Literature DB >> 19273164

The role of chemokines in acute renal allograft rejection and chronic allograft injury.

Michael Fischereder1, Bernd Schroppel.   

Abstract

Short and long term outcome of renal transplantation are determined by acute and chronic rejection processes. In acute transplant rejection, expression of chemokines occurs in different renal compartments where it is triggered through various stimuli e.g. brain death, ischemia, reperfusion, and HLA-mismatch. The induction of chemokine expression precedes the process of organ recovery and extends well into the late course of clinical allograft injury. Chemokines function mainly as chemoattractants for leukocytes, monocytes, neutrophils, and other effector cells from the blood to sites of infection or damage. Chemokines are also important in angiogenesis and fibrosis and can have anti-inflammatory functions. The study of chemokine biology in transplantation has broadened the understanding of acute and chronic transplant dysfunction. Data suggest that relatively few chemokine receptors play central roles in these developments, and chemokine blockade, either non-selective or specific, has shown promising results in experimental transplantation and is currently being investigated in human trials.

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Year:  2009        PMID: 19273164     DOI: 10.2741/3342

Source DB:  PubMed          Journal:  Front Biosci (Landmark Ed)        ISSN: 2768-6698


  8 in total

Review 1.  Role of chemokines, innate and adaptive immunity.

Authors:  Kurt A Zimmerman; Katharina Hopp; Michal Mrug
Journal:  Cell Signal       Date:  2020-04-20       Impact factor: 4.315

2.  Chemokines and their receptors in human renal allotransplantation.

Authors:  Denise J Lo; Tim A Weaver; David E Kleiner; Roslyn B Mannon; Lynn M Jacobson; Bryan N Becker; S John Swanson; Douglas A Hale; Allan D Kirk
Journal:  Transplantation       Date:  2011-01-15       Impact factor: 4.939

Review 3.  Immunologic monitoring in transplantation revisited.

Authors:  Paolo Cravedi; Peter S Heeger
Journal:  Curr Opin Organ Transplant       Date:  2012-02       Impact factor: 2.640

4.  CXCL10 and CXCL13 Expression were highly up-regulated in peripheral blood mononuclear cells in acute rejection and poor response to anti-rejection therapy.

Authors:  Youying Mao; Minmin Wang; Qin Zhou; Juan Jin; Yucheng Wang; Wenhan Peng; Jianyong Wu; Zhangfei Shou; Jianghua Chen
Journal:  J Clin Immunol       Date:  2010-12-30       Impact factor: 8.317

5.  Urinary CXCL9 and CXCL10 Levels and Acute Renal Graft Rejection.

Authors:  H S Ciftci; T Tefik; M K Savran; E Demir; Y Caliskan; Y D Ogret; T Oktar; O Sanlı; T Kocak; Y Ozluk; F S Oguz; I Kilicaslan; F Aydın; A Turkmen; I Nane
Journal:  Int J Organ Transplant Med       Date:  2019-05-01

6.  Lymphotoxin expression in human and murine renal allografts.

Authors:  Harald Seeger; Maja T Lindenmeyer; Clemens D Cohen; Carsten Jaeckel; Peter J Nelson; Jin Chen; Ilka Edenhofer; Nicolas Kozakowski; Heinz Regele; Georg Boehmig; Simone Brandt; Rudolf P Wuethrich; Mathias Heikenwalder; Thomas Fehr; Stephan Segerer
Journal:  PLoS One       Date:  2018-01-04       Impact factor: 3.240

7.  LPS-induced genes in intestinal tissue of the sea cucumber Holothuria glaberrima.

Authors:  Francisco Ramírez-Gómez; Pablo A Ortiz-Pineda; Gabriela Rivera-Cardona; José E García-Arrarás
Journal:  PLoS One       Date:  2009-07-08       Impact factor: 3.240

8.  Non-invasive imaging of allogeneic transplanted skin graft by 131I-anti-TLR5 mAb.

Authors:  Hukui Sun; Guangjie Yang; Ting Liang; Chao Zhang; Jing Song; Jiankui Han; Guihua Hou
Journal:  J Cell Mol Med       Date:  2014-10-06       Impact factor: 5.310

  8 in total

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