FOXP3

FOXP3 (forkhead box P3), also known as scurfin, is a protein involved in immune system responses.[5] A member of the FOX protein family, FOXP3 appears to function as a master regulator of the regulatory pathway in the development and function of regulatory T cells.[6][7][8] Regulatory T cells generally turn the immune response down. In cancer, an excess of regulatory T cell activity can prevent the immune system from destroying cancer cells. In autoimmune disease, a deficiency of regulatory T cell activity can allow other autoimmune cells to attack the body's own tissues.[9][10]

FOXP3
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 3QRF, 4WK8
Identifiers
Aliases	FOXP3, AIID, DIETER, IPEX, JM2, PIDX, XPID, forkhead box P3
External IDs	OMIM: 300292 MGI: 1891436 HomoloGene: 8516 GeneCards: FOXP3
Gene location (Human) Chr. X chromosome (human)[1] Band Xp11.23 Start 49,250,438 bp[1] End 49,270,477 bp[1]
Gene location (Mouse) Chr. X chromosome (mouse)[2] Band X A1.1|X 3.41 cM Start 7,573,644 bp[2] End 7,595,245 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • sequence-specific DNA binding • NF-kappaB binding • GO:0001106 transcription corepressor activity • nucleic acid binding • transcription factor activity, RNA polymerase II distal enhancer sequence-specific binding • GO:0001948 protein binding • histone deacetylase binding • GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity • NFAT protein binding • histone acetyltransferase binding • metal ion binding • DNA binding • protein homodimerization activity • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific • GO:0000980 RNA polymerase II cis-regulatory region sequence-specific DNA binding Cellular component • cell nucleus • intracellular • cytoplasm • nucleoplasm • macromolecular complex Biological process • negative regulation of cell proliferation • negative regulation of NF-kappaB transcription factor activity • B cell homeostasis • regulation of isotype switching to IgG isotypes • myeloid cell homeostasis • negative regulation of inflammatory response • positive regulation of interleukin-4 production • regulation of immunoglobulin production • regulation of transcription from RNA polymerase II promoter • regulation of T cell anergy • negative regulation of interleukin-6 production • tolerance induction to self antigen • regulation of transcription, DNA-templated • negative regulation of sequence-specific DNA binding transcription factor activity • positive regulation of T cell tolerance induction • negative regulation of immune response • negative regulation of interferon-gamma production • tolerance induction • regulatory T cell differentiation • positive regulation of transcription, DNA-templated • negative regulation of interleukin-2 production • positive regulation of histone acetylation • negative regulation of interleukin-5 production • negative regulation of cytokine biosynthetic process • negative regulation of chronic inflammatory response • CD4-positive, CD25-positive, alpha-beta regulatory T cell differentiation • positive regulation of transcription from RNA polymerase II promoter • negative regulation of activated T cell proliferation • positive regulation of gene expression • negative regulation of interleukin-4 production • negative regulation of interleukin-10 production • negative regulation of tumor necrosis factor production • T cell homeostasis • negative regulation of CREB transcription factor activity • negative regulation of T-helper 17 cell differentiation • T cell activation • positive regulation of immature T cell proliferation in thymus • negative regulation of interferon-gamma biosynthetic process • positive regulation of regulatory T cell differentiation • negative regulation of transcription from RNA polymerase II promoter • positive regulation of peripheral T cell tolerance induction • positive regulation of transforming growth factor beta1 production • negative regulation of transcription, DNA-templated • negative regulation of lymphocyte proliferation • negative regulation of histone acetylation • negative regulation of interleukin-17 production • response to virus • negative regulation of histone deacetylation • CD4-positive, CD25-positive, alpha-beta regulatory T cell lineage commitment • positive regulation of CD4-positive, CD25-positive, alpha-beta regulatory T cell differentiation • negative regulation of T cell proliferation • chromatin remodeling • cytokine production • negative regulation of T cell cytokine production • negative regulation of isotype switching to IgE isotypes • negative regulation of cytokine secretion • negative regulation of interleukin-2 biosynthetic process • T cell receptor signaling pathway • positive regulation of T cell anergy • transcription, DNA-templated • T cell mediated immunity • negative regulation of gene expression • anatomical structure morphogenesis • regulation of Wnt signaling pathway • regulation of regulatory T cell differentiation Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	50943	20371
Ensembl	ENSG00000049768	ENSMUSG00000039521
UniProt	Q9BZS1	Q99JB6
RefSeq (mRNA)	NM_001114377 NM_014009	NM_001199347 NM_001199348 NM_054039
RefSeq (protein)	NP_001107849 NP_054728	NP_001186276 NP_001186277 NP_473380
Location (UCSC)	Chr X: 49.25 – 49.27 Mb	Chr X: 7.57 – 7.6 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

While the precise control mechanism has not yet been established, FOX proteins belong to the forkhead/winged-helix family of transcriptional regulators and are presumed to exert control via similar DNA binding interactions during transcription. In regulatory T cell model systems, the FOXP3 transcription factor occupies the promoters for genes involved in regulatory T-cell function, and may inhibit transcription of key genes following stimulation of T cell receptors.[11]

Structure

The human FOXP3 genes contain 11 coding exons. Exon-intron boundaries are identical across the coding regions of the mouse and human genes. By genomic sequence analysis, the FOXP3 gene maps to the p arm of the X chromosome (specifically, Xp11.23).[5][12]

Physiology

Foxp3 is a specific marker of natural T regulatory cells (nTregs, a lineage of T cells) and adaptive/induced T regulatory cells (a/iTregs), also identified by other less specific markers such as CD25 or CD45RB.[6][7][8] In animal studies, Tregs that express Foxp3 are critical in the transfer of immune tolerance, especially self-tolerance.[13]

The induction or administration of Foxp3 positive T cells has, in animal studies, led to marked reductions in (autoimmune) disease severity in models of diabetes, multiple sclerosis, asthma, inflammatory bowel disease, thyroiditis and renal disease.[14] Human trials using regulatory T cells to treat graft-versus-host disease have shown efficacy.[15][16]

Further work has shown that T cells are more plastic in nature than originally thought.[17][18][19] This means that the use of regulatory T cells in therapy may be risky, as the T regulatory cell transferred to the patient may change into T helper 17 (Th17) cells, which are pro-inflammatory rather than regulatory cells.[17] Th17 cells are proinflammatory and are produced under similar environments as a/iTregs.[17] Th17 cells are produced under the influence of TGF-β and IL-6 (or IL-21), whereas a/iTregs are produced under the influence of solely TGF-β, so the difference between a proinflammatory and a pro-regulatory scenario is the presence of a single interleukin. IL-6 or IL-21 is being debated by immunology laboratories as the definitive signaling molecule. Murine studies point to IL-6 whereas human studies have shown IL-21. Foxp3 is the major transcription factor controlling T-regulatory cells (T_reg or CD4⁺ cells).[20] CD4⁺ cells are leukocytes responsible for protecting animals from foreign invaders such as bacteria and viruses.[20] Defects in this gene's ability to function can cause IPEX syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome as well as numerous cancers.[21] While CD4⁺ cells are heavily regulated and require multiple transcription factors such as STAT-5 and AhR in order to become active and function properly, Foxp3 has been identified as the master regulator for T_reg lineage.[20] Foxp3 can either act as a transcriptional activator or suppressor depending on what specific transcriptional factors such as deacetylases and histone acetylases are acting on it.[20] The Foxp3 gene is also known to convert naïve T-cells to T_reg cells, which are capable of an in vivo and in vitro suppressive capabilities suggesting that Foxp3 is capable of regulating the expression of suppression-mediating molecules.[20] Clarifying the gene targets of Foxp3 could be crucial to the comprehension of the suppressive abilities of T_reg cells.

Pathophysiology

In human disease, alterations in numbers of regulatory T cells – and in particular those that express Foxp3 – are found in a number of disease states. For example, patients with tumors have a local relative excess of Foxp3 positive T cells which inhibits the body's ability to suppress the formation of cancerous cells.[22] Conversely, patients with an autoimmune disease such as systemic lupus erythematosus (SLE) have a relative dysfunction of Foxp3 positive cells.[23] The Foxp3 gene is also mutated in IPEX syndrome (Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-linked).[24] Many patients with IPEX have mutations in the DNA-binding forkhead domain of FOXP3.[25]

In mice, a Foxp3 mutation (a frameshift mutation that result in protein lacking the forkhead domain) is responsible for 'Scurfy', an X-linked recessive mouse mutant that results in lethality in hemizygous males 16 to 25 days after birth.[5] These mice have overproliferation of CD4⁺ T-lymphocytes, extensive multiorgan infiltration, and elevation of numerous cytokines. This phenotype is similar to those that lack expression of CTLA-4, TGF-β, human disease IPEX, or deletion of the Foxp3 gene in mice ("scurfy mice"). The pathology observed in scurfy mice seems to result from an inability to properly regulate CD4⁺ T-cell activity. In mice overexpressing the Foxp3 gene, fewer T cells are observed. The remaining T cells have poor proliferative and cytolytic responses and poor interleukin-2 production, although thymic development appears normal. Histologic analysis indicates that peripheral lymphoid organs, particularly lymph nodes, lack the proper number of cells.

Role in cancer

In addition to FoxP3's role in regulatory T cell differentiation, multiple lines of evidence have indicated that FoxP3 play important roles in cancer development.

Down-regulation of FoxP3 expression has been reported in tumour specimens derived from breast, prostate, and ovarian cancer patients, indicating that FoxP3 is a potential tumour suppressor gene. Expression of FoxP3 was also detected in tumour specimens derived from additional cancer types, including pancreatic, melanoma, liver, bladder, thyroid, cervical cancers. However, in these reports, no corresponding normal tissues was analyzed, therefore it remained unclear whether FoxP3 is a pro- or anti-tumourigeneic molecule in these tumours.

Two lines of functional evidence strongly supported that FoxP3 serves as tumour suppressive transcription factor in cancer development. First, FoxP3 represses expression of HER2, Skp2, SATB1 and MYC oncogenes and induces expression of tumour suppressor genes P21 and LATS2 in breast and prostate cancer cells. Second, over-expression of FoxP3 in melanoma, glioma, breast, prostate and ovarian cancer cell lines induces profound growth inhibitory effects in vitro and in vivo. However, this hypothesis need to be further investigated in future studies.

Foxp3 is a recruiter of other anti-tumor enzymes such as CD39 and CD8.[21] The overexpression of CD39 is found in patients with multiple cancer types such as melanoma, leukemia, pancreatic cancer, colon cancer, and ovarian cancer.[21] This overexpression may be protecting tumorous cells, allowing them to create their “escape phase”.[21] A cancerous tumor's “escape phase” is where the tumor grows quickly and it becomes clinically invisible by becoming independent of the extracellular matrix and creating its own immunosuppressive tumor microenvironment.[21] The consequences of a cancer cell reaching the “escape phase” is that it allows it to completely evade the immune system, which reduces the immunogenicity and ability to become clinically detected, allowing it to progress and spread throughout the body. Some cancer patients have also been known to display higher numbers of mutated CD4⁺ cells. These mutated cells will then produce large quantities of TGF-β and IL-10, (a Transforming Growth Factor β and an inhibitory cytokine respectively,) which will suppress signals to the immune system and allow for tumor escape.[21] In one experiment a 15-mer synthetic peptide, P60, was able to inhibit Foxp3's ability to function. P60 did this by entering the cells and then binding to Foxp3, where it hinders Foxp3's ability to translocate to the nucleus.[26] Due to this, Foxp3 could no longer properly suppress the transcription factors NF-kB and NFAT; both of which are protein complexes that regulate transcription of DNA, cytokine production and cell survival.[26] This would inhibit a cell's ability to perform apoptosis and stop its own cell cycle, which could potentially allow an affected cancerous cell to survive and reproduce.

Autoimmune

Mutations or disruptions of the Foxp3 regulatory pathway can lead to organ-specific autoimmune diseases such as autoimmune thyroiditis and type 1 diabetes mellitus.[27] These mutations affect thymocytes developing within the thymus. Regulated by Foxp3, it's these thymocytes that during thymopoiesis, are transformed into mature Treg cells by the thymus.[27] It was found that patients who have the autoimmune disease systemic lupus erythematosus (SLE) possess Foxp3 mutations that affect the thymopoiesis process, preventing the proper development of T_reg cells within the thymus.[27] These malfunctioning T_reg cells aren’t efficiently being regulated by its transcription factors, which cause them to attack cells that are healthy, leading to these organ-specific autoimmune diseases. Another way that Foxp3 helps keep the autoimmune system at homeostasis is through its regulation of the expression of suppression-mediating molecules. For instance, Foxp3 is able to facilitate the translocation of extracellular adenosine into the cytoplasm.[28] It does this by recruiting CD39, a rate-limiting enzyme that's vital in tumor suppression to hydrolyze ATP to ADP in order to regulate immunosuppression on different cell populations.[28]

See also

• Autoimmune regulator (AIRE)
• Autoimmunity
• Central tolerance
• Immunity
• IPEX syndrome
• Lymphocytes
• Thymocyte

References

1. GRCh38: Ensembl release 89: ENSG00000049768 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000039521 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Brunkow ME, Jeffery EW, Hjerrild KA, Paeper B, Clark LB, Yasayko SA, Wilkinson JE, Galas D, Ziegler SF, Ramsdell F (January 2001). "Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse". Nature Genetics. 27 (1): 68–73. doi:10.1038/83784. PMID 11138001.
6. Hori S, Nomura T, Sakaguchi S (February 2003). "Control of regulatory T cell development by the transcription factor Foxp3". Science. 299 (5609): 1057–61. doi:10.1126/science.1079490. PMID 12522256.
7. Fontenot JD, Gavin MA, Rudensky AY (April 2003). "Foxp3 programs the development and function of CD4+CD25+ regulatory T cells". Nature Immunology. 4 (4): 330–6. doi:10.1038/ni904. PMID 12612578.
8. Fontenot JD, Rasmussen JP, Williams LM, Dooley JL, Farr AG, Rudensky AY (March 2005). "Regulatory T cell lineage specification by the forkhead transcription factor foxp3". Immunity. 22 (3): 329–41. doi:10.1016/j.immuni.2005.01.016. PMID 15780990.
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10. Zhang L, Zhao Y (June 2007). "The regulation of Foxp3 expression in regulatory CD4(+)CD25(+)T cells: multiple pathways on the road". Journal of Cellular Physiology. 211 (3): 590–7. doi:10.1002/jcp.21001. PMID 17311282.
11. Marson A, Kretschmer K, Frampton GM, Jacobsen ES, Polansky JK, MacIsaac KD, Levine SS, Fraenkel E, von Boehmer H, Young RA (February 2007). "Foxp3 occupancy and regulation of key target genes during T-cell stimulation". Nature. 445 (7130): 931–5. doi:10.1038/nature05478. PMC 3008159. PMID 17237765.
12. Bennett CL, Yoshioka R, Kiyosawa H, Barker DF, Fain PR, Shigeoka AO, Chance PF (February 2000). "X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3". American Journal of Human Genetics. 66 (2): 461–8. doi:10.1086/302761. PMC 1288099. PMID 10677306.
13. Ohki H, Martin C, Corbel C, Coltey M, Le Douarin NM (August 1987). "Tolerance induced by thymic epithelial grafts in birds". Science. 237 (4818): 1032–5. doi:10.1126/science.3616623. PMID 3616623.
14. Suri-Payer E, Fritzsching B (August 2006). "Regulatory T cells in experimental autoimmune disease". Springer Seminars in Immunopathology. 28 (1): 3–16. doi:10.1007/s00281-006-0021-8. PMID 16838180.
15. Brunstein CG, Miller JS, Cao Q, McKenna DH, Hippen KL, Curtsinger J, Defor T, Levine BL, June CH, Rubinstein P, McGlave PB, Blazar BR, Wagner JE (January 2011). "Infusion of ex vivo expanded T regulatory cells in adults transplanted with umbilical cord blood: safety profile and detection kinetics". Blood. 117 (3): 1061–70. doi:10.1182/blood-2010-07-293795. PMC 3035067. PMID 20952687.
16. Di Ianni M, Falzetti F, Carotti A, Terenzi A, Castellino F, Bonifacio E, Del Papa B, Zei T, Ostini RI, Cecchini D, Aloisi T, Perruccio K, Ruggeri L, Balucani C, Pierini A, Sportoletti P, Aristei C, Falini B, Reisner Y, Velardi A, Aversa F, Martelli MF (April 2011). "Tregs prevent GVHD and promote immune reconstitution in HLA-haploidentical transplantation". Blood. 117 (14): 3921–8. doi:10.1182/blood-2010-10-311894. PMID 21292771.
17. Zhou L, Chong MM, Littman DR (May 2009). "Plasticity of CD4+ T cell lineage differentiation". Immunity. 30 (5): 646–55. doi:10.1016/j.immuni.2009.05.001. PMID 19464987.
18. Bluestone JA, Mackay CR, O'Shea JJ, Stockinger B (November 2009). "The functional plasticity of T cell subsets". Nature Reviews. Immunology. 9 (11): 811–6. doi:10.1038/nri2654. PMC 3075537. PMID 19809471.
19. Murphy KM, Stockinger B (August 2010). "Effector T cell plasticity: flexibility in the face of changing circumstances". Nature Immunology. 11 (8): 674–80. doi:10.1038/ni.1899. PMC 3249647. PMID 20644573.
20. Rudensky AY (May 2011). "Regulatory T cells and Foxp3". Immunological Reviews. 241 (1): 260–8. doi:10.1111/j.1600-065X.2011.01018.x. PMC 3077798. PMID 21488902.
21. Hori S, Nomura T, Sakaguchi S (February 2003). "Control of regulatory T cell development by the transcription factor Foxp3". Science. 299 (5609): 1057–61. doi:10.1126/science.1079490. PMID 12522256.
22. Beyer M, Schultze JL (August 2006). "Regulatory T cells in cancer". Blood. 108 (3): 804–11. doi:10.1182/blood-2006-02-002774. PMID 16861339.
23. Alvarado-Sánchez B, Hernández-Castro B, Portales-Pérez D, Baranda L, Layseca-Espinosa E, Abud-Mendoza C, Cubillas-Tejeda AC, González-Amaro R (September 2006). "Regulatory T cells in patients with systemic lupus erythematosus". Journal of Autoimmunity. 27 (2): 110–8. doi:10.1016/j.jaut.2006.06.005. PMID 16890406.
24. Bennett CL, Christie J, Ramsdell F, Brunkow ME, Ferguson PJ, Whitesell L, Kelly TE, Saulsbury FT, Chance PF, Ochs HD (January 2001). "The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3". Nature Genetics. 27 (1): 20–1. doi:10.1038/83713. PMID 11137993.
25. van der Vliet, HJ; Nieuwenhuis, EE (2007). "IPEX as a Result of Mutations in FOXP3". Clin Dev Immunol. 2007: 89017. PMC 2248278.
26. Casares N, Rudilla F, Arribillaga L, Llopiz D, Riezu-Boj JI, Lozano T, López-Sagaseta J, Guembe L, Sarobe P, Prieto J, Borrás-Cuesta F, Lasarte JJ (November 2010). "A peptide inhibitor of FOXP3 impairs regulatory T cell activity and improves vaccine efficacy in mice". Journal of Immunology. 185 (9): 5150–9. doi:10.4049/jimmunol.1001114. PMID 20870946.
27. Hori S, Nomura T, Sakaguchi S (February 2003). "Control of regulatory T cell development by the transcription factor Foxp3". Science. 299 (5609): 1057–61. doi:10.1126/science.1079490. PMID 12522256.
28. Cai XY, Ni XC, Yi Y, He HW, Wang JX, Fu YP, Sun J, Zhou J, Cheng YF, Jin JJ, Fan J, Qiu SJ (October 2016). "Overexpression of CD39 in hepatocellular carcinoma is an independent indicator of poor outcome after radical resection". Medicine. 95 (40): e4989. doi:10.1097/md.0000000000004989. PMC 5059057. PMID 27749555.

Further reading

• Wu Y, Borde M, Heissmeyer V, Feuerer M, Lapan AD, Stroud JC, Bates DL, Guo L, Han A, Ziegler SF, Mathis D, Benoist C, Chen L, Rao A (July 2006). "FOXP3 controls regulatory T cell function through cooperation with NFAT". Cell. 126 (2): 375–87. doi:10.1016/j.cell.2006.05.042. PMID 16873067.
• Schmidt-Weber CB, Blaser K (September 2005). "The role of the FOXP3 transcription factor in the immune regulation of allergic asthma". Current Allergy and Asthma Reports. 5 (5): 356–61. doi:10.1007/s11882-005-0006-z. PMID 16091206.
• Li B, Samanta A, Song X, Furuuchi K, Iacono KT, Kennedy S, Katsumata M, Saouaf SJ, Greene MI (August 2006). "FOXP3 ensembles in T-cell regulation". Immunological Reviews. 212: 99–113. doi:10.1111/j.0105-2896.2006.00405.x. PMID 16903909.
• Ziegler SF (January 2007). "FOXP3: not just for regulatory T cells anymore". European Journal of Immunology. 37 (1): 21–3. doi:10.1002/eji.200636929. PMID 17183612.
• Bacchetta R, Gambineri E, Roncarolo MG (August 2007). "Role of regulatory T cells and FOXP3 in human diseases". The Journal of Allergy and Clinical Immunology. 120 (2): 227–35, quiz 236–7. doi:10.1016/j.jaci.2007.06.023. PMID 17666212.
• Ochs HD, Torgerson TR (2007). Immune dysregulation, polyendocrinopathy, enteropathy, X-linked inheritance: model for autoaggression. Advances in Experimental Medicine and Biology. 601. pp. 27–36. doi:10.1007/978-0-387-72005-0_3. ISBN 978-0-387-72004-3. PMID 17712989.
• Long E, Wood KJ (August 2007). "Understanding FOXP3: progress towards achieving transplantation tolerance". Transplantation. 84 (4): 459–61. doi:10.1097/01.tp.0000275424.52998.ad. PMID 17713426.
• Hartley JL, Temple GF, Brasch MA (November 2000). "DNA cloning using in vitro site-specific recombination". Genome Research. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.
• Chatila TA, Blaeser F, Ho N, Lederman HM, Voulgaropoulos C, Helms C, Bowcock AM (December 2000). "JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome". The Journal of Clinical Investigation. 106 (12): R75–81. doi:10.1172/JCI11679. PMC 387260. PMID 11120765.
• Wildin RS, Ramsdell F, Peake J, Faravelli F, Casanova JL, Buist N, Levy-Lahad E, Mazzella M, Goulet O, Perroni L, Bricarelli FD, Byrne G, McEuen M, Proll S, Appleby M, Brunkow ME (January 2001). "X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy". Nature Genetics. 27 (1): 18–20. doi:10.1038/83707. PMID 11137992.
• Schubert LA, Jeffery E, Zhang Y, Ramsdell F, Ziegler SF (October 2001). "Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation". The Journal of Biological Chemistry. 276 (40): 37672–9. doi:10.1074/jbc.M104521200. PMID 11483607.
• Kobayashi I, Shiari R, Yamada M, Kawamura N, Okano M, Yara A, Iguchi A, Ishikawa N, Ariga T, Sakiyama Y, Ochs HD, Kobayashi K (December 2001). "Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)". Journal of Medical Genetics. 38 (12): 874–6. doi:10.1136/jmg.38.12.874. PMC 1734795. PMID 11768393.
• Tommasini A, Ferrari S, Moratto D, Badolato R, Boniotto M, Pirulli D, Notarangelo LD, Andolina M (October 2002). "X-chromosome inactivation analysis in a female carrier of FOXP3 mutation". Clinical and Experimental Immunology. 130 (1): 127–30. doi:10.1046/j.1365-2249.2002.01940.x. PMC 1906506. PMID 12296863.
• Bassuny WM, Ihara K, Sasaki Y, Kuromaru R, Kohno H, Matsuura N, Hara T (June 2003). "A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes". Immunogenetics. 55 (3): 149–56. doi:10.1007/s00251-003-0559-8. PMID 12750858.
• Walker MR, Kasprowicz DJ, Gersuk VH, Benard A, Van Landeghen M, Buckner JH, Ziegler SF (November 2003). "Induction of FoxP3 and acquisition of T regulatory activity by stimulated human CD4+CD25- T cells". The Journal of Clinical Investigation. 112 (9): 1437–43. doi:10.1172/JCI19441. PMC 228469. PMID 14597769.
• Owen CJ, Jennings CE, Imrie H, Lachaux A, Bridges NA, Cheetham TD, Pearce SH (December 2003). "Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome". The Journal of Clinical Endocrinology and Metabolism. 88 (12): 6034–9. doi:10.1210/jc.2003-031080. PMID 14671208.

External links

• GeneReviews/NIH/NCBI/UW entry on IPEX Syndrome
• FOXP3+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)