Complement component C3–The “Swiss Army Knife” of innate immunity and host defense

D Ricklin, ES Reis, DC Mastellos, P Gros… - Immunological …, 2016 - Wiley Online Library
As a preformed defense system, complement faces a delicate challenge in providing an
immediate, forceful response to pathogens even at first encounter, while sparing host cells in …

[HTML][HTML] The complement system in age-related macular degeneration: A review of rare genetic variants and implications for personalized treatment

MJ Geerlings, EK de Jong, AI den Hollander - Molecular immunology, 2017 - Elsevier
Age-related macular degeneration (AMD) is a progressive retinal disease and the major
cause of irreversible vision loss in the elderly. Numerous studies have found both common …

[HTML][HTML] Complement in secondary thrombotic microangiopathy

LMP Palma, M Sridharan, S Sethi - Kidney international reports, 2021 - Elsevier
Thrombotic microangiopathy (TMA) is a condition characterized by thrombocytopenia and
microangiopathic hemolytic anemia (MAHA) with varying degrees of organ damage in the …

Complement, infection, and autoimmunity

P Conigliaro, P Triggianese, E Ballanti… - Current Opinion in …, 2019 - journals.lww.com
The relationship between the complement system and autoimmunity appears paradoxical as
both the deficiency and the activation contribute to inducing autoimmune diseases. In these …

[HTML][HTML] Implications of genetic variation in the complement system in age-related macular degeneration

S de Jong, G Gagliardi, A Garanto, A de Breuk… - Progress in Retinal and …, 2021 - Elsevier
Age-related macular degeneration (AMD) is the main cause of vision loss among the elderly
in the Western world. While AMD is a multifactorial disease, the complement system was …

[HTML][HTML] Regulation of regulators: Role of the complement factor H-related proteins

M Cserhalmi, A Papp, B Brandus, B Uzonyi… - Seminars in …, 2019 - Elsevier
The complement system, while being an essential and very efficient effector component of
innate immunity, may cause damage to the host and result in various inflammatory …

Functional characterization of 105 factor H variants associated with aHUS: lessons for variant classification

H Martín Merinero, Y Zhang, E Arjona… - Blood, The Journal …, 2021 - ashpublications.org
Atypical hemolytic uremic syndrome (aHUS) is a life-threatening thrombotic microangiopathy
that can progress, when untreated, to end-stage renal disease. Most frequently, aHUS is …

Complement and coagulation: cross talk through time

S Dzik - Transfusion Medicine Reviews, 2019 - Elsevier
Two complex protein defense systems—complement and coagulation—are based on
amplifying enzyme cascades triggered by specific local stimuli. Excess systemic activation of …

Pretransplant genetic susceptibility: clinical relevance in transplant-associated thrombotic microangiopathy

E Gavriilaki, T Touloumenidou… - Thrombosis and …, 2020 - thieme-connect.com
Transplant-associated thrombotic microangiopathy (TA-TMA) is a life-threatening
complication of allogeneic hematopoietic cell transplantation (HCT). We hypothesized that …

Effect of rare coding variants in the CFI gene on Factor I expression levels

S de Jong, EB Volokhina, A de Breuk… - Human Molecular …, 2020 - academic.oup.com
Factor I (FI) is one of the main inhibitors of complement activity, and numerous rare coding
variants have been reported in patients with age-related macular degeneration, atypical …