Clinical manifestations and treatment of EpsteinBarr virus infectionWord格式.docx
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Clinical manifestations and treatment of EpsteinBarr virus infectionWord格式.docx
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SheldonLKaplan,MD
DeputyEditor
JenniferMitty,MD,MPH
Disclosures
Alltopicsareupdatedasnewevidencebecomesavailableandourpeerreviewprocessiscomplete.
Literaturereviewcurrentthrough:
Feb2014.|Thistopiclastupdated:
三月18,2013.
INTRODUCTION
—
Epstein-Barrvirus(EBV)isawidelydisseminatedherpesvirusthatisspreadbyintimatecontactbetweensusceptiblepersonsandasymptomaticEBVshedders.EBVistheprimaryagentofinfectiousmononucleosis(IM),persistsasymptomaticallyforlifeinnearlyalladults,andisassociatedwiththedevelopmentofBcelllymphomas,Tcelllymphomas,Hodgkinlymphomaandnasopharyngealcarcinomasincertainpatients.ReactivationdiseaseisnotaprominentissuewithEBV,incontrasttoothercommonherpesviruses,butithasbeenassociatedwithanaggressivelymphoproliferativedisorderintransplantrecipients[1].(See"
Treatmentandpreventionofpost-transplantlymphoproliferativedisorders"
.)
TheclinicalmanifestationsandtreatmentofEBVinfectionswillbereviewedhere.ThediagnosisofEBVaspertainstoinfectiousmononucleosisisdiscussedseparately.(See"
Infectiousmononucleosisinadultsandadolescents"
EPIDEMIOLOGY
ThemajorityofprimaryEBVinfectionsthroughouttheworldaresubclinicalandinapparent.AntibodiestoEBVhavebeendemonstratedinallpopulationgroupswithaworldwidedistribution;
approximately90to95percentofadultsareEBV-seropositive.ThehostrangeofEBVisrestrictedtohumansandcertainsubhumanprimatesincludingsquirrelmonkeysandcottontopmarmosets[2].
VIROLOGY
Likeothermembersoftheherpesvirusfamily,EBVhasalatencyphase.ThehostcellsfortheorganisminhumansarelimitedtoBlymphocytes,Tlymphocytes,epithelialcellsandmyocytes.Unlikeherpessimplex(HSV)orcytomegalovirus(CMV),EBViscapableoftransformingBcellsbutdoesnotroutinelydisplayacytopathiceffect.AdetaileddiscussionofthevirologyofEBVisfoundelsewhere.(See"
VirologyofEpstein-Barrvirus"
PRIMARYINFECTION
EBVcancauseanumberofprimaryinfections,canleadtocomplications,andcaninduceavarietyofmalignancies.
Acuteinfectiousmononucleosis
Infectiousmononucleosis(IM)isthebestknownacuteclinicalmanifestationofEBV.IMoftenbeginswithmalaise,headache,andlow-gradefeverbeforedevelopmentofthemorespecificsignsoftonsillitisand/orpharyngitis,cervicallymphnodeenlargementandtenderness,andmoderatetohighfever[3].Affectedpatientsusuallyhaveperipheralbloodlymphocytosis,composedinlargemeasureofatypicallymphocytes(picture1).(See"
Thelymphadenopathycharacteristicallyissymmetricandinvolvestheposteriorcervicalchainmorethantheanteriorchain.Tonsillarexudateisafrequentcomponentofthepharyngitis;
theexudatecanhaveawhite,gray-green,ornecroticappearance.
Severefatiguemaybeprominent,whileotherlesscommonfindingsincludepalatalpetechiae,periorbitalorpalpebraledema,andmaculopapularormorbilliformrashes.Nausea,vomiting,andanorexiaarefrequentinpatientswithIM,probablyreflectingthemildhepatitisencounteredinabout90percentofinfectedindividuals.Splenomegalyoccursinasmanyas50percentofpatients,butjaundiceandhepatomegalyareuncommon.
MostpatientswithIMcausedbyEBVhaveprominentpharyngealsymptoms[4].Thereare,however,severalotherformsoftheillness.SomeindividualswithIMpresentwiththeso-called“glandular”formofthediseaseinwhichlymphnodeenlargementisoutofproportiontothepharyngealsymptoms;
othersdevelopasystemicformoftheinfectioninwhichfeverandfatiguepredominate,whilelymphadenopathyandpharyngitisaremildorabsent.SomepatientshavehepatitisintheabsenceofothertypicalfeaturesofIM.
MostindividualswithprimaryEBVinfectionrecoveruneventfullyanddevelopahighdegreeofdurableimmunity.Acutesymptomsresolveinonetotwoweeks,butfatigueoftenpersistsformonths.
PrimaryEBVinfectionininfantsandchildren
PrimaryEBVinfectionsinyounginfantsandchildrenarecommonandfrequentlyasymptomatic.Whensymptomsdooccur,avarietyofmanifestationshavebeenobserved,includingotitismedia,diarrhea,abdominalcomplaints,upperrespiratoryinfection,andIM[5].Asanexample,oneseriesreported32childrenyoungerthan4yearsofagewithIM,selectedfromapopulationof200childrenbyreviewofbloodsmears(morethan50percentmononuclearcellsandmorethan10percentatypicallymphocytes)[6].ThemajorityofthesechildrenhadclinicalevidencecompatiblewithIM(significantcervicaladenopathyandtonsillarpharyngitis);
respiratorysymptomswerefrequentlyprominent,especiallyinyounginfants.
ChildrencanhavesymptomaticprimaryEBVinfectionwithouttheproductionofheterophileantibodies;
asaresult,EBV-specificserologicstudiesarerequiredtoestablishthediagnosis.Intheaboveseriesof32children,interpretationoftheresultsofserologywasmostproblematicinchildrenbelowtheageoftwoyears[6].
▪Theheterophiletestwasparticularlyinsensitive(25percentpositiveforages10to24monthsversus75percentforages24to28months).
▪Anti-viralcapsidantigen(VCA)IgMwaslessfrequentlypositiveininfants(60percentcomparedwith100percentinolderchildrenandyoungadults);
inaddition,peaktitersofVCAantibodywerelower,andthedevelopmentofantibodiestoearlyantigenwaslesscommonininfants.
Despitethereductioninantibodyproduction,younginfantscanmountanEBV-specificcytotoxicTlymphocyteresponseduringacuteEBVinfectionandthatthelatentproteinsrecognizedareidenticaltothoserecognizedbyyoungadults[7].
Congenitalandperinatalinfections
IntrauterineinfectionwithEBVisrarebecausefewerthan5percentofpregnantwomenaresusceptibletothevirus.Inaddition,prospectivestudiesofsusceptible(ie,seronegative)womenhavenotfoundevidenceofcongenitalabnormalitiesamonginfantsofwomenwhodiddevelopprimaryEBVinfectionduringpregnancy[8].WhileisolatedcasesofinfantswithsomeevidenceforEBVinfectionandcongenitalanomalies(biliaryatresia,congenitalheartdisease,hypotonia,micrognathia,cataractsandthrombocytopenia)havebeenreported[9],theevidencearguesagainstEBVasasignificantcauseofcongenitalinfection.Specifically,noevidenceofEBVinfectionhasbeendemonstratedinlargestudiesofchildrenwithcongenitalanomaliesorincordbloodsamples[10].
Othermanifestations
EBVcanaffectvirtuallyanyorgansystemandhasbeenassociatedwithsuchdiversediseasemanifestationsaspneumonia,myocarditis,pancreatitis,mesentericadenitis,myositis,glomerulonephritis,andgenitalulceration[11].AlargenumberofothermanifestationshavebeenassociatedwithprimaryEBVinfection:
▪NeurologicsyndromescanincludeGuillain-Barré
syndrome,facialnervepalsy,meningoencephalitis,asepticmeningitis,transversemyelitis,peripheralneuritis,andopticneuritis[12].
▪Hematologicabnormalitiescanincludehemolyticanemia,thrombocytopenia,aplasticanemia,thromboticthrombocytopenicpurpura/hemolytic-uremicsyndrome,anddisseminatedintravascularcoagulation.
ChronicEBVinfection
ChronicEBVinfectionisararedisordercharacterizedbyongoingsymptomsofaninfectiousmononucleosissyndromewithactiveviremia.Thisentityisdiscussedelsewhere.(See"
COMPLICATIONS
EBVinfectionisassociatedwithanumberofacutecomplicationsand,incertainhosts,moredelayedeffects.
Rash
OneofthemorecommoncomplicationsofIMisamorbilliformrashfollowingtheadministrationofampicillin,andtoalesserextent,penicillin.Theincidenceinitiallywasreportedtobeashighas70to90percentbutisprobablylower[13].Themechanismresponsibleforthisrashisnotunderstoodbuthasbeenthoughttoinvolvecirculatingantibodiestoampicillin.DevelopmentofthisrashduringIMdoesnotappeartopresageanampicillinallergy;
patientshavesubsequentlytoleratedampicillinwithoutanadversereaction.
Oralhairyleukoplakia
AnotherEBV-mediatedmucocutaneousmanifestationisoralhairyleukoplakia(OHL),whichisanunusualdiseaseofthelingualsquamousepithelium[14].OHLgenerallyaffectsthelateralportionsofthetongue,althoughthefloorofthemouth,thepalate,orthebuccalmucosamayalsobeinvolved.Thelesionsaredescribedaswhitecorrugatedpainlessplaquesthat,unlikecandida,cannotbescrapedfromthesurfacetowhichtheyadhere(picture2).Theyarenotgenerallyassociatedwithfever.
TheOHLlesionsappeartoberelativelyspecificforHIVinfection,sincetheyareonlyrarelyobservedinpatientswithotherimmunodeficiencies[14,15].TheuseofhighlyactiveantiretroviraltherapyappearstohavereducedtheincidenceofOHL[16,17].
OHLisassociatedwithintenseEBVreplicationandtheactionofEBV-encodedproteinssuchaslatentmembraneprotein-1[14].Inaddition,studiesinwhichEBVreplicationhasbeensuppressedbyvalacyclovirhavedemonstratedpersistent,nonproductiveEBVinfectionandcontinuedEBVentryfromthebloodintothetongue[18].Theseobservationssuggestaroleforentry,persistence,andreactivationoforalepithelialEBVinthepathogenesisofOHL.
OHLisnotconsideredapremalignantlesion,beingunlikelytoprogresstosquamouscellcarcinoma[14].Treatmentwithzidovudine,acyclovir,ganciclovir,foscarnet,andtopicalpodophyllin
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