Rh BLOOD GROUP (004) Flashcards
memorization (39 cards)
The Rh blood group was discovered by _________ and __________ in 1940
Karl Landsteiner and Alex Weiner
Inheritance of Rh blood group:
Codominant alleles
Rh genes:
RhD gene - Chr 1
RhCE gene - Chr 1
RhAG gene - Chr 6
RHD gene expresses what antigen(s)?
D antigen
RHCE gene expresses what antigen(s)?
D, C, c, E, e antigens
RHAG gene expresses what antigen(s)?
Rh-associated glycoprotein of Rh antigens; co-expresser of Rh antigen
Nomenclatures of Rh Blood Group:
Fisher-Race
Wiener
Rosenfield
ISBT
Rh D nomenclature that has 5 Rh antigens; d = absence of D Ag
Fisher-Race
Rh D nomenclature that has 8 agglutinogens with equivalent blood factors:
Wiener
Rh D nomenclature that has no genetic basis; presence/absence of Ag
Rosenfield
Rh D nomenclature that is machine readable; uniform nomenclature:
ISBT (International Society of Blood Transfusions)
Fisher-Race terminologies
Dce
DCe
DcE
DCe
dce
dCe
dcE
dCE
Wiener blood factor terminologies:
Rho hr’ hr’’
Rho rh’ hr’’
Rho hr’ rh’’
Rho rh’ rh’’
hr’ hr’’
rh’ hr’’
hr’ rh’’
rh’ rh’’
Agglutinogens (Wiener Haplotype terminology)
Ro
R1
R2
Rz
r
r’
r’’
r^y
Rosenfield terminology:
Rh1 —> D
Rh2 —> C
Rh3 —> E
Rh4 —> c
Rh5 —> e
ISBT terminology:
004 001 —-> D
004 002 —-> C
004 003 —-> E
004 004 —-> c
004 005 —-> e
What is the most common haplotype in Asia?
DCe, R1, Rho rh’ hr’’ (70%)
Testing for Weak D utilizes the principle of:
Indirect Antiglobulin Testing (IAT)
Testing for Weak D is required for:
- Blood donors
- Babies born from Rh D-negative mothers
Note: Recipients of donated blood don’t require weak D testing
Reasons for Weak D testing:
Genetic Weak D
- Fewer D antigen present
- Quantitative problem
C trans
- Position effect
- D is trans to C
D mosaic/Partial D
- Missing portion of D Ag
- Qualitative problem
Rh antigens composition:
- Non-glycosylated proteins
- D is the major Rh Ag and the immunogenic
Arrangement from most immunogenic to least immunogenic Rh D antigens:
D > c > E > C > e
Rh antibodies composition:
- IgG immune antibodies
- DO NOT activate complement (extravascular RBC lysis)
- Reactivate at 37C and AHG phase (Clinically significant - may cause HTR and HDN)
Lacks all Rh antigens; demonstrates mild compensated hemolytic anemia, increase in Hb F:
Rh null syndrome (—/—)