MNS Blood group system powerpoint in.ppt

MNS BGS

2. Introduction:
•MNS, the second blood group system
discovered
•Second only to Rh in its complexity
•43 antigens are known
•the first blood group polymorphisms to be
defined at the level of protein sequence

3. History
•The first antibodies to the M and N red cell
antigens were found in rabbits immunized with
human red cells by Landsteiner and Levine in
1927.
•In 1947, Walsh and Montgomeryfound an
alloantibody, anti-S, detecting an antigen relating
to M and N.
•Anti-s, an alloantibody detecting the product of an
allele of S, was reported in 1951 by Levine et al

4. MNSs blood group system
•M, N, S, s, and U antigens are most
important
•The M and N antigens are located on GPA
•The S, s, U are located on GPB
•Considerable linkage disequilibrium b/w M,
N, S, s due to gene location on the
chromosome
•GYPA, GYPB and GYPE constitute a gene
cluster on chromosome4 at 4q28-q31

5. Development and distribution of
MNS antigens
•Well developed at birth
•GPA restricted to blood cells of erythroid
lineage and is often used as an erythroid
marker
•NOT present on lymphocytes, granulocytes,
megakaryocytes or platelets
•GPA –has been detected on renal
endothelium (incompletely sialylated)

6. MNSs antigens
Common
antigens
encoded by
MNS loci
M
N
S
s
Low frquency
antigens
<1%
He
Mi
a
M
c
Vw
Mur
M
g
V
r
M
e
Mt
a
St
a
Ri
a
Cl
a
Ny
a
Hut
Hil
M
v
Far
s
D
Mit
Dantu
Hop
Nob
En
a
KT
Or
DANE
TSEN
MINY
High
frequency
antigens
>99%
U
En
a
‘N’

7. Glycophorin
•Heavily glycosylated
glycoproteins rich in sialic
acid (N-acetyl neuraminic
acid)
•C-terminus & N-terminus
•N-glycans & O-glycans
•GPB is not N-glycosylated
•O-glycans contain most of
the sialic acid

8. GPA & GPB

9. MN antigens
•The M and N antigens are found on glycophorin-
A(CD235A) , the major red cell sialic acid-rich
glycoprotein( α-sialoglycoprotein 36 kD,131 AA)
•Defined by the 1
st
and 5
th
AA on this structure
•About 10
6
copies of MN-SGP/ red cell.
•The antigens exhibit dosage
•The antigens can be detected as early as 9 weeks
GA.

10. •M differs from N in the amino acid composition of
the extracellular tip of GPA:
–M has serineat position 1 and glycineat
position 5;
–N has leucineat position 1 and glutamicacid at
position 5.
•Carbohydrate , sialic acid also plays a part in the
expression of M&N antigens.

11. •M and N antigens are primarily red cell antigens
•Not detected on lymphocytes, monocytes,
granulocytes, or platelets
•MN antigens have been detected on renal capillary
endothelium

12. •Because MN antigens are at the outer end of
the GPA, they are easily destroyed or
removed by the routine blood bank enzymes
ficin, papain, and bromelin, and by less
common enzymes trypsin and pronase
•The antigens are also destroyed by ZZAP, a
solution of dithiothreitol (DTT) and papain

13. Ss antigens
•Located on a glycoprotein-Ss-SGP, δ-SGP, or
glycophorin-B (CD235B)
•AA on position 29 on GPB is critical to antigen
expression-
•S has methionine, whereas s has threonine
•Ss-SGP complexes with Rh protein, which
helps Ss-SGP stabilize and incorporate into
the red cell membrane
•Rh null red cells have greatly reduced Ss
expression

14. •There are 2.5x10
5
copies of Ss-SGP/red cell
•Ss antigens show dosage
•Well developed at birth and appear on red cells at
an early GA(12 wks)
•Less easily degraded by enzymes
•Like MN, Ss are considered red cell antigens

15. Phenotypes and frequencies
Reaction with anti- phenotype Phenotype
frequency
MNSsU whitesblacks
+0 M+N- 28 26
++ M+N+ 50 44
0+ M-N+ 22 30
+ 0 + S+s-U+ 11 3
+++S+s+U+ 44 28
0 + + S-s+U+ 45 69
0 0 0 S-s-U- 0 <1
0 0 (+)S-s-U+w 0 rare

16. Frequencies in the MNS system
Whites Blacks Indians
M 28 24 78
N 22 30 73
S 11 3 63
s 45 69 45

17. ‘N’
•The first 26 aa residues from the extracellular
terminus of GPB are identical to those of N-active
GPA ( GPA
N
).
•Consequently, GPB also demonstrates N activity
(‘N’), detected in homozygous M/M individuals
by some anti-N.
•Trypsin resistant N antigen

18. U (universal)
•Weiner et al. 1953-A high frequency blood group ag.
•Located on Ss-SGP very close to the red cell membrane
•Found in all individuals except about 1% of american
blacks, who lack Ss-SGP.
•U-cells are almost always S-s-, but S-s-cells are often U+
•Resistant to denaturation by sialidase, trypsin,
chymotrypsin, papain, and ficin.
Anti-U –
•A non-complement binding IgG antibodies (IgG1)
•Greater activity at temp <22°C than at body temperature

19. En(a-)
•Lack GPA and, consequently, MN antigen
expression (apart from the ‘N’ antigen carried on
GPB)
•En(a-) cells express normal Ss antigens but lack a
variety of GPA-borne high frequency antigens
collectively named En
a.
•En(a-) cells also lack Wr
b,
expression of which
results from an interaction between GPA and red
cell glycoprotein band3

20. Mk
•A new allele of M and N that lack all MNS antigens
•Have no GPA or GPB
•Red cells are M-N-S-s-U-En(a)Wr(a-b-)
•Showed all reactions characteristic of reduced sialic acid
•The Miltenberger subsystem-
A group of very low frequency antigens in the MNS
group, related to each other through the overlapping
specificity of a no. of low frequency alloantigens

21. Hybrid glycophorins-LFAs
•Lepore type-
Loss of GYPA and GYPB and the
formation of a novel gene that produces a
GP (A-B) hybrid. N terminal of GPA and C-
terminal of GPB
•Anti-lepore type-
GP(B-A) hybrid

22. Anti-M
•Naturally occuring, cold reactive saline
agglutinins
•Mostly IgM, 50 to 80 % are IgG or have an
IgG component
•Usually do not bind complement, regardless
of their of their Ig class
•Do not react with enzyme treated red cells

23. •The frequency of finding saline reactive
anti-M in routine blood donors-1 in 2500 to
5000
•More common in infants than adults
•Because of antigen dosage, M antibodies
react better with M+N-red cells (MM
genotype) than with M+N+ red cells
•Glucose dependent

24. •Some examples of anti-M are pH
dependent, reacting best at pH 6.5
•As long as anti-M does not react at 37 C, it
is not clinically significant in transfusion
•Anti-M rarely causes –hemolytic
transfusion reactions, decreased cell
survival, or hemolytic disease of newborn

25. Anti-N
•Cold reactive IgM or IgG saline agglutinin
that does not bind complement or react with
enzyme-treated red cells
•Demonstrates dosage
•Not clinically significant unless reacts at 37
C
•More rare than anti-M

26. Anti-N
f
•Anti-N also seen in kidney transplant
patients maintained on chronic
hemodialysis , regardless of their MN type,
who are dialized on equipment sterilized
with formaldehyde
•Ab disappeared after transplantation
•21 to 27 % of dialysis patients
[Am J Nephrol 1995]

27. Anti-S and Anti-s
•Mostly IgG, reactive at 37 C in the
antiglobulin phase
•Although seen less often than anti-M, more
likely to be clinically significant
•May bind complement
•Have been implicated with severe HTR
with hbnuria
•Have also caused HDN

28. Blood groups and their specific lectin.

29. Lectins with anti-N activity
•Anti-N lectins are common and highly specific,
while anti-M is rare
•Anti-N lectin B. purpureahas been found to be a
good typing reagent .
•Anti-N lectin from Vicia graminea, is easily
available & shows excellent specificity and
avidity.
•Saliva extracts of Vicia unijugaagglutinate both M
& N cells, but adsorption with pooled human M
cells gives a potent anti-N lectin
•A+ N reactivity - Molucella laevis
Bandeiraea simpicifolia

30. Lectins with anti-M activity
Iberis amara, I. umbellata,I. semperivens
•The best lectins are isolated from Iberis
amara.
•Other lectins with anti-M activity include
Japanese radishes and Escherichia coli .
•anti-M lectin from non-fimbrial E. coli is
the most specific

31. Glycophorins and malaria
•Invasion of host red cells by merozoites
involves interaction b/w receptors on
parasite and ligand on surface of cell
•Glycophorins
•GPA-deficient, En(a-), red cells are more
resistant to invasion

32. Phenotype Deficient
structure
% invasion
Normal 100
En(a-)GW GPA 8
En(a-)RL GPA 14
S-s-U- GPB 72
Ge:-2,-3,-4 leachGPC 57
Tn Gal+ sialic acid8
Trypsin treated
normal
GPA-T1,GPCT1 38
Trypsin treated S-
s-U-
GPA-T1, GPCT1,
GPB
5

33. Other pathogens:
•GPA
M
–uropathogenic E.coli strain 1H11165
•GP acts as a receptors for the bac. toxins that lyse
red cells
•Coating of red cells with antibodies to GPA &
GPB protects from lysis by hemolysins from E.
coli and vibrio cholerae respectively
•GPA also acts as a receptor for influenza virus