Can feeding strategies alter immune signaling and gut sepsis in critical illness?

Abstract

The insult necessitating admission to the intensive care unit propels the patient along a course involving increasing oxidative stress, immune dysregulation, and adverse outcomes. As the largest immune organ with the greatest microbial burden, the gastrointestinal (GI) tract may change the speed and direction the patient follows along this pathway. The gut's influence is mediated by a complex process of cross-talk immune signaling between the intestinal epithelium, the liver, and the microbiome. Agents that invoke this response vary from mitochondrial DNA, inflammatory cytokines, and bacterial organisms to short-chain fatty acids and bile salts. The site of action of these agents again varies widely from pattern-recognition receptors, G protein receptors, and farnesoid X receptors in the gut and liver to transcriptional factors in epithelial cells, hepatocytes, macrophages, and neutrophils. Whereas the initial focus of response may be local within the GI tract and liver, the process extends in a systemic manner to affect immune tissue and various organs at distant sites. The gut can modulate this cross-talk signaling through numerous strategies in the design of nutrition therapy. The physiologic response to luminal nutrients and short-chain fatty acids, and more novel approaches like using phosphorylated polyethylene glycol, bovine serum-derived immunoglobulin, and specialized proresolving molecules, may help slow disease progression and even reverse the patient's course toward one of health and recovery. The optimal benefit to be derived from nutrition therapy may have more to do with the degree to which immune cross-talk signaling can be modified by such innovative strategies.