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A. IgE reacting with mast cells
B. activation of cytotoxic T cells
C. IgG-allergen complexes that clog epithelial tissues
D. *complement-induced lysis of cells in the presence of antibodies
E. activation of natural killer cells
A. monozygotic twins’ serums
B. dizygotic twins’ serum
C. serums taken from different veins
D. serums of two patients with same diseases
E. *serums of one patient, the diseases taken in dynamics
A. They are the receptors for interleukin-2, which is produced by macrophages.when they attack the donor cells
B. *They are recognized by helper T cells, which then activate cytotoxic T cells to kill the donor cells
C. They induce the production of blocking antibodies that protect the graft
D. They induce IgE which mediates graft rejection
E. They induce complement depended cytolysis of the graft
A. type of antibody that combines with a toxin,
B. type of bacterium that resists phagocytosis.
C. type of enzyme that destroys toxins,
D. type of virus.
E. *inactivated toxin.
A. NADPH oxidase.
B. MPO.
C. G6PD.
D. No correct answer.
E. *all answers are true
A. ring precipitation
B. *in gel
C. on glass-slide
D. detailed
E. indirect
A. Micrococcus luteus
B. *Staphylococcus aureus
C. Escherichia coli
D. Streptococcus viridans
E. Salmonella typhi
A. Polymerase chain reaction (PCR)
B. ELISA
C. Method with the use of monoclonal antibodies
D. Radioimmune method (RIA)
E. *All of transferred
A. *serum of blood
B. pus
C. sputum
D. urine
E. liquor
A. For elimination of heterophiles antibodies
B. For diminishing of properdin’s activity
C. For the decline of lysozymes’ activity
D. *For elimination of complement
E. For oppressing of normal antibodies
A. The radial immunodiffusion of Manchini
B. The single dimension immunodiffusion in one dimension (Oudin procedure)
C. *The double immunodiffusion in two dimension (Ouchterlony)
D. The double diffusion in one dimension (Oakley-Fulthorpe)
E. The ring precipitation
A. Light chains
B. *Heavy chains
C. Domains
D. Fc- fragment
E. Fab-fragments
A. Cytotoxic T cells
B. *Hypervariable regions in domains of B cells
C. The major histocompatibility complex
D. Specific T cell receptors
E. Memory cells
A. Amino acid
B. Polysaccharidess
C. *Epitope
D. Protein
E. Porin
A. gamma interferon
B. phagocytosis
C. cytotoxic T cells
D. *enzymes released by polymorphonuclear cells
E. natural killers
A. type I
B. type II
C. type III
D. *type IV
E. all are correct
A. *IgE
B. IgM
C. IgA
D. only IgM and IgA
E. all of these
A. IgG
B. IgM
C. IgA
D. Only IgM and IgA
E. *all of these
A. IgG
B. IgM
C. *IgA
D. Only IgG and IgM
E. all of these
A. Atopic or anaphylactic
B. *Cytotoxic
C. Immune complex
D. Delayed
E. Autoimmune
A. B cell defect.
B. *Т cell defect.
C. Complement deficiency.
D. Phagocyte Deficiencies
E. No correct answer
A. Fluorescent antibody tests
B. Rocket electrophoresis
C. Double Diffusion in agar
D. *Immunoelectrophoresis
E. Ring precipitation
A. Specific antibody and complement
B. Specific antigen and complement
C. *Sheep red blood cells and hemolysin
D. Inactivated by temperature patient’s serum
E. Serum of guinea-pig
A.: 50
B.: 100
C. *1: 200
D.: 400
E.: 3600
A. Capsular polysaccharides
B. Recombinant surface antigens
C. Inactivated exotoxins
D. *DNA-based
E. All of the above
A. *potentially lethal graft-versus-host disease
B. high risk of T cell leukemia
C. inability to use a live donor
D. delayed hypersensitivity
E. autoimmune reaction
A. precipitin test
B. complement fixation test
C. agglutination test
D. coagglutination test
E. *indirect fluorescent-antibody test
A. DiGeorge's syndrome
B. *AIDS
C. Wiskott-Aldrich syndrome
D. Ataxia-telangiectasia
E. Chronic granulomatous disease
A. Determination of total quantity of lymphocytes in periferal blood (absolute and relative);
B. Determination of Т– and B–lymphocytes in peripheral blood;
C. Determination of the concentration of the main classes of immunoglobulins;
D. Determination of phagocitic activity of leukocytes.
E. *Determination of subpopulations of T lymphocytes (CD4+ and CD8+)
A. Single dose is immunogenic.
B. Dose is less.
C. Strict conditions of storage are essential.
D. Only humoral response is elicited.
E. It can mutate
A. Flow cytometry
B. Double diffusion immunoassay
C. *Immunoelectrophoresis
D. Direct immunosorbent assay
E. Indirect immunosorbent assay
A. lysis of antibody coated eucaryotic cells or bacteria
B. attract phagocytic cells
C. activation of phagocytic cells
D. *all of these are ways that the complement system aids in the defensive responses of an organism.
E. correct answers absent
A. Complement proteins
B. ABO antibodies
C. *MHC antigens
D. MHC antibodies
E. Mast cells
A. *MHC class I molecules
B. MHC class II molecules
C. MHC class III molecules
D. All of the above
E. None of the above
A. expression of antigen epitopes on B cells
B. expression of allergen epitopes on CD8 +T cells
C. IgE reaction with mast cells
D. reaction of allergen with the Ti and CD4 markers of B cells
E. *T helper cell reaction with the antigen epitope
A. Dysentery vaccines.
B. Cholera vaccines
C. *BCG
D. Diphtheria vaccines.
E. Solk polio vaccines
A. Salk.
B. *Sabin.
C. TAB.
D. Human diploid cell rabies vaccine.
E. DPT
A. hayfever
B. *allergic contact dermatitis
C. glomerulonephritis
D. penicillin reaction
E. blood transfusion reaction
A. Agglutination test
B. Precipitation test
C. Radial immunodiffusion test
D. *Radioimmune test
E. Immunoelectrophoresis
A. Matching the complement components of donor and recipient
B. Administering alpha interferon
C. *Removing mature T cells from the graft
D. Removing pre-B cells from the graft
E. Using monoclonal antibodies
A. Ability to cross the placenta
B. Isotype (class)
C. Ability to fix complement
D. *Affinity for antigen
E. Ability to opsonization
A. direct immunofluorescence
B. *indirect immunofluorescence
C. gel electrophoresis
D. countercurrent immunoelectrophoresis
E. all are correct
A. Direct immunosorbent assay
B. Double diffusion immunoassay
C. Flow cytometry
D. *Immunoelectrophoresis
E. Indirect immunosorbent assay
A. Fluorescent antibody tests
B. Rocket electrophoresis
C. Double Diffusion in agar
D. *Immunoelectrophoresis
E. Ring precipitation
A. atopic or anaphylactic
B. *cytotoxic
C. immune complex
D. delayed
E. autoallergy
A. herd immunity
B. seropositivity
C. cross reactivity
D. epidemic prophylaxis
E. *population immunity
A. *brucellosis
B. cholera
C. tularemia
D. typhoid
E. anthrax
A. *By flagellas
B. By bodies
C. By capsules
D. By hairs
E. By proteins
A. IgA
B. IgD
C. IgE
D. *IgG
E. IgM
A. *Streptococcal antigens induce antibodies cross-reactive with heart tissue
B. Streptococci are polyclonal activators of B cells
C. Streptococcal antigens bind to IgE on the surface of heart tissue and histamine is released
D. Streptococci are ingested by neutrophils that release proteases that damage heart tissue
E. Streptococci produce exotoxin B(protease) that destroy heart tissue
A. *IgM and IgG
B. Ig M and IgD
C. IgG and IgD
D. Ig An and IgD
E. IgA and IgG
A. *the thymus
B. the bursal equivalent
C. bone marrow
D. T cell-B cell interaction
E. stem cells originating in the bone marrow
A. the thymus
B. the bursal equivalent
C. T cell-B cell interaction
D. *stem cells originating in the bone marrow
E. gene encoding tyrosin kinase
A. other APCs
B. B lymphocytes
C. *Th lymphocytes
D. Neutrophils
E. NK cells
A. *the TcR
B. CD4
C. Class II MHC
D. membrane Ig
E. the BcR
A. CD 38 marker.
B. CD 25 marker.
C. CD 4 marker.
D. CD 3 marker
E. *CD 19 marker.
A. a hapten that combines with an antibody
B. *a substance that incites an antibody response and can combine specifically with these antibodies
C. a small molecule that attaches to cells
D. a carbohydrate
E. a protein that combines with antibodies
A. protein.
B. carbohydrate.
C. *glycoprotein.
D. fatty acid.
E. nucleic acid.
A. protein.
B. carbohydrate.
C. *glycoprotein.
D. fatty acid.
E. nucleic acid.
A. IgE
B. Gamma interferon
C. Class I MHC antigens
D. *Class II MHC antigens
E. Class III MHC antigens
A. IgE
B. Gamma interferon
C. Class I MHC antigens
D. *Class II MHC antigens
E. Class III MHC antigens
A. B-cells
B. T-killers
C. NK-cells
D. Mast cells
E. *T-helpers
A. IgE
B. Gamma interferon
C. Class I MHC antigens
D. *Class II MHC antigens
E. gM
A. IgE
B. Gamma interferon
C. Class I MHC antigens
D. *Class II MHC antigens
E. Class III MHC antigens
A. *T cells.
B. В cells.
C. monocytes.
D. granulocytes.
E. mast cells
A. bind to Class II MHC
B. function in signal transduction
C. bind to B7
D. *T cells
E. B1 and B2 cells
A. ICAM
B. TcR
C. *CD40L
D. CD16
E. CD8
A. all lymphocytes
B. B cells
C. *cytotoxic T cells
D. helper T cells
E. NK cells
A. helper Т cells.
B. *cytotoxic Т cells.
C. NK cells
D. both of the above.
E. none of the above.
A. Activation of lysozyme that degrades the cell wall
B. Acceleration of proteolysis of exotoxins
C. *Facilitation of phagocytosis
D. Inhibition of bacterial protein synthesis
E. Inhibition of bacterial metabolism
A. thymus
B. bursa of Fabricius.
C. bone marrow.
D. *all of the above are correct
E. all of the above are false
A. a hapten that combines with an antibody,
B. *a substance that incites an antibody response and can combine specifically with these antibodies.
C. a small molecule that attaches to cells.
D. a carbohydrate
E. a protein that combines with antibodies.
A. A hapten is complex antigen-antibody
B. *A hapten cannot induce an antibody by itself; rather, it must be bound to a carrier protein to be able to induce antibody
C. Haptens are big molecules of protein
D. Haptens must be processed by CD8 cells to become immunogenic
E. Haptens must be processed by MHC II to become immunogenic
A. epithelial cells
B. *macrophages
C. nerve cells
D. basophils
E. all of the above
A. *has a longer lag phase.
B. has a more rapid log phase.
C. persists for a longer plateau period.
D. attains a higher IgG titer.
E. produces antibodies with a higher affinity for the antigen.
A. perforations
B. *perforins
C. perforinse
D. performins
E. perporins
A. target cells from the same host.infected with any virus
B. *infected by virus A and identical at class I MHC loci of the cytotoxic T cells
C. infected by virus A and identical at class II MHC loci of the cytotoxic T cells
D. infected with a different virus and identical at class I MHC loci of the cytotoxic cells
E. infected with a different virus and identical at class II MHC loci of the cytotoxic cells
A. *mu chain
B. gamma chain
C. epsilon chain
D. alpha chain
E. kappa chain
A. *mu chain
B. gamma chain
C. epsilon chain
D. alpha chain
E. kappa chain
A. They are cell surface proteins on virtually all cells
B. They are recognition elements for cytotoxic T cells
C. They are codominantly expressed
D. *They are important in the skin test response to Mycobacterium tuberculosis
E. They are absent onto red blood cells
A. a hapten that combines with an antibody
B. *a substance that incites an antibody response and can combine specifically with these antibodies.
C. a small molecule that attaches to cells.
D. a carbohydrate
E. a protein that combines with antibodies.
A. *A hapten can combine with an antibody
B. A hapten can induce an antibody by itself
C. Haptens are big molecules of protein
D. Haptens must be processed by CD8 cells to become immunogenic
E. Haptens must be processed by MHC II to become immunogenic
A. *Are found mainly in the cortex region of the lymph node.
B. Are found in the red.pulp of the periarteriolar lymphoid sheath (PALS) of the spleen.
C. Make up 65-85% of the peripheral blood lymphocytes.
D. All of the above.
E. None of the above.
A. *Hypervariable regions of heavy and light chains
B. Constant regions of light chains
C. Constant regions of heavy chains
D. The hinge region
E. Constant regions of light and heavy chains
A. IgG
B. IgM
C. IgA
D. IgG and IgM
E. *IgM and IgA
A. *B lymphocytes
B. Monocytes
C. T lymphocytes
D. NK cells
E. be recognized by natural killers
A. are Rh(D)-negative
B. *are "universal recipients" of transfusions
C. have circulating anti-A and anti-B antibodies
D. have the same haplotype
E. are "universal donors" of transfusions
A. light chain variable region.
B. light chain constant region.
C. heavy chain variable region.
D. *heavy chain constant region.
E. Any of the above.
A. IgE
B. Gamma interferon
C. Class I MHC antigens
D. *Class II MHC antigens
E. Class III MHC antigens
A. lymphocytes.
B. myeloma cells.
C. *hybridomas.
D. spleen cells.
E. plasma cells.
A. the typing of tissue.
B. the identification and epidemiological study of infectious microorganisms.
C. the identification of tumor antigens.
D. the classification of leukemias.
E. *the manipulation of the immune response.
A. parasitic lysosomal degranulation.
B. aglutination of red blood cells.
C. *coating of microorganisms or other particles by antibody and/or complement.
D. adherence to mucosal epithelial cells.
E. antibody mediated viral inactivation.
A. are Rh(D)-negative
B. *are "universal recipients" of transfusions
C. have circulating anti-A and anti-B antibodies
D. have the same haplotype
E. are "universal donors" of transfusions
A. thymus
B. bursa of Fabricius.
C. bone marrow.
D. *all of the above are correct
E. E all of the above are false
A. A poptos
B. a poptosis
C. a pop tosis
D. apopstasis
E. *apoptosis
A. Th-1 cells produce gamma interferon and promote cell-mediated immunity
B. Th-2 cells produce interleukin-4 and -5 and promote antibody-mediated immunity
C. Both Th-1 and Th-2 cells have both CD3 and CD4 proteins on their outer cell membrane
D. *Before naive Th cells differentiate into Th-1 or Th-2 cells, they are, double- positives; ie, they produce both gamma interferon and intefleukin-4
E. Th-2 cells produce interleukin-10 and inhibit activity of Th-2 cells
A. lymph nodes.
B. spleen.
C. mucosa-associated lymphoid tissue.
D. GALT
E. *all of the above
A. *has a longer lag phase.
B. has a more rapid log phase.
C. persists for a longer plateau period.
D. attains a higher IgG titer.
E. produces antibodies with a higher affinity for the antigen.
A. NK cells
B. unbroken skin
C. cilia in trachea
D. *lysozyme in saliva
E. all of these
A. thymus
B. bursa of Fabricius.
C. bone marrow.
D. *all of the above are correct
E. all of the above are false
A. yolk sac.
B. foetal liver.
C. bone marrow.
D. *all of the above.
E. all of the above are wrong
A. all mature null cells
B. all mature lymphocytes
C. *all mature T lymphocytes
D. all mature monocytes
E. all mature K cells
A. serotonin
B. gamma interferon
C. *Interleukin-6
D. TNF
E. beta interferon.
A. The constant regions of H and L chains
B. *The hypervariable regions of H and L chains
C. The hypervariable regions of H chains
D. The variable regions of H chains
E. The variable regions of L chains
A. the constant regions of the light chains
B. the variable framework regions of the heavy & light chains
C. the variable regions of the heavy chains
D. *the hypervariable regions of both heavy & light chains
E. the constant regions of the heavy chains
A. precipitin test
B. complement fixation test
C. agglutination test
D. *indirect fluorescent-antibody test
E. coagglutination test
A. on all Tc lymphocytes
B. only on Th1 lymphocytes
C. *on all Th lymphocytes
D. on all NK cells
E. on all B lymphocytes
A. *IgG
B. IgM
C. IgA
D. IgD
E. IgE
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