Basic Principles of Immunology HARR Flashcards
From 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
Immunoglobulin
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 patches
B. Thymus and bone marrow
C. Spleen and mucosal-associated lymphoid tissue (MALT)
D. Lymph nodes and thoracic duct
Thymus and bone marrow
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
Plasma cells and memory B cells
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
Maturation and selection occur in the cortex; migration to the medulla; release of mature T cells to secondary lymphoid organs
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. CD1
B. CD2
C. CD3
D. CD4 or CD8
CD2
The CD2 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. CD1, CD2, CD4
B. CD2, CD3, CD8
C. CD1, CD3, CD4
D. CD2, CD3, CD4
CD2, CD3, CD4
Mature, peripheral helper T cells have the CD2
(E rosette), CD3 (mature T cell), and CD4 (helper) markers.
Which T cell expresses the CD8 marker and acts specifically to kill tumors or virally infected cells?
A. Helper T
B. T suppressor
C. T cytotoxic
D. T inducer/suppressor
T cytotoxic
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
Effective against virally infected cells
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 requires 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. Phagotaxis
Chemotaxis
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
Induction of an antiviral state
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
C3
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
IgG and IgM
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 56°C for 30 min
B. Keeping serum at room temperature of 22°C for 1 hour
C. Heating serum at 37°C for 45 min
D. Freezing serum at 0°C for 24 hours
Heating serum at 56°C for 30 min
Complement activity in serum in vitro is destroyed by heating the serum at 56°C for 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.
What is the purpose of C3a, C4a, and C5a, the
split products of the complement cascade?
A. To bind with specific membrane receptors of lymphocytes and cause release of cytotoxic
substances
B. To cause increased vascular permeability,
contraction of smooth muscle, and release of
histamine from basophils
C. To bind with membrane receptors of
macrophages to facilitate phagocytosis and the
removal of debris and foreign substances
D. To regulate and degrade membrane cofactor protein after activation by C3 convertase
To cause increased vascular permeability,
contraction of smooth muscle, and release of
histamine from basophils
C3a, C4a, and C5a are split products of the
complement cascade that participate in various biological functions such as vasodilation and smooth muscle contraction. These small peptides act as anaphylatoxins, e.g., effector molecules that participate in the inflammatory response to assist in the destruction and clearance of foreign antigens
Which region of the immunoglobulin molecule
can bind antigen?
A. Fab
B. Fc
C. CL
D. CH
Fab
The Fab (fragment antigen binding) is the region of the immunoglobulin molecule that can bind antigen. Two Fab fragments are formed from hydrolysis of the immunoglobulin molecule by papain. Each consists of a light chain and the VH and CH1 regions of the heavy chain. The variable regions of the light and heavy chains interact, forming a specific
antigen-combining site.