Harr - ISBB questions well answered 2023 passed

Harr - ISBBFrom the following, identify a specific component of the adaptive immune system that is formed in response to antigenic stimulation: A. Lysozyme B. Complement C. Commensal organisms D. Immunoglobulin D. Immunoglobulin is a specific part of the adaptive immune system and is formed only in response to a specific antigenic stimulation. Complement, lysozyme, and commensal organisms all act nonspecifically as a part of the adaptive immune system. These three components do not require any type of specific antigenic stimulation. Which two organs are considered the primary lymphoid organs in which immunocompetent cells originate and mature? A. Thyroid and Peyer's Patch B. Thymus and bone marrow C. Spleen and mucosal-associated lymphoid tissue (MALT) D. Lymph nodes and thoracic duct B. The bone marrow and thymus are considered primary lymphoid organs because immunocompetent cells either originate or mature in them. Some immunocompetent cells mature or reside in the bone marrow (the source of all hematopoietic cells) until transported to the thymus, spleen, or Peyer's patches, where they process antigen or manufacture antibody. T lymphocytes, after originating in the bone marrow, travel to the thymus to mature and differentiate. What type of B cells are formed after antigen stimulation? A. Plasma cells and memory B cells B. Mature B cells C. Antigen-dependent B cells D. Receptor-activated B cells A. Mature B cells exhibit surface immunoglobulin that may cross link a foreign antigen, thus forming the activated B cell and leading to capping and internalization of antigen. The activated B cell gives rise to plasma cells that produce and secrete immunoglobulins and memory cells that reside in lymphoid organs. T cells travel from the bone marrow to the thymus for maturation. What is the correct order of the maturation sequence for T cells in the thymus? A. Bone marrow to the cortex; after thymic education, released back to peripheral circulation B. Maturation and selection occur in the cortex; migration to the medulla; release of mature T cells to secondary lymphoid organs C. Storage in either the cortex or medulla; release of T cells into the peripheral circulation D. Activation and selection occur in the medulla; mature T cells are stored in the cortex until activated by antigen B. Immature T cells travel from the bone marrow to the thymus to mature into functional T cells. Once in the thymus, T cells undergo a selection and maturation sequence that begins in the cortex and moves to the medulla of the thymus. Thymic factors such as thymosin and thymopoietin and cells within the thymus such as macrophages and dendritic cells assist in this sequence. After completion of the maturation cycle, T cells are released to secondary lymphoid organs to await antigen recognition and activation. Which cluster of differentiation (CD) marker appears during the first stage of T-cell development and remains present as an identifying marker for T cells? A. CD 1 B. CD 2 C. CD 3 D. CD 4 or CD 8 C. CD 3 the CD 2 marker appears during the first stage of T-cell development and can be used to differentiate T cells from other lymphocytes. This T-lymphocyte receptor binds sheep red blood cells (RBCs). This peculiar characteristic was the basis for the classic E rosette test once used to enumerate T cells in peripheral blood. CD2 is not specific for T cells, however, and is also found on large granular lymphocytes (LGL or natural killer [NK]cells). Which markers are found on mature, peripheral helper T cells? A. CD 1, CD 2, CD 4 B. CD 2, CD 3, CD 8 C. CD 1, CD 3, CD 4 D. CD 2, CD 3, CD 4 D. Mature. peripheral helper T cells have the CD 2 (E rosette), CD 3 (mature T cell), and CE 4 (helper) markers. Which T cell expresses the CD8 marker and acts specifically to kill tumor or virally infected cells? A. Helper T B. T suppressor C. T cytotoxic D. T inducer/suppressor C. T cytotoxic cells recognize antigen in association with major histocompatibility complex (MHC) class I complexes and act against target cells that express foreign antigens. These include viral antigens and the human leukocyte antigens (HLA) that are the target of graft rejection. How are cytotoxic T cells (Tc cells) and natural killer (NK) cells similar? A. Require antibody to be present B. Effective against virally infected cells C. Recognize antigen in association with HLA class II markers D. Do not bind to infected cells B Both TC and NK cells are effective against virally infected cells, and neither requires antibody to be present to bind to infected cells. NK cells do not exhibit MHC class restriction, whereas activation of Tc cells require the presence of MHC class I molecules in association with the viral antigen. What is the name of the process by which phagocytic cells are attracted to a substance such as a bacterial peptide? A. Diapedesis B. Degranulation C. Chemotaxis D. Pahotaxis C Chemotaxis is the process by which phagocytic cells are attracted toward an area where they detect a disturbance in the normal functions of body tissues. Products from bacteria and viruses, complement components, coagulation proteins, and cytokines from other immune cells may all act as chemotactic factors. All of the following are immunologic functions of complement except: A. Induction of an antiviral state B. Opsonization C. Chemotaxis D. Anaphylatoxin formation A Complement components are serum proteins that function in opsonization, chemotaxis, and anaphylatoxin formation but do not induce an antiviral state in target cells. This function is performed by interferons. Which complement component is found in both the classic and alternative pathways? A. C1 B. C4 C. Factor D D. C3 D. C3 is found in both the classic and alternative (alternate) pathways of the complement system. In the classic pathway, C3b forms a complex on the cell with C4b2a that enzymatically cleaves C5. In the alternative pathway, C3b binds to an activator on the cell surface. It forms a complex with factor B called C3bBb which , like C4b2a3b, can split C5. Which immunoglobulin(s) help(s) initiate the classic complement pathway? A. IgA and IgD B. IgM only C. IgG and IgM D. IgG only C Both IgG and IgM are the immunoglobulins that help to initiate the activation of the classic complement pathway. IgM is a more potent complement activator, however. How is complement activity destroyed in vitro? A. Heating serum at 56oC for 30 min B. Keeping serum at room temperature of 22oC for 1 hour C. Heating serum at 37oC for 45 min D. Freezing serum at 0oC for 24 hours A complement activity in serum in vitro is destroyed by heating the serum at 56oC fir 30 min. In test procedures where complement may interfere with the test system, it may be necessary to destroy complement activity in the test sample by heat inactivation.