Biology:T helper 17 cell

From HandWiki
Short description: Subset of pro-inflammatory T helper cells

T helper 17 cells (Th17) are a subset of pro-inflammatory T helper cells defined by their production of interleukin 17 (IL-17). They are related to T regulatory cells and the signals that cause Th17s to actually inhibit Treg differentiation.[1] However, Th17s are developmentally distinct from Th1 and Th2 lineages. Th17 cells play an important role in maintaining mucosal barriers and contributing to pathogen clearance at mucosal surfaces; such protective and non-pathogenic Th17 cells have been termed as Treg17 cells.[2]

They have also been implicated in autoimmune and inflammatory disorders. The loss of Th17 cell populations at mucosal surfaces has been linked to chronic inflammation and microbial translocation. These regulatory Th17 cells can be generated by TGF-beta plus IL-6 in vitro.

Differentiation

Like conventional regulatory T cells (Treg), induction of regulatory Treg17 cells could play an important role in modulating and preventing certain autoimmune diseases. Treg17 (Regulatory Th17) cells are generated from CD4+ T cells.

Transforming growth factor beta (TGF-β), interleukin 6 (IL-6), interleukin 21 (IL-21) and interleukin 23 (IL-23) contribute to Th17 formation in mice and humans. Key factors in the differentiation of Th17 cells are signal transducer and the activator of transcription 3 (Stat3) and retinoic acid receptor-related orphan receptors gamma (RORγ) and alpha (RORα).[3] Th17 cells are differentiated when naive T cells are exposed to the cytokines mentioned above. These cytokines are produced by activated antigen presenting cells (APCs) after contact with pathogens.[4] The Th17 cells can alter their differentiation program ultimately giving rise to either protective or pro-inflammatory pathogenic cells. The protective and non-pathogenic Th17 cells induced by IL-6 and TGF-β are termed as Treg17 cells. The pathogenic Th17 cells are induced by IL-23 and IL-1β.[5] IL-21, produced by Th17 cells themselves, has also been shown to initiate an alternative route for the activation of Th17 populations.[6] Both interferon gamma (IFNγ) and IL-4, the main stimulators of Th1 and Th2 differentiation, respectively, have been shown to inhibit Th17 differentiation.[citation needed]

Similar to Th17 cells the Treg17 development depended on the transcription factor Stat3.[7]

Function

Th17 cells play a role in adaptive immunity protecting the body against pathogens. However, anti-fungal immunity appears to be limited to particular sites with detrimental effects observed.[8] Their main effector cytokines are IL-17A, IL-17F, IL-21, and IL-22,[9] as well as granulocyte-macrophage colony-stimulating factor (GM-CSF). IL-17 family cytokines (IL-17A and IL-17F) target innate immune cells and epithelial cells, among others, to produce G-CSF and IL-8 (CXCL8), which leads to neutrophil production and recruitment. In this way, Th17 cell lineage appears to be one of the three major subsets of effector T cells, as these cells are involved in regulation of neutrophils, while Th2 cells regulate eosinophils, basophils and mast cells, and Th1 cells regulate macrophages and monocytes.[10] Thus, three T helper cell subsets are able to influence the myeloid part of the immune system, largely responsible for innate defense against pathogens.

Treg17 cells with regulatory phenotype with in vivo immune-suppressive properties in the gut have also been identified as rTh17 cells.[11]

Treg17 cells produce IL-17 and IL-10 and low level of IL-22 and suppress autoimmune and other immune responses. CD4+ T cells polarized with IL-23 and IL-6 are pathogenic upon adoptive transfer in type 1 diabetes while cells polarized with TGF-beta and IL-6 are not pathogenic.,[12][13] The intracellular aryl hydrocarbon receptor (AhR), which is activated by certain aromatic compounds, is specifically expressed in Treg17 cells.[14] These cells are regulated by IL-23 and TGF-beta.[15][16][17] The production of IL-22 in this subset of Th17 cells is regulated by AhR and Treg17 cells are depend on activation of the transcription factor Stat3. In a steady state, TGF-beta and AhR ligands induce low expression of IL-22 along with high expression of AhR, c-MAF, IL-10, and IL-21 that might play a protective role in cell regeneration and host microbiome homeostasis.

Th17 cells mediate the regression of tumors in mice,[18][19] but were also found to promote tumor formation induced by colonic inflammation in mice.[20] Like other T helper cells, Th17 cells closely interact with B cells in response to pathogens. Th17 cells are involved in B cell recruitment through CXCL13 chemokine signaling, and Th17 activity may encourage antibody production.[21]

Treg17 cells regulate the function of Th17 cells that are important role in the host defense against fungal and bacterial pathogens and participate in the pathogenesis of multiple inflammatory and autoimmune disorders. Selective deletion of Stat3 caused spontaneous severe colitis because of the lack of Treg17 cells and increase in pathogenic Th17 cells. The mechanism of Treg17 cell action is expression of chemokine receptor CCR6, which facilitates trafficking into areas of Th17 inflammation. This is also seen in human disease such glomerulonephritis (GN) in the kidney. Conversion of pathogenic Th17 cells in vivo at the conclusion of an inflammatory disease process by TGF-β results in the generation of Treg17 like cells.[22] There is also conservation across species of Treg17 cells.

In disease

The dysregulation of Th17 and switch to Th17 pathogenic phenotype cells have been associated with autoimmune disorders and inflammation. In the case of autoimmune disorders, Th17 cell over activation can cause an inappropriate amount of inflammation, like in the case of rheumatoid arthritis. Th17 cells have also been shown to be necessary for maintenance of mucosal immunity. In HIV, the loss of Th17 cell populations can contribute to chronic infection.

Role in autoimmune disorders

Th17 cells, particularly auto-specific Th17 cells, are associated with autoimmune disease such as multiple sclerosis, rheumatoid arthritis, and psoriasis.[9] Th17 overactivation against autoantigen will cause type 3 immune complex and complement-mediated hypersensitivity. Rheumatoid arthritis or Arthus reaction belong to this category.[23] Apart from autoantigen reactivity, Th17 cells' inherent biology of low end MAP kinases signalling, especially Erk1/2 and p38, help their survival by refusing activation induced cell death (AICD).[24] Together, excessive activity against autoantigen and prolonged existence of Th17 cells have deleterious consequence in autoimmune disease like Rheumatoid arthritis.[25]

Bone erosion caused by mature osteoclast cells is common in patients with rheumatoid arthritis. Activated T helper cells such as Th1, Th2, and Th17 are found in the synovial cavity during the time of inflammation due to rheumatoid arthritis. The known mechanisms associated with the differentiation of osteoclast precursors into mature osteoclasts involve the signaling molecules produced by immune-associated cells, as well as the direct cell to cell contact of osteoblasts and osteoclast precursors. However, it has been suggested that Th17 can also play a more major role in osteoclast differentiation via cell to cell contact with osteoclast precursors.[26][27]

Th17 cells may contribute to the development of late phase asthmatic response due to its increases in gene expression relative to Treg cells.[28]

Contribution of Th17 cells in HIV pathogenesis

The depletion of Th17 cell populations in the intestine disrupts the intestinal barrier, increases levels of movement of bacteria out of the gut through microbial translocation, and contributes to chronic HIV infection and progression to AIDS.[29] Microbial translocation results in bacteria moving from out of the gut lumen, into the lamina propria, to the lymph nodes, and beyond into non-lymphatic tissues. It can cause the constant immune activation seen through the body in the late stages of HIV. Increasing Th17 cell populations in the intestine has been shown to be both an effective treatment as well as possibly preventative.[30]

Although all CD4+ T cells gut are severely depleted by HIV, the loss of intestinal Th17 cells in particular has been linked to symptoms of chronic, pathogenic HIV and SIV infection. Microbial translocation is a major factor that contributes to chronic inflammation and immune activation in the context of HIV.[31] In non-pathogenic cases of SIV, microbial translocation is not observed. Th17 cells prevent severe HIV infection by maintaining the intestinal epithelial barrier during HIV infection in the gut.[30] Because of their high levels of CCR5 expression, the coreceptor for HIV, they are preferentially infected and depleted.[32] Thus, it is through Th17 cell depletion that microbial translocation occurs.

Additionally, the loss of Th17 cells in the intestine leads to a loss of balance between inflammatory Th17 cells and Treg cells, their anti-inflammatory counterparts. Because of their immunosuppressive properties, they are thought to decrease the anti-viral response to HIV, contributing to pathogenesis. There is more Treg activity compared to Th17 activity, and the immune response to the virus is less aggressive and effective.[29]

Revitalizing Th17 cells has been shown to decrease symptoms of chronic infection, including decreased inflammation, and results in improved responses to highly active anti-retroviral treatment (HAART). This is an important finding—microbial translocation general results in unresponsiveness to HAART. Patients continue to exhibit symptoms and do not show as reduced a viral load as expected.[33] In an SIV-rhesus monkey model, it was found that administering IL-21, a cytokine shown to encourage Th17 differentiation and proliferation, decreases microbial translocation by increasing Th17 cell populations.[30] It is hopeful that more immunotherapies targeting Th17 cells could help patients who do not respond well to HAART.

In addition, Th17 cells are cellular reservoirs of virus in patients submitted to antiretroviral therapy (in addition to the major cell sanctuary which are follicular Th cells) and should contribute to the latency of the HIV infection.[34]

Contribution of Th17 cells in tuberculosis

Recent studies have recognized that Th17 T cells may play a role in tuberculosis. Polyfunctional T cells with Th17 T cell features are depleted in individuals that progress to active TB after infection. In freshly resected lung tissue, from individuals with active or previous TB, CD4+ T cells have been identified that are enriched for IL-17–producing cells, including antigen specific T cells.[35] A cohort study conducted in Peru demonstrated that individuals who progressed to develop active TB after infection were depleted in Th17 functioning T cells.[36]

Role of vitamin D

The active form of vitamin D (1,25-Dihydroxyvitamin D3) has been found to 'severely impair' [37] production of the IL-17 and IL-17F cytokines by Th17 cells. Thus, active form of vitamin D is a direct inhibitor for Th17 differentiation. In this way, oral administration of vitamin D3 was proposed to be a promising tool for the treatment of Th17-mediated diseases.[38] In young patients with asthma 1,25-Dihydroxyvitamin D3-treated dendritic cells significantly reduced the percentage of Th17 cells, as well as IL-17 production.[39]

History of research

Intensive research starting in 2004 in mouse models elucidated its transcription factors and the cytokines that provoke differentiation.[40]

References

  1. ↑ "Th17 cells and regulatory T cells in elite control over HIV and SIV". Current Opinion in HIV and AIDS 6 (3): 221–7. May 2011. doi:10.1097/COH.0b013e32834577b3. PMID 21399494. 
  2. ↑ "Modulation of autoimmune diseases by interleukin (IL)-17 producing regulatory T helper (Th17) cells". The Indian Journal of Medical Research 138 (5): 591–4. November 2013. PMID 24434314. 
  3. ↑ "The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+ T helper cells". Cell 126 (6): 1121–33. September 2006. doi:10.1016/j.cell.2006.07.035. PMID 16990136. 
  4. ↑ "Th17 cytokines in mucosal immunity and inflammation". Current Opinion in HIV and AIDS 5 (2): 120–7. March 2010. doi:10.1097/coh.0b013e328335c2f6. PMID 20543588. 
  5. ↑ "Modulation of autoimmune diseases by interleukin (IL)-17 producing regulatory T helper (Th17) cells". The Indian Journal of Medical Research 138 (5): 591–4. November 2013. PMID 24434314. 
  6. ↑ "IL-21 initiates an alternative pathway to induce proinflammatory T(H)17 cells". Nature 448 (7152): 484–487. July 2007. doi:10.1038/nature05970. PMID 17581588. Bibcode: 2007Natur.448..484K. 
  7. ↑ "CD4+ regulatory T cells control TH17 responses in a Stat3-dependent manner". Science 326 (5955): 986–91. November 2009. doi:10.1126/science.1172702. PMID 19797626. Bibcode: 2009Sci...326..986C. 
  8. ↑ "C-type lectins, fungi and Th17 responses". Cytokine & Growth Factor Reviews 21 (6): 405–12. December 2010. doi:10.1016/j.cytogfr.2010.10.001. PMID 21075040. 
  9. ↑ 9.0 9.1 "Th17 cells in autoimmune and infectious diseases". International Journal of Inflammation 2014: 651503. Aug 2014. doi:10.1155/2014/651503. PMID 25152827. 
  10. ↑ "The Th17 pathway and inflammatory diseases of the intestines, lungs, and skin". Annual Review of Pathology 8 (1): 477–512. January 2013. doi:10.1146/annurev-pathol-011110-130318. PMID 23157335. 
  11. ↑ "Control of TH17 cells occurs in the small intestine". Nature 475 (7357): 514–8. July 2011. doi:10.1038/nature10228. PMID 21765430. 
  12. ↑ "Preventative role of interleukin-17 producing regulatory T helper type 17 (Treg 17) cells in type 1 diabetes in non-obese diabetic mice". Clinical and Experimental Immunology 182 (3): 261–9. December 2015. doi:10.1111/cei.12691. PMID 26250153. 
  13. ↑ "Th17 polarized cells from nonobese diabetic mice following mycobacterial adjuvant immunotherapy delay type 1 diabetes". Journal of Immunology 184 (9): 4779–88. May 2010. doi:10.4049/jimmunol.0902822. PMID 20363968. 
  14. ↑ "The aryl hydrocarbon receptor: multitasking in the immune system". Annual Review of Immunology 32: 403–32. 2014. doi:10.1146/annurev-immunol-032713-120245. PMID 24655296. 
  15. ↑ "Stat3 programs Th17-specific regulatory T cells to control GN". Journal of the American Society of Nephrology 25 (6): 1291–302. June 2014. doi:10.1681/ASN.2013080904. PMID 24511136. 
  16. ↑ "Generation of pathogenic T(H)17 cells in the absence of TGF-β signalling". Nature 467 (7318): 967–71. October 2010. doi:10.1038/nature09447. PMID 20962846. Bibcode: 2010Natur.467..967G. 
  17. ↑ "TGF-beta and IL-6 drive the production of IL-17 and IL-10 by T cells and restrain T(H)-17 cell-mediated pathology". Nature Immunology 8 (12): 1390–7. December 2007. doi:10.1038/ni1539. PMID 17994024. 
  18. ↑ "Tumor-specific Th17-polarized cells eradicate large established melanoma". Blood 112 (2): 362–73. July 2008. doi:10.1182/blood-2007-11-120998. PMID 18354038. 
  19. ↑ "T helper 17 cells promote cytotoxic T cell activation in tumor immunity". Immunity 31 (5): 787–98. November 2009. doi:10.1016/j.immuni.2009.09.014. PMID 19879162. 
  20. ↑ "A human colonic commensal promotes colon tumorigenesis via activation of T helper type 17 T cell responses". Nature Medicine 15 (9): 1016–22. September 2009. doi:10.1038/nm.2015. PMID 19701202. 
  21. ↑ "Translational mini-review series on Th17 cells: function and regulation of human T helper 17 cells in health and disease". Clinical and Experimental Immunology 159 (2): 109–19. February 2010. doi:10.1111/j.1365-2249.2009.04037.x. PMID 19912252. 
  22. ↑ "Th17 cells transdifferentiate into regulatory T cells during resolution of inflammation". Nature 523 (7559): 221–5. July 2015. doi:10.1038/nature14452. PMID 25924064. Bibcode: 2015Natur.523..221G. 
  23. ↑ "Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages". Nature Immunology 6 (11): 1123–32. November 2005. doi:10.1038/ni1254. PMID 16200070. 
  24. ↑ "Inherent low Erk and p38 activity reduce Fas Ligand expression and degranulation in T helper 17 cells leading to activation induced cell death resistance". Oncotarget 7 (34): 54339–54359. August 2016. doi:10.18632/oncotarget.10913. PMID 27486885. PMC 5342346. https://www.oncotarget.com/article/10913/text/. 
  25. ↑ "Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages". Nature Immunology 6 (11): 1123–32. November 2005. doi:10.1038/ni1254. PMID 16200070. https://www.nature.com/articles/ni1254. 
  26. ↑ "Physiological functions of osteoblast lineage and T cell-derived RANKL in bone homeostasis". Journal of Bone and Mineral Research 29 (4): 830–42. April 2014. doi:10.1002/jbmr.2096. PMID 24014480. 
  27. ↑ "Prominent bone loss mediated by RANKL and IL-17 produced by CD4+ T cells in TallyHo/JngJ mice". PLOS ONE 6 (3): e18168. March 2011. doi:10.1371/journal.pone.0018168. PMID 21464945. Bibcode: 2011PLoSO...618168W. 
  28. ↑ "Th17/Treg ratio derived using DNA methylation analysis is associated with the late phase asthmatic response". Allergy, Asthma, and Clinical Immunology 10 (1): 32. 24 June 2014. doi:10.1186/1710-1492-10-32. PMID 24991220. 
  29. ↑ 29.0 29.1 "Critical loss of the balance between Th17 and T regulatory cell populations in pathogenic SIV infection". PLOS Pathogens 5 (2): e1000295. February 2009. doi:10.1371/journal.ppat.1000295. PMID 19214220. 
  30. ↑ 30.0 30.1 30.2 "Maintenance of intestinal Th17 cells and reduced microbial translocation in SIV-infected rhesus macaques treated with interleukin (IL)-21". PLOS Pathogens 9 (7): e1003471. 2013-07-04. doi:10.1371/journal.ppat.1003471. PMID 23853592. 
  31. ↑ "Anatomical localization of commensal bacteria in immune cell homeostasis and disease". Immunological Reviews 260 (1): 35–49. July 2014. doi:10.1111/imr.12186. PMID 24942680. 
  32. ↑ "Loss and dysregulation of Th17 cells during HIV infection". Clinical & Developmental Immunology 2013: 852418. 2013-01-01. doi:10.1155/2013/852418. PMID 23762098. 
  33. ↑ "Microbial translocation is a cause of systemic immune activation in chronic HIV infection". Nature Medicine 12 (12): 1365–71. December 2006. doi:10.1038/nm1511. PMID 17115046. 
  34. ↑ Gosselin, Annie; Monteiro, Patricia; Chomont, Nicolas; Diaz-Griffero, Felipe; Said, Elias A.; Fonseca, Simone; Wacleche, Vanessa; El-Far, Mohamed et al. (30 December 2009). "Peripheral Blood CCR4+CCR6+ and CXCR3+CCR6+ CD4+ T Cells Are Highly Permissive to HIV-1 Infection". The Journal of Immunology 184 (3): 1604–1616. doi:10.4049/jimmunol.0903058. PMID 20042588. 
  35. ↑ "Tissue-resident-like CD4+ T cells secreting IL-17 control Mycobacterium tuberculosis in the human lung". The Journal of Clinical Investigation 131 (10). May 2021. doi:10.1172/JCI142014. PMID 33848273. 
  36. ↑ "Multimodally profiling memory T cells from a tuberculosis cohort identifies cell state associations with demographics, environment and disease". Nature Immunology 22 (6): 781–793. June 2021. doi:10.1038/s41590-021-00933-1. PMID 34031617. 
  37. ↑ "Vitamin D suppresses Th17 cytokine production by inducing C/EBP homologous protein (CHOP) expression". The Journal of Biological Chemistry 285 (50): 38751–5. December 2010. doi:10.1074/jbc.C110.185777. PMID 20974859. 
  38. ↑ "1,25-Dihydroxyvitamin D3 inhibits the differentiation and migration of T(H)17 cells to protect against experimental autoimmune encephalomyelitis". PLOS ONE 5 (9): e12925. September 2010. doi:10.1371/journal.pone.0012925. PMID 20886077. Bibcode: 2010PLoSO...512925C. 
  39. ↑ "Vitamin D reduces the differentiation and expansion of Th17 cells in young asthmatic children". Immunobiology 219 (11): 873–9. November 2014. doi:10.1016/j.imbio.2014.07.009. PMID 25128460. 
  40. ↑ Korn, Thomas; Bettelli, Estelle; Oukka, Mohamed; Kuchroo, Vijay K. (2009). "IL-17 and Th17 Cells". Annual Review of Immunology (Annual Reviews) 27 (1): 485–517. doi:10.1146/annurev.immunol.021908.132710. (VK ORCID: 0000-0001-7177-2110. GS: h6h5FdoAAAAJ). ISSN 0732-0582. PMID 19132915. 



Retrieved from "https://handwiki.org/wiki/index.php?title=Biology:T_helper_17_cell&oldid=3517804"