Gut-associated lymphoid tissue

Gut-associated lymphoid tissue
Details
SystemLymphatic system
Identifiers
Acronym(s)GALT
FMA62820
Anatomical terminology

Gut-associated lymphoid tissue (GALT)[1] is a component of the mucosa-associated lymphoid tissue (MALT) which works in the immune system to protect the body from invasion in the gut.

Owing to its physiological function in food absorption, the mucosal surface is thin and acts as a permeable barrier to the interior of the body. Equally, its fragility and permeability creates vulnerability to infection and, in fact, the vast majority of the infectious agents invading the human body use this route.[2] The functional importance of GALT in body's defense relies on its large population of plasma cells, which are antibody producers, whose number exceeds the number of plasma cells in spleen, lymph nodes and bone marrow combined.[3] GALT makes up about 70% of the immune system by weight; compromised GALT may significantly affect the strength of the immune system as a whole.[4]

Structure

The gut-associated lymphoid tissue lies throughout the intestine, covering an area of approximately 260–300 m2.[5] In order to increase the surface area for absorption, the intestinal mucosa is made up of finger-like projections (villi), covered by a monolayer of epithelial cells, which separates the GALT from the lumen intestine and its contents. These epithelial cells are covered by a layer of glycocalyx on their luminal surface so as to protect cells from the acid pH.

New epithelial cells derived from stem cells are constantly produced on the bottom of the intestinal glands, regenerating the epithelium (epithelial cell turnover time is less than one week).[2][6] Although in these crypts conventional enterocytes are the dominant type of cells, Paneth cells can also be found. These are located at the bottom of the crypts and release a number of antibacterial substances, among them lysozyme, and are thought to be involved in the control of infections.

Underneath them, there is an underlying layer of loose connective tissue called lamina propria. There is also lymphatic circulation through the tissue connected to the mesenteric lymph nodes.

Both GALT and mesenteric lymph nodes are sites where the immune response is started due to the presence of immune cells through the epithelial cells and the lamina propria.

The GALT also includes the Peyer's patches of the small intestine, isolated lymphoid follicles present throughout the intestine and the appendix in humans.[2]

The following examples comprise lymphoid tissues that act as interfaces between immune system and incoming antigens either as food antigens or as pathogenic or commensal microbiota´s antigens:

GALT can be also divided into two categories considering the structure, from which the function arise. There can be found 1.) organised GALT made up from folicules – such as Peyer´s patches, mesenteric lymph nodes and even more organised appendix. Its main function is to induce immune reaction. 2.) diffuse GALT with single T and B cells, macrophages, eosinophiles, basophiles and mast cells, preferentially found in lamina propria. This part of GALT is made up from mature effector cells ready to perform their actions.

Peyer's patches

The Peyer's patch is an aggregate of lymphoid cells projected to the lumen of the gut which acts as a very important site for the initiation of the immune response. It forms a subepithelial dome where large number of B cell follicles with its germinal centers, T cells areas between them in a smaller number and dendritic cells are found. In this area, the subepithelial dome is separated from the intestinal lumen by a layer of follicle-associated epithelium. This contains conventional intestinal epithelial cells and a small number of specialized epithelial cells called microfold cells (M cells) in between. Unlike enterocytes, these M cells present a folded luminal surface instead of the microvilli, do not secrete digestive enzymes or mucus and lack a thick surface of glycocalix, so it can be in contact with microbiota and antigens presented in the content of gut.

Function

Intestinal microenvironments and niches.

Under normal circumstances, immune system of the whole organism needs intestinal source of antigens to train and regulate development of various immune cells. Without having such stimulation, many properties of immune systems do not develop, as it is shown on the case of germ-free animals. Because immune cells are in constant touch with bacterial and food antigens, the primary response is set up as tolerogenic. Still there must a robust defence in a case that pathogens cross either the border line of epithelium or produce harmful substances like bacterial toxins. Such a walking on the edge of a knife is ensured by diverse types of immune cells:

B-lymphocytes

Plasma B cells residing at lamina propria produce high levels of specific secretory IgA antibodies. These IgA are secreted into the lumen of the gut through the epithelial layer by transcytosis. Firstly epithelial cell binds a dimer of IgA via polymeric Ig receptor at the basolateral side and transports it in a vesicle into the luminal space. Then the receptor is proteolyticaly cleaved and the dimer of IgA is released with a portion of the receptor called the secretory component. The secretory component protects secreted antibodies against the digestive milieu in the gut.[7]

A high level of secretory IgA results from the interaction of B cells and intestinal antigen presenting dendritic cell (DC) in cooperation with follicular T helper cell (Tfh) in the germinal centers (GCs) of Peyer´s patches.[8] There are two main ways of IgA production 1) T-cell dependent resulting in sIgAs with high affinity and specificity and 2) T-cell independent generation of sIgA, which utilizes dendritic cells and their production of BAFF and APRIL cytokines. T-cell independently produced sIgAs have lower affinity and coat mainly commensals.[9][10] General functions of secretory IgAs are to coat any of the intestinal bacteria (commensal or pathogenic ones) to impair their motility and to prevent them from getting in prolonged and direct contact with the intestinal epithelium and the host intestinal immune system. This is called immune exclusion. Secreted IgAs bind to bacterial toxins and neutralize them as well.[8][9][10]

T-lymphocytes

Naïve CD4+T cells differentiate into Treg or various helper T cell subsets (Th1, Th2, Th17 or Tfh). In the gut-associated lymphoid tissue, the process of differentiation occurs via presentation of antigens derived from gut microbiota by antigen presenting cells such as dendritic cells or M cells in Peyer´s patches.[8] Typical process of an oral tolerance towards ingested food antigens can be described as continuous luminal sampling of antigens by DCs and their subsequent migration followed by priming of naïve T cells in mesenteric lymph nodes to become immunosuppressive T cells (Treg).[11] Antigens received in this way ensure tolerance against them. Commensal microbiota activates immune response as well - in a way that protects host intestinal tissue from damaging it by immune cell reactions. The final outcome of T cell populations in healthy individuals differs from the spectrum of T cells resulting from acute infection or chronic inflammation. Inappropriate stimulation (typically by segmented filamentous bacteria - SFB) of chronic Th1 or Th17 cell response plays a crucial role in pathological damage to the host.[12]

Several novel gut-associated lymphoid cells have been described. They are of different origins and follow different maturation processes but share the same GALT role – to rapidly respond to pathogens and secrete effector cytokines. Such multi-layered protection systems highlights the susceptibility of mucosal sites to invading agents. The mucosal route is the most frequent way for entering of pathogenic infections into the host.[13] Robust engagement of a variety of lymphoid cells patrolling the epithelial layer also reflects evolutionary pressure and arms race between immune systems and pathogens escaping its control.[14]

Intraepithelial lymphocytes (IELs)

Long-lived and residential intraepithelial lymphocytes are one of the largest populations of T-lymphocytes in the body.[14] In contrast to other peripheral lymphocytes, IEL do not circulate in the blood stream or lymphatic system but reside in the epithelial layer in intestine.[15] Such location in very special per itself – IELs patrol the condition within a single layer of cells and have dendritic look.[16] They provide the first line of defense in case of pathogen crossing the epithelial barrier. IELs encompass surprising diversity of origins and divide into two main categories – conventional and nonconventional. It is based on molecular surface properties and the place where they acquire their final effector cytotoxic program.[14]

Conventional IELs bear classical TCR receptor made up from α and β subunit together with CD4 or CD8 co-receptors. They represent a relative minority of the total intestinal IELs compared with unconventional IELs. They are derived from naïve T cells that encounter antigens in the periphery (typically antigens displayed by DC in the Peyer´s patches). After this activation, conventional IELs express gut-tropic molecules allowing them to home in intestinal tissue after trafficking through lymph stream and subsequent blood stream. Conventional intraepithelial cells are thus tissue-resident effector memory T cells, capable of rapid respond with cytolytic activity and release of cytokines such as INFγ and TNF.[14]

Unconventional IELs present majority of IEL cells in intestinal epithelial layer and acquire their effector program after exiting thymus as naïve cells and encountering antigens in GALT. After such stimulation, unconventional IELs (mainly γδ T cells) reside in the intestinal epithelium.[14] γδ T cells express TCR receptor made of γ and δ subunit and do not recognize antigen peptides presented in the MHC-bound form. The process of their activation is still largely unknown. Main property of γδ T cells is formation of long-lived memory populations in barrier tissues such as intestinal epithelium or in the skin. They perform immune memory in particular tissue even after clearance of pathogen or retreat of inflammation.[15]

Innate lymphoid cells (ILCs)

Innate lymphoid cells (ILCs) are the most recently discovered family of innate immune cells and term “innate” means they do not need antigen receptor gene rearrangement. Due to the development of novel method, such as single cell RNA sequencing, subtypes of innate lymphoid cells are described. Based on their transcriptional profile set by main transcription factors ILCs are divided into five distinct subsets: NK cells, ILC1s, ILC2s, ILC3s, and LTi cells. ILCs are prevalent at mucosal surfaces, playing a key role in mucosal immunity and homeostasis due to their ability of rapid secretion of immunoregulatory cytokines and thus communicating with other immune cells.[17]

Innate immunity

Beside adaptive specific immunity, an innate immunity plays a significant role in GALT because it provides more rapid response. Recognition of microbial non-self signature occurs by pattern recognition receptors (PRR) that can be found on dendritic cells, macrophages, monocytes, neutrophils and epithelial cells. PRRs bind to conserved microbial pattern like cell walls components (LPS, teichoic acid, flagellin, peptidoglycan) or viral or bacterial nucleic acid. PRRs are localized extracellularly as membrane-bound receptors (Toll-like receptors) or intracellularly (NOD-like and RIG-like receptors).[12] Varied palette of pattern recognition receptors is activated by various signals named PAMP (pathogen associated molecular patterns) or by signals connected to tissue damage named DAMP (damage associated molecular patterns).

Macrophages

Majority of antigen presenting cells (APCs) in intestine is derived from macrophages, which have very quick turnover. Macrophages are prevalent in lamina propria and submucosal deeper layers like muscularis layer. Macrophages can use their trans-epithelial dendrites (long cytoplasmic extensions) and directly contact epithelial layer and sample luminal bacteria.[16] Under healthy conditions macrophages engulf commensal bacteria and surrounding cellular debris, secrete IL-10, drive maturation of Treg and contribute to tissue homeostasis. Because of low expression of innate response receptors and co-stimulatory surface molecules, intestinal macrophages do not initiate inflammation. But upon infection or inflammation, the profile of macrophages changes and they start to secrete large amounts of TNF-α and become proinflammatory effector cells.[18]

Dendritic cells

DCs present less than 10% of lamina propria APC and typically do not reside in lower layers. Inherent production of retinoic acid and TGF-β (typical for gut-associated DCs) induces expression of gut-homing molecules and favor IgA switch during maturation of B cells in folicules. DCs also direct Treg and conventional IELs to receive their final phenotype of mature effector cells in intestine.[16]

Other animals

The adaptive immunity, mediated by antibodies and T cells, is only found in vertebrates. Whereas all of them have a gut-associated lymphoid tissue and the vast majority have a version of spleen and thymus, not all vertebrates show bone marrow, lymph nodes or germinal centers, what means that not all vertebrates can generate lymphocytes in bone marrow.[3] This different distribution of the adaptive organs in the different groups of vertebrates suggests GALT as the very first part of the adaptive immune system in vertebrates. It has been suggested that from this existing GALT, and due to the pressure put by commensal bacteria in gut that coevolved with vertebrates, later specializations as thymus, spleen or lymph nodes appeared as part of the adaptive immune system.[2]

Additional images

References

  1. ↑ Janeway Jr CA, Travers P, Walport M, Shlomchik MJ (2001). "The mucosal immune system". Immunobiology: The Immune System in Health and Disease (5th ed.). New York: Garland Science. ISBN 978-0-8153-3642-6.
  2. 1 2 3 4 Murphy K, Janeway Jr CA (2011). Janeway's immunobiology (Immunobiology: The Immune System (Janeway)). Garland Science. ISBN 978-0-8153-4243-4. OCLC 733935898.
  3. 1 2 Goldsby RA, Osborne BA, Kindt TJ, Kuby J (2007). Kuby immunology. W.H. Freeman. ISBN 978-0-7167-6764-0. OCLC 68207318.
  4. ↑ Vighi G, Marcucci F, Sensi L, Di Cara G, Frati F (September 2008). "Allergy and the gastrointestinal system". Clinical and Experimental Immunology. 153 (Suppl 1): 3–6. doi:10.1111/j.1365-2249.2008.03713.x. PMC 2515351. PMID 18721321.
  5. ↑ Helander HF, Fändriks L (June 2014). "Surface area of the digestive tract - revisited". Scandinavian Journal of Gastroenterology. 49 (6): 681–9. doi:10.3109/00365521.2014.898326. PMID 24694282.
  6. ↑ Slomianka L. "Blue Histology - Gastrointestinal Tract". School of Anatomy and Human Biology. The University of Western Australia. Retrieved 2017-01-30.
  7. ↑ Immunology. Male, David K., 1954- (8th ed.). [United States]: Elsevier/Saunders. 2013. ISBN 978-0-7020-5028-2. OCLC 814034128.{{cite book}}: CS1 maint: others (link)
  8. 1 2 3 Wang L, Zhu L, Qin S (October 2019). "Gut Microbiota Modulation on Intestinal Mucosal Adaptive Immunity". Journal of Immunology Research. 2019: 4735040. doi:10.1155/2019/4735040. PMC 6794961. PMID 31687412.
  9. 1 2 Zhang H, Luo XM (March 2015). "Control of commensal microbiota by the adaptive immune system". Gut Microbes. 6 (2): 156–60. doi:10.1080/19490976.2015.1031946. PMC 4615846. PMID 25901893.
  10. 1 2 Stephens WZ, Round JL (September 2014). "IgA targets the troublemakers". Cell Host & Microbe. 16 (3): 265–7. doi:10.1016/j.chom.2014.08.012. PMID 25211066.
  11. ↑ McCoy KD, Köller Y (August 2015). "New developments providing mechanistic insight into the impact of the microbiota on allergic disease". Clinical Immunology. 159 (2): 170–6. doi:10.1016/j.clim.2015.05.007. PMC 4553911. PMID 25988860.
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  13. ↑ Tlaskalová-Hogenová H, Stěpánková R, Kozáková H, Hudcovic T, Vannucci L, Tučková L, et al. (March 2011). "The role of gut microbiota (commensal bacteria) and the mucosal barrier in the pathogenesis of inflammatory and autoimmune diseases and cancer: contribution of germ-free and gnotobiotic animal models of human diseases". Cellular & Molecular Immunology. 8 (2): 110–20. doi:10.1038/cmi.2010.67. PMC 4003137. PMID 21278760.
  14. 1 2 3 4 5 McDonald BD, Jabri B, Bendelac A (August 2018). "Diverse developmental pathways of intestinal intraepithelial lymphocytes". Nature Reviews. Immunology. 18 (8): 514–525. doi:10.1038/s41577-018-0013-7. PMC 6063796. PMID 29717233.
  15. 1 2 Khairallah C, Chu TH, Sheridan BS (November 2018). "Tissue Adaptations of Memory and Tissue-Resident Gamma Delta T Cells". Frontiers in Immunology. 9: 2636. doi:10.3389/fimmu.2018.02636. PMC 6277633. PMID 30538697.
  16. 1 2 3 Faria AM, Reis BS, Mucida D (May 2017). "Tissue adaptation: Implications for gut immunity and tolerance". The Journal of Experimental Medicine. 214 (5): 1211–1226. doi:10.1084/jem.20162014. PMC 5413340. PMID 28432200.
  17. ↑ Jiao Y, Wu L, Huntington ND, Zhang X (February 2020). "Crosstalk Between Gut Microbiota and Innate Immunity and Its Implication in Autoimmune Diseases". Frontiers in Immunology. 11: 282. doi:10.3389/fimmu.2020.00282. PMC 7047319. PMID 32153586.
  18. ↑ Wang S, Ye Q, Zeng X, Qiao S (2019-03-18). "Functions of Macrophages in the Maintenance of Intestinal Homeostasis". Journal of Immunology Research. 2019: 1512969. doi:10.1155/2019/1512969. PMC 6442305. PMID 31011585.
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