Literature DB >> 21515369

Macrophages and T lymphocytes are the predominant cells in intimal arteritis of resected renal allografts undergoing acute rejection.

Hua-jun Sun1, Tong Zhou, Yong Wang, Yao-wen Fu, Yun-peng Jiang, Li-hong Zhang, Cheng-bin Zhang, Hong-lan Zhou, Bao-shan Gao, Ying-ai Shi, Shan Wu.   

Abstract

BACKGROUND: In acute renal allograft rejection, T-cell-mediated processes have been generally regarded as dominant. Although there is recent evidence that macrophages play important roles in acute vascular rejection, less is known about the exact proportion of immunocytes in the intimal arteritis of renal allografts with unfavorable outcomes.
METHODS: By immunohistochemical staining using nine primary antibodies, we classified the proportions of infiltrating immunocytes in intimal arteritis and glomerulitis in five allografts resected because of acute irreversible graft failure.
RESULTS: All five allografts had features of antibody-mediated rejection based on criteria established by the Banff classification. In intimal arteritis, CD3+ T-lymphocytes accounted for 30.6±13.3% of the immunocytes and macrophages for 40.4±9.2%. 45.4% of the T-cells were CD8+ cytotoxic T-cells. Neutrophils were also present but accounted for a relatively low proportion of the cells (8.8±8.6%). B-cells and plasma cells all accounted for <5% of the immunocytes. NK cells were readily detected (4.2±4.2%). When we compared types of arteritis, the CD15+ neutrophils accounted for as many as 27.8±15.1% of immunocytes in V3 vasculitis and only 1.0±1.4% in V2 vasculitis. CD3+ T-lymphocytes accounted for 25.8±7.3% of immunocytes in V3 vasculitis and 41.5±7.9% in V2 vasculitis. In glomerulitis, the immunocytes were mainly macrophages (53.1±9.1%) and neutrophils (34.6±9.9%).
CONCLUSION: Macrophages and T-lymphocytes accounted for the highest percentage of immunocytes in the intimal arteritis of irreversible renal failure associated with antibody-mediated rejection. 45.4% of the T-cells were CD8+ cytotoxic T-cells. Neutrophils and NK cells were also present in these lesions. The proportion of neutrophils in V3 vasculitis was much higher than in V2 vasculitis. These observations suggest that besides macrophages and T-lymphocytes, neutrophils may also play a role in the more severe arterial lesion. To our knowledge this is the first report of this observation. Macrophages and neutrophils were the main inflammatory cells in the glomerulitis of acute rejection.
Copyright © 2011 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21515369     DOI: 10.1016/j.trim.2011.04.002

Source DB:  PubMed          Journal:  Transpl Immunol        ISSN: 0966-3274            Impact factor:   1.708


  7 in total

Review 1.  Effector mechanisms of rejection.

Authors:  Aurélie Moreau; Emilie Varey; Ignacio Anegon; Maria-Cristina Cuturi
Journal:  Cold Spring Harb Perspect Med       Date:  2013-11-01       Impact factor: 6.915

2.  Blockade of p-selectin is sufficient to reduce MHC I antibody-elicited monocyte recruitment in vitro and in vivo.

Authors:  N M Valenzuela; L Hong; X-Da Shen; F Gao; S H Young; E Rozengurt; J W Kupiec-Weglinski; M C Fishbein; E F Reed
Journal:  Am J Transplant       Date:  2012-12-27       Impact factor: 8.086

3.  Morphologic Features and Clinical Impact of Arteritis Concurrent with Transplant Glomerulopathy.

Authors:  Deján Dobi; Zsolt Bodó; Éva Kemény; Krisztina Boda; Pál Szenohradszky; Edit Szederkényi; Zoltan G Laszik; Béla Iványi
Journal:  Pathol Oncol Res       Date:  2015-07-23       Impact factor: 3.201

4.  The Clinical and Pathologic Phenotype of Antibody-Mediated Vascular Rejection Diagnosed Using Arterial C4d Immunoperoxidase.

Authors:  Brian J Nankivell; Meena Shingde; Chow H P'Ng; Ankit Sharma
Journal:  Kidney Int Rep       Date:  2022-05-05

5.  A reproducible mouse model of chronic allograft nephropathy with vasculopathy.

Authors:  Abolfazl Zarjou; Lingling Guo; Paul W Sanders; Roslyn B Mannon; Anupam Agarwal; James F George
Journal:  Kidney Int       Date:  2012-08-08       Impact factor: 10.612

Review 6.  M2 Macrophages Serve as Critical Executor of Innate Immunity in Chronic Allograft Rejection.

Authors:  Hanwen Zhang; Zhuonan Li; Wei Li
Journal:  Front Immunol       Date:  2021-03-17       Impact factor: 7.561

7.  Single cell transcriptomics of mouse kidney transplants reveals a myeloid cell pathway for transplant rejection.

Authors:  Anil Dangi; Naveen R Natesh; Irma Husain; Zhicheng Ji; Laura Barisoni; Jean Kwun; Xiling Shen; Edward B Thorp; Xunrong Luo
Journal:  JCI Insight       Date:  2020-10-15
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.