Peyer's patch

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Peyer's patch
Peyer's patch (improved color).jpg
Cross section of ileum with a Peyer's patch circled.
System Immune system (Lymphatic system)
Latin noduli lymphoidei aggregati
Code TH H3.
TA A05.6.01.014
TH H3.
FMA 76466
Anatomical terminology

Peyer's patches (or aggregated lymphoid nodules, or occasionally PP for brevity) are organized lymphoid nodules, named after the 17th-century Swiss anatomist Johann Conrad Peyer. They are aggregations of gut associated lymphoid tissue that are usually found in the lowest portion of the small intestine, the ileum, in humans; as such, they differentiate the ileum from the duodenum and jejunum. The duodenum can be identified by Brunner's glands. The jejunum has neither Brunner's glands nor Peyer's patches.


Peyer's patches are observable as elongated thickenings of the intestinal epithelium measuring a few centimeters in length. About 100 are found in humans. Microscopically, Peyer’s patches appear as oval or round lymphoid follicles (similar to lymph nodes) located in the lamina propria layer of the mucosa and extending into the submucosa of the ileum. The number of Peyer's patches peaks at age 15-25 and then declines during adulthood.[1] In the distal ileum, they are numerous and they form a lymphoid ring. At least 46% of Peyer's patches are concentrated in the distal 25 cm of ileum in humans. It is important to note that there are large variations in size, shape, and distribution of Peyer's patches from one individual to another one.[2] In adults, B lymphocytes are seen to dominate the follicles' germinal centers. T lymphocytes are found in the zones between follicles. Among the mononuclear cells, CD4+/CD25+ (10%) cells and CD8+/CD25+ (5%) cells are more abundant in Peyer's patches than in the peripheral blood.[3]


Because the lumen of the gastrointestinal tract is exposed to the external environment, much of it is populated with potentially pathogenic microorganisms. Peyer's patches thus establish their importance in the immune surveillance of the intestinal lumen and in facilitating the generation of the immune response within the mucosa.

Pathogenic microorganisms and other antigens entering the intestinal tract encounter macrophages, dendritic cells, B-lymphocytes, and T-lymphocytes found in Peyer's patches and other mucosa-associated lymphoid tissue (MALT). Peyer's patches thus act for the gastrointestinal system much as the tonsils act for the respiratory system, trapping foreign particles, surveilling them, and destroying them.

Peyer's patches are covered by a special epithelium that contains specialized cells called microfold cells (M cells) which sample antigen directly from the lumen and deliver it to antigen-presenting cells (located in a unique pocket-like structure on their basolateral side). Dendritic cells and macrophages can also directly sample the lumen by extending dendrites through transcellular M cell-specific pores.[4][5] T cells, B-cells and memory cells are stimulated upon encountering antigen in Peyer's patches. These cells then pass to the mesenteric lymph nodes where the immune response is amplified. Activated lymphocytes pass into the blood stream via the thoracic duct and travel to the gut where they carry out their final effector functions.The maturation of B-lymphocytes takes place in the Peyer's patch.

Clinical significance[edit]

Although important in the immune response, excessive growth of lymphoid tissue in Peyer's patches is pathologic, as hypertrophy of Peyer's patches has been closely associated with idiopathic intussusception.

The hypertrophy of Peyer's patches has also been associated with susceptibility to transmissible spongiform encephalopathies (commonly known as prion diseases).

Salmonella typhi and poliovirus also target this section of the intestine.[6]


  1. ^ Cornes J S. Number, size, and distribution of Peyer's patches in the human small intestine: Part I The development of Peyer's patches[J]. Gut, 1965, 6(3): 225.
  2. ^ Van Kruiningen H J, West A B, Freda B J, et al. Distribution of Peyer's patches in the distal ileum[J]. Inflammatory bowel diseases, 2002, 8(3): 180-185.
  3. ^ Jung C, Hugot J P, Barreau F. Peyer's patches: the immune sensors of the intestine[J]. International journal of inflammation, 2010, 2010.
  4. ^ Lelouard H, Fallet M, de Bovis B, Méresse S, Gorvel JP. « Peyer's Patch Dendritic Cells Sample Antigens by Extending Dendrites Through M Cell-Specific Transcellular Pores » Gastroenterology 2011.
  5. ^ Bonnardel J, Da Silva C, Henri S, Tamoutounour S, Chasson L, Montañana-Sanchis F, Gorvel JP, Lelouard H.« Innate and adaptive immune functions of peyer's patch monocyte-derived cells. » Cell Reports 2015.
  6. ^ Pascall, C R; Stearn, E J; Mosley, J G (1980-07-05), "Short Reports", British Medical Journal, p. 26, PMC 1713722free to read, PMID 7407483, Unlike S hadar peritonitis, S typhi peritonitis is due to perforation of Peyer's patches.