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Questions and Answers
What is antigen processing and presentation?
What is antigen processing and presentation?
The process by which antigen presenting cells digest antigens acquired from the inside or outside the cell and display the resulting antigenic fragments on cell surface MHC molecules for recognition by T lymphocytes
Which cells are primarily responsible for digesting antigens in the antigen processing and presentation process?
Which cells are primarily responsible for digesting antigens in the antigen processing and presentation process?
Which of the following professional antigen presenting cells is NOT one of the three main types identified?
Which of the following professional antigen presenting cells is NOT one of the three main types identified?
What is the outcome of T lymphocytes recognizing antigenic fragments displayed on MHC molecules?
What is the outcome of T lymphocytes recognizing antigenic fragments displayed on MHC molecules?
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Antigen processing involves which of the following processes?
Antigen processing involves which of the following processes?
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What is the role of MHC molecules in antigen presentation?
What is the role of MHC molecules in antigen presentation?
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What are examples of non-professional antigen presenting cells?
What are examples of non-professional antigen presenting cells?
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Non professional cells only present antigens when they become infected
Non professional cells only present antigens when they become infected
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What unique function do dendritic cells perform that is crucial for T cell activation?
What unique function do dendritic cells perform that is crucial for T cell activation?
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Which mechanism allows dendritic cells to present antigens from infected and tumor cells to CD8+ T cells?
Which mechanism allows dendritic cells to present antigens from infected and tumor cells to CD8+ T cells?
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What property of dendritic cells significantly enhances their ability to stimulate T cell responses?
What property of dendritic cells significantly enhances their ability to stimulate T cell responses?
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Which statement contradicts the conventional understanding of antigen presentation mechanisms?
Which statement contradicts the conventional understanding of antigen presentation mechanisms?
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What is the term used to describe the process by which dendritic cells present ingested antigens through MHC class I?
What is the term used to describe the process by which dendritic cells present ingested antigens through MHC class I?
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What type of antigens do dendritic cells primarily present via the MHC class 1 and MHC class 2 pathways?
What type of antigens do dendritic cells primarily present via the MHC class 1 and MHC class 2 pathways?
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In which location are dendritic cells predominantly found compared to other sites?
In which location are dendritic cells predominantly found compared to other sites?
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Which statement accurately describes the characteristics of dendritic cells in relation to MHC expression?
Which statement accurately describes the characteristics of dendritic cells in relation to MHC expression?
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What can be inferred about the role of dendritic cells in the immune system based on their locations?
What can be inferred about the role of dendritic cells in the immune system based on their locations?
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Which of the following statements is true regarding their functionality in antigen presentation?
Which of the following statements is true regarding their functionality in antigen presentation?
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What triggers macrophages to express MHC class 2 and present antigens?
What triggers macrophages to express MHC class 2 and present antigens?
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In which location are macrophages most abundantly found?
In which location are macrophages most abundantly found?
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Which of the following statements about macrophages is accurate?
Which of the following statements about macrophages is accurate?
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Which factor is NOT necessary for macrophages to present antigens to CD4+ T cells?
Which factor is NOT necessary for macrophages to present antigens to CD4+ T cells?
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What is the primary role of macrophages in the context of cell-mediated immunity?
What is the primary role of macrophages in the context of cell-mediated immunity?
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What role do B lymphocytes play in the activation of helper T-cells during the humoral immune response?
What role do B lymphocytes play in the activation of helper T-cells during the humoral immune response?
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Which statement correctly describes the expression of MHC class II on B lymphocytes?
Which statement correctly describes the expression of MHC class II on B lymphocytes?
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Where are B lymphocytes primarily located within the body?
Where are B lymphocytes primarily located within the body?
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What type of antigens do B lymphocytes bind to during the humoral immune response?
What type of antigens do B lymphocytes bind to during the humoral immune response?
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What is the sequence of event regarding B lymphocytes and helper T-cells in the immune response?
What is the sequence of event regarding B lymphocytes and helper T-cells in the immune response?
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What is the primary role of antigen presenting cells (APCs) in relation to T cells?
What is the primary role of antigen presenting cells (APCs) in relation to T cells?
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Which statement correctly describes the process of co-stimulation provided by APCs?
Which statement correctly describes the process of co-stimulation provided by APCs?
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During antigen processing, which is a key step performed by APCs?
During antigen processing, which is a key step performed by APCs?
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What distinguishes the functions of professional APCs from non-professional APCs?
What distinguishes the functions of professional APCs from non-professional APCs?
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Which of the following functions is NOT performed by antigen presenting cells?
Which of the following functions is NOT performed by antigen presenting cells?
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Antigen presentation begins with (…)
Antigen presentation begins with (…)
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Which statement accurately describes the source of the peptides that are presented by MHC class I molecules?
Which statement accurately describes the source of the peptides that are presented by MHC class I molecules?
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What distinguishes the antigen processing pathway that generates MHC class II-associated peptides from that of MHC class I-associated peptides?
What distinguishes the antigen processing pathway that generates MHC class II-associated peptides from that of MHC class I-associated peptides?
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Which of the following best characterizes the role of professional antigen presenting cells (APCs) in relation to MHC molecules?
Which of the following best characterizes the role of professional antigen presenting cells (APCs) in relation to MHC molecules?
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What is the significance of acidic vesicular compartments in the context of antigen processing?
What is the significance of acidic vesicular compartments in the context of antigen processing?
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Which of the following peptides is least likely to be displayed by MHC class I molecules?
Which of the following peptides is least likely to be displayed by MHC class I molecules?
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What is the primary role of cathepsins in the processing of endocytosed antigens for MHC class II presentations?
What is the primary role of cathepsins in the processing of endocytosed antigens for MHC class II presentations?
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Which process is responsible for the uptake of extracellular proteins into the vesicular compartments of antigen presenting cells?
Which process is responsible for the uptake of extracellular proteins into the vesicular compartments of antigen presenting cells?
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What is the significance of the phagolysosome in antigen processing for MHC class II presentations?
What is the significance of the phagolysosome in antigen processing for MHC class II presentations?
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In the context of antigen processing, what is the expected length of peptides produced for MHC class II presentation?
In the context of antigen processing, what is the expected length of peptides produced for MHC class II presentation?
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Which component plays a critical role in the further degradation of proteins within endosomal or lysosomal vesicles during antigen processing?
Which component plays a critical role in the further degradation of proteins within endosomal or lysosomal vesicles during antigen processing?
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What is the correct sequence of the first step involved in the biosynthesis of MHC class II molecules?
What is the correct sequence of the first step involved in the biosynthesis of MHC class II molecules?
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What happens to the invariant chain (Ii) during the processing of MHC class II molecules?
What happens to the invariant chain (Ii) during the processing of MHC class II molecules?
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Which cells primarily recognize the MHC class II-peptide complexes once expressed on the surface of antigen presenting cells?
Which cells primarily recognize the MHC class II-peptide complexes once expressed on the surface of antigen presenting cells?
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Where is the invariant chain (Ii) specifically associated during the transport of MHC class II molecules?
Where is the invariant chain (Ii) specifically associated during the transport of MHC class II molecules?
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What outcome occurs after the stable association of peptides with MHC class II molecules?
What outcome occurs after the stable association of peptides with MHC class II molecules?
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What role does the transporter associated with antigen presentation (TAP) play in the processing of cytosolic antigens for MHC class I presentation?
What role does the transporter associated with antigen presentation (TAP) play in the processing of cytosolic antigens for MHC class I presentation?
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Which step in the sequence of MHC class I antigen processing occurs after the proteolytic degradation of proteins?
Which step in the sequence of MHC class I antigen processing occurs after the proteolytic degradation of proteins?
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What is the final outcome of the stable MHC class I-peptide complex in the immune response?
What is the final outcome of the stable MHC class I-peptide complex in the immune response?
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Which of the following correctly describes the origin of the proteins presented by MHC class I molecules?
Which of the following correctly describes the origin of the proteins presented by MHC class I molecules?
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What is the role of the Golgi apparatus in the process of MHC class I antigen presentation?
What is the role of the Golgi apparatus in the process of MHC class I antigen presentation?
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What is the primary effect of microbial product detection on antigen presenting cells (APCs)?
What is the primary effect of microbial product detection on antigen presenting cells (APCs)?
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What is the role of dendritic cells in the initiation of T cell responses?
What is the role of dendritic cells in the initiation of T cell responses?
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How do APCs respond to microbial products to enhance their function?
How do APCs respond to microbial products to enhance their function?
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Which of the following describes a response of APCs upon the activation of toll-like receptors?
Which of the following describes a response of APCs upon the activation of toll-like receptors?
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What is the significance of chemokine production by activated APCs?
What is the significance of chemokine production by activated APCs?
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What type of molecules are responsible for presenting lipid antigens to T-cells?
What type of molecules are responsible for presenting lipid antigens to T-cells?
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Which type of T-cells are primarily activated by lipid antigens presented by CD1?
Which type of T-cells are primarily activated by lipid antigens presented by CD1?
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Where are CD1 molecules typically found?
Where are CD1 molecules typically found?
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What distinguishes the T-cell activation by CD1 from that by MHC molecules?
What distinguishes the T-cell activation by CD1 from that by MHC molecules?
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Which statement is accurate regarding the structure of CD1 molecules?
Which statement is accurate regarding the structure of CD1 molecules?
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What types of T cells are activated by peptides derived from endogenously acquired proteins?
What types of T cells are activated by peptides derived from endogenously acquired proteins?
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Which statement accurately reflects the nature of T cells in terms of antigen recognition?
Which statement accurately reflects the nature of T cells in terms of antigen recognition?
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What is the role of the CD3 complex in T cells?
What is the role of the CD3 complex in T cells?
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Which statement best describes the predominant type of TCR found in lymphoid tissues?
Which statement best describes the predominant type of TCR found in lymphoid tissues?
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Which characteristic distinguishes alpha-beta TCR from gamma-delta TCR?
Which characteristic distinguishes alpha-beta TCR from gamma-delta TCR?
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What defines self MHC restriction in T cells?
What defines self MHC restriction in T cells?
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Which type of antigens are CD4+ T cells specifically designed to recognize?
Which type of antigens are CD4+ T cells specifically designed to recognize?
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Which component of the TCR is crucial for recognizing specific amino acid sequences of peptides?
Which component of the TCR is crucial for recognizing specific amino acid sequences of peptides?
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Which of the following are recognized by B cell receptors (BCRs)?
Which of the following are recognized by B cell receptors (BCRs)?
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What is the consequence of T cells being stimulated without co-stimulatory signals?
What is the consequence of T cells being stimulated without co-stimulatory signals?
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Which signal is primarily responsible for T cell activation?
Which signal is primarily responsible for T cell activation?
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Which of the following combinations properly represents the two signals required for T cell activation?
Which of the following combinations properly represents the two signals required for T cell activation?
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What type of antigens can B cell receptors (BCRs) recognize?
What type of antigens can B cell receptors (BCRs) recognize?
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What is the primary positive co-stimulatory signal provided by APCs to activate naive T cells?
What is the primary positive co-stimulatory signal provided by APCs to activate naive T cells?
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Which characteristic of dendritic cells enables them to effectively initiate primary T cell responses?
Which characteristic of dendritic cells enables them to effectively initiate primary T cell responses?
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What is the role of mature dendritic cells in relation to naive T cells?
What is the role of mature dendritic cells in relation to naive T cells?
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What effect does the interaction of APC CD90/86 with T cell CTLA4 have on T cell activation?
What effect does the interaction of APC CD90/86 with T cell CTLA4 have on T cell activation?
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Which of the following properties distinguishes dendritic cells from other professional APCs?
Which of the following properties distinguishes dendritic cells from other professional APCs?
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Study Notes
Antigen Processing And Presentation
- Antigen presenting cells (APCs) process and present antigens to T lymphocytes.
- APCs digest antigens acquired from inside or outside the cell.
- APCs display resulting antigenic fragments on cell surface MHC molecules.
- T lymphocytes recognize antigenic fragments presented on MHC molecules, initiating a cellular immune response.
- The three professional APCs are dendritic cells, macrophages, and B lymphocytes.
Dendritic Cells and T Cell Response
- Dendritic cells (DCs) are crucial for initiating T cell responses.
- They present antigens to naive CD4+ and CD8+ T cells.
- DCs express high levels of costimulatory molecules which are required for T cell activation.
- DCs can ingest infected and tumor cells.
- This allows DCs to present antigens to CD8+ T cells, even if the antigen is not directly expressed by the DC itself.
- This process, known as cross-presentation or cross-priming, is essential for generating CD8+ T cell responses against intracellular pathogens and tumors.
- Cross-presentation allows DCs to present antigens through MHC class I, even though the antigen was initially ingested through the MHC class II pathway.
Dendritic Cells
- Dendritic cells always express MHC-2
- Dendritic cells present intracellular and extracellular antigens
- Dendritic cells present antigens via MHC class 1 and MHC class 2 pathways
- Dendritic cells are located in the lymphoid tissue, connective tissue and epithelium -- with the highest concentration in the epithelial layer
Macrophages in Cell-Mediated Immunity
- Macrophages are key players in the effector phase of cell-mediated immunity.
- They present antigens to differentiated CD4+ T cells, which are crucial for triggering an immune response.
- Macrophages express MHC class 2, which is involved in antigen presentation.
- Macrophage expression of MHC class 2 is low but can be induced by various stimuli, including:
- Pathogen-associated molecular patterns (PAMPs)
- Damage-associated molecular patterns (DAMPs)
- Cytokines
- Macrophages are considered extracellular antigen presenters.
- They present antigens via MHC class 2.
- Macrophages are found in various locations, including:
- Lymphoid tissue
- Connective tissue
- Body cavities
- The majority of macrophages are located in lymphoid tissue, highlighting their importance in immunity.
B Lymphocyte Antigen Presentation
- B lymphocytes present antigens to helper T-cells (CD4+) after being activated by dendritic cells.
- This occurs during the humoral immune response.
- B lymphocytes present extracellular antigens that bind to specific Ig receptors.
- Presentation is facilitated by MHC II.
- MHC II is always expressed on B lymphocytes but becomes inducible upon activation.
- B lymphocytes are found in lymphoid tissue and blood.
Antigen-Presenting Cells (APCs)
- APCs are essential for T cell responses to protein antigens.
- APCs capture, digest, and display antigens to T cells.
- APCs convert protein antigens into peptides.
- APCs display peptide-MHC complexes for recognition by T cells.
- This process of converting proteins to peptides is called antigen processing.
- APCs provide co-stimulatory signals that help activate T cells.
Antigen Processing
- Antigen processing converts protein antigens into peptides
- MHC molecules are responsible for displaying these peptides to lymphocytes
- Protein antigens in acidic vesicular compartments of antigen-presenting cells (APCs) generate MHC class 2-associated peptides
- Protein antigens present in the cytosol generate MHC class 1-associated peptides
Antigen Processing for MHC Class II Presentation
- Antigen-presenting cells (APCs) internalize extracellular proteins through receptor-mediated endocytosis.
- B cells use their B cell receptor (BCR) to internalize specific antigens.
- Internalized proteins are processed within endosomal or lysosomal vesicles, which are acidic compartments containing proteolytic enzymes.
- Endosomes and lysosomes combine to form phagolysosomes, further degrading proteins.
- Proteins are degraded into peptides of 14-20 amino acids in length for MHC class II presentation.
- Cathepsins are the primary enzymes responsible for protein degradation within these compartments.
MHC Class II Antigen Processing - Step 3
- MHC Class II alpha and beta chains are synthesized in the endoplasmic reticulum.
- These chains are transported to the Golgi apparatus and then to endosomes.
- An invariant chain (Ii) is associated with the MHC Class II molecules during transport.
- In the endosomes, Ii dissociates, and processed peptides associate with the MHC Class II molecules.
- The stable MHC Class II-peptide complexes are transported to the cell surface.
- These complexes are then recognized by CD4+ T cells.
Cytosolic Antigen Processing for MHC Class 1
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Cytosolic proteins, including those from viruses, bacteria, and endocytosed antigens can be processed for MHC Class 1 presentation.
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The proteasome, a large protein complex, degrades ubiquitinated proteins in the cytosol, generating peptides.
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The transporter associated with antigen presentation (TAP) transports peptides from the cytosol to the endoplasmic reticulum (ER).
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Within the ER, MHC Class 1 molecules assemble with peptides. The interaction of TAP with MHC Class 1 allows efficient peptide loading.
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The MHC Class 1-peptide complex is transported through the Golgi apparatus to the cell surface.
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The complex is recognized by CD8+ T cells, initiating an immune response.
Antigen Presenting Cells and Microbial Products
- Antigen presenting cells (APCs) enhance their presentation of antigens in the presence of microbial products.
- APCs express Toll-like receptors (TLRs) that recognize and respond to microbial components.
- TLR activation triggers a cascade of events that lead to:
- Increased expression of major histocompatibility complex (MHC) molecules and co-stimulatory molecules, enhancing antigen presentation efficiency.
- Production of cytokines that activate immune cells involved in the adaptive immune response.
- Production of chemokines that recruit immune cells to the site of infection.
Dendritic Cells as Primary APCs to Naive T Cells
- Dendritic cells are the primary APCs responsible for presenting antigens to naive T cells.
- Dendritic cells capture antigens in peripheral tissues, such as the skin or mucosal surfaces, and migrate to draining lymph nodes where they interact with T cells.
- This antigen presentation to naive T cells initiates the adaptive immune response in peripheral lymphoid tissues.
CD1 Antigen Presentation Pathway
- CD1 molecules are a class 1-like non-polymorphic group of proteins
- CD1 proteins are found on antigen presenting cells (APCs) and some epithelial cells
- They function to present lipid antigens to T-cells
- CD1-mediated antigen presentation is not MHC-restricted
- NKT cells are an example of T-cells that recognize lipid antigens presented by CD1 molecules
T Cell Responses
- T cells are activated by the presentation of antigens by MHC class 1 or class 2 pathways.
- CD4+ T cells are activated by exogenously acquired proteins presented by MHC class 2.
- CD8+ T cells are activated by endogenously acquired proteins presented by MHC class 1.
- The T cell receptor (TCR) recognizes antigens presented in the correct MHC context.
- TCR is a member of the immunoglobulin superfamily and comes in two types: alpha-beta TCR and gamma-delta TCR.
- Alpha-beta TCR is MHC dependent and found in lymphoid tissues.
- Gamma-delta TCR is MHC independent and found on T lymphocytes at mucosal surfaces.
- Each T cell expresses only one TCR specificity.
- The CD3 complex is associated with the TCR and is composed of gamma, delta, epsilon, and Xi chains.
- The CD3 complex is invariant and does not contribute to specificity.
- The CD3 complex is necessary for TCR expression during T cell development.
- The CD3 complex transmits signals to the nucleus after antigen interaction with the TCR.
- T cells recognize peptides and are specific for amino acid sequences.
- T cells recognize anchor residues in peptide sequences, and only recognize foreign peptides when presented in the MHC context.
- Some T cells can recognize small chemicals called hapten conjugates.
- T cells from one individual only recognize foreign peptides when they are bound to MHC molecules of that individual (self-MHC restriction).
- CD4+ T cells are MHC class 2 restricted and recognize peptides from extracellular proteins.
- CD8+ T cells are MHC class 1 restricted and recognize peptides from cytosolic proteins.
B Cell Receptor (BCR)
- BCR does not interact with MHC molecules.
- BCR can recognize soluble and exposed antigens, including:
- Peptides
- Proteins
- Nucleic acids
- Polysaccharides
- Lipids
T Cell Activation
- Co-stimulatory signals are necessary for complete T cell activation.
- Signal 1: Antigen bound to MHC (specific signal)
- Signal 2: Interaction between CD28 on T-cells and B7 (CD90/CD86) on antigen-presenting cells (APCs) (co-stimulatory signal)
- Clonal anergy: Occurs when T cells are stimulated without co-stimulatory signals, resulting in a state of non-responsiveness.
Antigen Presentation
- T cell responses begin in peripheral lymphoid organs.
- Dendritic cells are the primary antigen presenting cells (APCs) for naive T cells.
- Dendritic cells are found in epithelia and tissues, capturing protein antigens and transporting them to draining lymph nodes.
- Dendritic cells express receptors that capture microbes and respond to microbial signals.
- Dendritic cells migrate to T-cell rich zones of lymph nodes through which naive T cells circulate.
- Mature dendritic cells express high levels of co-stimulatory molecules required to activate naive T cells.
Co-stimulation Regulation
- Co-stimulatory molecules regulate T cell activation.
- CD90/CD86 on APCs and CD28 on T cells lead to positive effects on T cell activation.
- CD90/CD86 on APCs and CTLA4 on T cells lead to negative effects on T cell activation.
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Understand antigen presentation