Literature DB >> 28722107

The peritoneum: healing, immunity, and diseases.

Annalisa Capobianco1, Lucia Cottone1,2, Antonella Monno1, Angelo A Manfredi1,3, Patrizia Rovere-Querini1,3.   

Abstract

The peritoneum defines a confined microenvironment, which is stable under normal conditions, but is exposed to the damaging effect of infections, surgical injuries, and other neoplastic and non-neoplastic events. Its response to damage includes the recruitment, proliferation, and activation of a variety of haematopoietic and stromal cells. In physiological conditions, effective responses to injuries are organized; inflammatory triggers are eliminated; inflammation quickly abates; and the normal tissue architecture is restored. However, if inflammatory triggers are not cleared, fibrosis or scarring occurs and impaired tissue function ultimately leads to organ failure. Autoimmune serositis is characterized by the persistence of self-antigens and a relapsing clinical pattern. Peritoneal carcinomatosis and endometriosis are characterized by the persistence of cancer cells or ectopic endometrial cells in the peritoneal cavity. Some of the molecular signals orchestrating the recruitment of inflammatory cells in the peritoneum have been identified in the last few years. Alternative activation of peritoneal macrophages was shown to guide angiogenesis and fibrosis, and could represent a novel target for molecular intervention. This review summarizes current knowledge of the alterations to the immune response in the peritoneal environment, highlighting the ambiguous role played by persistently activated reparative macrophages in the pathogenesis of common human diseases.
Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Entities:  

Keywords:  angiogenesis; autoimmune serositis; endometriosis; fibrosis; macrophages; peritoneal adhesions; peritoneal carcinomatosis; sterile inflammation

Mesh:

Year:  2017        PMID: 28722107     DOI: 10.1002/path.4942

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  25 in total

1.  Role of [68Ga]Ga-DOTA-FAPI-04 PET/CT in the evaluation of peritoneal carcinomatosis and comparison with [18F]-FDG PET/CT.

Authors:  Liang Zhao; Yizhen Pang; Zuoming Luo; Kaili Fu; Tingting Yang; Long Zhao; Long Sun; Hua Wu; Qin Lin; Haojun Chen
Journal:  Eur J Nucl Med Mol Imaging       Date:  2021-01-07       Impact factor: 9.236

Review 2.  Macrophages in Chronic Liver Failure: Diversity, Plasticity and Therapeutic Targeting.

Authors:  Arjuna Singanayagam; Evangelos Triantafyllou
Journal:  Front Immunol       Date:  2021-04-02       Impact factor: 7.561

3.  Analyzing material changes consistent with degradation of explanted polymeric hernia mesh related to clinical characteristics.

Authors:  Xinyue Lu; Melinda Harman; B Todd Heniford; Vedra Augenstein; Brittney McIver; William Bridges
Journal:  Surg Endosc       Date:  2022-03-07       Impact factor: 3.453

4.  [68Ga]Ga-DOTA-FAPI-04 PET/CT in the evaluation of gastric cancer: comparison with [18F]FDG PET/CT.

Authors:  Rong Lin; Zefang Lin; Zhenying Chen; Shan Zheng; Jiaying Zhang; Jie Zang; Weibing Miao
Journal:  Eur J Nucl Med Mol Imaging       Date:  2022-04-25       Impact factor: 10.057

5.  FOLFIRINOX in patients with peritoneal carcinomatosis from pancreatic adenocarcinoma: a retrospective study.

Authors:  E Bonnet; C Mastier; A Lardy-Cléaud; P Rochefort; M Sarabi; P Guibert; A Cattey-Javouhey; F Desseigne; C de La Fouchardière
Journal:  Curr Oncol       Date:  2019-08-01       Impact factor: 3.677

6.  Exosomal miR-106a derived from gastric cancer promotes peritoneal metastasis via direct regulation of Smad7.

Authors:  Meng Zhu; Ning Zhang; Shuixiang He; Xinlan Lu
Journal:  Cell Cycle       Date:  2020-04-08       Impact factor: 4.534

7.  Type I IFN, Ly6C+ cells, and Phagocytes Support Suppression of Peritoneal Carcinomatosis Elicited by a TLR and CLR Agonist Combination.

Authors:  Allison M Dyevoich; Karen M Haas
Journal:  Mol Cancer Ther       Date:  2020-03-18       Impact factor: 6.261

8.  Activation of B-1 Cells Promotes Tumor Cell Killing in the Peritoneal Cavity.

Authors:  Marcela A Haro; Allison M Dyevoich; James P Phipps; Karen M Haas
Journal:  Cancer Res       Date:  2018-09-17       Impact factor: 12.701

Review 9.  The Neutrophil's Choice: Phagocytose vs Make Neutrophil Extracellular Traps.

Authors:  Angelo A Manfredi; Giuseppe A Ramirez; Patrizia Rovere-Querini; Norma Maugeri
Journal:  Front Immunol       Date:  2018-02-20       Impact factor: 7.561

Review 10.  The Pathophysiological Relevance of the iNKT Cell/Mononuclear Phagocyte Crosstalk in Tissues.

Authors:  Filippo Cortesi; Gloria Delfanti; Giulia Casorati; Paolo Dellabona
Journal:  Front Immunol       Date:  2018-10-12       Impact factor: 7.561

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