Immune regulatory networks coordinated by glycans and glycan-binding proteins in autoimmunity and infection

被引:58
|
作者
Pinho, Salome S. [1 ,2 ,3 ]
Alves, Ines [1 ]
Gaifem, Joana [1 ]
Rabinovich, Gabriel A. [4 ,5 ]
机构
[1] Univ Porto, Inst Res & Innovat Hlth, i3S, P-4200135 Porto, Portugal
[2] Univ Porto, Sch Med & Biomed Sci, ICBAS, P-4050313 Porto, Portugal
[3] Univ Porto, Fac Med, P-4200319 Porto, Portugal
[4] Consejo Nacl Invest Cient & Tecn CONICET, Lab Glicomedicina, Inst Biol & Med Expt IBYME, RA-1428 Buenos Aires, Argentina
[5] Univ Buenos Aires, Fac Ciencias Exactas & Nat, RA-1428 Buenos Aires, Argentina
基金
欧洲研究理事会;
关键词
Immune response; Inflammation; Infection; Glycans; Glycosylation; Glycan-binding proteins; MANNOSE-CAPPED LIPOARABINOMANNAN; PATTERN-RECOGNITION RECEPTOR; T-CELL-ACTIVATION; LECTIN DC-SIGN; N-GLYCOSYLATION; DENDRITIC CELLS; CAMPYLOBACTER-JEJUNI; RHEUMATOID-ARTHRITIS; CANDIDA-ALBICANS; ANTIINFLAMMATORY ACTIVITY;
D O I
10.1038/s41423-023-01074-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system is coordinated by an intricate network of stimulatory and inhibitory circuits that regulate host responses against endogenous and exogenous insults. Disruption of these safeguard and homeostatic mechanisms can lead to unpredictable inflammatory and autoimmune responses, whereas deficiency of immune stimulatory pathways may orchestrate immunosuppressive programs that contribute to perpetuate chronic infections, but also influence cancer development and progression. Glycans have emerged as essential components of homeostatic circuits, acting as fine-tuners of immunological responses and potential molecular targets for manipulation of immune tolerance and activation in a wide range of pathologic settings. Cell surface glycans, present in cells, tissues and the extracellular matrix, have been proposed to serve as "self-associated molecular patterns" that store structurally relevant biological data. The responsibility of deciphering this information relies on different families of glycan-binding proteins (including galectins, siglecs and C-type lectins) which, upon recognition of specific carbohydrate structures, can recalibrate the magnitude, nature and fate of immune responses. This process is tightly regulated by the diversity of glycan structures and the establishment of multivalent interactions on cell surface receptors and the extracellular matrix. Here we review the spatiotemporal regulation of selected glycan-modifying processes including mannosylation, complex N-glycan branching, core 2 O-glycan elongation, LacNAc extension, as well as terminal sialylation and fucosylation. Moreover, we illustrate examples that highlight the contribution of these processes to the control of immune responses and their integration with canonical tolerogenic pathways. Finally, we discuss the power of glycans and glycan-binding proteins as a source of immunomodulatory signals that could be leveraged for the treatment of autoimmune inflammation and chronic infection.
引用
收藏
页码:1101 / 1113
页数:13
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