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Questions and Answers
Which cells primarily initiate the clonal expansion of naive T lymphocytes?
Which cells primarily initiate the clonal expansion of naive T lymphocytes?
What is the main function of major histocompatibility complex (MHC) molecules?
What is the main function of major histocompatibility complex (MHC) molecules?
Which type of MHC molecule presents peptides derived from intracellular proteins?
Which type of MHC molecule presents peptides derived from intracellular proteins?
What mechanism do dendritic cells use to internalize extracellular antigens?
What mechanism do dendritic cells use to internalize extracellular antigens?
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In which cellular structures are extracellular proteins processed for display by class II MHC molecules?
In which cellular structures are extracellular proteins processed for display by class II MHC molecules?
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What process occurs after the internalization and digestion of antigens by antigen-presenting cells?
What process occurs after the internalization and digestion of antigens by antigen-presenting cells?
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Which of the following best describes the property of MHC restriction?
Which of the following best describes the property of MHC restriction?
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Which of the following cells are NOT considered antigen-presenting cells (APCs)?
Which of the following cells are NOT considered antigen-presenting cells (APCs)?
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What is the primary purpose of CD4+ helper T cells in the immune response?
What is the primary purpose of CD4+ helper T cells in the immune response?
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What role do dendritic cells play in cross-presentation?
What role do dendritic cells play in cross-presentation?
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What is a key characteristic of naive CD8+ T lymphocytes in relation to infected cells?
What is a key characteristic of naive CD8+ T lymphocytes in relation to infected cells?
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What is the significance of the proteasome in the process of cross-presentation?
What is the significance of the proteasome in the process of cross-presentation?
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What mechanism allows CD8+ cytotoxic T lymphocytes to eliminate infected cells?
What mechanism allows CD8+ cytotoxic T lymphocytes to eliminate infected cells?
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What is the primary role of MHC molecules in antigen display?
What is the primary role of MHC molecules in antigen display?
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Which pathway is involved in the processing of cytosolic proteins for display by Class I MHC molecules?
Which pathway is involved in the processing of cytosolic proteins for display by Class I MHC molecules?
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What is required for the stabilization and transport of peptide-MHC complexes to the cell surface?
What is required for the stabilization and transport of peptide-MHC complexes to the cell surface?
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What type of antigens do B lymphocytes recognize?
What type of antigens do B lymphocytes recognize?
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Which mechanism is involved in the immune response to a microbe circulating in the blood?
Which mechanism is involved in the immune response to a microbe circulating in the blood?
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What is an essential factor for T cell activation in response to antigen exposure?
What is an essential factor for T cell activation in response to antigen exposure?
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From where can peptides that bind to Class I MHC molecules be derived?
From where can peptides that bind to Class I MHC molecules be derived?
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What is the role of follicular dendritic cells in the immune response?
What is the role of follicular dendritic cells in the immune response?
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The activation of CD4+ helper T cells is solely responsible for the production of antibodies.
The activation of CD4+ helper T cells is solely responsible for the production of antibodies.
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Cross-presentation allows dendritic cells to present antigens from infected or dying host cells to CD8+ T lymphocytes.
Cross-presentation allows dendritic cells to present antigens from infected or dying host cells to CD8+ T lymphocytes.
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CD8+ T lymphocytes require continuous signals from dendritic cells to recognize and eliminate infected cells.
CD8+ T lymphocytes require continuous signals from dendritic cells to recognize and eliminate infected cells.
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Cross-presentation occurs exclusively through the major histocompatibility complex (MHC) class II pathway.
Cross-presentation occurs exclusively through the major histocompatibility complex (MHC) class II pathway.
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CD8+ T lymphocytes are primarily activated by antigens found inside host cells.
CD8+ T lymphocytes are primarily activated by antigens found inside host cells.
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T lymphocytes can recognize peptide antigens regardless of the specific major histocompatibility complex (MHC) molecules present.
T lymphocytes can recognize peptide antigens regardless of the specific major histocompatibility complex (MHC) molecules present.
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Proteins in any nucleated cell are processed by class II MHC molecules and displayed for T cell recognition.
Proteins in any nucleated cell are processed by class II MHC molecules and displayed for T cell recognition.
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Dendritic cells primarily use phagocytosis to internalize extracellular antigens for class II MHC processing.
Dendritic cells primarily use phagocytosis to internalize extracellular antigens for class II MHC processing.
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Peptides bound to class I MHC molecules are derived exclusively from extracellular proteins.
Peptides bound to class I MHC molecules are derived exclusively from extracellular proteins.
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In antigen-presenting cells, microbial proteins are processed in intracellular vesicles called endosomes.
In antigen-presenting cells, microbial proteins are processed in intracellular vesicles called endosomes.
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The end products of antigen processing in antigen-presenting cells are uniform in length and sequence.
The end products of antigen processing in antigen-presenting cells are uniform in length and sequence.
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Class II MHC molecules present antigens only to CD8+ T lymphocytes.
Class II MHC molecules present antigens only to CD8+ T lymphocytes.
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Antigen-preseiting cells must internally process antigens to bind them to MHC molecules for T cell activation.
Antigen-preseiting cells must internally process antigens to bind them to MHC molecules for T cell activation.
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Peptide loading destabilizes class II MHC molecules before they are exported to the cell surface.
Peptide loading destabilizes class II MHC molecules before they are exported to the cell surface.
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Antigenic proteins can originate from non-infected host cells and their mutated genes.
Antigenic proteins can originate from non-infected host cells and their mutated genes.
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Binding of peptides to class II MHC molecules occurs in the cytosol.
Binding of peptides to class II MHC molecules occurs in the cytosol.
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The immune system often reacts in the same way to a microbe at different stages of its life cycle.
The immune system often reacts in the same way to a microbe at different stages of its life cycle.
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Cytokines secreted by activated APCs provide necessary signals for the stimulation of specific T cells.
Cytokines secreted by activated APCs provide necessary signals for the stimulation of specific T cells.
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The transport of peptide-MHC complexes to the cell surface occurs only if the class I MHC molecule does not find a peptide with an appropriate fit.
The transport of peptide-MHC complexes to the cell surface occurs only if the class I MHC molecule does not find a peptide with an appropriate fit.
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B lymphocytes can only recognize protein antigens and require them to be denatured to bind.
B lymphocytes can only recognize protein antigens and require them to be denatured to bind.
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Follicular dendritic cells play a crucial role in selecting high-affinity B cells during the humoral immune response.
Follicular dendritic cells play a crucial role in selecting high-affinity B cells during the humoral immune response.
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What is the significance of cross-presentation in the immune response?
What is the significance of cross-presentation in the immune response?
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How do CD8+ T lymphocytes differentiate into cytotoxic T lymphocytes (CTLs) without continuous signals from dendritic cells?
How do CD8+ T lymphocytes differentiate into cytotoxic T lymphocytes (CTLs) without continuous signals from dendritic cells?
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What role does the proteasome play in the process of cross-presentation?
What role does the proteasome play in the process of cross-presentation?
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In what way do tumors present a challenge for immune recognition by CD8+ T lymphocytes?
In what way do tumors present a challenge for immune recognition by CD8+ T lymphocytes?
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Can naive CD8+ T lymphocytes respond to intracellular antigens if the infected cells do not interact with dendritic cells?
Can naive CD8+ T lymphocytes respond to intracellular antigens if the infected cells do not interact with dendritic cells?
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What differentiates the processing pathways of antigens presented by class I and class II MHC molecules?
What differentiates the processing pathways of antigens presented by class I and class II MHC molecules?
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Explain how dendritic cells play a role in the activation of naive T lymphocytes.
Explain how dendritic cells play a role in the activation of naive T lymphocytes.
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Describe the mechanism by which antigen-presenting cells (APCs) internalize extracellular antigens.
Describe the mechanism by which antigen-presenting cells (APCs) internalize extracellular antigens.
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Discuss the significance of MHC restriction in T cell recognition.
Discuss the significance of MHC restriction in T cell recognition.
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How do proteolytic enzymes affect peptide generation in antigen processing?
How do proteolytic enzymes affect peptide generation in antigen processing?
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What role do intracellular vesicles, such as endosomes and lysosomes, play in antigen processing for class II MHC molecules?
What role do intracellular vesicles, such as endosomes and lysosomes, play in antigen processing for class II MHC molecules?
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Why is the interaction between T lymphocytes and MHC molecules crucial during the immune response?
Why is the interaction between T lymphocytes and MHC molecules crucial during the immune response?
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What happens to the peptides generated in the cytosolic processing pathway for class I MHC molecules?
What happens to the peptides generated in the cytosolic processing pathway for class I MHC molecules?
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What is the primary mechanism by which cytosolic proteins are recognized for antigen presentation by class I MHC molecules?
What is the primary mechanism by which cytosolic proteins are recognized for antigen presentation by class I MHC molecules?
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Explain the role of the endoplasmic reticulum in the transport of peptide-MHC complexes.
Explain the role of the endoplasmic reticulum in the transport of peptide-MHC complexes.
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Discuss how B lymphocytes differ from T lymphocytes in their recognition of antigens.
Discuss how B lymphocytes differ from T lymphocytes in their recognition of antigens.
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Describe the significance of second signals provided by APCs in T cell activation.
Describe the significance of second signals provided by APCs in T cell activation.
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What distinguishes the responses of the immune system to the same microbe at different stages of its life?
What distinguishes the responses of the immune system to the same microbe at different stages of its life?
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What happens if a class I MHC molecule does not find a peptide with the correct fit?
What happens if a class I MHC molecule does not find a peptide with the correct fit?
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What is the role of follicular dendritic cells in B cell activation?
What is the role of follicular dendritic cells in B cell activation?
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How can antigens from non-infected host cells contribute to immune responses?
How can antigens from non-infected host cells contribute to immune responses?
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The activation of CD4+ helper T cells is crucial for the production of potent ______.
The activation of CD4+ helper T cells is crucial for the production of potent ______.
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Naive CD8+ T lymphocytes respond to intracellular antigens through a process called ______.
Naive CD8+ T lymphocytes respond to intracellular antigens through a process called ______.
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CD8+ cytotoxic T lymphocytes are necessary to kill infected host cells when the antigens are ______ from antibodies.
CD8+ cytotoxic T lymphocytes are necessary to kill infected host cells when the antigens are ______ from antibodies.
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Dendritic cells process ingested antigens in structures called the ______, where they are degraded before presentation.
Dendritic cells process ingested antigens in structures called the ______, where they are degraded before presentation.
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Once CD8+ T cells have differentiated into CTLs, they can kill infected or tumor ______ without additional signals.
Once CD8+ T cells have differentiated into CTLs, they can kill infected or tumor ______ without additional signals.
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T lymphocytes recognize peptide antigens that are bound to and displayed by major ______ complex (MHC) molecules.
T lymphocytes recognize peptide antigens that are bound to and displayed by major ______ complex (MHC) molecules.
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Naive T lymphocytes must see the antigens presented by ______ cells to initiate clonal expansion.
Naive T lymphocytes must see the antigens presented by ______ cells to initiate clonal expansion.
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Extracellular proteins processed by specialized APCs are displayed by class ______ MHC molecules.
Extracellular proteins processed by specialized APCs are displayed by class ______ MHC molecules.
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Proteins in the cytosol are processed in proteolytic structures called ______ and displayed by class I MHC molecules.
Proteins in the cytosol are processed in proteolytic structures called ______ and displayed by class I MHC molecules.
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Antigens destined for the class II MHC pathway are usually ______ from the extracellular environment.
Antigens destined for the class II MHC pathway are usually ______ from the extracellular environment.
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After internalization, microbial proteins enter acidic intracellular vesicles called ______ or phagosomes.
After internalization, microbial proteins enter acidic intracellular vesicles called ______ or phagosomes.
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The binding of peptides to class II MHC molecules occurs after the ______ of antigens.
The binding of peptides to class II MHC molecules occurs after the ______ of antigens.
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Antigen-presenting cells are responsible for presenting antigens to ______ T lymphocytes.
Antigen-presenting cells are responsible for presenting antigens to ______ T lymphocytes.
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Peptides bind to newly synthesized ______ molecules in specialized vesicles.
Peptides bind to newly synthesized ______ molecules in specialized vesicles.
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The peptides that bind to class I MHC molecules are derived from cytosolic proteins following digestion by the ______ pathway.
The peptides that bind to class I MHC molecules are derived from cytosolic proteins following digestion by the ______ pathway.
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If a class I molecule finds a peptide with the right fit, the complex is stabilized and transported to the cell ______.
If a class I molecule finds a peptide with the right fit, the complex is stabilized and transported to the cell ______.
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B lymphocytes recognize proteins as well as ______ antigens, even in their native conformations.
B lymphocytes recognize proteins as well as ______ antigens, even in their native conformations.
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The immune system reacts in different ways even to the same microbe at different ______ of its life.
The immune system reacts in different ways even to the same microbe at different ______ of its life.
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Antigenic proteins may be produced in the cytoplasm from viruses that are living inside infected ______.
Antigenic proteins may be produced in the cytoplasm from viruses that are living inside infected ______.
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Follicular dendritic cells display antigens to germinal center B cells and select high-affinity ______ during humoral immune responses.
Follicular dendritic cells display antigens to germinal center B cells and select high-affinity ______ during humoral immune responses.
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Cytokines secreted by activated APCs provide necessary signals for the stimulation of specific ______.
Cytokines secreted by activated APCs provide necessary signals for the stimulation of specific ______.
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Match the following T cell types with their primary functions:
Match the following T cell types with their primary functions:
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Match the following processes to their descriptions in T cell activation:
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Match the following components involved in immune response with their roles:
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Match the following immune challenges with their characteristics:
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Match the following terms related to antigen presentation with their definitions:
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Match the type of antigen-presenting cell (APC) with its primary function:
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Match the major histocompatibility complex (MHC) class with its antigen source:
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Match the process with its description in antigen processing:
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Match the T cell type with its function:
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Match the pathway of antigen processing with the involved cell structure:
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Match the antigen processing step with its associated function:
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Match the antimicrobial response with its corresponding immune mechanism:
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Match the following processes with their associated pathways:
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Match the following types of MHC molecules with their primary antigen sources:
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Match the following features with the correct MHC class:
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Study Notes
Antigen Recognition by T Lymphocytes
- T lymphocytes recognize peptide antigens presented by MHC molecules on antigen-presenting cells (APCs).
- MHC restriction: T cells only recognize peptides when displayed by their own MHC molecules.
- Naive T cells need to recognize antigens presented by dendritic cells to activate and differentiate into effector and memory cells.
MHC Molecules in Antigen Presentation
- MHC molecules are expressed on APCs and display peptides derived from protein antigens.
- Class II MHC: presents peptides derived from extracellular proteins internalized by APCs (dendritic cells, macrophages, B cells).
- Class I MHC: presents peptides derived from proteins in the cytosol of any nucleated cell.
Processing & Presentation of Internalized Antigens (Class II MHC Pathway)
- Internalization & Digestion: Antigens are internalized by APCs through phagocytosis, receptor-mediated endocytosis, and enter acidic vesicles (endosomes/phagosomes).
- Peptide Binding: Peptides generated by proteolysis bind to newly synthesized MHC II molecules within specific vesicles.
- Transport to Cell Surface: Peptide-MHC II complexes are transported to the cell surface.
Processing & Presentation of Cytosolic Antigens (Class I MHC Pathway)
- Proteolysis: Cytosolic proteins are degraded by the proteasome pathway.
- Peptide Transport: Peptides are transported into the endoplasmic reticulum (ER).
- Binding to Class I MHC: Peptides bind to class I MHC molecules within the ER.
- Transport to Cell Surface: Stable peptide-MHC I complexes are transported to the cell surface.
Summary of MHC-Mediated Antigen Presentation
- MHC molecules ensure T cells only recognize cell-associated protein antigens.
- MHC class II presents extracellular antigens, while class I presents intracellular antigens.
- This ensures the appropriate type of T cell (helper or cytotoxic) responds to the specific microbe.
Induction of Immune Responses
- APCs express costimulators and secrete cytokines to activate specific T cells.
- These additional signals ensure T cells respond to microbial antigens and not harmless substances.
- B lymphocytes recognize diverse antigens, including non-protein antigens, in native conformations.
- Follicular dendritic cells display antigens to germinal center B cells during humoral immune responses.
The Need for Different Immune Responses
- The immune system responds differently to the same microbe depending on its stage of infection.
- Extracellular microbes: Combatted by antibodies that bind and neutralize the microbe.
- Intracellular microbes: Activation of CD8+ cytotoxic T lymphocytes (CTLs) is necessary to kill infected cells and eliminate the reservoir.
Cross-Presentation of Internalized Antigens to CD8+ T Cells
- Cross-Presentation: Dendritic cells can ingest infected cells, dead tumor cells, and present their antigens to naive CD8+ T cells.
- Mechanism: Ingested antigens are transported into the cytosol, processed by the proteasome, and presented by MHC class I molecules.
- This allows CD8+ T cells to respond to intracellular antigens from cells that are not themselves APCs.
- Once activated, CTLs can kill infected cells or tumor cells directly, without the need for further dendritic cell involvement.
Antigen Recognition by T Lymphocytes
- T lymphocytes recognize peptide antigens bound to and displayed by major histocompatibility complex (MHC) molecules on antigen-presenting cells (APCs).
- T cells are MHC restricted, meaning they can only see peptides displayed by their own MHC molecules.
- Dendritic cells are the main APCs responsible for initiating T cell activation and differentiation.
Antigen Processing and Presentation Pathways
-
MHC Class II Pathway:
- Processes extracellular antigens internalized by APCs like dendritic cells, macrophages, and B cells.
- Occurs in late endosomes and lysosomes.
- Peptides bind to newly synthesized MHC class II molecules within specialized vesicles.
- Peptide-MHC class II complexes are transported to the cell surface for T cell recognition.
-
MHC Class I Pathway:
- Processes cytosolic proteins, including viral proteins, proteins from phagocytosed microbes that escape into the cytosol, and mutated host proteins.
- Proteins are digested by proteasomes.
- Resulting peptides are transported into the endoplasmic reticulum (ER) and bind to class I MHC molecules.
- Peptide-MHC class I complexes are transported to the cell surface for T cell recognition.
Summary of Antigen Processing and Presentation
- MHC molecules are crucial for T cell recognition of cell-associated protein antigens.
- MHC class II presents extracellular antigens to CD4+ helper T cells.
- MHC class I presents intracellular antigens to CD8+ cytotoxic T lymphocytes (CTLs).
- APCs express costimulatory molecules and secrete cytokines to activate T cells in conjunction with antigen presentation.
Induction of Immune Responses
- Different immune mechanisms are required to combat microbes at different stages of their life cycle.
- Antibodies are effective against extracellular microbes, while CTLs are needed to eliminate intracellular microbes.
- CD4+ helper T cells are essential for antibody production.
- CD8+ CTLs are essential for killing infected cells and eradicating intracellular microbes.
Cross-Presentation of Internalized Antigens to CD8+ T Cells
- Cross-presentation allows dendritic cells to process antigens from infected cells or tumors and present them to naive CD8+ T cells.
- This process allows for activation of CD8+ T cells against viruses that do not directly infect dendritic cells or against tumor cells that cannot activate T cells directly.
- Once activated, CTLs can directly kill infected cells or tumor cells without the need for dendritic cells.
Antigen Recognition by T Lymphocytes
- T lymphocytes recognize peptide antigens bound to Major Histocompatibility Complex (MHC) molecules on antigen-presenting cells (APCs)
- Each individual has unique MHC molecules, so T cells can only recognize antigens presented by their own MHC molecules, a property called MHC restriction
- Dendritic cells are vital for initiating T cell activation and differentiation
Processing and Presentation of Protein Antigens
- Two pathways exist for antigen processing: MHC class I and MHC class II
- MHC class I presents intracellular antigens, while MHC class II presents extracellular antigens
MHC class II Antigen Presentation Pathway
- Extracellular antigens, such as microbes or proteins, are internalized by APCs like dendritic cells, macrophages, and B cells
- Antigens are processed in late endosomes and lysosomes
- Peptides generated from the processed antigens bind to newly synthesized MHC class II molecules in specialized vesicles
- Peptide-MHC class II complexes travel to the cell surface for recognition by CD4+ T cells
MHC class I Antigen Presentation Pathway
- Cytosolic proteins, derived from viruses, bacteria, or mutated host genes, are processed by proteasomes
- Peptides generated from proteasomal degradation are transported into the endoplasmic reticulum
- Peptides bind to newly synthesized MHC class I molecules in the ER
- Stable peptide-MHC class I complexes move to the cell surface for recognition by CD8+ T cells
Induction of Immune Responses
- MHC molecules ensure specific T cell recognition of cell-associated protein antigens
- APCs express costimulators and secrete cytokines to activate T cells
- These signals are crucial for a proper immune response to microbial antigens, preventing activation by harmless substances
- B cells can recognize both proteins and non-protein antigens in their native form
Cross-Presentation of Internalized Antigens to CD8+ T cells
- Cross-presentation occurs when dendritic cells internalize infected cells, dead tumor cells, or microbial antigens
- Internalized antigens are transported into the cytosol, processed by proteasomes, and presented via MHC class I molecules
- Cross-presentation allows naive CD8+ T cells to recognize antigens from infected cells that may not directly activate APCs
- This process is crucial for anti-viral and anti-tumor immune responses
Antigen Recognition by T lymphocytes
- T lymphocytes recognize peptide antigens that are bound and displayed by major histocompatibility complex (MHC) molecules of antigen-presenting cells (APCs).
- This property of T cells is called MHC restriction.
- Cells that capture microbial antigens and display them for recognition by T lymphocytes are called antigen-presenting cells (APCs).
- Naive T lymphocytes must be exposed to antigens presented by dendritic cells to initiate clonal expansion and differentiation.
Processing and Presentation of Protein Antigens
- Extracellular proteins internalized by APCs (dendritic cells, macrophages, B cells) are processed in endosomes and lysosomes and displayed by class II MHC molecules.
- Intracellular proteins are processed in proteasomes and displayed by class I MHC molecules.
- Two pathways are designed to sample all proteins present in the extracellular and intracellular environments.
Processing of Internalized Antigens for Display by Class II MHC Molecules
- Antigens destined for the class II MHC pathway are usually internalized from the extracellular environment.
- Dendritic cells and macrophages ingest microbes or microbial proteins by several mechanisms, including phagocytosis and receptor-mediated endocytosis.
- After internalization, microbial proteins enter acidic vesicles, called endosomes or phagosomes, which fuse with lysosomes.
- Proteolytic enzymes break down proteins in these vesicles, generating peptides of varying lengths and sequences.
- Peptides bind to newly synthesized MHC molecules in specialized vesicles.
- Peptide loading stabilizes class II MHC molecules, which are exported to the cell surface.
Processing of Cytosolic Antigens for Display by Class I MHC Molecules
- Peptides that bind to class I MHC molecules are derived from cytosolic proteins following digestion by the proteasome pathway.
- Antigenic proteins may be produced in the cytoplasm from viruses, from phagocytosed microbes that leak into the cytosol, and from mutated or altered host genes.
- Peptides must be transported into the endoplasmic reticulum to form peptide-MHC complexes.
- If a class I molecule finds a peptide with the right fit, the complex is stabilized and transported to the cell surface.
Cross-Presentation of Internalized Antigens to CD8+ T Cells
- Some viruses may infect only specific cell types and may not produce the signals needed to initiate T cell activation.
- How do naive CD8+ T lymphocytes respond to intracellular antigens of infected cells?
- A subset of classical dendritic cells can ingest infected host cells, dead tumor cells, microbes, and microbial and tumor antigens.
- These antigens are transported into the cytosol, where they are processed by the proteasome.
- The generated antigenic peptides enter the ER and bind to class I molecules, which display the antigens for recognition by CD8+ T lymphocytes.
- This process is called cross-presentation (or cross-priming).
- Once CD8+ T cells differentiate into CTLs, they kill infected host cells or tumor cells without the need for dendritic cells or signals other than antigen recognition.
Antigen Recognition by T Lymphocytes
- T lymphocytes recognize peptide antigens presented by MHC molecules on antigen-presenting cells (APCs).
- Different T cell clones recognize peptides only when presented by their own individual's MHC molecules, a phenomenon known as MHC restriction.
- Naive T cells require interaction with dendritic cells to initiate clonal expansion and differentiation into effector and memory cells.
Antigen Processing and Presentation
- MHC molecules are expressed on APCs and display peptides derived from protein antigens.
- Extracellular proteins are processed in late endosomes and lysosomes, presented by class II MHC molecules.
- Intracellular proteins are processed in proteasomes and presented by class I MHC molecules.
Processing of Internalized Antigens for Display by Class II MHC Molecules
- Antigens destined for the class II MHC pathway are internalized from the extracellular environment.
- Dendritic cells and macrophages internalize antigens via phagocytosis and receptor-mediated endocytosis.
- Proteins are broken down into peptides in acidic vesicles like endosomes and phagosomes.
Processing of Cytosolic Antigens for Display by Class I MHC Molecules
- Peptides presented by class I MHC molecules are derived from cytosolic proteins processed by the proteasome pathway.
- Antigenic proteins may originate from viruses, phagocytosed microbes, or mutated host genes.
- Peptides are transported into the endoplasmic reticulum (ER) for binding to class I MHC molecules.
Role of MHC Molecules in Antigen Display
- MHC molecules ensure that T cells only recognize cell-associated protein antigens.
- MHC molecules determine the type of T cell (helper or cytotoxic) that responds to a specific microbe.
Induction of Immune Responses
- APCs express costimulatory molecules and secrete cytokines to stimulate specific T cells in concert with antigens.
- These second signals ensure T cell activation only occurs in response to microbial antigens.
- B lymphocytes recognize proteins and non-protein antigens in their native conformations.
Cross-Presentation of Internalized Antigens to CD8+ T Cells
- Some viruses infect specific cell types and may not travel to lymph nodes or produce signals for naive CD8+ T cell activation.
- Dendritic cells can ingest infected host cells, dead tumor cells, microbes, and antigens.
- Cross-presentation occurs when dendritic cells transport ingested antigens into their cytosol, where they are processed by the proteasome.
- Processed peptides enter the ER and bind to class I molecules, presenting them for CD8+ T cell recognition.
- This process is known as cross-presentation (or cross-priming) and allows dendritic cells to prime naive CD8+ T cells against antigens from other infected or dying cells.
- Once activated, CTLs can kill infected host cells or tumor cells without the need for dendritic cells or additional signals.
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Test your knowledge on how T lymphocytes recognize antigens presented by MHC molecules. This quiz covers MHC restriction, the role of dendritic cells, and the pathways of antigen processing and presentation. Perfect for students studying immunology or related fields.