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support high-dimensional quantitative analysis of immune responses. Techniques include viral gene delivery, inducible gene expression, RNA-guided genome editing, and site-specific recombinases for applications related to biotechnology and cellular immunotherapy.
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tissue. Advances in chemical biology include synthetic molecules that modulate B cell activation, structurally complex carbohydrate tumor antigen and adjuvants synthesis, immunogenic chemotherapeutic agents and chemically homogeneous, synthetic vaccines.
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into induced neural stem cells. The team mixed the cells into an FDA-approved surgical glue that provided a physical support matrix. They administered the result to mice. Survival times increased from 160 to 220 percent, depending on the type of tumor.
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is the rational design and construction of synthetic systems that perform complex immunological functions. Functions include using specific cell markers to target cells for destruction and or interfering with immune reactions. US
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BagΓ³, Juli R.; Alfonso-Pecchio, Adolfo; Okolie, Onyi; Dumitru, Raluca; Rinkenbaugh, Amanda; Baldwin, Albert S.; Miller, C. Ryan; Magness, Scott T.; Hingtgen, Shawn D. (2016-02-02).
74:'s San Francisco biotech unit stated, βthe immune system will be the most convenient vehicle for , because they can move and migrate and play such important roles.β
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that can perform complex immunological tasks. Such strategies could produce organisms that perform multistep immune functions such as presenting
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formation and using small molecules to induce stem cells to differentiate into specific cell types. Dedifferentiation could be used to turn
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and are rarely allergenic. Synthetic antibody-recruiting small molecules have been created that redirect natural antibodies to
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484:"Therapeutically engineered induced neural stem cells are tumour-homing and inhibit progression of glioblastoma"
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Geering, Barbara; Fussenegger, Martin (2015-02-01). "Synthetic immunology: modulating the human immune system".
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Spiegel, David A. (2010-12-01). "Grand
Challenge Commentary: Synthetic immunology to engineer human immunity".
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Antibody therapeutics and other 'biologics' have proven to be effective in treating a diseases from
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The discipline emerged after 2010 following the development of genome editing technology including
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that became active only in the presence of a specific drug, allowing them to be turned on and off
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Deletion of a single transcription factor enables mature B cells to transform into T cells via
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and redifferentiation. Technologies that can control cell fate include strategies to induce
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production. Such engineered organisms have the potential be as safe and as inexpensive as
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67:. Another example is a T cell that targets only cells that display two separate markers.
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Design and construction of synthetic systems that perform complex immunological functions
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Therapeutic vaccines treat and immunize patients already infected with a given disease.
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Khan TA, Friedensohn S, de Vries ARG, Straszewski J, Ruscheweyh H-J, Reddy ST (2016).
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cells into inactive progenitors or to suppress rejection of transplanted organs.
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Researchers are exploring the creation of 'smart' organisms such as
544:"Ask the Expert - David Spiegel, Yale University... | ACS Network"
151:, in contrast, are generally inexpensive to produce, orally
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reactions, are administered by injection and are expensive.
229: β Interdisciplinary branch of biology and engineering
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to induce affinity maturation and isotype switching during
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in a specific manner, or providing integrated signals to
458:"Ordinary skin cells turned into brain tumor predators"
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therapy in which a patient's antigen-presenting target
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but precise in carrying out targeted interventions.
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59:. In 2015, one project created
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542:Cheung, Fred (May 25, 2012).
314:10.1016/j.tibtech.2014.10.006
91:Immunity-modulating organisms
25:Food and Drug Administration
456:Lavars, Nick (2016-02-24).
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70:In 2016, John Lin head of
163:Transdifferentiated cells
569:Arizona State University
302:Trends in Biotechnology
259:Nature Chemical Biology
562:"Synthetic immunology"
429:"Synthetic Immunology"
397:10.1126/sciadv.1501371
201:adoptive cell-transfer
107:to and co-stimulating
37:therapeutic antibodies
488:Nature Communications
352:MIT Technology Review
173:pluripotent stem cell
348:"Immune Engineering"
271:10.1038/nchembio.477
133:rheumatoid arthritis
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508:10.1038/ncomms10593
500:2016NatCo...710593B
389:2016SciA....2E1371K
221:Synthetic antibody
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169:dedifferentiation
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184:fibroblasts
598:Immunology
587:Categories
575:2016-02-25
571:iGem. 2013
553:2016-02-25
468:2016-02-26
442:2016-02-25
437:ETH Zurich
357:2016-02-25
234:References
205:autologous
177:autoimmune
121:probiotics
494:: 10593.
322:0167-7799
279:1552-4450
157:pathogens
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464:. Gizmag
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377:Sci. Adv
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287:21079593
215:See also
197:Provenge
191:Vaccines
117:antibody
101:bacteria
33:vaccines
31:agents,
517:4740908
496:Bibcode
406:4795664
385:Bibcode
113:B cells
105:antigen
65:in situ
61:T cells
47:History
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199:is an
137:cancer
72:Pfizer
57:CRISPR
53:TALENS
565:(PDF)
86:Types
522:PMID
411:PMID
326:PMID
318:ISSN
283:PMID
275:ISSN
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