All are true regarding the development of T-cells, except?
Cytolytic activity of membrane attack complex is modulated by ?
Which of the following statements about interleukin-1 is false?
Rosette formation with sheep RBCs (SRBCs) indicates functioning of -
Which cytokine activates macrophages?
Which of the following is considered the most professional antigen presenting cell (APC) in the immune system?
The idiotype of an antibody is determined by -
Which cells are known to cause rosette formation with sheep red blood cells?
Which immunoglobulin is known as the pentameric immunoglobulin?
Which of the following statements about interferons is true?
Explanation: ***T-cells are located in mantle layer of spleen*** - The **mantle layer** (or marginal zone) of the spleen is primarily associated with **B-lymphocytes**, which are involved in antibody production. - While T-cells are present in the spleen, they are predominantly found in the **periarteriolar lymphoid sheath (PALS)**, which is part of the white pulp, rather than the mantle layer. *T-cells are formed in bone marrow* - **Hematopoietic stem cells** in the **bone marrow** are the progenitors of all blood cells, including lymphocytes. - These stem cells differentiate into **lymphoid stem cells**, which then travel to the thymus to become T-cells. *Maturation of T-cells take place in thymus* - **T-cell precursors** migrate from the bone marrow to the **thymus**, where they undergo a complex process of differentiation and selection. - In the thymus, T-cells acquire their **T-cell receptors (TCRs)** and undergo positive and negative selection to ensure they are self-MHC restricted and tolerant to self-antigens. *In lymph nodes, T-cells are found in paracortical area* - The **paracortical area** (or paracortex) of the lymph node is the **T-cell zone**, rich in T-lymphocytes and dendritic cells. - This region is crucial for the interaction between T-cells and antigen-presenting cells, initiating adaptive immune responses.
Explanation: ***Correct Option: Factor S (vitronectin)*** - Vitronectin (S-protein) is a **plasma protein** that directly modulates the **cytolytic activity of the membrane attack complex (MAC)**. - It binds to the **C5b-7 complex** in the fluid phase, preventing its insertion into target cell membranes and thereby blocking the formation of the complete, functional MAC. - By inhibiting membrane insertion of C5b-7, vitronectin prevents the subsequent binding of **C8 and C9**, which are essential for the cytolytic pore formation. - This is a **direct modulation** of MAC's cytolytic activity at the MAC assembly stage. *Incorrect Option: Factor H* - Factor H is a regulatory protein that controls the **alternative pathway** of complement activation by promoting degradation of **C3b**. - By degrading C3b, Factor H prevents formation of **C5 convertase**, thereby reducing downstream MAC formation. - However, Factor H acts **early in the complement cascade** and does not directly modulate the cytolytic activity of already-formed MAC components. - Its effect is on **preventing MAC formation**, not on modulating MAC's cytolytic function itself. *Incorrect Option: Factor I* - Factor I is a **serine protease** that cleaves and inactivates C3b and C4b, requiring cofactors like Factor H or C4bp. - Like Factor H, it regulates complement activation **upstream** of MAC formation. - It does not directly interact with or modulate the cytolytic activity of the MAC. *Incorrect Option: Factor B* - Factor B is a component of the **alternative pathway C3 convertase** (C3bBb). - It **promotes complement activation** rather than modulating MAC's cytolytic activity. - Factor B functions early in the cascade and has no direct role in regulating MAC function.
Explanation: ***IL-1 inhibits IL-2 production by T-cells*** - This statement is false because **IL-1** actually **enhances the production of IL-2** by T-cells, which is crucial for T-cell proliferation and immune response. - **IL-1 acts synergistically with IL-6 and TNF-α** to promote inflammation and immune cell activation, where IL-2 plays a key role. *The primary source of IL-1 is the monocyte-macrophage system* - This statement is true; **monocytes and macrophages** are the main producers of **IL-1α and IL-1β** upon activation by various stimuli. - Other cells, such as neutrophils, dendritic cells, and endothelial cells, can also produce IL-1, but monocytes and macrophages are the predominant source. *IL-1 is an endogenous pyrogen* - This statement is true; **IL-1** is a potent **endogenous pyrogen** that acts on the hypothalamus to induce fever, a hallmark of the acute phase response. - It triggers prostaglandin synthesis in the hypothalamus, leading to an elevation in the body's thermoregulatory set point. *IL-1 promotes acute phase protein synthesis in the liver* - This statement is true; **IL-1** is a key mediator that stimulates **hepatocytes** to produce **acute phase proteins**, such as C-reactive protein and serum amyloid A. - This hepatic response is part of the innate immune system's effort to control infection and inflammation.
Explanation: ***T-cells*** - **T-cells** possess specific receptors, like **CD2** on their surface, that can bind to ligands on sheep red blood cells (SRBCs). - This binding leads to the formation of characteristic **rosettes**, where SRBCs cluster around the T-lymphocytes, indicating functional T-cells. *B-cells* - **B-cells** primarily function in **humoral immunity** by producing antibodies and do not typically form rosettes with sheep RBCs. - While B-cells have surface receptors, they are not CD2 and thus do not facilitate this specific type of rosette formation. *Neutrophils* - **Neutrophils** are **phagocytic cells** involved in innate immunity, primarily combating bacterial and fungal infections. - They lack the specific surface receptors (like CD2) required to form rosettes with sheep RBCs. *Monocytes* - **Monocytes** are precursors to macrophages and dendritic cells, involved in phagocytosis and antigen presentation. - They do not possess the necessary surface markers to form rosettes with sheep RBCs.
Explanation: ***IFN-γ (Interferon-gamma)*** - **IFN-γ is the classic macrophage-activating cytokine**, enhancing phagocytic and antimicrobial functions - Promotes expression of **MHC class I and II molecules**, increasing antigen presentation capacity - Produced mainly by **Th1 cells and NK cells** during cell-mediated immunity - Key cytokine in defense against **intracellular pathogens** (mycobacteria, viruses) *IL-8* - **IL-8 is a chemokine** (cytokine subfamily) primarily involved in **neutrophil chemotaxis** - Recruits neutrophils to sites of infection or inflammation - Does not directly activate macrophages like IFN-γ - Important in acute inflammatory responses *PAF (Platelet-Activating Factor)* - **Not a cytokine** - it is a **phospholipid mediator** - Involved in allergic and inflammatory responses - Functions include **platelet aggregation**, **vasodilation**, and **bronchoconstriction** - While it affects immune responses, it doesn't function as a macrophage-activating cytokine *Leukotriene B4* - **Not a cytokine** - it is a **lipid mediator** (eicosanoid) derived from arachidonic acid - Primarily acts as a **chemoattractant for neutrophils** - Promotes neutrophil and monocyte adhesion and migration to inflammatory sites - Does not directly activate macrophages
Explanation: ***Dendritic cells*** - **Dendritic cells** are specialized for capture, processing, and presentation of antigens to T lymphocytes. - They are often referred to as the "**professional APCs**" due to their superior ability to initiate primary T cell responses. *B cells* - While B cells can present antigens, they are generally less efficient than **dendritic cells** and primarily serve to present antigens to **helper T cells** during secondary immune responses. - Their main role is **antibody production** after activation, not initiating primary T cell responses. *T cells* - **T cells** are effector cells of the adaptive immune system and recognize antigen presented by APCs; they do not typically function as antigen-presenting cells themselves. - Some T cells, like **gamma-delta T cells**, can present antigens, but this is not their primary role. *NK cells* - **Natural Killer (NK) cells** are part of the innate immune system and primarily target and kill infected or cancerous cells without prior sensitization. - They do not present antigens in the classical sense and are not considered professional APCs.
Explanation: ***Amino end*** - The **idiotypic class** of an antibody is determined by the unique amino acid sequences within the **variable regions** of both the heavy and light chains, located at the **amino-terminal end** of the antibody. - These variable regions form the **antigen-binding sites**, giving each antibody its specific binding capabilities and thus its idiotype. *Fc region* - The **Fc (fragment crystallizable) region** is the tail region of an antibody that interacts with cell surface receptors and other immune system molecules. - It determines the **isotype (class)** of the antibody (e.g., IgG, IgM) and mediates effector functions but does not define the idiotype. *Hinge region* - The **hinge region** is a flexible segment in the middle of the heavy chains of IgG, IgA, and IgD antibodies. - It allows flexibility between the antigen-binding (Fab) arms, facilitating bivalent binding, but does not determine the idiotype. *Carboxy end* - The **carboxy end** (C-terminus) of the heavy and light chains typically corresponds to the constant regions of the antibody. - While it contributes to the antibody's overall structure and effector functions (especially the Fc region), it does not contain the unique sequences that define the **idiotype**.
Explanation: ***T cells*** - **T cells** are the classic cells known to form rosettes with sheep red blood cells, a phenomenon called **E-rosette formation** - This interaction is mediated by the **CD2 receptor** on human T cells binding to **CD58 (LFA-3)** on sheep red blood cells - E-rosette formation was historically used as a diagnostic test to identify and enumerate T cells before the advent of flow cytometry - This is a characteristic feature of **mature T cells** and was widely used in immunology laboratories *NK cells* - **NK cells** do NOT typically form rosettes with sheep red blood cells - NK cells lack the specific CD2-mediated interaction required for classical E-rosette formation - NK cells are identified by other markers such as CD16 and CD56, and by their ability to kill target cells without prior sensitization *Monocytes* - **Monocytes** do not form rosettes with sheep red blood cells - Their primary functions include phagocytosis, antigen presentation, and cytokine production - They are identified by surface markers like **CD14** and their characteristic morphology (large size, kidney-shaped nucleus) *All types of T cells* - While this option is technically correct since all mature T cells express CD2 and can form E-rosettes, the more conventional answer is simply **"T cells"** - Both CD4+ helper T cells and CD8+ cytotoxic T cells possess the CD2 receptor and can participate in rosette formation - The distinction between "T cells" and "All types of T cells" is subtle, but "T cells" is the standard textbook answer
Explanation: ***IgM*** - **IgM** is found as a **pentamer** in its secreted form, meaning it is composed of five immunoglobulin monomer units joined together. - This pentameric structure gives IgM a high valency, making it very effective at **binding multiple antigens** simultaneously and activating the **complement system**. *IgA* - **IgA** primarily exists as a **monomer** in serum and as a **dimer** in secretions like mucus, tears, and saliva. - Its main function is to provide **mucosal immunity**, protecting epithelial surfaces from pathogens. *IgG* - **IgG** is the most abundant immunoglobulin in serum and exists as a **monomer**. - It crosses the **placenta** to provide passive immunity to the fetus and is crucial for **opsonization** and neutralizing toxins and viruses. *IgE* - **IgE** is present in very low concentrations in serum and exists as a **monomer**. - It plays a critical role in **allergic reactions** and defense against **parasites** by binding to mast cells and basophils.
Explanation: **Interferons inhibit viral replication in host cells.** - Interferons are a crucial part of the **innate immune response** against viral infections. - They work by inducing an **antiviral state** in neighboring uninfected cells, preventing viral replication. - Interferons are **non-specific** antiviral cytokines with broad-spectrum activity. *Interferons are specific for particular viruses.* - This is incorrect. Interferons are **virus-non-specific** in their antiviral action. - While their production is triggered by viral infection, they can inhibit replication of various different viruses. - This broad-spectrum activity is a key feature distinguishing them from antibodies (which are specific). *Interferons have no effect on viral infections.* - This is false. Interferons are potent **antiviral cytokines** essential for host defense against viruses. - They activate immune cells (NK cells, macrophages) and induce expression of genes that inhibit viral processes. *Interferons are synthetic antiviral agents.* - This is incorrect. Interferons are **naturally produced proteins** by the body's cells (leukocytes, fibroblasts, dendritic cells) in response to viral infections. - While recombinant interferons are used therapeutically, interferons are biological molecules, not synthetic drugs.
Cells and Organs of Immune System
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Innate Immunity
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Adaptive Immunity
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Antigens and Antibodies
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Major Histocompatibility Complex
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Complement System
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Cytokines and Chemokines
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Hypersensitivity Reactions
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Autoimmunity and Autoimmune Diseases
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Immunodeficiency Disorders
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Transplantation Immunology
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Tumor Immunology
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