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CD4+CD25+ Regulatory T Cells: Origin, Function and Therapeutic Potential (Paperback, Softcover reprint of hardcover 1st ed. 2005) Loot Price: R5,167
Discovery Miles 51 670
CD4+CD25+ Regulatory T Cells: Origin, Function and Therapeutic Potential (Paperback, Softcover reprint of hardcover 1st ed....

CD4+CD25+ Regulatory T Cells: Origin, Function and Therapeutic Potential (Paperback, Softcover reprint of hardcover 1st ed. 2005)

B. Kyewski, Elisabeth Suri-Payer

Series: Current Topics in Microbiology and Immunology, 293

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Loot Price R5,167 Discovery Miles 51 670 | Repayment Terms: R484 pm x 12*

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The vertebrate immune system defends the organism against invading pathogens while at the same time being self-tolerant to the body's own constituentsthuspreservingitsintegrity. Multiplemechanismsactinconcert to ensure self-tolerance. During intrathymic development, the nascent T cell repertoire is purged from autoreactive T cells via negative selection, a process also known as recessive tolerance. Ridding of self-reactivity, however, isnotcomplete, asattestedbythepresenceofself-reactiveTcells intheperipheralTcellrepertoire. Hence, additionaltolerancemechanisms, collectively referred to as dominant tolerance, have been postulated on theoreticalgrounds(seethechapterbyA. Coutinhoetal. inthisvolume)and experimentalprooffortheirexistencehadbeenrepeatedlyclaimedinthepast 40years. Whilesomeoftheseclaims, largelybasedoninvitroexperiments, laterfellintodisrepute(i. e., theinfamousCD8suppressorcellsexpressingI-J molecules), concurrent, butlesswellpublicizedstringsofresearch, provided unremitting evidence for dominant tolerance mechanisms. These include the postnatal thymectomy model pioneered by Nishizuka and Sakakura in 1969, the dominant tolerance model in chicken and quail chimeras introducedbyleDouarinandcolleagues, andstudiesoninfectioustolerance by the Waldmann laboratory. A breakthrough in this ?eld was achieved by the identi?cation and isolation by Sakaguchi's and Shevach's groups of + + aCD4 CD25 TcellsubsetexertingsuppressiononeffectorTcellsbothin vitroandinvivo. Thisinstigatedanavalancheofpublicationsonsuppressor Tcells. Whilelargelyoverlookedforsomanyyears, thereisnowhardlyany aspectofimmunitythatdoesnotseemtobeaffectedbysuppressorTcells. This volume will hardly be more than a snapshot in thisfast-moving ?eld, yetwehopethatitwillofferinspirationandorientationtothescientistwho wouldliketoenterthis?eld. To date, many different cells have been described that can suppress + + other cells of the immune system: CD4 CD25 regulatory T cells (Treg), + ? CD4 CD25 regulatory T cells, T regulatory 1 cells (Tr1), T-helper 3 cells + ? (Th3), CD8 CD28 Tcells, NKTcells, aswellastolerogenicdendriticcells. Suppressive CD4 T cells fall at least into two categories. So called natural VI Preface + + CD4 CD25 Tregformpartoftheintra-thymicallyselectedTcellrepertoire andapparentlyconstituteadistinctlineage. Incontrast,"adaptive"regulatory Tcellsareinstructedintheperipherytobecomesuppressivecells, theyform + + amoreheterogeneousgroupincludingCD4 CD25 Treg, Tr1, andTh3cells. As natural Treg are so far the best characterized entity, the ?rst three contributionsofthisvolume(C. Cozzoetal., C. -S. Hsiehetal., andL.

General

Imprint: Springer-Verlag
Country of origin: Germany
Series: Current Topics in Microbiology and Immunology, 293
Release date: October 2010
First published: 2005
Editors: B. Kyewski • Elisabeth Suri-Payer
Dimensions: 235 x 155 x 18mm (L x W x T)
Format: Paperback
Pages: 332
Edition: Softcover reprint of hardcover 1st ed. 2005
ISBN-13: 978-3-642-06376-3
Categories: Books > Medicine > Clinical & internal medicine > Diseases & disorders > Immunology > General
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LSN: 3-642-06376-4
Barcode: 9783642063763

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