LU, CO, XG Flashcards
ISBT
005
FIRSTS
First autosomal linkage with Se in man
First autosomal crossing over in man
Antithetical pairs
Lua/Lub
Lu6/Lu9
Lu8/Lu14
Lu18/Lu19
Low incidence
Lu9, Lu14
Antigens
Weak on cord cells
Not in plasma
Fragile
Present on other tissues
Antigens on red cells
Variable # among different individuals: variable strength on different test cells
Variable # antigens in same person: MF agglutination
Anti-Lua
Mostly benign
More active at lower temperature
HTR extremely rare
HDFN none to mild
Anti-Lub
More significant
Mostly IgG1
Mild HDFN and HTR
Anti-Lu3
Not reported to cause HDFN
LuLu recessive
Mutations in LU gene
Can make anti-Lu
Very rare
Cells normal
In(Lu)
Dominant supressor
Mutations in KLF1 gene
Have trace Lu antigen, cannot make anti-Lu
0.03% frequency
Weakens other antigens: P1, i, CD44, AnWj, Knops
Lumod
X linked inhibitor
Have trace Lu antigen
Found in males of Australian family
Weak P1, enhanced i
Gene
LU: Chromosome 19
Gene product
BCAM. IgSF adhesion
LU disease association
May be associated with PV
CO high prevalence
Coa
CO cord cells
Expressed
CO enzyme DTT
Resistant to both
CO:-3
No AQP1
CO:-4
Normal AQP1, cells are CO:3
CO antibodies
Rare, not immunogenic
Implicated in HTR and HDFN
XG gene product
Single pass, linked to STS
X linked
X linked dominant in female
XG genetics
Xga+ male and an Xga- female will produce all Xga- males and Xga+ females