Table 1 Metabolic pathways and metabolic characteristics of different immune cells

From: Metabolic regulation of the immune system in health and diseases: mechanisms and interventions

Immune cell

Glycolysis

FAO

OXPHOS

References

Macrophage

M1 macrophages mainly rely on aerobic glycolysis

M2 macrophages mainly rely on OXPHOS and FAO

M2 macrophages mainly rely on OXPHOS and FAO

14,21

T cell

Naive T cell

In a quiescent state with low metabolic activity

A main energy source and default metabolic program

A main energy source and way of glucose metabolism

73,88,91

Effector T cell

With highly upregulated aerobic glycolysis, also known as the Warburg effect

Downregulated during T cell activation

Also upregulated, but less than aerobic glycolysis

80,91

Memory T cell

Not the default metabolic program; promoting rapid recall response of CD8+ memory T cells; depending on intracellular glycogen; main metabolic pathway for G6P

An energy source and the default metabolic program; with fatty acids as the preferent metabolites in the survival environment with limited glucose

An energy source and the default metabolic program

73,76,80,84,88,91,95,97

Treg cell

Not the default metabolic program

An energy source and the default metabolic program; with fatty acids as the preferent metabolites in the survival environment with limited glucose

An energy source and the default metabolic program

76,80,84,85,86,87,88,91,95,97

B cell

Naive B cell

In a quiescent state with low metabolic activity

In a quiescent state with low metabolic activity

In a quiescent state with low metabolic activity

113

Activated B cell

Upregulated; B cells with chronic BAFF stimulation rapidly increase glycolysis; aerobic glycolysis not highlighted in nonneoplastic B cells; B1 cells have a higher rate of glycolysis than B2 cells

Germinal center B cells carry out active FAO

Upregulated; B1 cells have a higher rate of OXPHOS than B2 cells

115,116,581

Neutrophil

Mainly rely on glycolysis for ATP production

Unclear

Very limited because of low mitochondrial density

134

Dendritic cell

Upregulated during pathogen infection

Upregulated in activated dendritic cells

Upregulated in activated dendritic cells

140,141

Natural killer cell

Indispensable for the anti-tumor effect

Enhance the responses against infection and cancer

Cover the metabolic demand at a quiescent state

149,150,151,152

Group 2 innate lymphoid cell

Upregulated in the activated state

Supports the function during helminth infection

Always at steady state

149,157,158

Group 3 innate lymphoid cell

Upregulated in the activated state

Unclear

Upregulated in the activated state

158,160

  1. FAO fatty acid oxidation, OXPHOS oxidative phosphorylation, FAS fatty acid synthesis, G6P glucose-6-phosphate