2.1256 |
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