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B. C + patient's serum + EA/wait/+ Ag
C. Ag + patient's serum + EA/wait/+ C
D. *Ag + patient's serum + C/wait/+ EA
E. patient's serum + EA +C/wait
A. Capsid’s proteins
B. Internal proteins
C. Nucleoproteins
D. *Nucleic acid
E. Glycoproteins of supercapsid
A. SS + V to expect > CC
B. CC + V to expect > SS
C. *V + SS to expect >CC
D. SS + CC to expect >V
E. CC + PS to expect >V
A. an estimation of the immune status
B. *serological diagnosis of infectious diseases
C. serological diagnosis of congenital immunodeficiency
D. serological identification of microorganisms
E. definition of group of blood
A. in diagnostics of Anthrax
B. for definition toxigenity of diphtheritic cultures
C. *for definition of groups of blood
D. In forensic medicine
E. for definition of class Ig
A. Coagglutination (COA)
B. *Latex agglutination (LA)
C. Enzyme-linked immunosorbent assay (ELISA)
D. Enzyme multiplied immunoassay test (EMIT)
E. Counterimmunoelectrophoresis (CIE)
A. complement+hemolysin
B. *red cells and hemolysin
C. patient’s serum
D. red blood cells of I (0) groups and hemolysin
E. specific antigen
A. decreased resistance to viral infections
B. increased hypcrsensitivity reactions
C. increased frequency of cancer
D. *decreased resistance to Neisseria bacteremia
E. all answers are true
A. Antigens which all of representatives of this kind have.
B. *Antigens whichare possessed by some representatives of this kind.
C. Antigens which are possessed by all of representatives of different kinds.
D. Antigens which are possessed by some representatives of different kinds.
E. Antigens which are possessed by a certain person.
A. detailed
B. indirect hemagglutination
C. *precipitation
D. on glass-slide
E. coagglutination
A. hydrophobic interactions
B. *connection of the active centers of antibodies and determinant groups of antigenes
C. Van-Der Waalse interactions
D. Brown movement
E. electrostatic interaction
A. DiGeorge's syndrome
B. *AIDS
C. Wiskott-Aldrich syndrome
D. Ataxia-telangiectasia
E. Chronic granulomatous disease
A. *sediment of red cells as a "button"
B. flocculation
C. luminescence
D. sediment of red cells as a "umbrella"
E. sediment of red cells in the test tube
A. sediment
B. discoloration
C. *even dimness
D. flocculation
E. gasification
A. SS + V to expect > CC
B. CC + V to expect > SS
C. *V + SS to expect >CC
D. SS + CC to expect >V
E. CC + PS to expect >V
A. Performing the test in a liquid environment
B. use of transparent antigens
C. *impossibility to set the amount of different antigens
D. the colloid particles of protein take part in the reaction
E. all of above are incorrect
A. antibodies in the blood serum, urine
B. autoantibodies in serum
C. *bacterial, viral antigens in a serum, urine, CSF.
D. incomplete antibodies in serum
E. incomplete antibodies on red blood cells
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. 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. tuberculosis.
B. enteric fever.
C. diphtheria.
D. rubella.
E. pertussis
A. B cell defect.
B. Т cell defect.
C. both В and Т cell defects.
D. Complement deficiency.
E. *Phagocyte Deficiencies
A. B cell defect.
B. *Т cell defect.
C. both В and Т cell defects.
D. Complement deficiency.
E. Phagocyte Deficiencies
A. B cell defect.
B. *Т cell defect.
C. both В and Т cell defects.
D. Complement deficiency.
E. Phagocyte Deficiencies
A. *B cell defect.
B. Т cell defect.
C. both В and Т cell defects.
D. Complement deficiency.
E. Phagocyte Deficiencies
A. contactant
B. ingestant
C. injectant
D. *inhalant
E. insectant
A. the causative agent of anthrax
B. anthrax toxins
C. spores of bacillus anthracis
D. *antibodies to a specific antigene of bacillus anthracis
E. normal antibodies
A. receive from donor blood
B. use for therapy
C. *use for serological identifying of microorganisms
D. use for serological diagnosis of infectious diseases
E. contains monoclonal antibodies
A. reaction of sedimentation of a soluble antigene
B. interaction an antigene-antibody
C. serological test
D. *the mechanism of realization of cellular immunity
E. passes in a solution of electrolit
A. in diagnostics of Anthrax
B. for definition toxigenity of diphtheritic cultures
C. *for definition of groups of blood
D. In forensic medicine
E. for definition of class Ig
A. ring precipitation
B. *in gel
C. on glass-slide
D. detailed
E. indirect
1043. Presumptive agglutination test allows to do a preliminary conclusion about selected pure culture. Choose faithful assertion concerning this test:
A. *used for the exposure of unknown microorganism by a specific serum
B. used only for determination of level of antibodies in the patient’s serum
C. a test is conducted in the wells of polystyrene plates
D. the account of test is conducted in 2-3 hours
E. allows to define the titre of incomplete antibodies
A. Agar is mixed with antiserum
B. Patient samples (serum) is diluted
C. All classes of immunoglobulins except IgE determination
D. *Measure Ag-Ab-Complement complex
E. Diameter of ring is proportional to concentration of antigens
A. sedimentation of a soluble antigene
B. *sedimentation of a corpuscular antigene
C. linkages complement
D. Immune hemolysis
E. Immune sticking
A. precipitation.
B. complement fixation.
C. *degranulation.
D. agglutination
E. asthma
A. *red blood cells - hemolysis
B. an antigene - hemolysis
C. serum– hemolysis
D. complement- hemolysis absence
E. hemolysin- hemolysis absence
A. immunodeficiency disease, muscles
B. autoimmune disease, nerves
C. allergy, cartilage
D. *autoimmune disease, joints
E. autoimmune disease, bones
A. K
B. O
C. Vi
D. *H
E. B
A. *that have differences in antigenic composition.
B. that have differences in size
C. that have differences in molecular weigh
D. that have differences in fermentative properties
E. that have differences in morphological structure
A. antigen and patient’s serum
B. antigen, antibody, complement
C. precipitated serum and bacteria
D. antigen and tanned red blood cell diagnosticum
E. *patient’s serum and molecular antigen
A. using the immunofluorescence test.
B. using the agglutination test.
C. using the Coombs test
D. *using the precipitation test.
E. using the latex-agglutination test
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. all are correct
A. interleukin-2
B. interleukin-10
C. *slow-reacting substance A (leukotrienes)
D. serotonin
E. bradykinin
A. Agar is mixed with antigen
B. Patient samples (serum) is not diluted
C. Only IgG determination
D. Measure Ag-Ab complex
E. *Diameter of ring is proportional to concentration of antigens
1056. Slide agglutination test allows to do a preliminary conclusion about selected pure culture. Choose faithful assertion concerning this test:
A. *used for the exposure of unknown microorganism by a specific serum
B. used only for determination of level of antibodies in the patient’s serum
C. a test is conducted in the wells of polystyrene plates
D. the account of test is conducted in 2-3 hours
E. allows to define the titre of incomplete antibodies
A. Between the constant parts of H- and L-chains
B. Between the variable parts of Н-chains
C. Between the constant parts of Н-chains
D. In the joint region of immunoglobuline
E. *Between the variable parts of H- and L- chains
A. Chemical structure
B. Foreignness
C. *Epitopes
D. In size electric charge
E. Size of molecular weight
A. By a chemical nature
B. Foreignness
C. *Determination groups
D. In size of electric potential
E. By size of molecular weight
A. Antigens
B. Bacteria
C. *Staphylococcus aureus
D. Streptococcus hemolyticus
E. Antiglobulin
A. Because they have complement binding point in the Fab fragment
B. Because their third domain adsorbs C2 and C4
C. *Because there is a place for attachment of C1 in a joint region
D. Because only their light chains are able to fix complement
E. Because there is similarity between their disulphide bridge and C1-C4
A. one monomer
B. two monomers
C. three monomers
D. four monomers
E. *five monomers
A. *B cell defect.
B. Т cell defect.
C. both В and Т cell defects.
D. Complement deficiency.
E. Phagocyte Deficiencies
A. *Cl, C4
B. B cells
C. Т cells
D. No correct answer
E. Phagocyte
A. *immunoglobulins’ classes.
B. antibodies.
C. immune complexes.
D. cytokines.
E. All of the above.
A. at participation of antibodies
B. *at participation of LPS
C. without formation membrane attack complex
D. at formation of a complex an antigen - antibody
E. at formation of R-forms of microorganisms
A. *to mix up an antiserum with gel. Bring an antigen in wells, done in gel
B. to mix up an antigen with gel. Bring a specific serum in wells, done in gel
C. To make wells in neutral gel. To bring in an antigen in one of them, in other is an antibody
D. To do a well in a centr in neutral gel, where to bring in an antigen. Make four wells, around and bring in the different types of antibodies into them
E. To mix antigen and specific antibody in the neutral gel
A. process of recognition of antigen by the receptors of macrophage
B. co-operating of antigen with dendritic cells
C. recognition of antibody by antigen’s epitopes
D. *co-operating of antigen with an antibody
E. all of assertions are true
A. *complement
B. antigenes
C. antibodies
D. red blood cells
E. hemolysin
A. without participation of antibodies
B. at participation properdin
C. without formation membrane attack complex
D. *at formation of an antigen – antibody complex
E. at formation L-transformations
A. synergism
B. *cascade
C. avalanche
D. amplified response
E. all are true
A. Specific serum, sheep red blood cells
B. *Viral material, red blood cells
C. Unknown antibodies, chicken red blood cells
D. Virus, sheep red blood cells
E. Pair serums, viral diagnosticum
A. sensiling dose
B. degranulation dose
C. *provocative dose
D. desensitizing dose
E. inhibition dose
A. the allergen directly on smooth muscle
B. the allergen on B lymphocytes
C. *allergic mediators released from mast cells and basophils
D. IgE on smooth muscle
E. the allergen on mast cells
A. *antigens
B. antibodies
C. either antigens or antibodies
D. limphocytes
E. cytokines
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. beta-globulins
B. Albumens
C. Glycoproteins
D. *Immunoglobulins
E. a-fetoprotein
A. Variable region of light chain.
B. Constant region of light chain
C. Variable region of heavy chain
D. *Constant region of of heavy chain
E. Any area
A. edema without a cellular infiltrate
B. an infiltrate composed of neutrophils
C. *an infiltrate composed of helper T cells and macrophages
D. an infiltrate composed of eosinophils
E. cellular infiltration
A. sediment
B. discoloration
C. even dimness
D. *formation of rings precipitation
E. gasification
A. it can be administered orally
B. *it provides antibody more rapidly
C. antibody persists for a longer period
D. it contains primarily IgM
E. it contains only antibacterial antibodies
A. to mark and target antigens for destruction by other components of the immune system.
B. to detect unknow antigen
C. to detect unknow antibody
D. *All are true
E. No correct unswer
A. *Agar is mixed with antiserum
B. Patient samples (serum) is not diluted
C. Only IgM determination
D. Measure Ag-Ab-Complement complex
E. Diameter of ring is not proportional to concentration of antigens
A. *serum
B. diagnosticum
C. culture
D. agglutinated serum
E. physiological solution
A. diagnosticum
B. cultures
C. *serum
D. agglutinated serum
E. physiological solution
A. *2th H and 2th L chains
B. th H-chains
C. th L- chains
D. th H-chains
E. th L-chains
A. *the class (isotype) of antibody
B. the site where antigen-antibody complexes are formed
C. the participation of macrophages
D. the participation of T cells
E. correct all
A. the class (isotype) of antibody
B. *the site where antigen-antibody complexes are formed
C. the participation of complement
D. the participation of T cells
E. interraction between antigen and antibody
A. Enzyme multiplied immunoassay test (EMIT)
B. Latex agglutination (LA)
C. Enzyme-linked immunosorbent assay (ELISA)
D. *Coagglutination (COA)
E. Counterimmunoelectrophoresis (CIE)
A. *Unknown bacteria
B. A level of specific antibodies is in a serum
C. Level of complement
D. Level of lysozymes
E. All of the above-mentioned right
A. bacteria
B. virus
C. levage of the surface of the tested object
D. *thermoextract animal’s skin
E. patient’s blood
A. Determination of subpopulations of T lymphocytes (CD4+ and CD8+);
B. Leukocyte migration inhibition test;
C. Examination of proliferative ability of T– and B–lymphocytes (lymphocyte blast transformation test);
D. Cutaneous tests of hypersensitivity;
E. Determination of Т– and B–lymphocytes in peripheral blood
A. antibodies
B. *antigens
C. immune complexes
D. cytokines
E. complement
A. *an inflammatory response
B. histaminesies.
C. autoimmune antigens.
D. IgE.
E. autoimmune antibodies
A. a minimum quantity causing partial hemolysis of red blood cells in hemolytic system
B. *a minimum quantity causing full hemolysis
C. a maximum quantity causing full hemolysis
D. minimum quantity at which hemolysis is absent
E. the maximum quantity causing partial hemolysis
A. *20-30 %
B. -40 %
C. -50 %
D. -60 %
E. -70 %
A. Patient’s serum labeled with an enzyme, specific antigen
B. Specific serum, virus, antigen, antiglobulin serum
C. Virus, antigen in wells, specific serum, substance
D. *Viral antigen in wells, patient’s serum, antiglobulins serum labeled with an enzyme, substance
E. Patient’s serum in wells, viral antigen, antiglobulins serum labeled with an enzyme
A. latex-agglutination
B. indirect hemagglutination
C. *precipitation
D. on glass-slide
E. coagglutination
A. natural active
B. artificial passive
C. *artificial active
D. natural passive
E. non are correct
A. Capsid’s proteins
B. Internal sproteins
C. Nucleoproteins
D. *Nucleic acid
E. Glycoproteins of envelope
A. bacterial diagnosticum and patient’s serum
B. *patient’s serum and tanned red blood cells diagnosticum
C. antigen and fluorescein-tagget antibodies
D. antigen and tanned red blood cells diagnosticum
E. antigen, antibody, complement
A. a humoral immune response has occurred
B. *a cell-mediated immune response has occurred
C. both the T and B cell systems are functional
D. only the B cell system is functional
E. a humoral immune response has decreased
A. *recurrent pyogenic infections.
B. AIDS
C. All answers are correct.
D. No correct answer
E. recurrent fungal infections
A. Determination of subpopulations of T lymphocytes (CD4+ and CD8+);
B. Leukocyte migration inhibition test;
C. Examination of proliferative ability of T– and B–lymphocytes (lymphocyte blast transformation test);
D. Cutaneous tests of hypersensitivity;
E. *Determination of Т– and B–lymphocytes in peripheral blood
A. Lipid
B. Glucose
C. Fat acids
D. *Proteins
E. Carbonhydrates
A. *IgG
B. IgM
C. IgD
D. IgE
E. IgA
A. natural, acquired, passive
B. artificial, acquired, passive.
C. artificial, acquired, active.
D. *natural, acquired, active
E. all answers are incorrect
A. *full hemolysis of red cells
B. hemolysis absence
C. partial hemolysis of red cells with intensity +++, ++
D. precipitate formation
E. agglutinate formation
A. partial hemolysis
B. *agglutination with intensity ++++, +++, ++
C. a phenomenon of spontaneous agglutination
D. sedementation of erythrocytes
E. Full hemolysis of erythrocytes
A. *an antigene - molecular
B. an antigene – corpuscular
C. antibodies – monoclonal
D. Antibodies – polyclonal
E. Antibodies – blocking
A. *an antigene - molecular
B. an antigene – corpuscular
C. antibodies – monoclonal
D. Antibodies – polyclonal
E. Antibodies – blocking
A. *T cell defect.
B. В cell defect.
C. Ataxia-telangiectasia
D. E. Chronic granulomatous disease
E. AIDS
A. It is easier
B. *It is more accurate
C. It requires less test material
D. It is more sensitive
E. It is less expensive
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