MNSs Flashcards

1
Q

MNSs

Inherited as _______alleles, meaning both inherited alleles are expressed in the individual’s red blood cells (RBCs).

A

co-dominant

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2
Q

MNSs

Located on Chromosome___

A

4

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3
Q

MNSs

The system consists of two genes:

• → Responsible for the M and N antigens.

• → Responsible for the S, s, and U antigens

A

GYPA (Glycophorin A)

GYPB (Glycophorin B)

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4
Q

Key Antigens in the MNSs System

• (4) are the four main antigens.

•___ antigen is only expressed when S and/or s are present.

A

M, N, S, and s

U

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5
Q

• Fully developed at birth (important for Hemolytic Disease of the Fetus and Newborn, HDFN).

• Located on RBCs and tissues but NOT in secretions.

A

MNSs

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6
Q

• M & N differ in only two amino acids at positions ____ and____on the Glycophorin A (GPA) protein.

A

1 and 5

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7
Q

S & s differ in one amino acid at position____ on the Glycophorin B (GPB) protein.

A

29

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8
Q

____antigen is expressed only if S and/or s are present.

A

U

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9
Q

• All MNSs antigens exhibit dosage, meaning their reactivity is stronger in______ individuals and weaker in_____ individuals.

A

homozygous

heterozygous

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10
Q

• Homozygous individuals (M+N− or M−N+) →_______

• Heterozygous individuals (M+N+) →_______

A

Stronger reaction

Weaker reaction

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11
Q

Antigens are destroyed by______, meaning that proteolytic enzymes like papain, ficin, trypsin, and bromelin will degrade the MNSs antigens, affecting serologic testing.

A

enzymes

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12
Q

• U antigen is always present if_______ are inherited.

A

S and/or s

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13
Q

• U-negative individuals are extremely rare (found only in ______ populations).

A

Black

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14
Q

• Approximately____% of S−s− individuals lack the U antigen.

A

85%

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15
Q

Antigen Frequency

U+
Black
White

A

High-incidence antigen (99%)
99.9%

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16
Q

Phenotype Frequency
Black
White

S-s-U (Very Rare)

A

<1
Extremely rare

17
Q

are typically IgM, react at cold temperatures (below 37°C), and are usually clinically insignificant unless reacting at 37°C.

A

M and N antibodies

18
Q

are mostly IgG, react at 37°C, and can cause Hemolytic Transfusion Reactions (HTRs) and Hemolytic Disease of the Fetus and Newborn (HDFN).

A

S and s antibodies

19
Q

_____individuals can develop anti-U, which can cause severe and fatal transfusion reactions and HDFN.

A

U-negative

20
Q

Can a Person Have No Expression of MNSS Antigens?

Yes, a person can completely lack MNSS antigens due to certain null phenotypes, which result from deletions or mutations in the (2) genes

A

GYPA (Glycophorin A) and
GYPB (Glycophorin B) genes

21
Q

Deletion of the GYPB gene, which codes for S, s, and U

A

U-phenotype

22
Q

Deletion of the GYPA gene, which codes for M and N

A

En (a-) phenotype

23
Q

Deletion of both GYPA and GYPB genes

A

M^k phenotype (Silent Gene/Null Gene)*

24
Q

• This occurs when the GYPB gene is deleted, meaning there is no production of S or s antigens.

A

U− Phenotype (S−S−U−)

25
Q

• This results from the deletion of the GYPA gene, which encodes M and N antigens.

A

En(a−) Phenotype

26
Q

reacts with multiple parts of the Glycophorin A protein.

27
Q

• This occurs when both GYPA and GYPB genes are deleted.
• All MNSS antigens are absent.

A

M^k Phenotype (Silent Gene/Null Gene)*

28
Q

_____ is usually IgG (50-80%) but can be IgM.

29
Q

• Naturally occurring antibodies (do not require prior sensitization).
• Found in individuals who lack M or N antigen.
• Can be either IgG or IgM.
• Do not bind complement, meaning they are usually not clinically significant.

A

Anti-M and Anti-N

30
Q

_____ is clinically insignificant because it cannot cross the placenta.

_____can rarely cause mild hemolytic disease of the fetus and newborn (HDFN).

A

• IgM Anti-M

• IgG Anti-M

31
Q

• Clinically significant because they are primarily IgG.

• IgG antibodies can bind complement, leading to cell lysis.

• Cause severe hemolytic transfusion reactions (HTR) and HDFN.

A

Anti-S, Anti-s, and Anti-U

32
Q

• Usually IgG.
• Can cause HTR and HDFN.

• If optimal reactivity occurs at 10-22°C, AHG testing should be performed without incubating at 37°C.

A

Anti-S and Anti-s

33
Q

• U- individuals must be registered in rare donor registries.
• Causes severe and fatal HTR and HDFN.

34
Q

• Found in S−s− (U−) individuals.
• Requires U− blood for transfusion.
• Extremely rare and mostly found in the Black population (<1%).

35
Q

• Highly clinically significant.
• Reacts strongly with S+ or s+ red cells.