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INTERMIDIATE EXAMINATION
DATE: 21-Nov-03
Student number:…………………………………………………………………
Centre:……………………………………………………………………………
INSTRUCTIONS TO CANDIDATES
3. Section A has 60 multiple choice questions (MCQS) and section B has 6 essay questions
4. Answer all the questions in section A, and answer ANY four (4) from Section B.
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20. Dolicos biflorus seeds produce a lectin which is able to react specifically with A1 red cells.
What is the chemical nature of the lectin?
a) Lipid
b) Protein
c) Steroid
d) Carbohydrate
21. Blood groups MN and P are not likely to cause a transfusion reaction or HDN. Why?
a) They are extremely rare
b) They produce cold antibodies
c) They are only found in rats
d) Their antibodies have an IgM class
22. The average shelf life of blood stored in Citrate Phosphate Dextrose (CPD) is..
a) 21 days
b) 35 days
c) 46 days
d) 64 days
23. Sensitized rhesus negative mother has ……… in the plasma.
a) Anti-c
b) Anti-E
c) Anti-D
d) Anti-d
24. Which class of antibodies is incriminated in Haemolytic Disease of Newborn (HDN)?
a) IgA
b) IgM
c) IgE
d) IgG
25. H antigen is present on all red cells except…
a) O+ Bombay cells
b) B+ cells
c) O+ cells
d) A+ cells
26. The commonest ABO blood group in Zambia is….
a) A
b) B
c) O
d) AB
27. Which of the following would produce a positive Direct Coombs Test (DAT)?
a) Plain red cells
b) Red cells digested with papain
c) Red cells washed in LISS
d) Red cells coated with complement
28. This amino acid is an ingredient of LISS
a) Alanine
b) Glycine
c) Methionine
d) Phenylalanine
29. Which blood group antigens serve as receptors for the entry of Plasmodium vivax
into red cells.
a) ABO antigens
b) Kell antigens
c) Duffy antigens
d) Kidd antigens
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30. MNS are seen as one blood group genetically. What is the difference between MN and S
blood groups serologically speaking then?
a) There is no genetic linkage between MN and S
b) MN produce cold antibodies where as S produce warm antibodies
c) MN is found in serum, and S on red cells
d) MN has soluble antigens, and S has insoluble antigens.
31. As a BTS officer how would you treat donor blood tested positive with VDRL.
a) Store at 22C for 72 hours before release for crossmatch
b) Store at 2 - 6C for 72 hours before release for crossmatch
c) Discard it right away
d) Issue it for cross-matching right away
32. In HIV infection, what best describes ‘window period’?
a) Time interval between appearance of anti-HIV and AIDS
b) Time interval between HIV infection and AIDS
c) Time interval between ARC and AIDS
d) Time interval between HIV infection and appearance of anti-HIV
33. How can one best describe the term ‘Complement Fixation’?
a) Consumption of compliment factors in serum by activation
b) Addition of compliment factors to serum
c) Inactivation of compliment factors in serum
d) Heamolysis of indicator red cells
34. A mother with rhesus genotype Cde/CDe and a father cDe/CdE are unlikely to have a
child with the following genotype.
a) Cde/CdE
b) CDe/cDe
c) Cde/cDe
d) CDe/Cde
35. Other than agglutination which phenomenon would render a cross match incompatible?
a) Rouleaux formation
b) Pan agglutination
c) Polyagglutination
d) Haemolysis
36. Fresh blood should not be older than 72 hours at 2 – 8C after collection. One of the
following clinical condition would warrant transfusion with fresh blood.
a) Hypo chromic microcytic anaemia (Hb 5.6g/l)
b) Bleeding due to intrauterine foetal death (PT 68 sec, APTT 150 sec)
c) Severe malarial infestation (B/S numerous)
d) Advanced Protein Calorie Malnutrition (Albumin 13g/l)
37. One of these transfusion reactions can be prevented by a cross match
a) Fever due to transfused incompatible MHC molecules
b) Urticaria caused by transfused allergens
c) Fever due to transfused cytokines such as TNF.
d) Intravascular haemolysis of donor cells
38. In ABO the expression of A gene will not affect the expression of B gene if
concurrently present at the same locus. Therefore, in group AB both anti-A and anti-B
bring about agglutination. What is this genetic feature called?
a) Recessiveness
b) Dominance
c) Penetrance
d) Codominace
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39. One of the antibodies below would not cause HDN or haemolytic transfusion reaction
being a cold antibody.
a) Anti-M
b) Anti-D
c) Anti-A
d) Anti-B
40. What does the term Du imply?
a) Strongly reacting D antigen
b) D negative
c) Defective D antigen
d) Weakly reacting D antigen
41. The first blood group to be discovered was….
a) Rh
b) ABO
c) Kidd
d) Kell
42. Which blood group was discovered in macacus monkey?
a) Rh
b) ABO
c) Kidd
d) Kell
43. The best way of extracting an antibody from a mixture is…
a) Absorption technique
b) Elution technique
c) Membrane fusion
d) Differential centrifugation
44. During monoclonal antibody preparation membrane fusion between splenocytes and
myeloma cells is achieved by use of this chemical.
a) Aminopterin
b) Polyethylene glycol
c) Propanol
d) Hypoxanthine
45. The system below is responsible for intravascular haemolysis of red cells in haemolytic
transfusion reaction.
a) Alternative complement
b) Classical complement
c) Coagulation
d) Phagocytosis
46. One of these is a light chain of a typical antibody.
a) -chain
b) -chain
c) -chain
d) -chain
47. How many light chains are present on IgM?
a) 5
b) 6
c) 10
d) 2
48. This chemical is often used to colour the anti-A grouping sera yellow.
a) Eosin
b) Tartrazine
c) Methylene blue
d) Methyl violet
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49. One of the following would exclude a prospective blood donor from donation panel
a) Fever characterising malaria
b) Infestation with round worms (Ascaris lumbricoides)
c) Colour blindness
d) Dental caries
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59. One of these substances below is able to opsonise red cells to enhance phagocytosis.
a) C4b
b) C3b
c) Interleukin –2 (IL2)
d) Tumour Necrosis Factor (TNF)
60. The reaction below would result from transfusing blood with incompatible MHC
molecules
a) Fever
b) Haemolysis
c) Blood pressure
d) Bleeding
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5. Explain the cascade of reactions that occur in classical complement
activation. What is the role of classical complement in haemolytic
transfusion reaction? (20 marks)
6. How would one use blood groups in paternity tests? Give examples and
state limitations. (20 marks)
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EXAMINATION COUNCIL OF HEALTH SCIENCES
INTERMEDIATE EXAMINATIONS
Diploma in Biomedical Sciences
DATE:13-Nov-03
Centre …………………………………………………..
INSTRUCTIONS TO CANDIDATES
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PART A - PRACTICAL PAPER
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