Microbiology chapter
MICROBIOLOGY

Immune Response

150 practice questions · 81 study notes
Start chapter practice

Questions

QUESTION 1
Which cellular effect is attributed to silica particles, beryllium sulphate and endotoxins as adjuvants?
QUESTION 2
What is the usual outcome of antigen presentation by non-professional antigen-presenting cells?
QUESTION 3
Why is Freund’s complete adjuvant unsuitable for human use?
QUESTION 4
Which antigen can elicit antibody production without T-cell participation?
QUESTION 5
What is the first step in the immune response involving antigen-processing cells?
QUESTION 6
Which pattern describes the effects of therapeutic corticosteroid doses on immune responses in humans?
QUESTION 7
How does incorporation of protein antigens into the water phase of a water-in-oil emulsion prolong the antigenic stimulus?
QUESTION 8
An immunosuppressive drug selectively inhibits helper T-cell activity without being cytotoxic to lymphocytes or having antimitotic activity. Which drug fits this description?
QUESTION 9
What do cytotoxic T cells do after recognising target-cell antigens associated with MHC Class I molecules?
QUESTION 10
Which MHC class is associated with antigen presentation to helper T cells?
QUESTION 11
What is the antibody preparation directed against thymus cells called?
QUESTION 12
How do antimetabolites inhibit the cell division and differentiation required for humoral and cellular immune responses?
QUESTION 13
For how long may pneumococcal polysaccharide persist in humans after a single injection?
QUESTION 14
Which component accounts for the adjuvant effect of Gram-negative bacilli?
QUESTION 15
What determines differences in immune response to the same antigen among different individuals of a species?
QUESTION 16
In guinea pigs, tuberculoprotein administered before BCG immunisation inhibits delayed hypersensitivity to tuberculin while preserving circulating antibody production. What is this phenomenon called?
QUESTION 17
Which step of antibody production comprises antigen entry, distribution and fate in tissues, and contact with appropriate immunocompetent cells?
QUESTION 18
Which cell produces the interleukin-1 signal described in the immune response?
QUESTION 19
For certain antigens that induce tolerance at both high and low doses, what response is produced by intermediate doses?
QUESTION 20
An indurated skin nodule with mononuclear cell infiltration develops 48–72 hours after antigen administration. Which immune response does this represent?
QUESTION 21
Which process characterises an efferent block in immunological tolerance?
QUESTION 22
Which activities constitute the central functions of antibody production?
QUESTION 23
Which intervention can prolong the duration of immunological tolerance?
QUESTION 24
Which antigen administration pattern generally induces T cell tolerance?
QUESTION 25
Which material from sensitised donors was used to passively transfer delayed hypersensitivity in guinea pigs?
QUESTION 26
Following cytokine stimulation, B cells that have combined with their respective antigens clonally proliferate and differentiate into which cells?
QUESTION 27
Which pair serves as effector cells in cell-mediated immunity?
QUESTION 28
Which interferon is produced by fibroblasts?
QUESTION 29
T cells stimulated by antigens, mitogens or exposure to IL-2 produce which interferon?
QUESTION 30
Which comparison of antibody appearance after primary antigenic stimulation is supported by the source?
QUESTION 31
Which cells release the biologically active substances defined as cytokines in this description?
QUESTION 32
Which event during immune elimination may cause tissue damage associated with serum sickness?
QUESTION 33
A person develops an antibody response after a subsequent stimulus with the same antigen. What is this response called?
QUESTION 34
After an antigen-presenting cell engulfs an antigen, where is the antigen degraded into fragments before presentation within a class II histocompatibility molecule?
QUESTION 35
Why can polysaccharide antigens persist for months or years while protein antigens are generally eliminated within days or weeks?
QUESTION 36
A viral protein generated within an infected cell is processed by cytosolic proteasomes. Through which molecule is the resulting peptide displayed, and which T cells recognise it?
QUESTION 37
Which statement correctly describes the relationship between humoral and cellular immune responses?
QUESTION 38
Why were mediators previously named for their demonstrated biological effects grouped under the term cytokines?
QUESTION 39
Cytotoxic CD8 T cells are activated by contact with antigen presented along with which molecules?
QUESTION 40
Increasing an antigen dose beyond a certain level inhibits the antibody response and induces tolerance. What is this phenomenon called?
Page 1 of 4
Next

Study notes

Definition and scope of the immune response
The immune response encompasses specific reactions to antigenic stimuli and has a broader scope than protection against infection. →
Humoral and cellular immune responses
The immune response has two forms that usually develop and act together. →
Functions of antibody-mediated and cell-mediated immunity
Antibody-mediated immunity and cell-mediated immunity contribute to host defence and also participate in immune-mediated disease. →
Humoral immune response
This introductory passage identifies the alternative name and initiating stimulus of humoral immunity. →
Three steps of antibody production
Antibody production proceeds through an afferent limb, central functions, and an efferent limb. →
Primary and secondary antibody responses
Antibody responses are distinguished by whether the antigenic stimulus is initial or subsequent. →
Repeated antigen exposure and vaccine antibody responses
Repeated antigen stimulation influences antibody levels and explains the priming and booster roles of vaccine doses. →
Antigen processing and presentation pathways
Engulfed antigens and antigens generated within cells undergo different processing and presentation pathways. →
Non-immune antigen removal and primary versus secondary immune responses
The passage describes initial removal of particulate antigens and compares the timing, cells, and antibody characteristics of primary and secondary responses. →
Professional antigen-presenting cells and T-cell dependence
Antigen presentation can initiate an adaptive immune response or promote tolerance, while some antigens elicit antibodies without T-cell participation. →
B cells as antigen-presenting cells
B cells can present antigens to T cells, particularly during the secondary immune response. →
First signal for helper T-cell activation
Helper T-cell activation requires two signals; the supplied text describes the first signal. →
Immune elimination of circulating antigen
Immune elimination accelerates antigen clearance once specific antibody appears. →
Immune elimination and persistence of antigens
Antigen elimination involves immune complex formation, while the duration of antigen persistence is related to metabolism. →
Antigen persistence and the initiation of an immune response
The passage describes prolonged persistence of pneumococcal polysaccharide and the cellular steps that initiate an immune response. →
Cytokine signals supporting B cell activation
The passage describes cytokine production and the subsequent proliferation and differentiation of antigen-bound B cells. →
Memory B cells and cytotoxic T-cell responses
Activated lymphocytes can generate immediate effector responses and form memory cells for subsequent antigen encounters. →
Genetic control of antigen responsiveness
Individuals within a species can differ in their immune response to the same antigen because of genetic differences. →
Embryonic development of antibody production and self-reactive clone elimination
Embryonic immune development includes the maturation of lymphoid organs and the elimination of cells that recognise self-antigens. →
Postnatal development of immunocompetence
Immunocompetence is incomplete at birth and develops progressively as the infant grows. →
Effects of nutritional deficiency on immune responses
Malnutrition adversely affects immunity, with different effects on serum components, cellular responses, and antibody synthesis. →
Effect of antigen administration route on immune responses
The route of antigen administration influences the strength of the humoral response, the antibody type produced and whether tolerance develops. →
Effect of injection site on hepatitis B vaccine immunogenicity
For some antigens, the site of injection influences the immune response. →
Antigen dose and immunological paralysis
The antibody response depends on antigen dose, with different effects at low, optimal and excessive doses. →
Simultaneous antigens and antigenic competition
Administering two or more antigens together can alter their individual antibody responses. →
Antibody responses to mixed vaccines
Combining vaccine antigens can leave their responses independent or potentiate a response, depending on the combination described. →
Antigenic competition after prior diphtheria immunisation
Previous exposure to one antigen can affect responses to other antigens during subsequent polyvalent immunisation. →
Adjuvants: definition and immune effects
Adjuvants enhance antigen immunogenicity and can affect antibody responses, cellular immunity, and the development of adjuvant diseases. →
Adjuvant actions: prolonged antigen release and macrophage activation
The passage describes ways in which adjuvants prolong antigenic stimulation or activate macrophages. →
Microbial adjuvants and immunosuppressive agents
The passage contrasts agents that enhance immune responses with agents used to inhibit immunity, including in transplantation. →
Antimetabolites, cyclosporine and antibody preparations for immunosuppression
These agents inhibit immune responses through interference with nucleic acid synthesis, selective inhibition of helper T cells, or antibody preparations directed against lymphocytes. →
Immune suppression by ALS, irradiation and homologous antibody
These interventions affect different components of immunity, and their effects depend on the target cells, timing or specificity of the intervention. →
Combined immunisation with toxoid and antitoxin
Combined immunisation for diphtheria and tetanus requires attention to administration sites and the form of toxoid used. →
Immunomodulatory effects of intravenous immunoglobulin
Intravenously administered immunoglobulin has effects relevant to diseases of presumed immunopathologic origin. →
Cell-mediated immunity and delayed hypersensitivity
Cell-mediated immunity is an antigen-specific response mediated by effector T cells. Delayed hypersensitivity illustrates its cellular basis. →
Scope of cell-mediated immunity in infectious diseases
Cell-mediated immunity participates in delayed hypersensitivity and responses to infections caused by obligate and facultative intracellular parasites. →
Antigenic stimuli that induce cell-mediated immunity
The nature of the antigenic stimulus influences the induction of cell-mediated immunity (CMI). →
Antigen recognition and T-cell responses in cell-mediated immunity
Cell-mediated immunity (CMI) depends on T cell–dependent antigens and specific recognition by T cells. →
MHC-associated antigen recognition by helper and cytotoxic T cells
T cells recognise antigens presented with MHC molecules; helper and cytotoxic T cells differ in the MHC class involved and their resulting actions. →
Cytokines: definition and terminology
Cytokines are biologically active mediators with regulatory effects on other cells. →
Nature and regulatory role of cytokines
Cytokines mediate communication between cells during host responses. →
Cytokines: production, local action and pleiotropy
Cytokines are hormone-like substances that act at very low concentrations and influence several cell types. →
Interleukin-1: properties, cellular sources and production
Interleukin-1 (IL-1) is a stable polypeptide whose production responds to inflammatory stimuli and inhibitory agents. →
Immunological effects of interleukin-1
Interleukin-1 (IL-1) stimulates responses in T cells, B cells and neutrophils. →
Broad effects and cellular targets of an unnamed mediator
This continuation describes a mediator's effects and targets, but the supplied target and immediate context do not explicitly name the mediator. →
IL-1: pyrogenic and inflammatory effects
IL-1 contributes to fever and to inflammatory changes in septic shock and bacterial meningitis. →
IL-1 in severe infection and IL-2 as T cell growth factor
The passage identifies a beneficial effect of IL-1 and the growth-factor role and cellular source of IL-2. →
LAK cells and the stem cell growth effect of interleukin-3
The passage describes an antitumour killer-cell response and introduces interleukin-3. →
Interleukin-3 and interleukin-4: functional names
The target passage completes the description of interleukin-3 and introduces the former name of interleukin-4. →
IgE synthesis in atopic hypersensitivity and interleukin-5 terminology
The passage links a cytokine effect to atopic hypersensitivity and then introduces interleukin-5. →
Colony-stimulating factors and functional groups of lymphokines
The passage explains colony-stimulating factor activity and groups lymphokines by the cells they affect. →
IL-3 as multi-CSF
IL-3 has broad effects on hematopoietic cell growth and may produce additional effects through other cytokines. →
CSFs in blood cell production and the types of TNF
The passage describes how colony-stimulating factors meet changing blood cell requirements and introduces tumour necrosis factor. →
Cytokines: cellular sources and major functions
The cytokine table connects interleukins, colony-stimulating factors, tumour necrosis factors, interferons and other mediators with their cellular sources and functions. →
Interferons: classification and cellular sources
Interferons were originally identified as antiviral agents and are classified as cytokines. →
Transforming growth factor beta and leukemia inhibitory factor
The passage describes growth-promoting and regulatory actions of two cytokines. →
Exogenous and endogenous regulation of cytokine production
Cytokine production responds to external stimuli as well as internal hormonal and biochemical factors. →
Cytokine feedback, therapeutic applications and IL-17
Cytokines regulate one another, several have therapeutic applications, and IL-17 participates in autoimmune inflammation. →
Potential future therapeutic uses of cytokines
The passage describes possible future applications that depend on a better understanding of cytokine properties. →
Detection of cell-mediated immunity
Cell-mediated immunity (CMI) can be assessed using skin testing and in vitro correlates. →
Migration inhibitory factor test
The migration inhibitory factor test assesses cell-mediated immunity through inhibition of cell migration after exposure to a relevant antigen. →
Transfer factor and antigen-specific transfer of immunity
Transfer factor (TF) is a leucocyte extract associated with passive transfer of cell-mediated immunity (CMI). →
Physical properties and stability of transfer factor
Transfer factor (TF) is a small, dialysable substance with resistance to several forms of treatment. →
Potency and systemic effects of transfer factor
Transfer factor (TF) produces demonstrable cell-mediated immunity (CMI) in the recipient. →
Transfer factor: serial transfer and proposed mechanism
Transfer factor (TF) transfers cell-mediated immunity (CMI) reflecting the donor's antigen sensitivities, although its mechanism remains unknown. →
Immunological tolerance: specificity and experimental induction
Immunological tolerance is antigen-specific unresponsiveness induced by contact with that antigen. →
Host factors affecting immunological tolerance
The ease of inducing tolerance varies with the host's species, strain and degree of immunocompetence. →
Induction of immunological tolerance in adults
Adult tolerance induction is influenced by temporary immunosuppression and prior immunisation against the antigen. →
Antigen physical state and tolerogenicity
The physical form of an antigen affects its ability to induce tolerance, and processing can change its immunological behaviour. →
Antigen dose and immunological tolerance
Induction and duration of immunological tolerance depend on the dose and repetition of antigen exposure. →
Routes of tolerance induction and persistent tolerant infections
Tolerance depends partly on antigen administration route and can also occur naturally during persistent viral infection. →
Mechanisms and selective expression of immunological tolerance
The source describes proposed mechanisms of tolerance, differences between lymphocyte responses, and selective loss of an immune response. →
Categories of theories of immune response
Theories of immune response attempt to explain its versatility, specificity, memory and other features. →
Instructive theories of antibody production
Instructive theories explain antibody specificity through instructions provided by the antigen to an immunocompetent cell. →
Selective theories of antibody production
Selective theories place the emphasis on the immunocompetent cell's restricted immunological range. →
Clonal selection theory of antibody formation
Clonal selection places immunological specificity at the cellular level and is described as the most relevant and accepted theory. →
Side chain theory of antibody formation
The side chain theory is presented as an abandoned explanation of the immune response. →
Historical theories of antibody formation
Template and natural selection theories offered different explanations for antibody specificity and the secondary response. →
Idiotypes, antibody diversity and patterns of immune response
The passage explains idiotype-mediated regulation and the genetic basis of antibody diversity, followed by key features of immune responses and antibody-producing cells. →
T-cell function and antigen-specific immunological tolerance
The target describes T-cell-mediated effects and defines immunological tolerance. Its opening continuation refers to monoclonal antibodies. →
Instructive versus selective theories of immunity
Theories of immunity are divided into instructive and selective categories according to the specificity attributed to immunocompetent cells. →
NEETx
Learn. Practise. Remember.