rev bras hematol hemoter. 2017;39(4):293–294
w w w . r b h h . o r g
Revista
Brasileira
de
Hematologia
e
Hemoterapia
Brazilian
Journal
of
Hematology
and
Hemotherapy
Scientific
Comment
Kidd
system
antigens
and
kidney
disease
夽
Melca
Maria
Oliveira
Barros
∗UniversidadeFederaldeSãoPaulo(Unifesp),SãoPaulo,SP,Brazil
TheKidd blood group system(ISBT009), identified in1951,
wastheninth bloodgroup systemandit isconsideredthe
ninthmostclinicallyimportant.AntigensoftheKiddblood
group system are expressed on type 3 glycoproteins, also
known as the urea transporter B(UT-B). The JK protein is
expressedonredbloodcells(RBCs)andintheendotheliumof
thedescendingvasarectaandepithelialsurfacesoftherenal
innermedulla.1 Evidenceofthefunctionofthe Kiddblood
groupsystemfirstcametolightfromtheobservationin1982
thatJk(a-b-)RBCswereresistanttolysisin2Mureain
con-trasttoRBCswithnormalKiddantigens.RBCshavingnormal
JKphenotypeswilllysewithin30sastheureaistransported
into the cells,followed bya rapidosmoticinflux ofwater.
Becauseofthelackofureatransportandthereforenowater
uptake,Jk(a-b-)cellsremainintactaftertwominutes,which
demonstratestheroleoftheJKproteininfacilitatingrapid
ureatransportacrosstheRBCmembrane.2Themajor
physio-logicroleforureatransportersisintheurinaryconcentrating
mechanism.However,noclinicalsequelawasfoundintwo
patientswiththeJknullphenotypesuggestingthepresence
ofcompensatorymechanisms.3
ThepaperbyCapriolietal.4publishedinthisissueofthe
RevistaBrasileiradeHematologiaeHemoterapiainvestigates
pos-sible relationsbetween the absence ofJka or Jkb antigens
inpatientswithchronic kidney disease.Thisisinteresting
becauseindividualswiththeJk(a-b-) phenotypehad lower
urine-concentratingability,howeverifpatientswithchronic
kidneydiseasepresentsomedifferenceintheKiddphenotype,
thedistributionremainsunknown.Moreover,thelocationof
the JK antigens on renal cells raises fascinating questions
DOIoforiginalarticle:http://dx.doi.org/10.1016/j.bjhh.2017.05.007.
夽
SeepaperbyCapriolietal.onpages301–5.
∗ Correspondenceto:DepartamentodeMedicina,DisciplinadeHematologia,UniversidadeFederaldeSãoPaulo(Unifesp),RuaDiogode
Farias,VilaClementino,04023-900SãoPaulo,SP,Brazil.
E-mailaddress:[email protected]
about the impact of the Kidd system antigens on kidney
disease.
Capriolietal.,4foundnodifferenceinphenotype
frequen-cies orthe distribution ofJka and Jkbantigenswhen they
comparedpatientswithchronickidneydiseaseandcontrols,
howeverthenullphenotypewasnotobservedinthegroups.
ThissuggeststhattheabsenceofJkaorJkbdoesnotinfluence
thedevelopmentofchronickidneydiseaseinthesechronic
kidneydiseasepatients,althoughtheinfluenceoftheabsence
ofbothhasnotbeenstudied.Severalcasereportssuggesta
roleoftheKiddSystemonrenalgraftsurvivalinkidney
trans-plants. Lerutet al.5 demonstratedinaretrospective cohort
studyof370kidneytransplantsthatmismatchofthe
recipi-ent/graftattheJKlocuswasassociatedwithmoreinterstitial
inflammationthanwhentheywerematchedasobservedat
biopsyofthetransplantedkidney,althoughoverallgraft
sur-vivalwasnotinfluenced.
TheauthorssuggestthatintheabsenceofUT-B,another
transporter,suchasUT-A,wouldnotallowureatoaccumulate
intherenalmedulla,therebyprotectingagainstrenal
dysfunc-tion,howevernofunctionalexperimentswereperformedto
affirmthis conclusion.Finally, whilethefunctionofthe JK
proteinisknown,futurestudieswouldbeexpectedtoresult
inamorecompleteunderstandingabouttheimpactofKidd
systemantigensonkidneydisease.
Conflicts
of
interest
Theauthordeclaresnoconflictsofinterest.
http://dx.doi.org/10.1016/j.bjhh.2017.07.004
1516-8484/©2017PublishedbyElsevierEditoraLtda.onbehalfofAssociac¸ ˜aoBrasileiradeHematologia,HemoterapiaeTerapiaCelular.
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1.HamiltonJR.Kiddbloodgroupsystem:areview. Immunohematology.2015;31(1):29–35.
2.HeatonDC,McLoughlinK.Jk(a-b-)redbloodcellsresisturea lysis.Transfusion.1982;22(1):70–1.
3.SandsJM,GargusJJ,FröhlichO,GunnRB,KokkoJP.Urinary concentratingabilityinpatientswithJk(a-b-)bloodtypewho lackcarrier-mediatedureatransport.JAmSocNephrol. 1992;2(12):1689–96.
4.CaprioliTV,VisentainerJ,SellAM.Lackofassociationbetween Kiddbloodgroupsystemandchronickidneydisease.RevBras HematolHemoter.2017;39(4):301–5.