HHE Sponsored supplement: Sepsis | Page 14

the glycocalyx affects vascular permeability. In an experimental study, an increase in urinary albumin and ultrastructural changes of the glomerular filtration barrier was observed with a decreased expression of syndecan-1, hyaluronic acid and sialic acid, all glomerular glycolic components. 60 Clinical studies reveal a strong relationship between deterioration of the endothelial glycocalyx and severity of sepsis. It has been related to the activity of TNFα. 61 Renal cells are especially sensitive; deterioration has also been described in the lung and hepatic sinusoidal endothelium. 53 • The intestine: the intestine can house around 500 species of bacteria. 62 The passage of viable and non-viable micro-organisms, and their products, such as endotoxins, through the anatomically intact intestinal barrier is termed bacterial translocation. It can be a physiological mechanism of stimulation of the immune system that under certain conditions can be overcome and initiate systemic inflammatory processes. 63,64 The intestne comprises 25% lymphoid tissue and 70–80% of the immunoglobulin-secreting cells are found in the intestine. For many years, the intestine was thought to be the ‘motor of sepsis’. 65 Alteration of intestinal epithelial integrity, the increase in permeability and alteration of the gut microbiome are also documented in sepsis. 66 The response to infection is dependent on the causative organism(s), the host’s response and other environmental and therapeutic factors Factors affecting response to infection The response to infection is dependent on factors associated with the causative organism(s), the ability of the host to respond and other environmental and therapeutic factors. 67 Micro-organism Bacterial products, fundamentally components of the cell wall, activate the immune system by manufacturing and releasing inflammatory mediators responsible for the systemic response. Endotoxin, or, more precisely, bacterial lipopolysaccharide (LPS), is recognised as the most potent microbial mediator involved in the pathogenesis of sepsis and septic shock. LPS is a highly antigenic molecule part of the cell wall of gram-negative bacteria that binds in body fluids to the soluble binding protein (LBP) that serves to facilitate its binding to the CD14 monocyte membrane receptor. LBP is dissociated and the resulting complex makes contact with the TLR4. Other components of the bacterial wall are: peptidoglycan, muramyl dipeptide, and lipoteichoic acid. Other bacterial products produce a systemic response: Staphylococcal enterotoxin B, toxic shock syndrome toxin-1, Pseudomonas exotoxin A, and M protein of haemolytic group A streptococci. 68 Influenza A virus infection will induce a pro-inflammatory innate immune response through the recognition of viral RNA by TLR7 and retinoic acid-inducible gene 1 (RIG-I) molecules, that induce the production of the pro- inflammatory cytokine-mediated NF-κB route and activate the antiviral response. 52 Host Immunosuppression is accompanied by an increased incidence of sepsis and worse prognosis. 69 14 HHE 2018 | hospitalhealthcare.com Genetics Parental death through infection before the age of 50 years, presents an increased risk of dying of infection (5.8-times) for an individual. This observation was made after studying the causes of premature deaths in 1000 families with adopted children, verifying the relationship with the death of the biological parents with that of the adopted parents. This relative risk is higher than death due to cancer or cardiovascular diseases, and suggests a significant genetic susceptibility to death by infection and, by extension, to sepsis. 70 Other articles extend the studies on gene polymorphisms of other responsible molecules in the cell signalling mechanism during the immune response in the process of systemic inflammatory response. Polymorphisms in TLR4 and CD14 have been associated with survival and the development of septic shock. These polymorphisms would code for proteins with less responsiveness to lipopolysaccharide. These patients would present an inadequate early expression of pro-inflammatory proteins in response to endotoxin (tolerance to endotoxin). 71–74 A number of different proteins are involved in iron metabolism. The delicate connection between innate immunity and iron homeostasis might seem obvious, but it is difficult to prove. It seems certain that a balance between both systems is fundamental in the defence against micro-organisms, because poor management of iron reserves in any cell compartment would be harmful to the host and beneficial to the invading pathogen. 75 Modifiable factors Adipose tissue has a role in immune regulation. 76 It has been observed that adipocytes and some cells of the immune system, such as T lymphocytes and macrophages, have similar characteristics in terms of the production of pro-inflammatory cytokines. Adipose tissue secretes biologically active molecules (adipokines), among which are TNFα, IL-6, leptin and adiponectin. These molecules participate in physiological processes including regulation of energy balance, glucose metabolism and vascular remodelling, and seem to be involved in a protective effect observed in obese patients. 77 Leptin, for example, acts directly on macrophages increasing its phagocytic activity and the production of pro-inflammatory cytokines. Adiponectin reduces the activity of macrophages and occurs in smaller amounts in obese individuals. 78,79 Pregnant women also have low levels of adiponectin. This immune alteration is especially important in influenza A infection. 80 This increased severity of influenza in pregnant women could explain the increased susceptibility to infection of this condition. Indeed, the foetus behaves as a semi-allograft (expressed as both maternal and paternal antigens). To avoid rejection, during pregnancy, there are changes in both innate and adaptive immunity (immune tolerance and active suppression of the immune response). 81 They occur both locally at the maternal–foetal interface, and systemically. In addition to the foetus being physically protected by trophoblasts, local adaptations occur to prevent maternal