[HTML][HTML] Cytokine storm—definition, causes, and implications

D Jarczak, A Nierhaus - International journal of molecular sciences, 2022 - mdpi.com
The human innate and adaptive immune systems consist of effector cells producing
cytokines (interleukins, interferons, chemokines, and numerous other mediators). Usually, a …

Therapeutic targeting of the complement system: from rare diseases to pandemics

P Garred, AJ Tenner, TE Mollnes - Pharmacological reviews, 2021 - ASPET
The complement system was discovered at the end of the 19th century as a heat-labile
plasma component that “complemented” the antibodies in killing microbes, hence the name …

[HTML][HTML] Meningococcal vaccination: recommendations of the advisory committee on immunization practices, United States, 2020

SA Mbaeyi - MMWR. Recommendations and Reports, 2020 - cdc.gov
This report compiles and summarizes all recommendations from CDC's Advisory Committee
on Immunization Practices (ACIP) for use of meningococcal vaccines in the United States …

Infectious complications of biological and small molecule targeted immunomodulatory therapies

JS Davis, D Ferreira, E Paige, C Gedye… - Clinical microbiology …, 2020 - Am Soc Microbiol
The past 2 decades have seen a revolution in our approach to therapeutic
immunosuppression. We have moved from relying on broadly active traditional medications …

[HTML][HTML] Immunotherapy in sepsis-brake or accelerate?

F Steinhagen, SV Schmidt, JC Schewe… - Pharmacology & …, 2020 - Elsevier
Sepsis, a life threating syndrome characterized by organ failure after infection, is the most
common cause of death in hospitalized patients. The treatment of sepsis is generally …

How I diagnose and treat atypical hemolytic uremic syndrome

F Fakhouri, N Schwotzer… - Blood, The Journal of …, 2023 - ashpublications.org
Our understanding and management of atypical hemolytic uremic syndrome (aHUS) have
dramatically improved in the last decade. aHUS has been established as a prototypic …

Complement deficiencies and dysregulation: Pathophysiological consequences, modern analysis, and clinical management

J Schröder-Braunstein, M Kirschfink - Molecular immunology, 2019 - Elsevier
Complement defects are associated with an enhanced risk of a broad spectrum of infectious
as well as systemic or local inflammatory and thrombotic disorders. Inherited complement …

Management of infection in PNH patients treated with eculizumab or other complement inhibitors: Unmet clinical needs

C Girmenia, W Barcellini, P Bianchi, E Di Bona, AP Iori… - Blood Reviews, 2023 - Elsevier
This article presents the results of group discussion among an ad hoc constituted panel of
experts aimed at identifying and addressing unmet clinical needs (UCNs) in the …

[HTML][HTML] Non-capsulated Neisseria meningitidis sepsis in a paroxysmal nocturnal hemoglobinuria patient treated with ravulizumab: case report and review of the …

N Galli, L Pettine, M Panigada, L Daprai… - Frontiers in …, 2023 - frontiersin.org
Paroxysmal nocturnal haemoglobinuria (PNH) is a rare acquired haematopoietic stem cell
disease characterized by complement-mediated intravascular hemolysis, thrombosis, and …

[HTML][HTML] Characteristics of and meningococcal disease prevention strategies for commercially insured persons receiving eculizumab in the United States

CH Bozio, C Isenhour, LA McNamara - PLoS One, 2020 - journals.plos.org
Introduction Eculizumab is a licensed treatment for several rare, complement-mediated
diseases. Eculizumab use is associated with an approximately 2,000-fold increased …