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Questions and Answers
What is the primary advantage of utilising highly specific antigen receptors in adaptive immunity?
What is the primary advantage of utilising highly specific antigen receptors in adaptive immunity?
What is the outcome of the resolution phase of an immune response?
What is the outcome of the resolution phase of an immune response?
What is the primary role of T cells in immune responses?
What is the primary role of T cells in immune responses?
What is the outcome of T cell activation?
What is the outcome of T cell activation?
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What is the primary mechanism of adaptive immunity?
What is the primary mechanism of adaptive immunity?
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What is the primary function of CD4+ and CD8+ T cells?
What is the primary function of CD4+ and CD8+ T cells?
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What is the primary function of cytotoxic T cells?
What is the primary function of cytotoxic T cells?
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What is the main difference between effector and memory T cells?
What is the main difference between effector and memory T cells?
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What is the role of antigen-presenting cells in T cell activation?
What is the role of antigen-presenting cells in T cell activation?
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What is the significance of MHC class I in T cell activation?
What is the significance of MHC class I in T cell activation?
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What is the primary function of helper T cells?
What is the primary function of helper T cells?
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What is the difference between naïve and effector T cells?
What is the difference between naïve and effector T cells?
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What is the primary function of γδ T cells in the immune system?
What is the primary function of γδ T cells in the immune system?
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What determines the differentiation of T cells into specific subsets?
What determines the differentiation of T cells into specific subsets?
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What is the term used to describe the process of T cell differentiation into specific subsets based on the cytokine environment?
What is the term used to describe the process of T cell differentiation into specific subsets based on the cytokine environment?
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What is the function of Th2 cells?
What is the function of Th2 cells?
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What is the primary function of Tregs?
What is the primary function of Tregs?
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What is the role of the third signal in T cell activation?
What is the role of the third signal in T cell activation?
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What is the primary function of T-Bet in Th1 and Th2 cross-regulation?
What is the primary function of T-Bet in Th1 and Th2 cross-regulation?
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Which of the following cytokines is involved in the differentiation of Th1 cells?
Which of the following cytokines is involved in the differentiation of Th1 cells?
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What is the primary function of GATA-3 in Th1 and Th2 cross-regulation?
What is the primary function of GATA-3 in Th1 and Th2 cross-regulation?
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Which of the following cell subsets is involved in B cell activation and Ab production?
Which of the following cell subsets is involved in B cell activation and Ab production?
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What is the primary function of IL-4 in Th1 and Th2 cross-regulation?
What is the primary function of IL-4 in Th1 and Th2 cross-regulation?
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Which of the following cytokines is involved in the differentiation of Th17 cells?
Which of the following cytokines is involved in the differentiation of Th17 cells?
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What is the primary requirement for CD8+ T cell activation, in addition to the two signals provided by the APC?
What is the primary requirement for CD8+ T cell activation, in addition to the two signals provided by the APC?
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How do CD4+ Th cells help activate CD8+ T cells?
How do CD4+ Th cells help activate CD8+ T cells?
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What is the consequence of the requirement for CD8+ T cells to be activated by related antigens presented by BOTH MHC I and MHC II on the same APC?
What is the consequence of the requirement for CD8+ T cells to be activated by related antigens presented by BOTH MHC I and MHC II on the same APC?
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What is the role of CD40L in CD8+ T cell activation?
What is the role of CD40L in CD8+ T cell activation?
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Why are CD4+ Th cells necessary for CD8+ T cell activation?
Why are CD4+ Th cells necessary for CD8+ T cell activation?
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What is the consequence of CD4+ Th cells recognizing related antigen on the APC?
What is the consequence of CD4+ Th cells recognizing related antigen on the APC?
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T cell activation requires only one signal from the antigen-presenting cell.
T cell activation requires only one signal from the antigen-presenting cell.
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Adaptive immunity can only be achieved through natural exposure to pathogens.
Adaptive immunity can only be achieved through natural exposure to pathogens.
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CD4+ T cells are involved in the humoral immune response.
CD4+ T cells are involved in the humoral immune response.
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The primary role of T cells is to recognize and eliminate infected cells and present antigens to B cells.
The primary role of T cells is to recognize and eliminate infected cells and present antigens to B cells.
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Effector-memory T cells are like naïve T cells upon activation.
Effector-memory T cells are like naïve T cells upon activation.
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The resolution phase of an immune response results in the expansion of immune cells.
The resolution phase of an immune response results in the expansion of immune cells.
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T cells can recognize pathogens with stereotypical PAMPs.
T cells can recognize pathogens with stereotypical PAMPs.
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CD4+ T cells are involved in the destruction of intracellular pathogens.
CD4+ T cells are involved in the destruction of intracellular pathogens.
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CD8+ T cells can recognize antigens presented by antigen-presenting cells through MHC class II.
CD8+ T cells can recognize antigens presented by antigen-presenting cells through MHC class II.
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Antigen recognition is the only step required for T cell activation.
Antigen recognition is the only step required for T cell activation.
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Naïve T cells are a type of memory T cell.
Naïve T cells are a type of memory T cell.
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T cell activation only occurs in peripheral infected organs.
T cell activation only occurs in peripheral infected organs.
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Co-stimulatory molecules are necessary for the activation of CD8+ T cells but not CD4+ T cells.
Co-stimulatory molecules are necessary for the activation of CD8+ T cells but not CD4+ T cells.
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CD8+ T cells can be activated by a single signal provided by the APC.
CD8+ T cells can be activated by a single signal provided by the APC.
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The protein Lck is involved in the activation of T cells through its interaction with ITAM.
The protein Lck is involved in the activation of T cells through its interaction with ITAM.
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CD40L binds to CD40L on the APC, which stimulates it to make more costimulatory CD80/CD86.
CD40L binds to CD40L on the APC, which stimulates it to make more costimulatory CD80/CD86.
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The production of cytokine, mainly IL-2, is induced by the first signal of T cell activation.
The production of cytokine, mainly IL-2, is induced by the first signal of T cell activation.
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CD8+ T cells can be activated by unrelated antigens presented by the APC.
CD8+ T cells can be activated by unrelated antigens presented by the APC.
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CD4+ Th cells help activate CD8+ T cells by providing cytokines and CD28.
CD4+ Th cells help activate CD8+ T cells by providing cytokines and CD28.
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CD80 and CD86 are co-stimulatory molecules found in mice.
CD80 and CD86 are co-stimulatory molecules found in mice.
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T cell activation results in the suppression of transcription factors and gene expression.
T cell activation results in the suppression of transcription factors and gene expression.
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CD80/CD86 is the murine equivalent of human B7.1/B7.2.
CD80/CD86 is the murine equivalent of human B7.1/B7.2.
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The clonal expansion of T cells is a result of antigen recognition by the TCR/MHC interaction.
The clonal expansion of T cells is a result of antigen recognition by the TCR/MHC interaction.
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Viruses are naturally trophic for dendritic cells, allowing for efficient activation of CD8+ T cells.
Viruses are naturally trophic for dendritic cells, allowing for efficient activation of CD8+ T cells.
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Almost all effector T cells die once the antigen is eliminated.
Almost all effector T cells die once the antigen is eliminated.
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Cross presentation of exogenous antigens to MHC-I is important for CD4+ T cell activation
Cross presentation of exogenous antigens to MHC-I is important for CD4+ T cell activation
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CD80/86-CD28 is enough for CD8+ T cell activation
CD80/86-CD28 is enough for CD8+ T cell activation
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MHC class I molecules only present peptides from endogenous antigens
MHC class I molecules only present peptides from endogenous antigens
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The third signal in T cell activation is antigen recognition
The third signal in T cell activation is antigen recognition
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Th1 cells produce TNFα/IFNγ and mediate humoral immune responses
Th1 cells produce TNFα/IFNγ and mediate humoral immune responses
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Study Notes
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T cell development and activation involves five key learning outcomes: the role of T cells in immune responses, the maturation and selection process for CD4+ and CD8+ T cells, stages and development of T cell-mediated immunity (CMI), the 2 steps to T cell activation, and the 3rd signal and T cell differentiation.
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Adaptive immunity is an immune response that becomes more powerful following repeated encounters with the same antigen, utilizing highly specific antigen receptors that allow for recognition of pathogens lacking stereotypical PAMPs, highly specific responses for a given pathogen, and immunological memory.
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The advantages of adaptive immunity include highly diverse populations of cells, pathogen-specific cells expanding and improving in the repertoire, and resolution (contraction) and memory.
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Specific immunity can be achieved through natural exposure (e.g., chickenpox) or artificially by vaccination (e.g., MMR/COVID).
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T cells are long-lived and can be reactivated, making them essential for immune responses.
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T cell terminology includes naïve, effector, and memory T cells, with naïve T cells being the precursors of effector T cells.
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Effector T cells are further divided into effector-memory and central memory T cells, with effector-memory T cells having a more rapid response to antigen.
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The magnitude of T cell response involves the activation of naïve T cells, the expansion of effector T cells, and the contraction and homeostasis of memory T cells.
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T cell activation requires two signals: antigen recognition (MHC/antigen-TCR) and costimulation (CD80/86-CD28), with the 3rd signal (cytokine environment) dictating the type of T effector cell.
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CD4+ T cells (Th cells) recognize antigen presented by MHC class II and assist other white blood cells, while CD8+ T cells (Tc cells) recognize antigen presented by MHC class I and kill infected cells.
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The 3rd signal (cytokine environment) directs T cell differentiation into different subsets, including Th1, Th2, Th17, Tregs, and Tfh cells.
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Cytokines produced by antigen-presenting cells (APCs) and other cells create a cytokine environment that influences T cell differentiation.
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Differentiation of Th cells is induced by different cytokines, producing different types of effector CD4+ T cells, each with distinct functions.
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Th1 cells are involved in anti-inflammatory responses, peripheral tolerance, and bacterial infections, while Th2 cells are involved in pro-inflammatory responses, B cell activation, and helminth infections.
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Th17 cells are involved in pro-inflammatory responses, bacterial infections, and autoimmune diseases.
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Tregs are involved in anti-inflammatory responses, peripheral tolerance, and autoimmune diseases.
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TfH cells are involved in B cell activation and antibody production.
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Cross-presentation of exogenous antigens to MHC-I is important for CD8+ T cell (CTL) activation, which requires Th help and CD40-CD40L interaction.
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The dynamics of T cell response involve antigen recognition, activation, antigen elimination, contraction/homeostasis, and memory.
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Description
Test your knowledge on the role of T cells in immune responses, their maturation and selection process, and the stages of T cell mediated immunity. Learn about the two steps to T cell activation and the third signal in T cell differentiation.