Skip to main content

Table 1 Comparison between secondary lymphoid organs and tertiary lymphoid structures

From: Tertiary lymphoid structural heterogeneity determines tumour immunity and prospects for clinical application

Characteristics

Secondary lymphoid organs

Tertiary lymphoid structures

References

Examples

Spleen, regional lymph nodes, peyer’s patches, ILFs, tonsils and NALT

Chronic Infection, autoimmune diseases, transplant rejection, cancer

[29,30,31,32,33,34]

Origin

During embryogenesis

After birth

[29, 35, 36]

Induction and development

LTo (FAP + podoplanin+,

LTβR+), LTi, endothelial

cells, retinoic acid

LTo (FAP + podoplanin+, LTβR+),

ILC3/LTi, endothelial cells,

NKT, Th17,

chronic inflammation, cytokines

(LT, TNF, LIGHT, IL-17), chemokines

(CXCL13, CCL19, CCL21)

[10, 37,38,39,40]

Location

Defined-relatively immutable

Variable (non-lymphoid organ or tissue site)

[29, 35, 41, 42]

Structure

B and T cell compartments, HEVs, lymphatic vessels

Variable (from mixed T and B cells to T and B cell compartments), HEVs, lymphatic vessels

[2, 35, 36, 42, 43]

Capsule

Defined

Rare

[2, 36, 42]

Self-tolerance

Maintained

Disturbed (autoantibody production etc.)

[2, 10, 44, 45]

Durability

Permanent (but can collapse)

Transient

[39]

  1. ILFs: isolated lymphoid follicle; NALT: nasal associated lymphoid tissue; FAP: fibroblast activation protein-α; ILC3: innate lymphocyte 3; NKT: natural killer T cells; LTs: leukotrienes; TNF: tumour necrosis factor