BB LEC (Semis- Other Blood Groups- Quiz 2) Flashcards

1
Q

Found and soluble in plasma and saliva

A

Lewis Blood Group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
1
Q

“Plasma antigen”

A

Lewis Blood Group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

“Not” a true blood group antigen because it is acquired from the body tissues/Secretions

A

Lewis Blood Group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Expression of the Lewis antigens are influenced by? (2pts)

A

Hh and Sese genes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

This blood group is weak during pregnancy

A

Lewis Blood Group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

When was Lewis blood group first reported?

A

1946

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Lewis blood group is named after the?

A

one of the first individuals to make the antibody

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

In Lewis Blood group, the antibody, Anti-Le^a, is an agglutinated RBCs from about ______ of English people

A

25%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Are the antigens in Lewis Blood group antithetical?

A

NO

It was believed that both antigen were antithetical but proven otherwise

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Le genes (Le/FUT3) are located at the short arm of?

A

chromosome 19p13.3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

The Le gene of Lewis blood group is linked to? (2pts)

A

Se and H genes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

The gene does not actually code for the production of Lewis antigens but rather produce…?

A

specific L-fucosyltransferase to type 1 precursor substance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

The system depends on 3 genes to produce the Lewis antigen. These genes are:

A

H, Se, Le genes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

The two alleles at the secretor locus (Lewis blood group):

A

Se and se

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

The two alleles at the Lewis locus:

A

Le and le

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Le gene codes for?

A

L-fucosyltransferase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

The L-fucosyltransferase that is coded by the Le gene adds fucose to ____________________ to form Leª and fucose to _________________ to form Leᵇ

A

N-acetylglucosamine of Type-1 precursor; H structure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Lewis typing may be impossible until about?

A

6 years of age

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

This was formed by Se by adding fucose to terminal galactose on type 1 precursor

A

H structure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

These antigens are also found on lymphocytes and platelets

A

Lewis antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

This Lewis antigen is from the genetic interaction of LeLe and Sese

A

Lewis Le (a-b+)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Lewis antigens are resistant to treatment by enzymes…?`

A

Ficin and Papain, Dithiothreitol, and Glycine-acid EDTA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Le gene adds “L-fucose” to the ______________ and;
H gene adds “L-fucose” to ________of the precursor substance forming the Leᵇ antigen

A

N-acetylglucosamine; galactose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Le gene adds _________ to the N-acetylglucosamine of the type 1 precursor substance to form the Leª

A

“L-fucose”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

This is secreted regardless of secretor’s status

A

Leª substance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

The antibodies from this blood group are IgM and Naturally occurring

A

Lewis Blood Group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

The antibodies from this blood group react at room temperature and at 37C

A

Lewis Blood Group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

The year the antithetical “k” or “Cellano” was first described by Levine and group

A

1949

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

The antibodies from this blood group react at immediate spin, bind complement, trigger in-vitro hemolysis, and do not cause HDFN

A

Lewis Blood Group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

The year Kpª antigen and the null phenotype (Ko) were first described

A

1957

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

The year Jsᵇ antigen was first described (antithetical to Jsª, and both are related to Kell system)

A

1963

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

The year the antibody Anti-K was first identified in the serum of Mrs. Kelleher. Discovery by Robin Coomb

A

1946

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

The year the low-incidence antigen K24 was found

A

1985

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

The year both Jsª and Jsᵇ were officially added to the Kell system

A

1965

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

The year Jsª were first described, named after the first producer, “John Sutter”

A

1958

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

The year Kpᵇ was first described

A

1958

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

The year the K11 antigen was first reported

A

1971

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

The year the Kpᶜ antigen joined the Kell system

A

1979

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

The Kel gene is found on _____________ and consist of _________ exons

A

chromosome 7q33/34; 19 exons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

5 sets of alleles that produce the Kell system’s antithetical antigens exist within the Kell locus and these are:

A
  • K and k
  • Kpª and Kpᵇ
  • Jsª and Jsᵇ
  • K11 and K17
  • K14 and K24
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

The different Kell antigens are due to ____________ that results in amino acid substitutions

A

single base mutations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

The Kell Antigens are located on a _________ glycoprotein with ______ amino acids

A

type II; 719 amino acids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

Kell glycoprotein of the Kell antigens is a member of what family?

A

Neprilysin family

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

The Kell antigen expression is dependent on the presence of?

A

Xk protein

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

The N-terminal domain of the kell glycoprotein is intracellular, and the large external C-terminal domain is highly folded by ___________ and has _______ amino acids with ______ cysteine
residues

A

disulfide linkages; 665; 15

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q

The kell glycoprotein is linked with XK protein by a disulfide bond at ______ of Kell protein, to the _________of the XK glycoprotein

A

Cys72; Cys347

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q
  • Found only on RBCs
  • Appears on fetal red cells earlier than Rh proteins
A

Kell Antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
39
Q

Can be detected on fetal RBCs as early as 10 weeks gestation and is fully developed at birth

A

K antigen “Kell”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
39
Q

The Kell glycoprotein has been characterized as a ____________ which is central to zinc binding and catalytic activity

A

Zinc endopeptidase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
40
Q
  • With 3,500 to 18,000 sites per RBC
  • Low prevalence antigen
A

K antigen “Kell”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
40
Q

k antigen “Cellano” can be detected as early as?

A

7 weeks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
41
Q

Very immunogenic (second only to D)

A

K antigen “Kell”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
42
Q

Other term for:
- Kpᵇ antigen
- Kpª antigen

A
  • Kpᵇ antigen- “Rautenberg”
  • Kpª antigen “Penny”
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
43
Q

Gene encoding for this antigen is associated with suppression of other Kell antigens

A

Kpª antigen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
43
Q

Found in 2% of whites

A

Kpª antigen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
44
Q

Found in 20% of blacks

A

Jsª antigen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
45
Q

The K0 - Kell null Phenotype was identified in what year and by whom?

A

Bruce Chown, Marion Lewis, and Kiroko Kaita in 1957

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
46
Q

Resistant to ficin and papain, and are sensitive to trypsin and chymotrypsin. This is destroyed by Glycine-acid EDTA

A

Kell Antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
47
Q

A patient’s red cells lack the entire Kell glycoprotein, therefore, no Kell antigen

A

K0 - Kell null Phenotype

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
47
Q

This reduces the disulfide bonds of the protein

A

Sulfhydryl reagents (such as 2-mercaptoethanol, Dithiothreitol, 2-aminoethyl-isothiouronium bromide)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
47
Q

The most commonly encountered antibody next to ABO and Rh

A

Anti-K

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
48
Q

Associated with severe HTRs and severe HDFN

A

Anti-K

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
49
Q
  • Usually IgG (Predominantly IgG1) and reacts at AHG phase (IAT)
  • Stimulated by pregnancy or transfusion and persists for years
A

Anti-K

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
50
Q

Patients with this antibody should receive antigen-negative

A

Anti-K

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
50
Q

Are not commonly detected because individuals who lack these high-incidence antigens/antibodies (?) are scarce

A

Anti-Kpª, Anti-Kpᵇ, Anti-Kpᶜ, Anti-Jsª, Anti-Jsᵇ

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
51
Q

Antigens that are only found in Asians

A

Kpᶜ

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
51
Q

Found in erythroid tissues, brain, lymphoid organs, heart, skeletal muscle

A

Kx Blood Group “Xk”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
52
Q

Discovered in a young male medical student in 1961. He was initially a Kell null but showed weak expression to some Kell antigens

A

McLeod Phenotype

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
53
Q

True or False: The XK gene that encodes for the Xk protein is dependent to KEL gene

A

False. Xk protein is independent to KEL gene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
54
Q

Kx antigen is present on all RBCs except those of?

A

Mcleod phenotype

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
55
Q

Rare and are common in males via inheritance of X-linked through a carrier mother

A

McLeod Phenotype

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
56
Q

The McLeod phenotype RBC lacks ______ and ______, with decreased expression of other Kell antigens

A

Kx and Km

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
57
Q

People with McLeod phenotype are known to have the?

A

McLeod Syndrome (a
neuroacanthocytosis syndrome)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
57
Q

Individual with McLeod Syndrome present…? (2pts)

A

Muscle and Nerve disorders

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
58
Q
  • Muscle dystrophy - with increase CK-MM and Carbonic anhydrase III
  • Cardiomegaly
  • Chronic Granulomatous Disease
  • Acanthocytosis, Reticulocytosis, Bilirubinemia, Low haptoglobin, and Splenomegaly
A

McLeod Syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
59
Q

A multiply transfused hemophiliac who in 1950 was found out to produce antibodies against an antigen name Fyª

A

Mr. Duffy (Duffy Blood Group)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
60
Q

In what year did Sanger and colleagues report that majority of the African Americans tested were Fy (a-b-)

A

1955

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
61
Q

Most commonly encountered Duffy antigens

A

Fyª and Fyᵇ

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
61
Q

Can be detected at 6 weeks gestation and are fully developed at birth

A

Duffy antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
61
Q

In what year did Ikin et. al describe the Anti-Fyᵇ in the serum of Mrs. Hahn following the birth of her third child

A

1951

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
61
Q

In 1975, it was observed that _______ RBCs are resistant to Plasmodium knowlesi and Plasmodium vivax

A

Fy(a-b-)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
62
Q

There are about ________to ________ Fyª and Fyᵇ sites on Fy(a+b-) and Fy(a-b+) RBCs respectively

A

13,000 to 14,000

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
63
Q

Found in other body tissues such as the brain, Colon, Endothelium, Lungs, Spleen, Thyroid, Thymus, and Kidneys

A

Duffy antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
63
Q

These antigens are destroyed by proteolytic enzymes (Ficin, Papain, Bromelin, Chymotrypsin)

A

Duffy antigens

64
Q

Duffy Antigens reside on a glycoprotein of?

A

336 amino acids

65
Q

The glycoprotein of Duffy antigen is predicted to traverse the cell membrane ______ times and with _____ predicted disulfide bridges

A

seven; two

66
Q

Duffy glycoprotein is a member of the superfamily of chemokine receptors known as?

A

“Duffy antigen receptor for chemokines”

66
Q

The amino acid of:
- Fyª
- Fyᵇ

A
  • Fyª - glycine
  • Fyᵇ - aspartic acid
66
Q

The amino acid at _________ on Duffy glycoprotein defines Fyª and Fyᵇ polymorphism

A

position 42

67
Q

Binds variety of proinflammatory cytokines

A

“Duffy antigen receptor for chemokines”

68
Q

The gene of Duffy antigens is located near the centromere on the long arm of?

A

chromosome 1q23.2

68
Q

The Duffy gene was linked to a visible, inherited abnormality of?

A

chromosome 1

69
Q

The three alleles at the Fy locus

A

Fya, Fyb, and Fy

70
Q

These encodes Fyª and Fyᵇ

A

Fyª and Fyᵇ

70
Q

A duffy antigen that is a major allele in blacks

A

Fy

70
Q

Duffy Antibodies are usually _____ and reacts at _____

A

IgG; AHG

71
Q

Common and usually in a mixture of antibodies

A

Anti-Fyª

71
Q
  • Enhanced in a low ionic strength medium
  • Rarely binds complement
A

Duffy Antibodies

71
Q

Discovered in 1951 from an antibody detected in the serum of Mrs. Kidd who had in infant with HDFN

A

Kidd Blood Group

72
Q

The antithetical partner of Jkª was found on?

A

1953

73
Q

In what year was the null phenotype Jk(a-b-) was described?

A

1959

74
Q

This antibody is present on RBCs positive for Jkª or Jkᵇ

A

Jk3

75
Q

These antibodies are a significant cause of Hemolytic transfusion reactions

A

Kidd antibodies

75
Q
  • Found in most populations
  • Both are well developed at birth
A

Jkª and Jkᵇ

75
Q

Jkª can be detected on fetal RBCs at _______ gestation while Jkᵇ can be detected at _______ gestation

A

11 weeks; 7 weeks

76
Q

The Jk gene is located on?

A

chromosome 18q12.3

76
Q

These antigens are not found on other blood cells

A

Jkª and Jkᵇ (Kidd antigens)

77
Q

Phenotypes of the Kidd Blood group

A
  1. Jk(a+b-)
  2. Jk(a+b+)
  3. Jk(a-b+)
  4. Jk(a-b-)
78
Q

Resist lysis in 2M Urea and is associated with a dominant gene In (Jk)

A

Jk(a-b-)

78
Q

“Null”. Lacks the 3 antigens. Common in Filipinos, Chinese, Japanese, and Indonesians

A

Jk(a-b-)

78
Q

Weak and demonstrates dosage (reacts strongly with RBCs with double dose antigen)

A

Anti-Jkª and Anti-Jkᵇ (Kidd antibodies)

79
Q

Found in combination with other antibodies

A

Anti-Jkª and Anti-Jkᵇ (Kidd antibodies)

79
Q

Antibody reactivity of Anti-Jkª and Anti-Jkᵇ can be enhanced by using?

A

LISS or PEG

79
Q

Stimulated by pregnancy or transfusion

A

Anti-Jkª and Anti-Jkᵇ (Kidd antibodies)

80
Q

Known to be notorious for its danger in causing severe/fatal delayed HTR and some HDFN

A

Anti-Jkª and Anti-Jkᵇ

81
Q
  • An IgG that reacts at AHG phase
  • Associated with both immediate and delayed HTRs and mild HDFN
A

Anti-Jk3

82
Q

The antigen for that agglutinin is “I” is for?

A

“individuality”

82
Q

I Blood Group was discovered by? and in what year?

A

Discovered by Weiner and his coworkers in 1956

83
Q

They discovered the anti-i

A

Marsh and Jenkins

84
Q

“I” is a _________ carbohydrate while “i” is a ________ carbohydrate, both are formed
due to the activity of glycosyl transferase

A

branched; linear

85
Q

The reactivity of Anti-Jk3 is enhanced by?

A

enzyme pretreatment of the RBCs

86
Q

Infant RBCs are rich in what “I” antigen?

A

“i”

86
Q
  • Both are high-prevalence antigens
  • Expressed in a reciprocal relationship
A

I and i Antigens

87
Q

This antigen is undetectable in infant RBCs

A

“I” antigen

87
Q

During the first ________ of life, the quantity of “i” decreases

A

18 months

88
Q

Adult RBCs are rich in what “I” antigen?

A

“I”

”i” antigen is trace

89
Q

These antigens are precursors for the synthesis of ABO and Lewis antigens

A

I and i antigens

89
Q

This antigen has more and more adult i present in adult RBCs compared to cord blood RBCs

A

“Adult-i”

90
Q

Adults that retain their “i” antigen

A

“Adult-i”

91
Q

“i” antigen activity is defined by at least _____ repeating N-acetyllactosamine units in linear form

A

two

92
Q

Encodes the N-acetylglucosaminyltransferase that adds N- Acetylglucosamine (G1cNAc) to form the branches

A

IGnt gene (GCNT2)

92
Q

This antigen activity is associated with a branched form of “i”

A

“I” antigen

92
Q

found on chromosome 6p24

A

IGnt gene (GCNT2)

93
Q

Other sources of I and i antigens:

A
  • Membranes of leukocytes and platelets
  • Also found in serum, saliva, human milk, amniotic fluid, urine, and ovarian cyst fluid
94
Q

Diseases that can alter the expression of I and i antigens and can cause increased “i” antigen expression.
(State at least 3)

A
  • Acute Leukemia
  • Hypoplastic anemia
  • Megaloblastic anemia
  • Sideroblastic anemia
  • Thalassemia
  • Sickle cell disease
  • Paroxysmal nocturnal hemoglobinuria
  • Chronic hemolytic anemia
94
Q
  • Not associated with in-vivo RBC destruction
  • Weak, naturally occurring, saline-reactive IgM agglutinin
  • Stronger antibodies agglutinate test cells at room temperature and binds complement
A

Benign antibody of Anti-I

94
Q

Common autoantibody found in virtually all sera

A

Anti-I

94
Q

True or False: Antigens (“I” and “i”) in secretions do not correlate with RBC expression and are thought to develop under separate genetic control

A

TRUE

95
Q

How can you enhance anti-i reactivity?

A

By incubating in cold

95
Q

Detected by polyspecific AHG reagent

A

Benign antibody of Anti-I

95
Q
  • With strong agglutination to adult RBCs (weak with cord blood or adult i RBCs)
  • Production can be stimulated by microorganisms carrying I-like antigen
A

Anti-I

95
Q

Tested at 4C and with enzyme treated RBCs

A

Anti-I

96
Q

Anti-I production can be stimulated by microorganisms carrying I-like antigens except in patients with?

A

M. pneumoniae infection

96
Q

Patients with this infection may experience acute abrupt hemolysis as the infection begins

A

Patients with M. pneumoniae infection

96
Q

A strong IgM agglutinin with higher titers and a broad thermal range of activity (may reach 30-32C)

A

Pathogenic autoanti- I

97
Q

In pathogenic autoanti-I, when the circulation cools in response to low ambient temperatures, the antibodies will attach in-vivo and cause _________ and a ______________

A

autoagglutination; Vascular occlusion, or hemolytic anemia

98
Q

Reacts with adult and cord RBCs at room temperature and at 4C

A

Pathogenic autoanti- I

98
Q

A rare antibody that gives strong reactions with cord RBCs and adult-i RBCs

A

Autoanti-i

99
Q

Exist as IgG or IgM in the serum of most Adult-i individuals

A

Alloanti-I

100
Q

Not common in healthy individuals

A

Autoanti-i

100
Q
  • With weaker reactions to adult RBCs
  • Most are IgM and react with saline suspended cells and at 4C
  • IgG types are rare but are associated with HDFN
A

Autoanti-i

100
Q

Some patients with autoanti-i are associated with? (2pts)

A

Infectious mononucleosis and lymphoproliferative
disorder

101
Q

The P blood Group or “P1PK” is comprised with?

A

P, P1, Pᵏ, and Luke

101
Q

These antigens are not considered as a single blood group

A

P, P1, PK, Luke

102
Q

These antigens are assigned to the Globoside blood group system (028)

A

P and PX2

102
Q

These antigens are assigned to the P1PK blood group system (003)

A

P1 and Pᵏ

102
Q

This antigen is assigned to the Globoside collection (209)

A

LKE

103
Q

Introduced in 1927 by Landsteiner and Levine

A

P blood Group or “P1PK”

104
Q

Discovered via injection of human RBCs into rabbits which produced new antibodies

A

P blood Group or “P1PK”

105
Q

In the P blood Group or “P1PK” the antibody was initially called?

A

“Anti-P”

106
Q

The finding of Anti-P divided the human RBCs into?

A

“P+” or “P-”

106
Q

An Antibody to a high-prevalence antigen that Sanger later showed was related to the P blood group

A

anti-PP1Pᵏ

106
Q

In what year did Levine and his colleagues describe Anti-Tjª which is now known as
anti-PP1Pᵏ?

A

1951

107
Q

Sanger influenced the renaming and formation of the P blood group system
- P+ became _____
- P- became _____ and
- rare P null became ______

A
  • P+ became “P₁”
  • P- became “P₂” and
  • rare P null became “p”
108
Q

In 1959, __________ described the antigen Pᵏ

A

Matson and coworkers

109
Q

The antigen is expressed on all RBCs except those of very rare p phenotypes. Not readily detected unless P is absent

A

Antigen Pᵏ

110
Q

The 2 common phenotypes of P Blood Group

A

P1 and P2

111
Q

Describes RBCs that react with Anti-P1 and Anti-P

A

P1

112
Q

Describes RBCs that do not react with Anti-P1 but react with Anti-P

A

P2

112
Q

The 3 rare phenotypes of P Blood Group

A

p, P₁ᵏ, and P₂ᵏ

112
Q

This phenotype does not react with Anti-P1, Anti-P, or Anti-Pᵏ

A

“p”

112
Q

Reacts with Anti-Pᵏ but does not react with Anti-P1 or Anti-P

A

P₂ᵏ phenotypes

112
Q

These phenotypes are rare and are common in Japan, North Sweden, and in Ohio

A

“p” phenotypes (P null)

113
Q

Reacts with Anti-P1 and Anti-Pᵏ but not with Anti-P

A

P₁ᵏ phenotype

114
Q

The P Blood Group Antigens are synthesized by?

A

glycosyltransferases

adds sugar to a precursor substance

115
Q

This P blood group antigen can be found on platelets, epithelial cells, and fibroblasts

A

“P”

116
Q

These P Blood Group Antigens have been found in plasma as glycosphingolipids and
glycoproteins in hydatid cyst fluid

A

P and Pᵏ

117
Q

The reactivity of these antibodies is greatly enhanced by testing with enzyme-treated RBC

A

P antibodies

118
Q

Poorly expressed at birth (may even take 7 years for full expression)

A

P1 antigen

119
Q

The Antigen strength of P1 antigen varies from?

A

inheritance to Race

119
Q

Pᵏ synthesis is carried out by?

A

4- α- galactosyltransferase (Gb3, Pᵏ synthase)

119
Q

Deteriorates rapidly on storage

A

P1 antigen

119
Q

Blacks have stronger expression of _____ than whites

A

P1

119
Q

Strong antibodies to P1 have also been found in patients with __________

A

Fascioliasis

119
Q

The common precursor of P antigen

A

Lactosylceramide (Gb2, Ceramide
dihexose, or CDH)

119
Q

The discovery of anti-P1 in two P1-individuals infected with _____________ led to the discovery of P1 and Pk substances in _____________

A

Echinococcus
granulosus worms; hydatid cyst fluid

119
Q

Differences among P1+ individuals may be controlled __________ or via _______________

A

genetically; homozygous/heterozygous inheritance

120
Q

This is a bovine liver fluke disease

A

Fascioliasis

121
Q

This converts Pᵏ to P

A

β-N- acetylgalactosaminyltransferase (Gb4 synthase)

121
Q

P synthesis formation is carried out by?

A

3-β-N- acetylgalactosaminyltransferase (Gb4 synthase)

121
Q

This gene is located on chromosome 3q25 and encodes the 3-B-N- acetylgalactosaminyltransferase

A

Globoside gene (B3GALNT1)

122
Q

Tippett and colleagues described an antibody in the serum of a ______________ in 1965

A

Hodgkin’s lymphoma patient

122
Q

This gene is located on chromosome 22q13.2 and encodes the 4-a- galactosyltransferase

A

P1PK gene (A4GALT)

122
Q

Luke antigens (LKE) divided the population into three phenotypes:

A
  • 84% = Luke (+)
  • 14% = Luke (w) (means weakly positive)
  • 2% = Luke (-)
123
Q

All p and Pᵏ phenotypes are?

A

Luke (-)

124
Q

The group under P Blood group since the antibody reacted in all RBCs except 2% of P1 and P2 phenotypes

A

Luke Antigens (LKE)

125
Q

Common, naturally occurring IgM antibody in the serum of P1(-) individuals and is poorly developed on fetal RBCs

A

Anti-P1

125
Q

Anti-PP1Pᵏ was first discovered in the serum of Mrs. Jay, a “p” individual with?

A

adenocarcinoma of the stomach

126
Q

Formerly “Anti-Tjª”

A

Anti-PP1Pᵏ

126
Q

Reaction varies especially if old RBCs are used

A

Anti-P1

126
Q
  • Weak, cold-reactive saline agglutinin (reacts at 4C)
  • Stronger types react at room temperature
  • Rare types react at 37 C and bind complement
  • These types are detected at the AHG phase (polyspecific reagent)
  • May cause in-vivo RBC destruction, immediate or delayed HTRs
A

Anti-P1

127
Q

Produced by “p” individuals early in life without RBC sensitization and reacts with all RBCs except those of the “p” phenotype

A

Anti-PP1Pᵏ

128
Q

A component of anti-PP1Pᵏ in “p” individuals and is naturally occurring in the sera of Pᵏ individuals

A

Alloanti-P

128
Q

A P Blood group antibody that is rare and IgMs that reacts at room temp

A

Anti-LKE

129
Q
  • Can be separated by adsorption
  • Reacts over a wide thermal range and bind cocomplement
A

anti-P, anti-P1, and anti-Pᵏ

130
Q

Produced early in life without RBC sensitization; Can cause
HTRs and HDFN

A

Anti-PP1Pᵏ

131
Q

HLA detectable on RBCs

A

Bennet-Goodspeed Antigens

132
Q

Enumerate the Bennet-Goodspeed Antigens

A
  • Bgª antigen = HLA-B7
  • Bgᵇ antigen = HLA-B17
  • Bgᶜ antigen = HLA-A28
133
Q

IMPORTANCE OF STUDYING OTHER BLOOD GROUP SYSTEM (FINALLLYYY!!!!)

A
  1. Avoid Hemolytic Transfusion Reactions and Hemolytic Disease of the Fetus and
    the Newborns
  2. Avoid confusion brought up by insignificant antibodies
  3. Avoid mistyping
  4. Properly find and identify potential donors to rare blood group patients