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An overview of the key components and mechanisms of the adaptive immune system, including the roles of t lymphocytes, b lymphocytes, dendritic cells, and other immune cells. It covers topics such as antigen presentation, t cell activation, antibody production, and the regulation of immune responses. The document delves into the specific functions of different immune cell types, their interactions, and the cytokines involved in shaping the adaptive immune response. It also discusses the importance of immunological memory and the implications of immune system dysfunction, such as in the case of hiv infection. The comprehensive coverage of adaptive immunity and immune cell biology makes this document a valuable resource for students and researchers interested in understanding the complex and dynamic nature of the human immune system.
Typology: Exams
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Rationale: B lymphocytes, or B cells, are the cells that differentiate into plasma cells that produce antibodies, which are crucial for the humoral immune response.
Rationale: Opsonization is the process where antibodies bind to the surface of pathogens and enhance their ingestion and destruction by phagocytes.
A. Interleukin-1 (IL-1) B. Interleukin-2 (IL-2) C. Interferon-gamma (IFN-γ) D. Tumor necrosis factor (TNF)
Rationale: IL-1 is a pro-inflammatory cytokine produced by activated macrophages and is a key mediator in the inflammatory response.
Rationale: MHC class I molecules present endogenously synthesized peptides to CD8+ T cells, which are cytotoxic T cells.
binding Rationale: Clonal selection is the process by which an antigen selectively binds to and activates B or T cells with specific receptors, leading to their proliferation.
Rationale: Type I hypersensitivity reactions are immediate allergic reactions mediated by IgE antibodies, such as in the case of asthma or anaphylaxis.
Rationale: The complement system can be activated through three pathways: classical, lectin, and alternative, all of which lead to the destruction of pathogens.
Rationale: IL-12, produced by dendritic cells and macrophages, is crucial for the differentiation of naive T cells into Th1 cells, which are involved in cell-mediated immunity.
Rationale: Treg cells play a critical role in maintaining immune tolerance by suppressing the immune response and preventing autoimmunity.
Rationale: dsDNA antibodies are a hallmark of systemic lupus erythematosus and are used as a diagnostic criterion for the disease.
Rationale: The adaptive immune system is characterized by its ability to remember specific pathogens, leading to an enhanced response upon subsequent exposures.
C. Crossing the placenta D. Binding to Fc receptors
Rationale: The variable regions of antibodies contain the antigen-binding sites, allowing for the specific recognition and binding of antigens.
Rationale: HIV primarily targets CD4+ T cells, which are essential for orchestrating the immune response, leading to immunodeficiency.
Rationale: Somatic hypermutation involves the mutation of B cell receptor genes, resulting in an increased affinity for the antigen during the immune response.
Rationale: Dendritic cells are crucial for initiating the adaptive immune response by capturing antigens and presenting them to T cells. Question: Which of the following cell types is responsible for presenting antigens to T cells? A) B cells B) Macrophages C) Natural killer cells D) Neutrophils
Rationale: Macrophages play a crucial role in antigen presentation to T cells through major histocompatibility complex (MHC) molecules.
Question: What is the primary function of cytotoxic T cells in the immune response? A) Phagocytosis of pathogens B) Secretion of antibodies C) Killing of infected cells D) Activation of B cells
Rationale: Cytotoxic T cells are specialized in identifying and eliminating virus-infected or cancerous cells through the release of cytotoxic molecules. Question: Which of the following is a hallmark of adaptive immunity? A) Rapid response upon reinfection B) Limited specificity C) Non-specific cellular responses D) Lack of memory
Rationale: Adaptive immunity provides a swift and targeted response upon re-exposure to a pathogen due to the presence of memory cells. Question: What is the role of cytokines in immune regulation? A) Direct killing of pathogens B) Activation of complement system C) Communication between immune cells
D) Antigen presentation to T cells
Rationale: Cytokines act as signaling molecules that facilitate communication and coordination between different immune cells. Question: Which type of hypersensitivity reaction is mediated by IgE antibodies? A) Type I B) Type II C) Type III D) Type IV
Rationale: Type I hypersensitivity reactions involve the release of histamine and other mediators by mast cells and basophils triggered by IgE antibodies. Question: What is the primary function of regulatory T cells in the immune system? A) Phagocytosis of pathogens B) Suppression of immune responses C) Production of antibodies D) Activation of cytotoxic T cells
Rationale: Regulatory T cells play a crucial role in maintaining immune tolerance and preventing autoimmune reactions by suppressing excessive immune responses. Question: Which of the following cell types is responsible for antibody production? A) T cells B) Natural killer cells C) B cells D) Dendritic cells
Rationale: B cells are specialized in producing antibodies in response to specific antigens encountered by the immune system. Question: What is the main function of MHC class II molecules? A) Presentation of endogenous antigens B) Presentation of exogenous antigens C) Recognition of self-antigens D) Activation of cytotoxic T cells
Rationale: MHC class II molecules present antigens derived from extracellular pathogens to CD4+ T helper cells.
Question: Which of the following cells is responsible for antibody class switching? A) Plasma cells B) Memory B cells C) Follicular dendritic cells D) T helper cells
Rationale: T helper cells play a crucial role in guiding B cells to undergo class switching and produce different classes of antibodies. Question: What is the primary function of natural killer cells in the immune response? A) Phagocytosis of pathogens B) Antibody production C) Killing of virus-infected cells D) Antigen presentation to T cells
Rationale: Natural killer cells are adept at recognizing and eliminating virus-infected or cancerous cells without prior sensitization. Question: Which of the following cytokines is involved in promoting inflammation and fever during infection? A) Interleukin- 4 B) Tumor necrosis factor-alpha
C) Interferon-gamma D) Transforming growth factor-beta
Rationale: Tumor necrosis factor-alpha is a pro-inflammatory cytokine that plays a key role in initiating immune responses and promoting inflammation. Question: What is the primary function of dendritic cells in the immune system? A) Antibody production B) Phagocytosis of pathogens C) Antigen presentation to T cells D) Killing of infected cells
Rationale: Dendritic cells are professional antigen-presenting cells that play a crucial role in initiating adaptive immune responses by presenting antigens to T cells. Question: Which of the following is a characteristic feature of memory B cells? A) Short lifespan B) Ability to produce antibodies C) Immediate response upon reinfection D) Lack of specificity
Rationale: Memory B cells exhibit a rapid and enhanced response upon re-exposure to a pathogen due to their ability to quickly differentiate into plasma cells. Question: What is the primary role of complement proteins in the immune system? A) Phagocytosis of pathogens B) Direct killing of infected cells C) Opsonization and lysis of pathogens D) Antibody production
Rationale: Complement proteins enhance the immune response by promoting opsonization of pathogens and facilitating their lysis. Question: Which of the following is a characteristic feature of the adaptive immune response? A) Non-specific recognition of pathogens B) Lack of memory C) Specificity for particular antigens D) Rapid response upon primary exposure
Rationale: The adaptive immune response is characterized by its specificity for unique antigens, allowing targeted and precise immune reactions.
Rationale: Calcineurin is a calcium-dependent phosphatase that plays a crucial role in the T cell activation pathway by dephosphorylating the nuclear factor of activated T cells (NFAT), allowing its translocation to the nucleus.
Rationale: Dendritic cells are professional antigen-presenting cells that capture, process, and present antigens to T cells, initiating the adaptive immune response.
Rationale: Toll-like receptors recognize specific molecular patterns associated with pathogens and initiate signaling cascades that lead to the production of cytokines and activation of immune responses.
Rationale: IL-12 is crucial for the differentiation of naïve T cells into Th cells, which are important in cell-mediated immunity against intracellular pathogens.
B) Phagocytosis C) Complement activation D) Apoptosis
Rationale: Somatic recombination is a process by which different gene segments encoding antigen receptors are rearranged, leading to the generation of a diverse repertoire of receptors on lymphocytes.
Rationale: CTLs recognize and kill infected or abnormal cells by inducing apoptosis, thereby eliminating the source of antigens in the body.
Rationale: ICAM-1 (Intercellular Adhesion Molecule-1) plays a key role in stabilizing the interaction between T cells and antigen-presenting cells, facilitating signal transduction and T cell activation.
Rationale: Tregs play a crucial role in immune tolerance by suppressing excessive immune responses, maintaining self-tolerance, and preventing autoimmunity.
Rationale: Complement proteins participate in the opsonization and lysis of pathogens, enhancing their recognition and elimination by phagocytes and promoting inflammation.
Rationale: B cells are specialized lymphocytes that produce antibodies in response to specific antigens, mediating humoral immune responses.
Rationale: The MHC molecules present antigens to T cells and play a crucial role in antigen recognition and activation of immune responses.
B) Memory B cells C) Follicular dendritic cells D) T helper cells
Rationale: T helper cells provide signals to B cells, inducing class switching and the production of different antibody isotypes to tailor immune responses to specific pathogens.
Rationale: Mast cells release histamine and other inflammatory mediators in response to allergens, contributing to the symptoms of allergic reactions.
Rationale: Central tolerance mechanisms eliminate self-reactive lymphocytes during development to prevent autoimmune responses and maintain self-tolerance.
Rationale: CD28 on T cells interacts with B7 molecules on antigen- presenting cells, providing a co-stimulatory signal necessary for T cell activation and proliferation.
Rationale: Memory B cells retain the ability to rapidly differentiate into plasma cells and produce specific antibodies upon re-exposure to an antigen, contributing to the secondary immune response.
Rationale: Peripheral tolerance mechanisms induce T cell anergy or deletion of self-reactive lymphocytes outside the central lymphoid organs to prevent autoimmunity.
Rationale: NK cells are part of the innate immune system and function by recognizing and killing virus-infected cells or tumor cells without prior sensitization.
Rationale: B lymphocytes produce antibodies that can neutralize pathogens, facilitate their clearance by phagocytes, or activate the complement system to eliminate pathogens.
Rationale: The proteasome degrades intracellular proteins into peptide fragments that can be loaded onto MHC class I molecules for presentation to CD8+ T cells.
D) IFN-γ
Rationale: IL-4 is crucial for the differentiation of naïve T cells into Th2 cells, which are important for antibody-mediated immune responses and allergic reactions.
Rationale: The Fc region of an antibody can bind complement proteins, initiating the classical complement cascade and promoting the lysis of pathogens.
Rationale: Macrophages are key immune cells that produce pro- inflammatory cytokines such as TNF-α and IL-1 in response to infection, promoting inflammation.
Rationale: CTLs recognize antigenic peptides presented by MHC class I molecules on infected cells through the T cell receptor (TCR), leading to target cell killing.