Immune Hemolysis Flashcards

1
Q

What types of antibodies does the DAT (Coombs) Test detect? Where is the antibody?

A

IgG antibodies or complement C3 on patients red cells

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2
Q

What types of antibodies does IAT (Coombs) Test detect? Where is the antibody?

A

detects IgG antibodies against RBC, its found in the patient serum

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3
Q

Where does the majority of immune hemolytic anemia occur- extravascular or intravascular?

A

mostly in extravascular (Ab-coated RBC ingested by macrophages) with the exception of ABO transfusion rxn

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4
Q

Which antibody are the spleen and liver best at removing from the blood?

A

spleen is most efficient clearing RBC coated with IgG and liver is more efficient in clearing sensitized by IgM (and complement over C3)

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5
Q

Name some common causes of autoimmune hemolytic anemia.

A

many are idiopathic, other are associated with autoimmune disease, lymphoproliferative disorder (esp CLL) infection, etc.

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6
Q

What smear/lab results would be suggestive of hemolysis due to warm autoantibodies?

A

DAT will be positive for IgG +/- C3 peripheral blood shows spherocytes, not bite cells, young shift cells may be present

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7
Q

How might you treat someone with hemolysis duet o warm autoantibodies?

A

corticosteroids splenectomy (relapse) rituximab transfusion (although crossmatch may be difficult)

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8
Q

Cold agglutinin syndrome is _____ antibody-mediated.

A

IgM, and most commonly target I or i antigens Note: hemolysis is more likely if antibody binds RBC at or near body temperature (measured by thermal amplitude), most are clinically benign

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9
Q

Cold agglutinin syndrome can be a complication of the which infections?

A

mycoplasma, EB virus or lymphoproliferative disorders

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10
Q

What is the smear/lab result indicating cold agglutinin (think antibodies).

A

DAT positive for C3 and negative for IgG smear shows groups of RBC that appear to be clumping together, clumping can be seen macroscopically

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11
Q

What is acrocyanosis?

A

slugging of blood that may occur with cold agglutinin syndrome can be clinically apparent with livedo reticular or associated with Raynaud’s syndrome

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12
Q

What can we do to treat cold agglutinin disease?

A

alternative immunosuppression and avoid cold exposure (corticosteroids or splenectomy are often ineffective)

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13
Q

Given the mechanism of drug-induced hemolysis, name the likely antibody and location of hemolysis: drug binds RBC membrane, antibody binds to drug-membrane complex. (haptenic)

A

IgG antibody, extravascular hemolysis (often Beta-lactam)

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14
Q

Given the mechanism of drug-induced hemolysis, name the likely antibody and location of hemolysis: drug binds antibody in plasma, immune complex deposits on RBC membrane. (immune complex)

A

IgM antibodies with complement fixation, intravascular hemolysis (often quinidine)

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15
Q

Given the mechanism of drug-induced hemolysis, name the likely antibody and location of hemolysis: drug stimulate immune system to make autoantibodies.

A

IgG antibodies, extravascular

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16
Q

This theory explains why some drugs can cause hemolysis with first exposure.

A

“induced-fit” hypothesis: where drug increases affinity of pre-formed antibody to RBC membrane

17
Q

What are consequences of hemolytic disease in a fetus?

A

severe hemolysis may cause liver injury from extra medullary hematopoiesis, hydrous fetalis, and intrauterine death unconjugated bilirubin may cause brain damage (kernicterus)

18
Q

Why is ABO fetus-mother incompatibility usually mild or asymptomatic?

A

ABO antibodies are IgM, don’t cross placenta well ABO antigens compete with antibody for RBC binding ABO antigens re less well developed at birth

19
Q

Why does maternofetal ABO incompatibility make sensitization to non-ABO antigens less likely?

A

ABO antibodies tend to destroy cells before they can cause an immune reaction

20
Q

How can you treat hemolytic disease of the newborn?

A

exchange transfusion (O neg RBC) for severe anemia phototherapy for hyperbilirubinemia intrauterine transfusion or early delivery in select cases **prevention is best treatment

21
Q

How do you prevent non-ABO immune hemolysis in the fetus?

A

prevent sensitization of the mother: never give Rh+ blood to Rh- woman Administer Rh immune globulin after delivery or abortion

22
Q
A
23
Q

What might be expected on the smear of a person undergoing hemolytic anemia? What is the most important lab result in this situation?

A

polychromasia, many spherocytes, H-J body; most important lab test is reticulocyte count

24
Q

Which of the following are not a cause of hemolysis: prosthetic valve, mild hypothyroidism, chemotherapy/radiation, chronic GI blood loss?

A

only mechanical valve would cause hemolysis, the rest simply lead to anemia

25
Q

What is microangiopathic hemolytic anemia?

A

intravascular hemolysis; can be caused by mechanical damage