MNSs System Flashcards

1
Q

What Chromosome is GYPA and GYPB located on?

A

Chromosome 4

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2
Q

What are the GYPA and GYPB antigen characteristics?

A
  • Single pass glycoprotein
  • AKA sialoglycoprotein
  • Glycosylated = sugar attached to an amino acid
  • 60% of RBC membrane carbohydrate (sialic acid)
  • Accounting for 80% of the net negative charge
  • 2-4% of the membrane protein
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3
Q

How many antigen sites are on GYPA?

A

1 million

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4
Q

How many antigen sites are on GYPB?

A

200,000

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5
Q

What are the High prevalent MNS antigens?

A

U, Ena, ‘N’, ENKT, ENEP, ENEH, ENAV, ENDA, ENEV

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6
Q

What is the structure of the carbohydrate chains attached to the MNS amino acids?

A

GalNAc - Gal - NANA or (N-Acetylneuraminic acid)

- NANA

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7
Q

What is the function of GYPA/GYPB structures?

A

GPA-deficient red cells are more resistant to invasion by Plasmodium falciparum merozoites
Sialic acid appears to be essential for adhesion of the parasite to the red cells.

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8
Q

What is the function of GYPA on the membrane?

A

GPA associates with band 3, which affects the expression of Wrb of the DI system

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9
Q

What is the function of GYPB on the membrane?

A

GPB associates with Rh proteins and Rh-associated protein (RHAG).
Rh null cells have reduced S and s. (Serologically weak or negative)

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10
Q

What are the amino acids that code for M?

A

SERINE-Serine-Threonine-Threonine-GLYCINE

Serine/Leucine at position 1 and Glycine/Glutamic Acid at position 5

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11
Q

What are the amino acids that code for N?

A

LEUCINE-Serine-Threonine-Threonine-GLUTAMIC ACID

Serine/Leucine at position 1 and Glycine/Glutamic Acid at position 5

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12
Q

What are the amino acids that code for S and s?

A

LEUCINE-Serine-Threonine-Threonine-GLUTAMIC ACID

amino acid difference for S/s – Methionine/Threonine 48 at position 29

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13
Q

What is ‘N’?

A

The first 5 amino acids on GYPB are the same as N antigen.

If GPYB present will have ‘N’ antigen and people usually don’t make anti-N

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14
Q

What is linkage disequilibrium in the MNS system?

A

MNS inherited as haplotypes: MS, Ms, NS, Ns
S is found twice as often with M than with N
M+, it is likely also S+; a cell that is M-S+ is not as common

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15
Q

What are the general MNS antigen frequencies?

A

M an N are present in approx 75% of whites and blacks
S is present in 50% of whites and 30% of Blacks
s is present 90% of whites and blacks
U negative is present in 1% of blacks

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16
Q

What are the most common MNS haplotypes

A

Ns > Ms > MS > NS

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17
Q

What is the effect of ficin/papain to MNSs antigens?

A

MN is destroyed

Ss are variable and less effected because S and s are further down the polypeptide and less accessible

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18
Q

What is the chlorine on S antigens?

A

Destroyed

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19
Q

What is the effect of Trypsin on MNSs antigens>

A

MN is destroyed

Ss are resistant

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20
Q

What is the effect of chymotrypsin?

A

MN is resistant

Ss are destroyed

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21
Q

What is the effect of DTT on MNSs antigens?

A

MNSs are not destroyed by DTT

MN are destroyed by ZZAP

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22
Q

What is effect of nueraminidase?

A

treating cells with nueraminidase will cleave the sialic acid residues and destroys antibody reactivity only in some antibody

23
Q

What are characteristics of anti-M?

A

Naturally occurring
Seen in children with bacterial infections
IgM; 50% will have IgG
May be enhanced by lowering pH
Anti-M not reacting at 37C is not clinically significant

24
Q

What are the characteristics of anti-N?

A

Naturally occurring
IgM; rarely IgG
Not common because of ‘N’ present in most people
Anti-N not reacting at 37C is not clinically significant

25
What are the characteristics of anti-S?
Can be naturally occurring IgG Can cause HDFN and TRN RXN Can be enhance my incubating at room temp
26
What are the characteristics of anti-s?
IgG Can cause HFN and TRN RXN May be enhanced by lowering pH to 6.0
27
What can make clinically significant anti-N
M+N-S-s- U- lack GPYB so no 'N'
28
What is Glycine Soya?
Ficin control that reacts with all cells that reduced sialic acid residues Can be used to screen for U- donors because S-s-U- cells have reduced sialic acid
29
How does allo anti-M form in M+ people?
antibody is directed to a portion of M not present on patients own cells auto and DAT are negative Usually reacts at RT or 4C
30
What is anti-Nf
RT, rarely 37 Not clinically significant for transfusion Rare antibody found in patients (N+ or N-) dialyzed with equipment cleaned with formaldehyde Trace formaldehyde can chemically modify the M and N antigens on the patient’s blood that goes through the dialysis equipment.
31
What is anti-N lectin?
Nvg - made from the lectin Vicia graminea, which has anti-N specificity when diluted appropriately When not diluted will react with GYPB - 'N'
32
Why doesn't anti-N reagents react with 'N'
GYPB is less abundant on RBC's
33
What cells have more 'N'?
S SGP is 1.5x more prevalent on the red cell than s SGP. Therefore, S+ rbcs have more ‘N’ than S-s+ rbcs. U neg cells (lack GPB) also lack ‘N’.
34
That is the effect of enzymes to 'N'?
Destroyed by Papain/ficin like M and N Resistant to trypsin Destroyed by chymotrypsin
35
What is anti-GPB?
Antibody that can be made by N- U- individuals
36
What is Ena?
``` High freq present on GYPA Rare deletion results in M- N- Ena- Wrb -phenotype Reduced sialic acid residue Glycine Soya will be positive in Ena- Present on cords DTT resisant ```
37
Anti-EnaTS
Trypsin Senstive - does not react with En(a+) cells treated with trypsin, ficin or papain.
38
Anti-EnaFS
Ficin sensitive - represents those Ena antibodies that recognize a ficin-sensitive (papain sensitive, trypsin resistant) determinant
39
Anti-EnaFR
Ficin resistant - represents those antibodies that react with a ficin-resistant (papain resistant, trypsin-resistant) determinant
40
Anti-Ena characteristics?
IgM or IgG seen at IAT Can cause TXN RXN or HDFN (Transfuse Ena- units) Can be an autoantibody Ena neg individuals who make anti-Ena often make anti-Wrb (Ena required for Wrb expression) Anti-Ena is directed against different portions of GPr Extremely difficult to find Ena- blood. Look at siblings
41
U antigen Characteristics
Resistant to all chemicals U negative found in 1% of blacks U antigen is present on cord cells
42
Anti-U characteristics?
IgG reacts at IAT Can cause TXN RXN and HDFN Can be auto antibody Most commonly found in blacks Not all Anti-U are compatible with U negative RBC’s (seen in U variants) Some can tolerate blood from Uvar donors Patients who are also N negative can make anti-U and anti-N (Anti-GPB)
43
What is Uvar?
``` 16% of serological S-s- have U var Uvar is a hybrid gene Weak U antigen is detected absorption and elution 23% are He+ Can make anti-U ```
44
What is MkMk phenotype?
Extremely rare phenotype (Mk is not a gene) Caused by GYP*01N allele that produces no GPA or GPB. Homozygous = Cells are M-N-S-s-U- ‘N’-, En(a-), Wr(a-b-) Heterzygous = Cells will express MNS antigens produced by the normal allele -For example, Mk/Ns will type M-N+S-s+.
45
Mc
Single amino acid change in GYPA produces low frequency antigen Intermediate between M and N antigens. Reacts with most anti-M and some rabbit anti-N, but negative with Nvg lectin. Often present with M1 antigen (see MN CHO section)
46
Mg
Single amino acid change in GYPA produces low frequency antigen Found more often among Swiss. Previously used as an adjunct in paternity testing. Anti-Mg is common. Antibody can be made in rabbits.
47
He (Henshaw)
Single amino acid change in GYPB produces low frequency antigen Antithetical to ‘N’ – He positive cells do not express ‘N’ Positive in 23% Uvar
48
Dantu and Sta
Dantu is found in blacks Sta is found in very low frequency, but seen in Japanese and Asians These are hybrid antigens Carry a protease resistant N which is probably ‘N’ Ficin-treated cells will react with Nvg lectin Anti-Dantu may be found in reagent anti-S
49
What is Mur?
Rare in European and African ethnicity, but higher prevalence in Chinese (7%) and Thais (10%) Form of Hybrid of GPYB Anti-Mur causes HTR/HDFN and is the most common blood group antibody after anti-A/-B in Hong Kong and Taiwan. Screen cells used in Southeast Asian labs should include a Mur+ cell.
50
MN CHO Blood Group Collection
``` Abnormal glycosylation (sialic acid or GluNAc) on GPA resulted in 6 antigens, now grouped in a separate blood group collection called MN CHO Antigens: M1, Hu, Tm, Can, Sext, Sj ```
51
What is M1?
Low prevalence (0.5% W, 16.5% B), found only on M+ cells, but is not an enhanced M Anti- M1 made primarily by M- (and some M+N+) individuals Anti-M and anti- M1 are not the same. Some anti-M react only with M1+ cells Amino acids are same in M and M1 but there is abnormal glycosylation GlcNAc is substituted for NANA on 1st GlcNAc This in inhibits glycosylation of amino acids 3 and 4
52
What is Tm?
Amino acids 1-5 look like N | Like M1 there is a GlcNAc substituted for the 1st NANA which inhibits glycosylation of amino acids 3 and 4
53
What is T and Tn?
Abnormal glycosylation results in polyagglutination T is when both NANA are removed and just GalNAc-Gal are present Tn is where the terminal NANA and GAL are removed exposing the GalNAc Reacts with human anti-A