Literature DB >> 22169380

Drugs that inhibit complement.

Hubert Schrezenmeier1, Britta Höchsmann.   

Abstract

The complement system is an important part of the innate immune system. Complement plays a crucial role in the pathophysiology of many disorders. Despite the pivotal role of the complement system, an approved targeted inhibitor of a complement factor became available only recently. Eculizumab is a humanized monoclonal antibody that inhibits complement factor C5. It is a targeted, disease modifying, treatment of paroxysmal nocturnal hemoglobinuria (PNH). It was approved be the US FDA and the European Commission in 2007. In this review we will update the experience with eculizumab in PNH and discuss potential use of eculizumab in other disorders (e.g. cold agglutinin disease; atypical HUS) and new approaches to complement inhibition with drugs other than eculizumab. Copyright Â
© 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22169380     DOI: 10.1016/j.transci.2011.11.012

Source DB:  PubMed          Journal:  Transfus Apher Sci        ISSN: 1473-0502            Impact factor:   1.764


  8 in total

1.  Acute necrotizing herpetic tonsillitis: a report of two cases.

Authors:  Walaa M Borhan; Mohammed A Dababo; Lester D R Thompson; M Saleem; N Pashley
Journal:  Head Neck Pathol       Date:  2013-12-14

2.  Eculizumab treatment in severe pediatric STEC-HUS: a multicenter retrospective study.

Authors:  Lucas Percheron; Raluca Gramada; Stéphanie Tellier; Remi Salomon; Jérôme Harambat; Brigitte Llanas; Marc Fila; Emma Allain-Launay; Anne-Laure Lapeyraque; Valerie Leroy; Anne-Laure Adra; Etienne Bérard; Guylhène Bourdat-Michel; Hassid Chehade; Philippe Eckart; Elodie Merieau; Christine Piètrement; Anne-Laure Sellier-Leclerc; Véronique Frémeaux-Bacchi; Chloe Dimeglio; Arnaud Garnier
Journal:  Pediatr Nephrol       Date:  2018-03-23       Impact factor: 3.714

3.  Development of a disease-specific quality of life questionnaire for patients with aplastic anemia and/or paroxysmal nocturnal hemoglobinuria (QLQ-AA/PNH)-report on phases I and II.

Authors:  Martha Groth; Susanne Singer; Cathrin Niedeggen; Andrea Petermann-Meyer; Alexander Röth; Hubert Schrezenmeier; Britta Höchsmann; Tim H Brümmendorf; Jens Panse
Journal:  Ann Hematol       Date:  2016-11-11       Impact factor: 3.673

4.  Gemcitabine-induced haemolytic uremic syndrome, although infrequent, can it be prevented: A case report and review of literature.

Authors:  Esther U Cidon; Pilar A Martinez; Tamas Hickish
Journal:  World J Clin Cases       Date:  2018-10-26       Impact factor: 1.337

5.  Gemcitabine induced hemolytic uremic syndrome.

Authors:  Seyed-Ali Sadjadi; Pavan Annamaraju
Journal:  Am J Case Rep       Date:  2012-05-25

Review 6.  Complement diagnostics: concepts, indications, and practical guidelines.

Authors:  Bo Nilsson; Kristina Nilsson Ekdahl
Journal:  Clin Dev Immunol       Date:  2012-11-14

7.  Rational engineering of a minimized immune inhibitor with unique triple-targeting properties.

Authors:  Christoph Q Schmidt; Hongjun Bai; Zhuoer Lin; Antonio M Risitano; Paul N Barlow; Daniel Ricklin; John D Lambris
Journal:  J Immunol       Date:  2013-04-24       Impact factor: 5.426

8.  Eculizumab as a bridge to immunosuppressive therapy in severe cold agglutinin disease of anti-Pr specificity.

Authors:  Roman Shapiro; Ian Chin-Yee; Selay Lam
Journal:  Clin Case Rep       Date:  2015-09-29
  8 in total

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