Journal of Emerging and Rare Diseases Volume: 1.1 Open Access Journal J Emerg Rare Dis Volume: 1.1 1 Article Information Article Type: Short Communication Journal Type: Open Access Volume: 1 Issue: 1 Manuscript ID: JER-1-101 Publisher: Boffn Access Inc. Received Date: October 04, 2017 Accepted Date: October 25, 2017 Published Date: November 03, 2017 Tissue damage in post infectious sequelae is caused by a synergism between microbial and neutrophils-derived agonists: a concern for a disregard for already published data Isaac Ginsburg 1 * Erez Koren 1 # Peter Vernon Van Heerden 2 * 1 Faculty of Dental Medicine, Institute for Dental Sciences the Hebrew University Hadassah, Jerusalem, Israel 2 General Intensive Care Unit, Hadassah University Hospital, Jerusalem, Israel # Currently at Teva Pharmaceutical Industries Ltd., Kfar Saba, Israel Abstract Post infectious sequelae such as sepsis and septic shock are poorly understood and annually take the lives of millions over the world. Severe microbial infections caused by Gram Positive and Gram Negative bacteria and by fungi are the main causes, which are aggravated by the rapid development of antibiotic resistance. It is unfortunate that today all the clinical trials of sepsis which tested the efficacy of single antagonists failed. Sepsis was recently redefined as a synergistic multifactorial episode where no unique alarmin had been identified, which if inhibited could control the deleterious biochemical and immune immunological events characteristic of sepsis. An apparent “breakthrough “in our understanding of sepsis pathogenicity was published in 2009 in Nature Medicine arguing that the main cause of mortality in sepsis is the release from neutrophils (PMNs) nets of highly toxic nuclear histone. This caused endothelial cell dysregulation leading to organ failure. However, this concept downplays the concept that concomitantly with the activation of PMNs, a plethora of additional pro- inflammatory agents is also released. These can act in synergy with histone to injure cells. Furthermore, since many additional clinical disorders not related to sepsis also reported high levels of circulating histones, this toxic agent may be considered just another marker of cell damage. The failure to treat sepsis by the administration of only single antagonists should be replaced by cocktails of appropriate anti inflammatory agents. In 2009, two provocative articles were published in Nature Medicine suggesting that the main cause of death in sepsis is due do the release from neutrophils (PMNs) nets adhering to endothelial cells of highly bactericidal nuclear histones [1,2]. Dysregulation of endothelial cell functions then can leads to organ failure and demise of the patient. Cell damage and death could potentially be inhibited by heparin, activated protein C and by antibodies to histones [2]. However, these exciting and promising papers were soon followed by publications suggesting that high levels of circulating nuclear histones were also detected in other clinical disorders unrelated to sepsis, hinting that histones might not be the sole alarmin active agent in sepsis pathogenicity [3-9]. This assumption is based on a recent suggestion which re-defined sepsis as a multi-factorial synergistic phenomenon, where no single alarmin is generated which if neutralized successfully, might prevent the aftermath of severe microbial infections [9]. We also previously suggested that histone may not be a “unique evil alarmin” agent but only an additional “member of the gang” [8]. It is conceivable that concomitantly with PMN activation, consequent upon adherence to endothelial cell, the PMNs also release into the surrounding media a burst of NADPH- activated oxidants such as superoxide, nitric oxide (NO), peroxynitrite, HOCl and highly cationic peptides such as LL37, elastase, cathepsins C and G, many acid hydrolases and also TH1 cytokines probably have a role in the pathogenesis of cell damage in inflammation [10-27]. These toxic agents most probably do not act alone but in synergy (a crosstalk) with nuclear cationic histone and with additional cationic peptides to injure cells. Furthermore, the role played by the microbial cell-wall components LPS, lipoteichoic acid (LTA) and peptidoglycan (PPG) released following bacteriolysis induced either by antibiotics or by certain cationic peptides and their interactions with PMN products have not been clearly considered in the numerous publications on the role of histones in sepsis published in the literature [28-30]. It is therefore enigmatic and concerning that screening no less than 52 publications via Google Scholar and PUBMED, published since 2009, regarding the role of histones in the pathophysiology of sepsis revealed a disregard for a large number of publications on these subjects [10-30]. *Corresponding author: Isaac Ginsburg Faculty of Dental Medicine Institute for Dental Sciences the Hebrew University Hadassah, Jerusalem, Israel E-mail: Ginsburg@mail.huji.ac.il Peter Vernon Van Heerden General Intensive Care Unit Hadassah University Hospital Jerusalem, Israel E-mail: Vernon@hadassah.org.il Citation: Ginsburg I, Koren E, Heerden PVV (2017) Tissue damage in post infectious sequelae is caused by asynergism between microbial and neutrophils-derived agonists: a concern for a disregard for already published data. J Emerg Rare Dis 1: 1:101 Copyright: © 2017 Manor Y. 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