Chapter 8 Concepts Flashcards

1
Q

How many RBC antigens are formally recognized internationally?

A

300 RBC antigens

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2
Q

Blood group antigens are defined by (structure-wise):

A

Carbohydrates (sugars) attached to the glycoprotein or glycolipid structures or by amino acids on a protein

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3
Q

Lewis, P, and I carbohydrate antigen blood groups

A

(like ABO and H) are not encoded by their genes but rather their genes encode specific GLYCOSYLTRANSFERASES that in turn synthesize the carbohydrate epitopes

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4
Q

How do Lewis, P, and I carbohydrate blood groups synthesize the carboyhydrate epitopes?

A

By sequential addition of sugars to a precursor

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5
Q

MNS, Duffy, Kell, and Kidd antigen blood groups

A

Significant in routine transfusion medicine and antibodies to these antigens are MORE COMMONLY encountered

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6
Q

A blood group system is one or more antigens produces by alleles at a single gene locus or at loci so closely linked that:

A

crossing over does not occur or is very rare

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7
Q

Most blood group genes are located on the autosomal chromosomes and demonstrate:

A

Straightforward Mendelian inheritance

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8
Q

Most blood group alleles are _____ and express a corresponding antigen.

A

Codominant (For example, a person who inherits alleles K and k expresses both K and k antigens on their RBCs. Some genes code for more than one antigen - i.e. the glycophorin B structure, which carries S and s antigen, also carries the U antigen)

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9
Q

Allele

A

One of two or more different genes that may occupy a specific locus on a chromosome

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10
Q

Silent, or amorphic, alleles exist that make:

A

no antigen but they are rare

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11
Q

When paired chromosomes carry the same silent (amorphic) allele:

A

a null phenotype results which can be very helpful when evaluating antibodies to unknown high-prevalence antigens

(For example, an antibody reacting with all test cells except those with the phenotype Lu(a-b-) may be directed against an antigen in the Lutheran System.

In some blood group systems, the null phenotype results in RBC abnormalities.

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12
Q

Some blood group systems have regulator or modifying genes, which alter:

A

antigen expression

These are not necessarily located at the same locus as the blood group genes they affect and may segregate independently.

(For example, RBCs with the dominant type of Lu(a-b-) have suppressed expression of all antigens in the Lutheran blood group system as well as many other antigens, including P1 and i)

Therefore, this modifying gene is inherited independently of the genes coding for Lutheran, P1, and i antigens.

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13
Q

Blood group antigens are detected by alloantibodies which occur:

Allo- Prefix indicating differences within a species (e.g., an alloantibody is produced in one individual against the red blood cell antigens of another individual)

A

Naturally (i.e., without a known immune stimulus) or as a response by the immune system after exposure to non-self RBC antigens introduced by blood transfusion or pregnancy.

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14
Q

Phenotype Nomenclature:

For letter antigens, a plus sign or a minus sign written on the same line as the antigen is used to designate that the antigen is present or absent

A

Phenotype Nomenclature Continued

For antigens that have superscripts, the letter of the superscript is placed in parentheses on the same line as the letter defining the antigen - for example Fy(a+) and Jk(a-)

For antithetical antigens, both results are written within the parentheses - Fy(a-b+)

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15
Q

Serologic tests:

determine only RBC phenotype NOT

A

genotype

A genotype is composed of the actual genes that an individual has inherited and can be determined by family or DNA studies

Sometimes the genotype can be inferred by the phenotype (probably interpretation)

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16
Q

Antibody Nomenclature

are described by their antigen notation with the prefix -

A

anti-

17
Q

To facilitate computer storage and retrieval of bloos group information and to help standardize blood group system and antigen names…

A

the International Society of Blood Transfusion (ISBT) formed the Working Party on Terminology for Red Cell Surface Antigens of 1980

The numeric system was not intended to replace the traditional terminology but rather to enable communication on computer systems where numbers are necessary.

The first three numbers represent system, collection, or low- or high- prevalence series, and the second three digits identify the antigen

Antigens within the system are number sequentially in order of discovery

18
Q

Collections are antigens that have

A

a biochemical, serologic, or genetic relationship but do not meet the criteria for a system - assigned a 200 number

19
Q

001 ABO

002 MNS

003 P1PK

004 Rh

005 Lutheran

006 Kell

007 Lewis

008 Duffy

009 Kidd

010 Diego

011 Yt

012 Xg

A

ABO 9q 4Ags

MNS 4q 46Ags

P1PK 22q 2Ags

RH 1p 52Ags

LU 19q 20Ags

KEL 7q 32Ags

LE 19p 6Ags

FY 1q 5Ags

JK 18q 3Ags

DI 17q 22Ags

YT 7q 2Ags

XG X 2Ags

20
Q

ISBT Collection Names:

A

Cost

Li

Er

Vel

21
Q

Low prevelance Series Ags: <1% of most random populations

High Prevelance Series Ags: >90% of most random populations

A

Low: 700 Series

High: 901 Series

22
Q

Lewis Blood Group System (007):

A

Lewis antigens are not intrinsic to RBCs but are on type 1 glycosphingolipids that are passively adsorbed onto the RBC membrane from the plasma.

23
Q

Lewis Blood Group System (007):

Antibody anti-Le^a

A