WO2012092382A3 - Role of microrna in t cell immune response - Google Patents
Role of microrna in t cell immune response Download PDFInfo
- Publication number
- WO2012092382A3 WO2012092382A3 PCT/US2011/067615 US2011067615W WO2012092382A3 WO 2012092382 A3 WO2012092382 A3 WO 2012092382A3 US 2011067615 W US2011067615 W US 2011067615W WO 2012092382 A3 WO2012092382 A3 WO 2012092382A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- mir
- cell
- mirna
- inhibitor
- cell activation
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
- C12N15/1136—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against growth factors, growth regulators, cytokines, lymphokines or hormones
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/10—Type of nucleic acid
- C12N2310/11—Antisense
- C12N2310/113—Antisense targeting other non-coding nucleic acids, e.g. antagomirs
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/10—Type of nucleic acid
- C12N2310/14—Type of nucleic acid interfering N.A.
- C12N2310/141—MicroRNAs, miRNAs
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- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- General Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Microbiology (AREA)
- Plant Pathology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The present disclosure provides methods for increasing or decreasing T cell activation. The methods include contacting a T cell with an miRNA nucleic acid or an inhibitor of an miRNA. In some embodiments, the disclosed methods for increasing T cell activation include activating a T cell and contacting the activated T cell with an effective amount of an miRNA nucleic acid (such as one or more of miR-21, miR-101a, miR-377, let-7b, let-7c, or miR-574); or an inhibitor of an miRNA (for example, an inhibitor of one or more of miR-99a, miR-467b, miR- 467d, miR-199a, or miR-192), thereby increasing T cell activation, for example as compared to a control. In other embodiments, the disclosed methods for decreasing T cell activation include contacting a T cell (such as an activated T cell) with an effective amount of an inhibitor of an miRNA (for example, an inhibitor of one or more of miR-21, miR-101a, miR-377, let-7b, let-7c, or miR-574); or an miRNA nucleic acid (such as one or more of miR-99a, miR-467b, miR-467d, miR-199a, or miR-192), thereby decreasing the T cell activation, for example as compared to a control.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201061428112P | 2010-12-29 | 2010-12-29 | |
US61/428,112 | 2010-12-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2012092382A2 WO2012092382A2 (en) | 2012-07-05 |
WO2012092382A3 true WO2012092382A3 (en) | 2012-08-23 |
Family
ID=45476693
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2011/067615 WO2012092382A2 (en) | 2010-12-29 | 2011-12-28 | Role of microrna in t cell immune response |
Country Status (1)
Country | Link |
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WO (1) | WO2012092382A2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2890789A1 (en) * | 2012-08-31 | 2015-07-08 | Aptamir Therapeutics, Inc. | Mirna modulators of chronic visceral inflammation |
CN104474558B (en) * | 2014-12-25 | 2018-02-06 | 宜春学院 | Application of the microRNA in preparing synovium of joint apoptosis of fibroblasts biological agent |
US11285144B2 (en) | 2016-08-03 | 2022-03-29 | The Broad Institute, Inc. | Use of CDK8 inhibitors to treat diseases of inflammation and autoimmunity |
US11266676B2 (en) * | 2016-10-27 | 2022-03-08 | The Regents Of The University Of California | MicroRNA in T cell activation |
CN108359730A (en) * | 2018-04-26 | 2018-08-03 | 东南大学 | The application of miR-21 and its target gene in preparing diagnosis and/or prevention Osteoarthritis reagent or drug |
EP3954773A1 (en) * | 2020-08-12 | 2022-02-16 | Royal College of Surgeons in Ireland | Compositions and methods for the treatment of diseases by enhancing arginase 2 in macrophages |
-
2011
- 2011-12-28 WO PCT/US2011/067615 patent/WO2012092382A2/en active Application Filing
Non-Patent Citations (6)
Title |
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P. T. JINDRA ET AL: "Costimulation-Dependent Expression of MicroRNA-214 Increases the Ability of T Cells To Proliferate by Targeting Pten", THE JOURNAL OF IMMUNOLOGY, vol. 185, no. 2, 15 July 2010 (2010-07-15), pages 990 - 997, XP055022232, ISSN: 0022-1767, DOI: 10.4049/jimmunol.1000793 * |
SONKOLY E ET AL: "MiR-155 is overexpressed in patients with atopic dermatitis and modulates T-cell proliferative responses by targeting cytotoxic T lymphocyte-associated antigen 4", JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, MOSBY, INC, US, vol. 126, no. 3, 1 September 2010 (2010-09-01), pages 581 - 589.E20, XP027255745, ISSN: 0091-6749, [retrieved on 20100731] * |
SONKOLY ENIKÖ ET AL: "MicroRNAs and immunity: novel players in the regulation of normal immune function and inflammation.", SEMINARS IN CANCER BIOLOGY APR 2008 LNKD- PUBMED:18291670, vol. 18, no. 2, April 2008 (2008-04-01), pages 131 - 140, XP002671998, ISSN: 1096-3650 * |
VAN DER FITS LESLIE ET AL: "MicroRNA-21 expression in CD4+ T cells is regulated by STAT3 and is pathologically involved in Sézary syndrome.", THE JOURNAL OF INVESTIGATIVE DERMATOLOGY MAR 2011 LNKD- PUBMED:21085192, vol. 131, no. 3, 18 November 2010 (2010-11-18), pages 762 - 768, XP002671997, ISSN: 1523-1747 * |
WEN PAN ET AL: "MicroRNA-21 and MicroRNA-148a Contribute to DNA Hypomethylation in Lupus CD4(+) T Cells by Directly and Indirectly Targeting DNA Methyltransferase 1", JOURNAL OF IMMUNOLOGY, AMERICAN ASSOCIATION OF IMMUNOLOGISTS, US, vol. 184, no. 12, 15 June 2010 (2010-06-15), pages 6773 - 6781, XP002637321, ISSN: 0022-1767, [retrieved on 20100517], DOI: 10.4049/JIMMUNOL.0904060 * |
XUE Q ET AL: "Human activated CD4<+> T lymphocytes increase IL-2 expression by downregulating microRNA-181c", MOLECULAR IMMUNOLOGY, PERGAMON, GB, vol. 48, no. 4, 26 November 2010 (2010-11-26), pages 592 - 599, XP027578530, ISSN: 0161-5890, [retrieved on 20101229] * |
Also Published As
Publication number | Publication date |
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WO2012092382A2 (en) | 2012-07-05 |
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