Medical Microbiology

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intheinductionofantigen-antibodycomplexes—someofwhichwereformed
inthepresenceofantigenexcess—andoccasionallyinducedastateofshock.
&Immunecomplexesinthepresenceofantibodyexcess.Theso-called
Arthusreactionisobservedwhenanindividualisexposedtorepeatedsmall
dosesofanantigenoveralongperiodoftime,resultingintheinductionof
complexesandanantibodyexcess.Furtherexposuretotheantigen,particu-
larlydermalexposure,inducesatypicalreactionofedemaanderythema
whichpeaksafterthreetoeighthoursanddisappearswithin 48 hours,
butwhichsometimesleadstonecrosis.Arthus-typereactionsoftenrepresent
occupationaldiseasesinpeopleexposedtorepeateddosesofenvironmental
antigens:farmer’slung(thermophilicActinomycesinmoldyhay),pigeon
breeder’slung(proteininthedustofdriedfecesofbirds),cheeseworker’s
lung(sporesofPenicilliumcasei),furrier’slung(proteinsfrompelthairs),
malt-worker’slung(sporesofAspergillusclavatusandA.fumigatus).

TypeIV:HypersensitivityorDelayedType,
Cell-MediatedHypersensitivity

Intracutaneousinjectionofasolubleantigenderivedfromaninfectious
pathogeninducesadelayeddermalthickeningreactioninthosepeople
whohavesufferedapreviousinfection.Thisdelayedskinreactioncanserve
asatesttoconfirmimmunityagainstintracellularbacteriaorparasites.
Formostcases,thetimebetweenadministrationoftheantigenandthe
swellingreactionis 48 – 72 hours—asdescribedaboveforcellulardelayedtype
hypersensitivity(DTH)reactionsintheskin(p.99).Asobservedforantibody-
dependenthyper-reactionsoftypesI-III,thetypeIVresponseispathogenic
anddiffersfromprotectiveimmuneresponsesonlyintermsoftheextentand
consequencesofthetissuedamage,butnotintermsofthemechanismofaction.
ThebalancebetweenautoimmunediseaseandtypeIVimmunopathologyin
suchcasesisreadilyillustratedbytypeIVreactions(e.g.,aggressivehepatitis
inhumansorlymphocyticchoriomeningitisinmice).Shouldthecausal
infectiouspathogenbeknown,theresponseistermedatypeIVreaction,
ifthecausalagentisunknown(ornotyetdetermined)thesamecondition
maybetermed“autoimmunedisease.”Thereaderisreferredtothemany
examplesoftypeIVresponsesalreadydiscussedwithinvariouschapters
(DTH[p.99],immuneprotectionandimmunopathology[Tables2. 9 and


  1. 10 ,pp. 104 and 1 05],transplantationimmunology[seebelow],andauto-
    immunity[p. 11 0ff.]).
    AutoimmuneTcellsareusuallydirectedagainstautoantigensthatwould
    otherwisebeignored(sincetheyareonlyexpressedintheextralymphatic
    periphery).AutoaggressiveCD4+Tcellsapparentlyrespondagainstmyelin


114 2 BasicPrinciplesofImmunology

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