Antigen-Based Immune Therapeutics for Type 1 Diabetes Magic Bullets or Ordinary Blanks英文文献资料.docVIP
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Antigen-Based Immune Therapeutics for Type 1 Diabetes Magic Bullets or Ordinary Blanks英文文献资料
HindawiPublishingCorporation
ClinicalandDevelopmentalImmunology
Volume2011,ArticleID286248,15pages
doi:10.1155/2011/286248
ReviewArticle
Antigen-BasedImmuneTherapeuticsforType1Diabetes:
MagicBulletsorOrdinaryBlanks?
SlobodanCulina,1,2ChristianBoitard,1,2,3andRobertoMallone1,2,3
1
2
3
INSERM,U986,DeARLabAvenir,SaintVincentdePaulHospital,82avenueDenfertRochereau,75674ParisCedex14,France
Universit′eParis-Descartes,75006Paris,France
AssistancePubliqueH?opitauxdeParis,H?otelDieu,ServicedeDiab′etologie,75181Paris,France
CorrespondenceshouldbeaddressedtoRobertoMallone,roberto.mallone@inserm.fr
Received16January2011;Revised7March2011;Accepted8March2011
AcademicEditor:AzizAlamiChentou?
Copyright?2011SlobodanCulinaetal. This is an open access article distributed under the Creative Commons Attribution
License,whichpermitsunrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalworkisproperly
cited.
Theidealdrugofmodernmedicineistheonethatachievesitstherapeutictargetwithminimaladversee?ects.Immunetherapyof
Type1diabetes(T1D)isnoexception,andknowledgeoftheantigenstargetedbypathogenicTcellso?ersauniqueopportunity
towardsthisgoal.Di?erentantigenformulationsarebeingconsidered,suchasproteinsorpeptides,eitherintheirnativeform
ormodi?edadhoc,DNAplasmids,andcell-basedagents.Translationfrommousetohumanshouldtakeintoaccountimportant
di?erences,particularlyinthetimescaleofautoimmuneprogression,andintervention.Criticalparameterssuchasadministration
route,dosingandintervalremainlargelyempiricalandneedtobefurtherdissected. T1Dstagingthroughimmunesurrogate
markersbeforeandaftertreatmentwillbekeyinunderstandingtherapeuticactionsandto?nallyturnordinaryblanksintomagic
bullets.
1.Introduction
2.TranslatingtheNODMouseintoHuman
Type 1diabetes(T1D),one ofthe most commonautoim-
munediseases,stemsfromdefectsincentralandperipheral
tolerance that lead to progressive T-cell-mediated destruc-
tionof insulin-producing β cells in pancreatic islets. Clin-
ically, this destruction
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