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A) It differentiates in the medulla of lymph nodes and the bone marrow.
B) It dedicates 10-20% of total protein synthesis to antibody production.
C) Levels of MHC class II molecules are elevated.
D) It undergoes extensive proliferation in germinal centers.
E) It produces secreted immunoglobulin instead of the membrane-bound form.
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A) The expression of Myc protein is perturbed.
B) A chromosomal translocation involving a proto-oncogene and an immunoglobulin gene occurs.
C) Overproduction of the Bcl-2 protein prolongs the lifetime of B-lineage cells.
D) Cell division restraints on mutated B cells are lifted.
E) In addition to a chromosomal translocation event,mutations elsewhere in the genome are usually involved.
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A) If further heavy-chain and light-chain gene rearrangements are possible,it undergoes apoptosis.
B) Somatic hypermutation.
C) Decrease in production of IgD.
D) Continued rearrangement of heavy-chain genes.
E) Continued rearrangement of light-chain genes.
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A) These antibodies bind to airborne bacteria such as Haemophilus influenzae.
B) λ light chains are used almost exclusively by these IgD antibodies.
C) Two-thirds of these IgD antibodies possess κ light chains.
D) These IgD antibodies recruit basophils and induce the secretion of antibacterial peptides.
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A) The cells acquire a state of unresponsiveness called anergy.
B) IgD is retained in the cytosol.
C) IgD on the cell surface fails to activate the B cell when bound to self antigen.
D) The cells have a much longer life-span than mature B cells.
E) The cells die by apoptosis.
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A) VDJ is successfully rearranged and μ heavy chain is made.
B) V-J is rearranging at the light-chain locus.
C) μ heavy chain and λ or κ light chain is made.
D) V is rearranging to DJ at the heavy-chain locus.
E) D-J is rearranging at the heavy-chain locus.
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A) They lack N nucleotides.
B) They possess polyspecificity for bacterial polysaccharide antigens.
C) They arise early in embryonic development preceding the development of the majority subset of B cells.
D) They have little or no IgD on the cell surface.
E) All of the above.
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A) B-cell development is blocked at the immature B-cell stage.
B) They are usually male because the Btk gene is on the X chromosome.
C) They suffer from an immune deficiency known as X-linked agammaglobulinemia (XLA) .
D) Recurrent infections with extracellular bacteria are common.
E) They benefit from treatment with immunoglobulin infusions.
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A) in the bone marrow
B) after encounter with foreign antigen in secondary lymphoid organs
C) in mature B cells
D) to establish self-tolerance of the B-cell repertoire
E) to express an excess of IgM over IgD on the surface of mature B cells.
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A) BCL-2
B) Myc
C) CD5
D) CD19
E) BTK.
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A) subendosteum
B) bone marrow
C) thymus
D) blood
E) secondary lymphoid organs.
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A) Kit
B) CD19
C) TdT
D) Pax-5
E) RAG-1 and RAG-2.
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A) They do not express CD19 at the cell surface.
B) Rearrangement of light-chain genes commences.
C) Nonproductive rearrangement of both heavy-chain loci has already occurred.
D) Allelic exclusion of the immunoglobulin light-chain loci has already occurred.
E) μ is assembled with VpreBλ5.
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A) CCL19: lymph-node dendritic cells
B) CXCL13: follicular dendritic cells
C) CCL21: stromal cells of secondary lymphoid tissues
D) All of the above are correctly matched.
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