Shiga toxin (Stx) classification, structure, and function

AR Melton-Celsa - Microbiology spectrum, 2014 - Am Soc Microbiol
Shiga toxin (Stx) is one of the most potent bacterial toxins known. Stx is found in Shigella
dysenteriae 1 and in some serogroups of Escherichia coli (called Stx1 in E. coli). In addition …

Immunosuppressive medications

AC Wiseman - Clinical Journal of the American Society of …, 2016 - journals.lww.com
Immunosuppressive agents are commonly used in the nephrologist's practice in the
treatment of autoimmune and immune-mediated diseases and transplantation, and they are …

Atypical hemolytic‐uremic syndrome: an update on pathophysiology, diagnosis, and treatment

R Raina, V Krishnappa, T Blaha, T Kann… - Therapeutic …, 2019 - Wiley Online Library
Atypical hemolytic uremic syndrome (aHUS), a rare variant of thrombotic microangiopathy, is
characterized by microangiopathic hemolytic anemia, thrombocytopenia, and renal …

Statistical validation of rare complement variants provides insights into the molecular basis of atypical hemolytic uremic syndrome and C3 glomerulopathy

AJ Osborne, M Breno, NG Borsa, F Bu… - The Journal of …, 2018 - journals.aai.org
Atypical hemolytic uremic syndrome (aHUS) and C3 glomerulopathy (C3G) are associated
with dysregulation and overactivation of the complement alternative pathway. Typically …

Endothelial cells: source, barrier, and target of defensive mediators

LT Roumenina, J Rayes, M Frimat… - Immunological …, 2016 - Wiley Online Library
Endothelium is strategically located at the interface between blood and interstitial tissues,
placing thus endothelial cell as a key player in vascular homeostasis. Endothelial cells are …

Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome

DM Connaughton, P Bhai, P Isenring, M Mahdi… - Journal of Molecular …, 2023 - Springer
Atypical hemolytic uremic syndrome (aHUS) is characterized by microangiopathic hemolytic
anemia, thrombocytopenia, and renal impairment. Complement and coagulation gene …

[HTML][HTML] Risk of atypical HUS among family members of patients carrying complement regulatory gene abnormality

G Ardissino, S Longhi, L Porcaro, G Pintarelli… - Kidney International …, 2021 - Elsevier
Introduction Atypical hemolytic uremic syndrome (aHUS) is mainly due to complement
regulatory gene abnormalities with a dominant pattern but incomplete penetrance. Thus …

Defining the genetics of thrombotic microangiopathies

P Vieira-Martins, C El Sissy, P Bordereau… - … and Apheresis Science, 2016 - Elsevier
The spectrum of the thrombotic microangiopathies (TMA) encompasses a heterogeneous
group of disorders with hereditary and acquired forms. Endothelial cell injury in the …

Adults with septic shock and extreme hyperferritinemia exhibit pathogenic immune variation

KF Kernan, L Ghaloul-Gonzalez, B Shakoory… - Genes & …, 2019 - nature.com
Post-hoc subgroup analysis of the negative trial of interleukin-1β receptor antagonist
(IL1RA) for septic shock suggested that patients with features of macrophage activation …

Diagnostic approach to microangiopathic hemolytic disorders

K Kottke‐Marchant - International journal of laboratory …, 2017 - Wiley Online Library
Thrombotic micro‐angiopathies (TMA) are a group of related disorders that are
characterized by thrombosis of the microvasculature and associated organ dysfunction, and …