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MLT 106 Unit 4( Other Major Blood Group System) Flashcards | StudBud
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MLT 106 Unit 4( Other Major Blood Group System)
MLT 106 Unit 4( Other Major Blood Group System)
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1
Both antibodies are usually considered to be clinically significant, bind complement & associated with HTR & HDFN
Anti-S & Anti-s
Anti-M & Anti-N
Anti-U & Anti-P
2
Contains only one antibody specificity, either anti-IgG or antibody to specific complements like C3d or C3b
Polyspecific AHG reagents
Monoclonal AHG production
Polyclonal AHG production
Monospecific AHG reagents
3
Importance and appreciation of antigen-typing technique include, EXCEPT!
Performed for patients who have history of clinically significant antibody
The two are correct
Blood units should be antigen- negative to the clinically significant ab
4
Poorly expressed at birth, take up to 7 years,inhibited by a rare dominant gene In(Lu) type Lu(a-b-) RBCs
The Pk antigen
The M antigen
The P1 antigen
The S antigen
5
Required anti-human immunoglobulins are, EXCEPT?
Anti-IgG
Anti-IgM
Anti-Complement (anti-C3d,C3b,C4b,& C4d)
6
—-% of the errors are misidentification of the recipient or blood at bedside
47%
74%
80%
20%
7
Which statement is CORRECT about the steps taken to use additional panel cells
If the antibody panel does NOT clearly identify one specific antibody
The serum may contain either one or both of the antibodies
Test selected cells in all phases just as original panel
This cell will determine the specificity of antibodies
8
Newborn red cells have a linear structure with repeating N-acetyllactosamine units
Anti-i
i antigen
I antigen
Anti-I
9
Also called “Rule-out’’ technique, it is performed ONLY if there’s homozygous expression of the antigen ( 0 +)
Exclusion
Inclusion
Antigen typing
Evaluation of Panel
10
When donor units of an ABO group other than the recipient’s own type have been transfused(Test for unexpected anti-A &B)
Neonatal transfusion
Intrauterine transfusions
Transfusion of plasma products
Transfusion of Non-Group specific blood
11
Lutheran Null Phenotype Lu(a-b-) can result through three different methods, EXCEPT!
Dominant InLu suppressor gene
Recessive X-Linked gene
Recessive LuLu gene
Recessive InLu gene
12
For whole blood NO ALTERNATIVE IS ALLOWED
False
True
13
Located on smaller glycoprotein called glycophorin B ( GPB), which is similar to GPA
M & N antigens
S & s antigens
Se antigens
Lewis antigens
14
Are generally IgM and can not cross the placenta to cause HDN
Kell Blood group system
Lewis antibodies
The P antigens
MNS antibodies
15
Most commonly encountered antibody of the Lewis system. IgM & Clinically insignificant
Anti-S
Anti- Le a
Anti-Le b
Anti-M
16
Discovery and use of the reagent led to the finding of, EXCEPT!
Duffy
Polyclonal AHG Production
Kell
Kidd
17
Contains multi-antibodies to human IgG and C3d in each reagent bottle
Polyclonal AHG production
Monoclonal AHG production
Monospecific AHG reagents
Polyspecific AHG reagents
18
Produced by people of S-s-U- phenotype, is seen in African American. IgG & react at 37oC( very clinically significant)
Anti-P
Anti-U
Anti-M
Anti-S
19
Anti-Lu a often displays a characteristic loose, mixed field reaction during in vitro testing
False
True
20
Antigen should be examined to see if the pattern of reactivity matches a pattern of antigen-positive cells.
Exclusion technique
Antigen typing
Additional panel cells
Inclusion technique
21
Enzyme adds sugar L-fucose to type 2 precursor chain
B gene
A gene
H gene
Se gene
22
For the most part clinically insignificant unless detected at 37 oC IgM
Anti-P1
P1 antigen
Anti-P
Anti-Pk
23
Fairly rare antibody, autoantibody. Seen in infectious Mononucleosis
I antigen
Anti-I
Anti-i/ Autoanti-i
S antigen
24
Once an antibody is positive, additional testing is required to ID the antibody & determine its significance
Exclusion
Evaluation of panel
Inclusion
Antigen typing techniques
25
What is the primary purpose of a crossmatch ?
Misidentification
To prevent collection of sample from wrong Patient
To prevent a transfusion reaction & provide Pt with adequate qty of blood
To select blood products with acceptable survival rate
26
The DAT can detect a level of 100 to 500 IgG molecules per RBC and —- to —— molecules of C3d per RBC
400 to 1100
100 to 200
300 to 500
500 to 1100
27
Testing Pt serum with donor RBCs is the last blood bank test performed before component is given
False
True
28
Produced by Jk(a-b-) individuals
Anti-JK3
Anti-JKb
Anti-JKa
Anti-JK1
29
Is associated with poor expression of Kell system antigens( McLeod phenotype)
Acantocytosis
Anisocytosis
Lack of Kx gene
Lack of XK gene
30
Techniques that may aid in the identification of anti-Le a & anti-Le b:
Lewis system Antibodies
Helicobacter pylori
The MNS system antibodies
Neutralization of the Antibodies & use of enzyme
31
Production of the trans-membrane carrier molecule for Duffy glycoprotein
Fy Gene
The Duffy blood group system
Fy a
Fy b
32
Found on RBCs, lymphocytes, granulocytes,& monocytes. Synthesized by the sequential action of glycosyltransferases
P antigen
Anti-P
Pk antigen
P1 antigen
33
When phenotyping the patient is DIFFICULT, b’ce of a positive DAT or recent transfusion
Differential adsorption
Elution technique
Homologous adsorption
Auto adsorption
34
We do an auto control, If crossmatch is incompatible
True
False
35
Was developed to promote efficient utilization of blood & to establish realistic blood ordering level of certain procedu
Non-hemolyzed specimens
Maximum Surgical Blood Ordering Schedule ( MSBOS)
Yersinia Enterocolitica
Negative Antibody Screen
36
Is used to adsorb Bg-like antibodies from serum
Centrifugation
RESt
HLA antigens
Human Platelet concentration
37
Is located on chromosome 19. It codes for the production of enzyme that adds L-Fucose to type 1 precursor chain
Lewis Antigens
Secretor gene ( Se)
Secretor genotype
Lewis gene
38
The true Lewis phenotype ( Le(a-b+) ) resulting after ———-of age.
6-7 months
5-10 years
10 days
6-7 years
39
Is the final check on ABO blood group compatibility and may detect any antibodies in Pt’s serum
Group specific
Exclusion
Antiglobulins
Crossmatch
40
Bacterial contamination of cells leading to cell agglutination
False positives
False negative
41
The most common bacterial contaminant is —-!
Human globulins
Inadequate sealing
Saline and glasswares
Yersinia enterocolitica
42
Lewis antigens are not well developed at birth, but begin to appear shortly thereafter
False
True
43
Not intrinsic to RBCs but are on type I glycosphingolipids that are passively ADSORBED ONTO the RBC membrane from plasma
Lewis Antigens
Lewis Phenotype
Secretor Gene( Se)
Lewis Genotype
44
It is a powerful biphasic hemolysin
P antigen
Anti-P1
Anti-P
Anti-Pk
45
Agglutination or hemolysis in the crossmatch is considered evidence of ——?
Incompatibility
Compatibility
46
The number of IgG molecules sensitized on RBC and the rate at which sensitization occurs can be influenced by: EXCEPT!
Ratio of serum to cell
Centrifugation for reading
Counting the negative reactions
Washing of RBC
47
The XK gene responsible for Kc protein
The Kc blood group system
The kell system antigen
The kell system phenotype
Kell null phenotype
48
Adults have almost all I antigen= I adult
True
False
49
The Fy gene Plays a role in susceptibility to red cells invasion by ———-.
Mycoplasma pneumonia
Infectious mononucleosis
Plasmodium vivax
Kidd syndrome
50
Is not destroyed by neuraminidase or purified trypsin
Duffy
Kidd
McLeod
Kell
51
No secretions, lack Se and Le genes that add fucose to type 1 chain
Le( a-b-)
Le(a+b+)
Le(a+b-)
Le(a-b+)
52
No secretions, lack Se and Le genes that add fucose to type 1 chain
Le( a-b-)
Le(a+b+)
Le(a+b-)
Le(a-b+)
53
Uses Hybridoma technology which fuses mouse spleen lymphocytes with myeloma cells
Monoclonal AHG production
Monospecific AHG Reagents
Polyclonal AHG production
Polyspecific AHG reagents
54
If IgG antibodies are detected, it dissociate the antibodies from the RBC surface to allow for identification & classif-
Homologous adsorption
Elution technique
Inclusion technique
Differential adsorption
55
Associated with Mycoplasma pneumonia, which often develop strong cold agglutinins with I specificity
Autoanti-I
Anti-i
Anti-I
Autoanti- i
56
What’s NOT true about anti-M & anti-N antibodies?
Clinically significant
Cold IgM & shows Dosage
Naturally occurring
Require exposure
57
( Less than 4 months old) use serum/plasma of MOTHER and INFANT for initial testing
Intrauterine
Prenates
Preoperative autologous
Neonates
58
Secretors gene are found in approximately—-% of the random population
80%
20%
75%
15%
59
What is the secondary purpose of compatibility testing?
Prevent sample mixups
To select blood products with acceptable survival rates
To prevent collection of sample from wrong patient
To prevent a transfusion reaction
60
Will remove these insignificant antibodies, which may interfere with the detection of clinically significant antibodies
Auto adsorption
Homologous adsorption
RESt
Autoantibody
61
Patient labeling requirements include, EXCEPT?
Initials of the person drawing the blood
Address
Identification number
Patient’s full name
62
Interpreting the significance of positive DAT requires the knowledge of the—, —-, &—-, EXCEPT?
Patient’s history of illness
Recent transfusion therapy
Drug therapy
The patient’s diagnosis
63
Results of autocontrol & antibody screening test determine patterns that may identify the cause of the incompatibility
When crossmatch are positive
When crossmatch results are negative
When antigen Jka is negative
When antigen Fy are positive
64
Are well developed at birth & are destroyed by proteolytic enzymes ( ficin, papain,&bromelin
Both Fya & Fyb
Fy3
Fy4
Fy6
65
The following are biological significance of Anti-Le a EXCEPT?
Reacts at 37 o C to cause HDFN
Kidney transplant rejection
Helicobacter pylori
Peptic ulcers
66
In extreme cases, when there is no time to do Pretransfusion testing, O Rh-negative blood can be used
False
True
67
Secretes everything. Lea, Leb, A,B,& H
Le(a+b+)
Le(a-b+)
Le(a-b-)
Le(a+b-)
68
Are resistant to malaria invasion. EXCEPT!
Cells that are Fy( a-b-)
Lack of Fy(a+b-)
Lack of the Fy6 receptor
69
Usually IgM and rarely clinically significant ( incubated at 37oC)
Anti-M
Anti-N
Anti-s
Anti-S
70
Which statement is INCORRECT about anti-S,-s, and -U ?
Require exposure & warm IgG
Shows minimal dosage
Clinically significant
Results from homozygosity
71
Weak secretions stated, insignificant and rare
Le(a+b+)
Le(a-b-)
Le( a+b-)
Le(a-b+)
72
ABO grouping and Rh typing, repeat weak-D testing is NOT required.
True
False
73
Lewis antigen strength may decline dramatically during ———
Pregnancy
Prenatal
Neutralization
Blood Transfusion
74
Advantage of monoclonal AHG production is —-
Overly sensitive
Over-specificity
Cheaper
Higher titer of antibody than polyclonal AHG
75
Examples of clerical errors include, EXCEPT?
Mix-up of samples
Misidentification of recipient
Mis-labeled tubes
76
Found on glycophorin A ( GPA) , the major sialic acid rich glycoprotein (SGP)
S & s antigens
Lewis antigens
Se Antigens
M&N antigens
77
Appeared to be Kell null but demonstrated weak expression of k, Kpb and Jsb
The McLeod syndrome
Ko ( Kell null) phenotype
Fy Gene
The Duffy Blood group system
78
Which method is the antigen-antibody complex composed of SOLID PRECIPITATES and is removed from test by Centrifugation
Neutralization method
Absorption methods
Adsorption method
Human platelet concentration method
79
Blood transfused exceeding the patient’s total blood volume within 24 hrs or 4 to 5 units of RBC units in 1 hr
Intrauterine transfusions
Neonatal transfusions
Transfusion of plasma products
Massive transfusions
80
Detection of incomplete antibodies to potential donor red cells
Indirect Antiglobulin Testing ( AIT)
DAT Panel
Direct Antiglobulin Testing (DAT)
81
Are not destroyed by enzymes
Kell
P antigen
Kidd antigens
Duffy
82
The primary objective of crossmatch is to——?
To detect recipient antibodies that react with donor RBC antigens
To prevent collection of a sample from wrong patient
To select blood products with acceptable survival rates
To prevent a transfusion reaction
83
If ABO/Rh of fetus is determined to, group specific blood can be given provided there’s no fetomaternal ABO or Rh inco
Neonatal transfusions
Massive transfusion
Intrauterine transfusions
Transfusion of plasma products
84
Are produced by TISSUE CELLS and are found in plasma & body secretions
Lewis antigens
Lewis gene
Secretor gene
Lewis phenotype