MNSs Flashcards

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1
Q

What are the primary antigens in the MNSs blood group system, and how are they inherited

A

The primary antigens in the MNSs blood group system are M, N, S, and s1
. These antigens are inherited through two codominant alleles, M and N, located on chromosome 42
. The possible genotypes are MM, MN, NN, SS, Ss, and ss2
.

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2
Q

Explain the clinical significance of anti-M and anti-N antibodies in transfusion medicine.

A

Anti-M and anti-N antibodies can cause hemolytic transfusion reactions (HTRs) if transfused with incompatible blood2
. These reactions are generally mild but can lead to symptoms such as fever, chills, and hemoglobinuria2

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3
Q

How do the S and s antigens differ in their expression and clinical relevance?

A

The S and s antigens are also part of the MNSs blood group system1
. The S antigen is more prevalent and can be adsorbed onto red blood cells, while the s antigen is less common2
. Anti-S antibodies are usually not clinically significant, but anti-s antibodies can occasionally cause mild hemolytic reactions2
.

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4
Q

What is the genetic basis for the distribution of M, N, S, and s antigens in different human populations?

A

The distribution of M, N, S, and s antigens varies among different human populations due to genetic diversity2
. The M and N alleles are co-dominant, leading to a variety of genotypes (MM, MN, NN) and phenotypes2
. The S and s alleles follow a similar pattern, resulting in different antigen expressions2
.

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5
Q

Discuss the potential complications of transfusions involving patients with high-titer anti-S or anti-s antibodies.

A

While rare, high-titer anti-S or anti-s antibodies can cause hemolytic transfusion reactions (HTRs)2
. These reactions can lead to symptoms such as jaundice, anemia, and fever2
. It’s crucial to screen for these antibodies and ensure compatible blood is used for transfusions.

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6
Q
A
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7
Q

How can the presence of anti-M antibodies affect prenatal care, and what steps should be taken if they are detected in a pregnant woman?

A

Anti-M antibodies can cause hemolytic disease of the fetus and newborn (HDFN) if they are IgG antibodies and cross the placenta. This can lead to fetal anemia and hydrops fetalis. If anti-M antibodies are detected in a pregnant woman, regular monitoring of the antibody titer and fetal health through ultrasound and Doppler studies is essential. In severe cases, intrauterine transfusions may be necessary to manage fetal anemia.

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8
Q

Describe the differences in clinical significance between anti-M and anti-S antibodies in terms of their potential to cause hemolytic reactions.

A

Anti-M antibodies are generally IgM and can cause mild to moderate hemolytic transfusion reactions (HTRs), but their clinical significance varies. They are more concerning in a prenatal context if they are of the IgG class. Anti-S antibodies, while less common, can cause more severe hemolytic reactions as they are typically IgG and can lead to significant hemolysis of transfused red blood cells. Thus, proper matching for S antigen is crucial in transfusion settings.

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