Literature DB >> 27179705

Complement-here, there and everywhere, but what about the transplanted organ?

R M Montero1, S H Sacks2, R A Smith1.   

Abstract

The part of the innate immune system that communicates and effectively primes the adaptive immune system was termed "complement" by Ehrlich to reflect its complementarity to antibodies having previously been described as "alexine" (i.e protective component of serum) by Buchner and Bordet. It has been established that complement is not solely produced systemically but may have origin in different tissues where it can influence organ specific functions that may affect the outcome of transplanted organs. This review looks at the role of complement in particular to kidney transplantation. We look at current literature to determine whether blockade of the peripheral or central compartments of complement production may prevent ischaemic reperfusion injury or rejection in the transplanted organ. We also review new therapeutics that have been developed to inhibit components of the complement cascade with varying degrees of success leading to an increase in our understanding of the multiple triggers of this complex system. In addition, we consider whether biomarkers in this field are effective markers of disease or treatment.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Complement; Kidney transplantation; Mirococept; Therapeutics

Mesh:

Substances:

Year:  2016        PMID: 27179705     DOI: 10.1016/j.smim.2016.04.007

Source DB:  PubMed          Journal:  Semin Immunol        ISSN: 1044-5323            Impact factor:   11.130


  6 in total

1.  C3 glomerulonephritis secondary to mutations in factors H and I: rapid recurrence in deceased donor kidney transplant effectively treated with eculizumab.

Authors:  Neetika Garg; Yuzhou Zhang; Anne Nicholson-Weller; Eliyahu V Khankin; Nicolò Ghiringhelli Borsa; Nicole C Meyer; Susan McDermott; Isaac E Stillman; Helmut G Rennke; Richard J Smith; Martha Pavlakis
Journal:  Nephrol Dial Transplant       Date:  2018-12-01       Impact factor: 5.992

2.  Human Tamm-Horsfall protein, a renal specific protein, serves as a cofactor in complement 3b degradation.

Authors:  Diana C J Rhodes
Journal:  PLoS One       Date:  2017-07-24       Impact factor: 3.240

3.  Complement Activation During Ischemia/Reperfusion Injury Induces Pericyte-to-Myofibroblast Transdifferentiation Regulating Peritubular Capillary Lumen Reduction Through pERK Signaling.

Authors:  Giuseppe Castellano; Rossana Franzin; Alessandra Stasi; Chiara Divella; Fabio Sallustio; Paola Pontrelli; Giuseppe Lucarelli; Michele Battaglia; Francesco Staffieri; Antonio Crovace; Giovanni Stallone; Marc Seelen; Mohamed R Daha; Giuseppe Grandaliano; Loreto Gesualdo
Journal:  Front Immunol       Date:  2018-05-23       Impact factor: 7.561

4.  Effect of the Anti-C1s Humanized Antibody TNT009 and Its Parental Mouse Variant TNT003 on HLA Antibody-Induced Complement Activation-A Preclinical In Vitro Study.

Authors:  M Wahrmann; J Mühlbacher; L Marinova; H Regele; N Huttary; F Eskandary; G Cohen; G F Fischer; G C Parry; J C Gilbert; S Panicker; G A Böhmig
Journal:  Am J Transplant       Date:  2017-03-31       Impact factor: 8.086

Review 5.  Inflammaging and Complement System: A Link Between Acute Kidney Injury and Chronic Graft Damage.

Authors:  Rossana Franzin; Alessandra Stasi; Marco Fiorentino; Giovanni Stallone; Vincenzo Cantaluppi; Loreto Gesualdo; Giuseppe Castellano
Journal:  Front Immunol       Date:  2020-05-07       Impact factor: 7.561

Review 6.  Complement Components in the Diagnosis and Treatment after Kidney Transplantation-Is There a Missing Link?

Authors:  Małgorzata Kielar; Agnieszka Gala-Błądzińska; Paulina Dumnicka; Piotr Ceranowicz; Maria Kapusta; Beata Naumnik; Grzegorz Kubiak; Marek Kuźniewski; Beata Kuśnierz-Cabala
Journal:  Biomolecules       Date:  2021-05-21
  6 in total

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