Immunology T Cell Activation Quiz
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Questions and Answers

Which receptor is crucial for the stabilization of the interaction between T cells and MHC on antigen-presenting cells?

  • CD4 or CD8 (correct)
  • PD-1
  • CTLA-4
  • CD28
  • What is the role of IL-2 in T cell activation?

  • Inhibits CD8+ T cell function
  • Drives T cell proliferation (correct)
  • Activates CD4+ T cells
  • Induces apoptosis in T cells
  • Which of the following statements about co-stimulation in T cell activation is true?

  • CD28 binding to B7 is essential for full T cell activation. (correct)
  • Co-stimulatory receptors are only important for naive T cells.
  • Signal 2 is not necessary if Signal 1 is present.
  • Co-stimulation occurs through the interaction of CD3 with MHC.
  • What happens to T cells when they receive only Signal 1 from resting APCs?

    <p>They become anergic.</p> Signup and view all the answers

    What characteristic distinguishes activated T cells from naive T cells regarding IL-2 receptors?

    <p>Activated T cells upregulate the alpha chain of IL-2 receptors.</p> Signup and view all the answers

    Which cytokine is involved in driving Th1 differentiation during T cell activation?

    <p>IL-12</p> Signup and view all the answers

    Which of the following proteins is NOT a signal transduction protein located on T cells?

    <p>CD8</p> Signup and view all the answers

    Which statement correctly describes the role of integrins during T cell activation?

    <p>Integrins assist in stabilizing the interaction between T cells and APCs.</p> Signup and view all the answers

    What is the primary function of naive CD4+ T lymphocytes upon activation?

    <p>Differentiate into Th1, Th2, or Th17 cells</p> Signup and view all the answers

    Which phase follows after antigen recognition in cellular immune response?

    <p>Activation</p> Signup and view all the answers

    What is the role of CD8+ T lymphocytes in the immune response?

    <p>Kill infected cells</p> Signup and view all the answers

    What is true about memory T lymphocytes?

    <p>They have a feature that allows quick response to re-exposure</p> Signup and view all the answers

    What is the end result of an effective T cell response?

    <p>Inflammation and clearing of infection</p> Signup and view all the answers

    What do both naive and effector T lymphocytes express?

    <p>CD3 along with CD4 or CD8</p> Signup and view all the answers

    During which phase do T cells specialize into effector and memory T cells?

    <p>Differentiation</p> Signup and view all the answers

    What is essential for naive T lymphocytes to recognize antigens?

    <p>Interaction with antigen-presenting cells (APCs)</p> Signup and view all the answers

    Study Notes

    Cellular Immune Response I Lecture Notes

    • Lecture Outline: The lecture covers the main phases of T lymphocyte responses, antigen recognition, activation signals, CD8+ T cell activation, functional responses of activated T lymphocytes, memory T cells, and T lymphocyte migration to infection sites.

    • T Lymphocyte Responses Phases: The lecture outlines the stages involved in T lymphocyte responses.

    • Antigen Recognition by T Lymphocytes: The role of CD4, CD8, and adhesion molecules is crucial to antigen recognition by T lymphocytes.

    • CD4+ T Lymphocyte Activation: Activation signals and co-stimulation molecules are essential for CD4+ T lymphocyte activation.

    • CD8+ T Lymphocyte Activation: The mechanisms of activating CD8+ T lymphocytes are described.

    • Activated T Lymphocyte Functional Responses: The lecture details the functional responses of activated T lymphocytes.

    • Memory T Lymphocyte Features: The lecture explores the characteristics of memory T lymphocytes, and their significance in the immune response.

    • Effector T Lymphocyte Migration: The process by which effector T lymphocytes migrate to infection sites is examined.

    Types of Intracellular Microbes and T Cell-Mediated Immunity

    • T Cell-Mediated Immunity (CMI): T lymphocytes play a vital role in CMI, providing defense against infections caused by intracellular microbes.

    • Intracellular Microbes: There are two types of infections caused by intracellular microbes: phagocytosis by phagocytes in immunity's early defense phase, and the microbes that can resist phagocytosis, and the microbes that infect the cell cytoplasm.

    Objectives

    • Objective 1: This objective asks what the main phases of T lymphocyte responses are.

    • Objective 2a: This objective aims to describe how T lymphocytes recognize antigens.

    • Objective 2b: This objective investigates the role of CD4, CD8, and adhesion molecules.

    • Objective 4: This objective focuses on the activation mechanisms of CD8+ T lymphocytes.

    • Objective 5: This objective details the functional responses of T cells after activation, including cytokine production, clonal expansion, and differentiation into effector cells.

    • Objective 6: This objective is the end point of the cellular immune response, where the immune system returns to a steady state after clearing an infection.

    • Objective 7: How effector T cells migrate to an infection site.

    T Cell Activation and Costimulation

    • How T Cells Recognize Ags: The initial step in T cell responses involves multiple receptors on the T cell engaging ligands on antigen-presenting cells (APCs).

    • T-Cell Activation Signals: T cell activation entails recognition of antigen-MHC complexes, co-receptor interactions, adhesion molecules to strengthen the binding, and the involvement of costimulatory receptors in the activation process.

    Surface Molecules of T Cells

    • T Cell Surface Molecules: The key surface molecules of T lymphocytes are detailed for their roles in the functional responses.

    T Cell Activation: Costimulation

    • T Cell Activation: T cell activation is dependent on antigen, and also requires costimulation from APCs.

    • Normal and Abnormal T Cell Activation: During normal activation, APCs express costimulators to activate T cells, whereas resting APCs, lack this expression, leading to T cell tolerance.

    How are CD8+ T Lymphocytes Activated?

    • Activation of CD8+ T Cells: The activation of CD8+ T cells follows a similar activation path to CD4+ T cells, involving dendritic cells or infected tissue cells and presenting microbe-derived antigens, costimulation, and helper T cells, which stimulate the expansion and differentiation of CD8 T cells.

    How are T-Cells Fully Activated?

    • T Cell Activation Pathways: T cell activation involves a series of steps initiated by antigen recognition, resulting in enzyme activation, recruitment of adaptor proteins, and production of active transcription factors on the surface of antigen-presenting cells (APCs).

    What are the Functional Responses of T Cells after Activation

    • Functional T Cell Responses Post Activation: Following T cell activation, a series of functional responses occur within 1-2 hrs or up to 3-4 days, including cytokine production, clonal expansion, and differentiation into effector cells.

    Memory T Lymphocytes

    • Memory T Lymphocytes: Memory T cells survive infection clearance and can be found in lymphoid organs, peripheral tissues, and the bloodstream. They can rapidly respond to subsequent infections of the same pathogen.

    End Point of Cellular Immune Response

    • Homeostasis after Immune Response: After clearing an infection, the immune system returns to a stable state by eliminating excess T cells via apoptosis and by retaining memory cells. 

    Migration of Effector T Cells

    • Effector T Cell Migration: Effector T cells migrate to infection sites, guided by adhesion molecules like L-selectin and chemokine receptors. They preferentially target sites where the infection has occurred.

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    Description

    Test your knowledge about T cell activation and the roles of various receptors and cytokines. This quiz covers interactions between T cells and MHC, the importance of IL-2, and co-stimulation. Perfect for students or enthusiasts in immunology.

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