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1
Q

Define antigen

A

A cell-surface protein capable of stimulating antibody production in an individual lacking that cell-surface protein

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2
Q

Define immunogen

A

the specific part, or parts, of an antigen that invoke the formation of antibody​

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3
Q

define antibody

A

Immunoglobulin produced in response to the introduction of a foreign antigen stimulated by the immunogenic part of the antigen. The antibody produced may result in removal of that antigen​

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4
Q

Why do IgM antibodies cause diresct agglutination while IgG require potentiators or AHG for agglutination.

A

IgM antibodies are large

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5
Q

difference between a direct and indirect test—-

A
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6
Q

what is an indirect antiglobulin test (IAT)? what is commonly used as a reagent and how?

A

testing antigen-antibody aggluttination to identify patient antibodies
mix patient sample with donor RBCs
incubated for binding
washing

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7
Q

describe fully an IAT

A

Primary - Incubation step
Secondary - Agglutination step

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8
Q

Explain the difference between an antigen and an immunogen

A

An antigen is any substance capable of inducing an immune response and can include non-immunogenic substances.

Immunogen specifically refers to the part of an antigen that can trigger the production of antibodies

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9
Q

What are antithetical antigens, and provide examples?

A

Antithetical antigens = antigens that are the result of alternative alleles at the same locus (different versions of the same antigen, determined by genetic variation).
Examples = M and N, S and s, and Fya and Fyb.

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10
Q

Describe the types of antibodies commonly found in blood groups and their characteristics.

A

Blood group antibodies are usually IgM or IgG, although some may be IgA.
IgM - naturally occurring,
IgG - immune.

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11
Q

what is the difference between IgM and IgG in terms of agglutination ability

A

IgM antibodies = directly agglutinate antigen-positive red cells in saline

IgG antibodies = most require potentiators or AHG to effect agglutination.

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12
Q

Why are ABO antibodies termed “naturally acquired”?

A

produced without requiring stimulation by foreign red cells
Most adults have antibodies to the A and/or B antigens naturally occurring to those ABO antigens they lack.

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13
Q

Discuss the factors influencing immunogenicity.

A

recognition of the substance as foreign

the molecular weight (typically at least 10,000 Daltons),

the composition of the substance (protein, carbohydrate, or lipid-based),

the amount and frequency of its introduction

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14
Q

define immunogenicity

A

ability to provoke an immune response

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15
Q

Explain why some IgG antibodies require potentiators or AHG for agglutination.

A

IgG is too small

AHG contains an antibody to IgG and so recognises and binds to the Fc portion of any IgG antibody.

Adding AHG allows cross-linking of red cells and therefore agglutination.

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16
Q

What factors contribute to the production of immune antibodies?

A

immunogenicity of the antigen concerned,

the amount and frequency of the stimulation involved,

the recipient’s immune response capability.

17
Q

Why does red cell antibody production not routinely occur after transfusion or pregnancy????????????

A
18
Q

What factors contribute to the production of immune antibodies?

A

Immunogenicity of the antigen: Some antigens are more likely to stimulate an immune response than others.

Amount and frequency of antigen exposure: Sufficient exposure to the antigen over time is required to trigger an immune response.

Recipient’s immune response capability: The recipient’s overall immune health and genetic factors influence their ability to generate antibodies.

Immunomodulatory factors: Certain medications, medical conditions, or immune-suppressing treatments may affect the immune response

19
Q

Discuss the clinical significance of blood group antibodies.

A

medicine and prenatal care:
etermine compatibility between donor and recipient blood or tissues, preventing adverse reactions such as hemolytic transfusion reactions or hemolytic disease of the fetus and newborn (HDFN).

Blood group antibodies can cause agglutination or hemolysis of incompatible red blood cells, leading to serious health complications or even death if not properly managed.

20
Q

What are the different ways blood group antigens can be introduced into circulation, and how do they lead to antibody formation?

A

transfusion of mismatched blood,

fetal-maternal blood exchange during pregnancy,

or transplantation of tissues containing foreign antigens.

When the recipient’s immune system encounters these foreign antigens, it may produce antibodies against them through the process of sensitisation, leading to antibody formation.

21
Q

What percentage of transfused patients, pregnant women, and transplant patients are likely to produce red cell antibodies?????????????????

A

Transfused patients: Approximately 2-9% may produce antibodies after transfusion, depending on various factors.
Pregnant women: About 1% may develop antibodies due to fetal-maternal blood exchange.
Transplant patients: Less than 2% may produce antibodies after transplantation.

22
Q

Explain the primary and secondary stages of agglutination in antigen-antibody reactions.

A

Primary stage: Occurs when antibody meets its corresponding antigen, leading to reversible binding via weak forces. This stage is also known as sensitisation.

Secondary stage: Involves cross-linking of red cells by antibody molecules, leading to visible agglutination. It depends on red cell dilution and attraction/repulsion forces.

23
Q

How does AHG facilitate the agglutination of red cells coated with IgG antibodies?

A

AHG contains antibodies to IgG and recognizes and binds the Fc portion of IgG antibodies. This binding allows for cross-linking of red cells coated with IgG antibodies, facilitating agglutination.

24
Q

Describe the blood group nomenclature system outlined in the lecture.

A

The blood group nomenclature system represents antigens, phenotypes, genes, and Rh haplotypes using various symbols and conventions, including capital letters, superscript/subscript letters and numbers, and positive/negative symbols enclosed in brackets.

25
Q

How are antigens represented in blood group nomenclature?

A

using capital letters, superscript letters, subscript numbers, non-subscript numbers, or a combination of these symbols. For example, A, B, K, Fya, Fyb, etc.

26
Q

Explain how phenotypes indicating RBC antigen presence are represented.

A

Phenotypes indicating RBC antigen presence are represented using positive and negative symbols enclosed in brackets. For example, Fy(a+b-), K-k+, Kp(a-b+), etc.

27
Q

How are genes causing the production of an antigen denoted in blood group nomenclature?

A

Genes causing the production of an antigen are denoted in text by the use of italics and superscript numbers or letters. For example, B, K, Fya, K11, etc.

28
Q

Discuss the shorthand used for Rh haplotypes in blood group nomenclature.

A

Rh haplotypes are represented using superscript symbols and letters or subscript numbers or letters. For example, r/, r//, ry, R1, R2, Ro, Rz, etc.

29
Q

why may anti-Jk^a react more strongly to Jk(a+b-)(homozygous for Jka) than Jk(a+b+)(heterozygous)?
and how does this show the dosage effect?

A

more Jka antigens on surface = more antibody binding to cell = stronger reaction
dosage effect shown as the absence of the competing antigen (Jk^b) allows for a higher expression (dosage) of Jk^a antigens and a stronger antibody-antigen interaction.

30
Q

what does IAT (indirect antiglobulin technique) detect?

A

IgG antibodies at 37*C
complement fixing antibodies
Rh antibodies

31
Q

which antibodies in the panel are clinnically insignificant and can be ruled out?

A

Cw, Kpa, P1, Lua, Lea, Leb

32
Q

what are the three methods of performing antibody identification?

A

traditional tube technique
gel column agglutination technology
solid phase technology

33
Q

why is column agglutination tech so commonly used?

A

lower sample volume required
reproducible results due to standardisation
stable reaction endpoints
eliminates washing steps
control cell not often required

34
Q

what is haemolytic disease of the foetus/newborn (HDFN) (erythroblastosis fetalis)?
what causes it?

A

destruction of red blood cells (hemolysis) in a fetus or newborn due to an incompatibility between the blood types of the mother and baby
—anemia, jaundice, and in severe cases, fetal hydrops (accumulation of fluid in fetal tissues)

35
Q

what is the purpose of the enzyme treatment panel in antibody identification?

A

altering the antigenic properties of RBCs through enzymatic digestion.

36
Q

what enzymes are used in the enzyme treatment panel?

A

papain, ficin, or bromelain

37
Q
A