Table 1.
Components | Characteristics | References |
---|---|---|
Follicle-associated epithelium (FAE) |
- Specialized epithelial layer that overlies lymphoid follicles of PPs - Function as barrier between the intestinal lumen and PPs |
[7] |
Microfold (M) cells |
- Specialized enterocytes, present in the FAE - Transport of luminal antigens to PPs - Low level of glycocalyx covering and flat apical surface for efficient interactions with particulate antigens - Binding the S-IgA for efficient capturing and transporting of luminal antigens - Expression of diverse glycan signatures on the apical membrane for recognition of certain bacteria or immune complexes - Presence of M cell pockets on the basolateral membrane for the migration of immune cells into the intraepithelial |
[11, 18–23] |
Subepithelial dome (SED) |
- Areas located between the FAE and B cell follicles of PPs - Containing the high density of DCs - Direct interactions between M cells and DCs |
[29–31] |
Large B cell follicles |
- Network of diverse populations of B cells - Antigen encounter - Complex interactions with T cells, DCs or FDCs - Initial activation of naïve B cells |
[32] |
Germinal centers (GCs) |
- Clonal expansion and differentiation of B cells - Undergo SHM and CSR - Generation of IgA-secreting B cells |
[32–35] |
Small T cell zone |
- Network of diverse populations of T cells - Delivering activation signals from CD4 + T cells to B cells |
[32] |
High endothelial venules (HEVs) |
- Entry of lymphocytes to PPs - High expression of MADCAM-1, a ligand for α4β7 integrin, and CXCL13, a ligand for CXCR5 for B cell entry |
[18] |
Efferent lymphatics | - Leave effector cells generated in the PPs to MLN | [32] |