» Articles » PMID: 36189219

The Expanding Impact of T-regs in the Skin

Overview
Journal Front Immunol
Date 2022 Oct 3
PMID 36189219
Authors
Affiliations
Soon will be listed here.
Abstract

As the interface between the body and the environment, the skin functions as the physical barrier against external pathogens and toxic agents. In addition, the skin is an immunologically active organ with a plethora of resident adaptive and innate immune cells, as well as effector molecules that provide another layer of protection in the form of an immune barrier. A major subpopulation of these immune cells are the Foxp3 expressing CD4 T cells or regulatory T cells (T-regs). The canonical function of T-regs is to keep other immune cells in check during homeostasis or to dissipate a robust inflammatory response following pathogen clearance or wound healing. Interestingly, recent data has uncovered unconventional roles that vary between different tissues and we will highlight the emerging non-lymphoid functions of cutaneous T-regs. In light of the novel functions of other immune cells that are routinely being discovered in the skin, their regulation by T-regs implies that T-regs have executive control over a broad swath of biological activities in both homeostasis and disease. The blossoming list of non-inflammatory functions, whether direct or indirect, suggests that the role of T-regs in a regenerative organ such as the skin will be a field ripe for discovery for decades to come.

Citing Articles

Exosome-derived microRNAs: emerging players in vitiligo.

Li W, Pang Y, He Q, Song Z, Xie X, Zeng J Front Immunol. 2024; 15:1419660.

PMID: 39040109 PMC: 11260631. DOI: 10.3389/fimmu.2024.1419660.


Regulatory T cells in skin regeneration and wound healing.

Knoedler S, Knoedler L, Kauke-Navarro M, Rinkevich Y, Hundeshagen G, Harhaus L Mil Med Res. 2023; 10(1):49.

PMID: 37867188 PMC: 10591349. DOI: 10.1186/s40779-023-00484-6.

References
1.
Arruda L, Malmegrim K, Lima-Junior J, Clave E, Dias J, Moraes D . Immune rebound associates with a favorable clinical response to autologous HSCT in systemic sclerosis patients. Blood Adv. 2018; 2(2):126-141. PMC: 5787873. DOI: 10.1182/bloodadvances.2017011072. View

2.
Maurer M, Paus R, Czarnetzki B . Mast cells as modulators of hair follicle cycling. Exp Dermatol. 1995; 4(4 Pt 2):266-71. DOI: 10.1111/j.1600-0625.1995.tb00256.x. View

3.
Conteduca G, Rossi A, Megiorni F, Parodi A, Ferrera F, Tardito S . Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata. Clin Exp Med. 2012; 14(1):91-7. DOI: 10.1007/s10238-012-0224-3. View

4.
Marangoni R, Lu T . The roles of dermal white adipose tissue loss in scleroderma skin fibrosis. Curr Opin Rheumatol. 2017; 29(6):585-590. DOI: 10.1097/BOR.0000000000000437. View

5.
Varga J, Marangoni R . Systemic sclerosis in 2016: Dermal white adipose tissue implicated in SSc pathogenesis. Nat Rev Rheumatol. 2017; 13(2):71-72. DOI: 10.1038/nrrheum.2016.223. View