The effect of enteral stimulation on the immune response of the intestinal mucosa and its application in nutritional support.


Journal

European journal of clinical nutrition
ISSN: 1476-5640
Titre abrégé: Eur J Clin Nutr
Pays: England
ID NLM: 8804070

Informations de publication

Date de publication:
11 2021
Historique:
received: 02 09 2020
accepted: 01 02 2021
revised: 22 01 2021
pubmed: 21 2 2021
medline: 1 4 2022
entrez: 20 2 2021
Statut: ppublish

Résumé

The intestine plays a fundamental role as a regulator of the mucosal immune response, mostly through the production and secretion of secretory Immunoglobulin A (sIgA) by the gut-associated lymphoid tissue (GALT). Enteral stimulation, a balance between the commensal microbiota and pathogenic microorganisms, in addition to an adequate nutritional status is required for the optimal immune function of the intestine. Fasting subjects or those supported only with parenteral nutrition, show a progressive anatomical and physiological deterioration of the GALT, triggering a series of alterations resulting in a decrease in the intestinal immune response, modification in the type of microbiota, and changes that lead to or aggravate malnutrition. Patients with malnutrition present an increase in the rate of nosocomial infections, hospital length of stay, and mortality. An adequate nutritional assessment at hospital admission and avoiding long periods of fasting are paramount to prevent these unfavorable outcomes. Herein, we present a mini-state of the art review on the role and importance of enteral stimulation by GALT-mediated immune response.

Identifiants

pubmed: 33608653
doi: 10.1038/s41430-021-00877-7
pii: 10.1038/s41430-021-00877-7
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1533-1539

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Nature Limited part of Springer Nature.

Références

Kang W, Kudsk KA. Is there evidence that the gut contributes to mucosal immunity in humans? J Parenter Enter Nutr. 2007;31:246–58.
doi: 10.1177/0148607107031003246
Cesta MF. Normal structure, function, and histology of mucosa-associated lymphoid tissue. Toxicol Pathol. 2006;34:599–608.
pubmed: 17067945 doi: 10.1080/01926230600865531
Elmore SA. Enhanced histopathology of mucosa-associated lymphoid tissue. Toxicol Pathol. 2006;34:687–96.
pubmed: 17067953 pmcid: 1797898 doi: 10.1080/01926230600939989
Fukatsu K, Kudsk KA. Nutrition and gut immunity. Surg Clin North Am. 2011;91:755–70.
pubmed: 21787966 pmcid: 3144400 doi: 10.1016/j.suc.2011.04.007
Pierre JF. Gastrointestinal immune and microbiome changes during parenteral. Am J Physiol - Gastrointest Liver Physiol. 2017;312:G246–56.
pubmed: 28154012 pmcid: 5401992 doi: 10.1152/ajpgi.00321.2016
Pierre JF, Busch RA, Kudsk KA. The gastrointestinal immune system: implications for the surgical patient. Curr Probl Surg. 2016;53:11–47.
pubmed: 26699624 doi: 10.1067/j.cpsurg.2015.10.005
Jonker MA, Hermsen JL, Sano Y, Heneghan AF, Lan J, Kudsk KA. Small intestine mucosal immune system response to injury and the impact of parenteral nutrition. Surg [Internet] 2012;151:278–86.
doi: 10.1016/j.surg.2010.10.013
Szefel J, Kruszewski WJ, Buczek T. Enteral feeding and its impact on the gut immune system and intestinal mucosal barrier. Prz Gastroenterol. 2015;10:71–7.
pubmed: 26557936 pmcid: 4631273
Gommerman JL, Rojas OL, Fritz JH. Re-thinking the functions of IgA+plasma cells. Gut Microbes. 2015;5:652–62.
doi: 10.4161/19490976.2014.969977
Woof JM, Ken MA. The function of immunoglobulin A in immunity. J Pathol. 2006;208:270–82.
pubmed: 16362985 doi: 10.1002/path.1877
Anastasilakis CD, Ioannidis O, Gkiomisi AI, Botsios D. Artificial nutrition and intestinal mucosal barrier functionality. Digestion. 2013;88:193–208.
pubmed: 24247113 doi: 10.1159/000353603
Suzuki K, Fagarasan S. How host-bacterial interactions lead to IgA synthesis in the gut. Trends Immunol. 2008;29:523–31.
pubmed: 18838301 doi: 10.1016/j.it.2008.08.001
Pabst O. New concepts in the generation and functions of IgA. Nat Rev Immunol. 2012;12:821–32.
pubmed: 23103985 doi: 10.1038/nri3322
Kudsk KA, Croce MA, Fabian TC, Minard G, Tolley EA, Poret HA, et al. Enteral versus parenteral feeding effects on septic morbidity after blunt and penetrating abdominal trauma. Ann Surg. 1992;215:503–13.
pubmed: 1616387 pmcid: 1242485 doi: 10.1097/00000658-199205000-00013
Sano Y, Gomez FE, Kang W, Lan J, Maeshima Y, Hermsen JL, et al. Intestinal polymeric immunoglobulin receptor is affected by type and route of nutrition. J Parenter Enter Nutr. 2007;31:356–7.
doi: 10.1177/0148607107031005351
Hermsen JL, Sano Y, Gomez FE, Maeshima Y, Kang W, Kudsk KA. Parenteral nutrition inhibits tumor necrosis factor- α-mediated IgA response to injury. Surg Infect (Larchmt) 2008;9:33–40.
doi: 10.1089/sur.2007.029
Heneghan AF, Pierre JF, Tandee K, Shanmuganayagam D, Wang X, Reed JD, et al. Parenteral nutrition decreases paneth cell function and intestinal bactericidal activity while increasing susceptibility to bacterial enteroinvasion. J Parenter Enter Nutr. 2014;38:817–24.
doi: 10.1177/0148607113497514
Ikeda S, Kudsk KA, Fukatsu K, Johnson CD, Le T, Reese S, et al. Enteral feeding preserves mucosal immunity despite in vivo MAdCAM-1 blockade of lymphocyte homing. Ann Surg. 2003;237:677–85.
pubmed: 12724634 pmcid: 1514523 doi: 10.1097/01.SLA.0000064364.40406.EA
Li J, Kudsk KA, Gocinski B, Dent D, Glezer J, Langkamp-Henken B, et al. Effects of parenteral and enteral nutrition on gut-associated lymphoid tissue. J Trauma - Inj Infect Crit Care. 1995;39:44–51.
doi: 10.1097/00005373-199507000-00006
Hermsen JL, Sano Y, Kudsk KA. Food fight! Parenteral nutrition, enteral stimulation and gut-derived mucosal immunity. Langenbeck’s Arch Surg. 2009;394:17–30.
doi: 10.1007/s00423-008-0339-x
Fukatsu K. Role of nutrition in gastroenterological surgery. Ann Gastroenterol Surg. 2019;3:160–8.
pubmed: 30923785 pmcid: 6422822 doi: 10.1002/ags3.12237
Fukatsu K. Impact of the feeding route on gut mucosal immunity. Curr Opin Clin Nutr Metab Care. 2014;17:164–70.
pubmed: 24500441 doi: 10.1097/MCO.0000000000000033
Elke G, van Zanten ARH, Lemieux M, McCall M, Jeejeebhoy KN, Kott M, et al. Enteral versus parenteral nutrition in critically ill patients: an updated systematic review and meta-analysis of randomized controlled trials. Crit Care/ 2016;20:1–14.
McCoy KD, Burkhard R, Geuking MB. The microbiome and immune memory formation. Immunol Cell Biol. 2019;97:625–35.
pubmed: 31127637 doi: 10.1111/imcb.12273
Huus KE, Bauer KC, Brown EM, Bozorgmehr T, Woodward SE, Serapio-Palacios A, et al. Commensal bacteria modulate immunoglobulin a binding in response to host nutrition. Cell Host Microbe. 2020;27:1–13.
doi: 10.1016/j.chom.2020.03.012
Miyasaka EA, Feng Y, Poroyko V, Falkowski NR, Erb-Downward J, Gillilland MG, et al. Total parenteral nutrition–associated lamina propria inflammation in mice is mediated by a MyD88-dependent mechanism. J Immunol. 2013;190:6607–15.
pubmed: 23667106 doi: 10.4049/jimmunol.1201746
Amarasinghe JJ, D’Hondt RE, Waters CM, Mantis NJ. Exposure of Salmonella enterica serovar typhimurium to a protective monoclonal IGA triggers exopolysaccharide production via a diguanylate cyclase-dependent pathway. Infect Immun. 2013;81:653–64.
pubmed: 23230292 pmcid: 3584880 doi: 10.1128/IAI.00813-12
Cullender TC, Chassaing B, Janzon A, Kumar K, Muller CE, Werner JJ, et al. Innate and adaptive immunity interact to quench microbiome flagellar motility in the gut. Cell Host Microbe. 2013;14:571–81.
pubmed: 24237702 pmcid: 3920589 doi: 10.1016/j.chom.2013.10.009
McClave SA, Taylor BE, Martindale RG, Warren MM, Johnson DR, Braunschweig C, et al. Guidelines for the provision and assessment of nutrition support therapy in the adult critically Ill patient: society of critical care medicine (SCCM) and American society for parenteral and enteral nutrition (A.S.P.E.N.). J Parenter Enter Nutr. 2016;40:159–211.
doi: 10.1177/0148607115621863
Okamoto K, Fukatsu K, Hashiguchi Y, Ueno H, Shinto E, Moriya T, et al. Lack of preoperative enteral nutrition reduces gut-associated lymphoid cell numbers in colon cancer patients: a possible mechanism underlying increased postoperative infectious complications during parenteral nutrition. Ann Surg. 2013;258:1059–64.
pubmed: 23187750 doi: 10.1097/SLA.0b013e31827a0e05
Patel JJ, Kozeniecki M, Biesboer A, Peppard W, Ray AS, Thomas S, et al. Early trophic enteral nutrition is associated with improved outcomes in mechanically ventilated patients with septic shock: a retrospective review. J Intensive Care Med. 2016;31:471–7.
pubmed: 25315218 doi: 10.1177/0885066614554887
Gustafsson UO, Scott MJ, Schwenk W, Demartines N, Roulin D, Francis N, et al. Guidelines for perioperative care in elective colonic surgery: Enhanced recovery after surgery (ERAS®) society recommendations. World J Surg. 2013;37:259–84.
pubmed: 23052794 doi: 10.1007/s00268-012-1772-0
Higashizono K, Fukatsu K, Watkins A, Watanabe T, Noguchi M, Ri M, et al. Influences of short-term fasting and carbohydrate supplementation on gut immunity and mucosal morphology in mice. J Parenter Enter Nutr. 2019;43:516–24.
doi: 10.1002/jpen.1446
Bourke CD, Berkley JA, Prendergast AJ. Immune dysfunction as a cause and consequence of malnutrition. Trends Immunol. 2016;37:386–98.
pubmed: 27237815 pmcid: 4889773 doi: 10.1016/j.it.2016.04.003
Correia MITD, Perman MI, Waitzberg DL. Hospital malnutrition in Latin America: a systematic review. Clin Nutr. 2017;36:958–67.
pubmed: 27499391 doi: 10.1016/j.clnu.2016.06.025
Cederholm T, Jensen GL, Correia MITD, Gonzalez MC, Fukushima R, Higashiguchi T. et al. GLIM criteria for the diagnosis of malnutrition – A consensus report from the global clinical nutrition community. Clin Nutr. 2019;38:1–9.
pubmed: 30181091 doi: 10.1016/j.clnu.2018.08.002
Pérez Romero MT, Serralde-Zuniga AE, Reyes Ramírez AL, del C, Alfonso Baruch E, Gulías Herrero A. et al. Prevalence of malnutrition at admission in hospitalized adults at INCMNSZ in Mexico City. Rev Mex Endocrinol Metab y Nutr. 2017;4:12–6.
Waitzberg DL, Ravacci GR, Raslan M. Desnutrición hospitalaria. Nutr Hosp. 2011;26:254–64.
pubmed: 21666960
Rangel AG, Sepúlveda FR, Domínguez RS, Maldonado GM. Evaluación del estado nutricional y su impacto en pacientes post operados de anastomosis intestinal. Nutrición y fuga anastomosis. Nutr Clin y Diet Hosp. 2016;36:82–8.
Morris HJ, Carrillo OV, Llauradó G, Alonso ME, Bermúdez RC, Lebeque Y, et al. Effect of starvation and refeeding on biochemical and immunological status of Balb/c mice: an experimental model of malnutrition. Immunopharmacol Immunotoxicol. 2011;33:438–46.
pubmed: 21105863 doi: 10.3109/08923973.2010.531732
Kau AL, Planer JD, Liu J, Rao S, Yatsunenko T, Trehan I, et al. Functional characterization of IgA-targeted bacterial taxa from undernourished Malawian children that produce diet-dependent enteropathy. Sci Transl Med. 2015;7:276ra24.
pubmed: 25717097 pmcid: 4423598 doi: 10.1126/scitranslmed.aaa4877
Lochs H, Dejong C, Hammarqvist F, Hebuterne X, Leon-Sanz M, Schütz T, et al. ESPEN guidelines on enteral nutrition: gastroenterology. Clin Nutr. 2006;25:260–74.
pubmed: 16698129 doi: 10.1016/j.clnu.2006.01.007
Hernández Centeno JR, Fernández Galicia JC, González Bravo F, Ramírez Barba EJ, Zavala Martín J, Montiel Ramírez AE, et al. Inicio temprano de la alimentación enteral en pacientes con reconexión intestinal. Nutr Clin y Diet Hosp. 2013;33:18–22.
Reddy V, Raghuramulu N, Bhaskaram C. Secretory IgA in protein-calorie malnutrition. Arch Dis Child. 1976;51:871–4.
pubmed: 827242 pmcid: 1546061 doi: 10.1136/adc.51.11.871
Elmadfa I, Meyer AL. The role of the status of selected micronutrients in shaping the immune function. Endocr, Metab Immune Disord - Drug Targets. 2019;19:1100–15.
doi: 10.2174/1871530319666190529101816
Kudsk KA, Hermsen JL, Genton L, Faucher L, Gomez FE. Injury stimulates an innate respiratory immunoglobulin a immune response in humans. J Trauma - Inj Infect Crit Care. 2008;64:316–23.
doi: 10.1097/TA.0b013e3181627586
Sano Y, Hermsen JL, Kang W, Gomez FE, Lan J, Maeshima Y, et al. Parenteral nutrition maintains pulmonary IgA antibody transport capacity, but not active transport, following injury. Am J Surg. 2009;198:105–9.
pubmed: 19249732 pmcid: 2755078 doi: 10.1016/j.amjsurg.2008.08.018
Kondrup J, Ramussen HH, Hamberg O, Stanga Z, Camilo M, Richardson R, et al. Nutritional risk screening (NRS 2002): a new method based on an analysis of controlled clinical trials. Clin Nutr. 2003;22:321–36.
pubmed: 12765673 doi: 10.1016/S0261-5614(02)00214-5
Heyland DK, Dhaliwal R, Jiang X, Day AG. Identifying critically ill patients who benefit the most from nutrition therapy: the development and initial validation of a novel risk assessment tool. Crit Care. 2011;15:R268.
pubmed: 22085763 pmcid: 3388687 doi: 10.1186/cc10546
The Veterans Affairs Total Parenteral Nutrition Cooperative Study Group. Perioperative total parenteral nutrition in surgical patients. The Veterans Affairs Total Parenteral Nutrition Cooperative Study Group. N. Engl J Med. 1991;325:525–32.
doi: 10.1056/NEJM199108223250801

Auteurs

Gabriela Quiroz-Olguín (G)

Clinical Nutrition Service, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México, Mexico.
Centro de Investigación en Ciencias de la Salud. Facultad de Ciencias de la Universidad Anáhuac México Norte, Huixquilucan, Mexico.

Gabriela Gutiérrez-Salmeán (G)

Centro de Investigación en Ciencias de la Salud. Facultad de Ciencias de la Universidad Anáhuac México Norte, Huixquilucan, Mexico.

Juan G Posadas-Calleja (JG)

Department of Critical Medicine, University of Calgary, Calgary, Canada.

María F Padilla-Rubio (MF)

Clinical Nutrition Service, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México, Mexico.

Aurora E Serralde-Zúñiga (AE)

Clinical Nutrition Service, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Ciudad de México, Mexico. aurora.serraldez@incmnsz.mx.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH