Literature DB >> 28035470

The clinical and laboratory features of Chinese Han anti-factor H autoantibody-associated hemolytic uremic syndrome.

Di Song1,2,3, Xiao-Rong Liu4, Zhi Chen5, Hui-Jie Xiao6, Jie Ding6, Shu-Zhen Sun7, Hong-Yan Liu8, Wei-Yi Guo1,2,3, Su-Xia Wang1,2,3, Feng Yu9,10,11,12, Ming-Hui Zhao1,2,3,13.   

Abstract

BACKGROUND: Anti-complement factor H (CFH) autoantibody-associated hemolytic uremic syndrome (HUS) is a severe sub-type of HUS.
METHODS: We assessed the clinical and renal pathological features, circulating complement levels, and genetic background of Chinese pediatric patients with this sub-type of HUS. Thirty-three consecutive patients with acute kidney injury who tested positive for serum anti-CFH autoantibodies were enrolled in this study.
RESULTS: All of the eight patients who underwent renal biopsies presented with changes typical of thrombotic microangiopathy, especially changes in chronic characteristics. Compared to patients in remission and normal control subjects, patients with acute disease had significantly lower plasma CFH levels and significantly higher plasma complement 3a (C3a), C5a, and terminal complement complex (SC5b-9) levels. The CFH-anti-CFH immunoglobin G (IgG) circulating immunocomplex (CFH-CIC) titers were more closely correlated with CFH plasma levels than anti-CFH IgG levels. Of the 22 patients, four (18%) were homozygous for CFHR3-1Δ and ten were heterozygous for CFHR1 or CFHR3 deletions. Most patients responded well to a combination of plasma and immunosuppressive therapies, with a remission rate of 87%. At the end of the follow-up, nine patients reached the combined end-points, including two with end-stage renal disease and seven with relapses.
CONCLUSION: Plasma C3a, C5a, and SC5b-9 levels predicted disease activity in anti-CFH autoantibody-associated HUS patients enrolled in this study. These patients responded well to plasma therapy combined with immunosuppression.

Entities:  

Keywords:  Autoantibody; Complement factor H; Hemolytic uremic syndrome; Immunosuppression; Plasma therapy; Thrombotic microangiopathies

Mesh:

Substances:

Year:  2016        PMID: 28035470     DOI: 10.1007/s00467-016-3562-7

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  35 in total

1.  Guidelines on the diagnosis and management of the thrombotic microangiopathic haemolytic anaemias.

Authors:  Sarah L Allford; Beverley J Hunt; Peter Rose; Samuel J Machin
Journal:  Br J Haematol       Date:  2003-02       Impact factor: 6.998

2.  Syndromes of thrombotic microangiopathy.

Authors:  James N George; Carla M Nester
Journal:  N Engl J Med       Date:  2014-11-06       Impact factor: 91.245

3.  Eculizumab reduces complement activation, inflammation, endothelial damage, thrombosis, and renal injury markers in aHUS.

Authors:  Roxanne Cofiell; Anjli Kukreja; Krystin Bedard; Yan Yan; Angela P Mickle; Masayo Ogawa; Camille L Bedrosian; Susan J Faas
Journal:  Blood       Date:  2015-04-01       Impact factor: 22.113

4.  Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.

Authors:  Marina Noris; Jessica Caprioli; Elena Bresin; Chiara Mossali; Gaia Pianetti; Sara Gamba; Erica Daina; Chiara Fenili; Federica Castelletti; Annalisa Sorosina; Rossella Piras; Roberta Donadelli; Ramona Maranta; Irene van der Meer; Edward M Conway; Peter F Zipfel; Timothy H Goodship; Giuseppe Remuzzi
Journal:  Clin J Am Soc Nephrol       Date:  2010-07-01       Impact factor: 8.237

5.  Functional analyses indicate a pathogenic role of factor H autoantibodies in atypical haemolytic uraemic syndrome.

Authors:  Stefanie Strobel; Peter F Hoyer; Christoph J Mache; Endre Sulyok; Wei-Shih Liu; Heiko Richter; Martin Oppermann; Peter F Zipfel; Mihály Józsi
Journal:  Nephrol Dial Transplant       Date:  2009-08-07       Impact factor: 5.992

6.  Complement factor I deficiency associated with recurrent meningitis coinciding with menstruation.

Authors:  C González-Rubio; A Ferreira-Cerdán; I M Ponce; J Arpa; G Fontán; M López-Trascasa
Journal:  Arch Neurol       Date:  2001-11

7.  Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome.

Authors:  Cynthia Abarrategui-Garrido; Rubén Martínez-Barricarte; Margarita López-Trascasa; Santiago Rodríguez de Córdoba; Pilar Sánchez-Corral
Journal:  Blood       Date:  2009-09-10       Impact factor: 22.113

8.  Serum complement factor H is associated with clinical and pathological activities of patients with lupus nephritis.

Authors:  Feng-mei Wang; Feng Yu; Ying Tan; Di Song; Ming-hui Zhao
Journal:  Rheumatology (Oxford)       Date:  2012-09-06       Impact factor: 7.580

9.  Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics.

Authors:  Lianne M Geerdink; Dineke Westra; Joanna A E van Wijk; Eiske M Dorresteijn; Marc R Lilien; Jean-Claude Davin; Martin Kömhoff; Koen Van Hoeck; Amerins van der Vlugt; Lambertus P van den Heuvel; Nicole C A J van de Kar
Journal:  Pediatr Nephrol       Date:  2012-03-13       Impact factor: 3.714

10.  Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.

Authors:  Peter F Zipfel; Matthew Edey; Stefan Heinen; Mihály Józsi; Heiko Richter; Joachim Misselwitz; Bernd Hoppe; Danny Routledge; Lisa Strain; Anne E Hughes; Judith A Goodship; Christoph Licht; Timothy H J Goodship; Christine Skerka
Journal:  PLoS Genet       Date:  2007-02-01       Impact factor: 5.917

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  8 in total

1.  Immunological features and functional analysis of anti-CFH autoantibodies in patients with atypical hemolytic uremic syndrome.

Authors:  Wei-Yi Guo; Di Song; Xiao-Rong Liu; Zhi Chen; Hui-Jie Xiao; Jie Ding; Shu-Zhen Sun; Hong-Yan Liu; Su-Xia Wang; Feng Yu; Ming-Hui Zhao
Journal:  Pediatr Nephrol       Date:  2018-10-12       Impact factor: 3.714

2.  IgM Autoantibodies to Complement Factor H in Atypical Hemolytic Uremic Syndrome.

Authors:  Massimo Cugno; Silvia Berra; Federica Depetri; Silvana Tedeschi; Samantha Griffini; Elena Grovetti; Sonia Caccia; Donata Cresseri; Piergiorgio Messa; Sara Testa; Fabio Giglio; Flora Peyvandi; Gianluigi Ardissino
Journal:  J Am Soc Nephrol       Date:  2021-03-12       Impact factor: 10.121

3.  Clinical and Immunological Profile of Anti-factor H Antibody Associated Atypical Hemolytic Uremic Syndrome: A Nationwide Database.

Authors:  Mamta Puraswani; Priyanka Khandelwal; Himanshi Saini; Savita Saini; Bahadur Singh Gurjar; Aditi Sinha; Rajashri Pramod Shende; Tushar Kanti Maiti; Abhishek Kumar Singh; Uma Kanga; Uma Ali; Indira Agarwal; Kanav Anand; Narayan Prasad; Padmaraj Rajendran; Rajiv Sinha; Anil Vasudevan; Anita Saxena; Sanjay Agarwal; Pankaj Hari; Arvind Sahu; Satyajit Rath; Arvind Bagga
Journal:  Front Immunol       Date:  2019-06-07       Impact factor: 7.561

4.  Anti-Factor H Antibodies in Egyptian Children with Hemolytic Uremic Syndrome.

Authors:  Shereen Shawky; Hesham Safouh; Mona Gamal; Mohammed M Abbas; Azza Aboul-Enein; Toshihiro Sawai; Yosra Fahmy; Heba Selim
Journal:  Int J Nephrol       Date:  2021-11-18

5.  Anti-factor H antibody and its role in atypical hemolytic uremic syndrome.

Authors:  Rupesh Raina; Guneive Mangat; Gordon Hong; Raghav Shah; Nikhil Nair; Brian Abboud; Sumedha Bagga; Sidharth Kumar Sethi
Journal:  Front Immunol       Date:  2022-08-23       Impact factor: 8.786

6.  Clinical features of children with anti-CFH autoantibody-associated hemolytic uremic syndrome: a report of 8 cases.

Authors:  Qian Li; Xinxin Kong; Minle Tian; Jing Wang; Zhenle Yang; Lichun Yu; Suwen Liu; Cong Wang; Xiaoyuan Wang; Shuzhen Sun
Journal:  Ren Fail       Date:  2022-12       Impact factor: 3.222

7.  Patient-specific iPSC-derived endothelial cells reveal aberrant p38 MAPK signaling in atypical hemolytic uremic syndrome.

Authors:  Danni Zhou; Ying Tan; Xiaoling Liu; Ling Tang; Hao Wang; Jiaxi Shen; Wei Wang; Lenan Zhuang; Juan Tao; Jun Su; Tingyu Gong; Xiaorong Liu; Ping Liang; Feng Yu; Minghui Zhao
Journal:  Stem Cell Reports       Date:  2021-08-12       Impact factor: 7.765

8.  Early relapse rate determines further relapse risk: results of a 5-year follow-up study on pediatric CFH-Ab HUS.

Authors:  Johannes Hofer; Magdalena Riedl Khursigara; Markus Perl; Thomas Giner; Alejandra Rosales; Gerard Cortina; Siegfied Waldegger; Therese Jungraithmayr; Reinhard Würzner
Journal:  Pediatr Nephrol       Date:  2020-10-07       Impact factor: 3.714

  8 in total

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