Medical Microbiology

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Indirectimmunofluorescenceandenzymehistology.Inthistechniquethe
specificor“first”antibodycanbeunlabeled.Theantigen–antibodycom-
plexesthatformarethendetectedusingalabeledor“second”antibody,di-
rectedagainstthefirstantibody(Fig.2.26b).Insteadoffluorochromes,enzy-
me-labeledantibodiesarenowfrequentlyusedfortissuesections.Theen-
zymecatalyzestheformationofacolorsignalfollowingadditionofapre-
viouslycolorlessdetectorsubstance.Thiscolorprecipitateallowsthedirect
observationofsignalsusingalightmicroscopic,andexhibitslittlebleaching.
Indirectimmunofluorescencecanbeusedforthequalitativeandquanti-
tativeanalysisofantibodiesdirectedagainstparticularmicrobialantigens,or
self-tissueantigens,withinapatientsserum.Inthequantitativetest,theanti-
genisfixedinawellortoatissuesectiononaslide.Thepatientsampleis
repeatedlydilutedbyafactoroftwoandaddedtotheantigenorsectionthen
renderedvisiblewithalabeledanti–antibody.
Therearetwomainmethodsofamplifyingtheimmunohistologicalcolor
signal:


ImmunologicalTestMethods 127

AntigenDetectionMethods

Fig.2. 26 Immunofluorescence(a,b)isparticularlysuitableforthedetectionof
antigens,orspecificantibodies,fixedonplastic(solidphase)(ELISA)orpresent
withinatissuesection(immunohistology).Fordirectimmunofluorescence(a)
thespecificprimaryantibodyislabeledwithafluorochrome,oranenzyme(ELISA
=enzyme-linkedimmunosorbentassay).Thetermindirectimmunofluorescenceis
usedwhenitisnottheprimaryantibodybeingdetected,butasecondaryantibody
whichisdirectedagainsttheunlabeledprimaryantibodyandhasalsobeenlabeled
withafluorochromeorenzyme(b).Inmostcases,thismethodachievesacertain
degreeofamplification.However,anevenhigherlevelofamplificationcanbe
achievedusingpreformedcomplexesofsecondaryantibodyandenzyme(c).
Fortheperoxidasemethodthedetectorenzymeisbounddirectlytothesecondary
antibody(peroxidasecatalyzesacolorreaction).Inthebiotin-avidinmethodthe
detectorenzymesarecoupledtoeitherbiotinoravidin.

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Kayser, Medical Microbiology © 2005 Thieme
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