Biology 2e
2nd Edition
ISBN: 9781947172517
Author: Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher: OpenStax
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Chapter 42, Problem 27CTQ
In mammalian adaptive immune systems, T cell receptors are extraordinarily diverse. What function of the immune system results from this diversity and how is this diversity achieved?
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The classical complement pathway is initiated by C1q binding to the surface of a pathogen. In some cases, C1q can directly bind the pathogen, for instance by recognizing proteins of bacterial cell walls, but in most cases C1q binds to IgM antibodies that are bound to the pathogen surface. How does this IgM-binding feature of C1q contribute to rapid, innate immune responses rather than to slow, adaptive responses?
C1q induces B lymphocytes to begin secreting antibody within hours of pathogen exposure.
Natural antibody that binds to many microbial pathogens is produced prior to pathogen exposure.
C1q binds to C-reactive protein which then binds to IgM on the pathogen surface.
C1q directly induces inflammation, recruiting phagocytes and antibodies from the blood into the infected tissue.
C1q binds to dendritic cells in the infected tissue, inducing them to secrete inflammatory cytokines.
Immune systems of animals are very complex. For an animal's immune system to work properly, certain cells must be able to recognize other specific types of cells, so that they can bind to and communicate with them. These types of interactions allow an immune system to decide if and when to launch an immune response.
For example, dendritic cells must be able to recognize and interact with T-cells, but they do not need to recognize adipocyte cells. Which of the following describes a difference between T-cells and adipocyte cells that would allow dendritic cells to recognize one, but not the other?
A. Adipocyte cells must have a cell wall, while T-cells lack one.
B. T-cells and adipocyte cells must have different types of lipids that compose their plasma membranes.
C. Adipocyte cells must lack endoplasmic reticulum, while T-cells possess endoplasmic reticulum.
D. T-cells and adipocyte cells must have some differences in the carbohydrates and/or…
Immune cells from the innate immunity arm are capable of participating in adaptive immunity. describe how it is possible for innate immune cells to contribute to adaptive immunity?
Chapter 42 Solutions
Biology 2e
Ch. 42 - Figure 42.11 Which of the following statements...Ch. 42 - Figure 42.14 Based on what you know about MHC...Ch. 42 - Figure 42.16 The Rh antigen is found on Rh...Ch. 42 - Which of the following is a barrier against...Ch. 42 - Although interferons have several effects, they...Ch. 42 - Which organelle do phagocytes use to digest...Ch. 42 - Which innate immune system component uses MHC I...Ch. 42 - Which of the following is both a phagocyte and an...Ch. 42 - Which immune cells bind MHC molecules on APCs via...Ch. 42 - What “self” pattern is identified by NK cells?...
Ch. 42 - The acquired ability to prevent an unnecessary or...Ch. 42 - A memory B cell can differentiate upon reexposure...Ch. 42 - Foreign particles circulating in the blood are...Ch. 42 - The structure of an antibody is similar to the...Ch. 42 - The first antibody class to appear in the serum in...Ch. 42 - What is the most abundant antibody class detected...Ch. 42 - Breastfed infants typically are resistant to...Ch. 42 - Allergy to pollen is classified as: an autoimmune...Ch. 42 - A potential cause of acquired autoimmunity is...Ch. 42 - Autoantibodies are probably involved in: reactions...Ch. 42 - Which of the following diseases is not due to...Ch. 42 - Different MHC I molecules between donor and...Ch. 42 - If a series of genetic mutations prevented some,...Ch. 42 - Explain the difference between an epitope and an...Ch. 42 - What is a naïve B or T cell?Ch. 42 - How does the Th1 response differ from the Th2...Ch. 42 - In mammalian adaptive immune systems, T cell...Ch. 42 - How do B and T cells differ with respect to...Ch. 42 - Why is the immune response after reinfection much...Ch. 42 - What are the benefits and costs of antibody cross...
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- The T-cell receptor gene segments are arranged in a similar pattern to immunoglobulin gene segments and are rearranged by the same enzymes. While B cells and T cells differ markedly in their functions during an immune response, the two lymphocyte subsets share the enzymatic machinery and overall scheme for generating antigen receptor diversity. This is because: B cells and T cells recognize the same form of antigen expressed by an infecting pathogen. Animals with B cells developed first, and later evolving species then developed T cells. B cells and T cells both need enormous antigen receptor diversity to provide protection against the diversity of pathogens. Antibody and T-cell receptor gene segments are both flanked by similar recombination signal sequences. B cells and T cells both secrete their antigen receptor proteins after they are activated by antigen-binding.arrow_forwardWhich proteins involved in the activation of T cells have the capacity for transduction without the need to be activated by a family of kinases?arrow_forwardWhat is the relationship and differences between receptor-mediated endocytosis and TLR in relation to innate immunity?arrow_forward
- Describe the roles that phagocytic and nonphagocytic cells and plasma proteins such as complement and interferon play in innate immunity?arrow_forwardThe entry of naive T cells from the blood into lymph nodes and mucosal lymphoid tissues occurs by a process that involves similar steps and similar adhesion molecules to the process by which leukocytes are recruited into sites of inflammation. Yet naive T cells do not enter tissues at sites of inflammation, but rather, home to lymphoid tissues. Which class of adhesion molecules direct the specific homing of naive T cells to lymphoid tissues?arrow_forwardHuman immune system a) Pathogen-associated molecular patterns are conserved molecular structures produced by microorganisms, but not by host cells. b) A virus-infected host cell that displays a viral antigen via MHC class I molecules may become a target of cytotoxic T cells. c) Secreted MHC Class I proteins present in blood plasma can function as opsonins. d) Both (a) and (b) are correct and (c) is incorrect e) Statements (a), (b) and (c) are all correctarrow_forward
- Some viruses have mechanisms to down-regulate MHC class I protein expression on the surface of cells in which the virus is replicating. This immune evasion strategy might prevent effector CD8 cytotoxic T cells from recognizing and killing the virus-infected cells. Would this immune evasion strategy also prevent the initial activation of virus-specific CD8 T cells? Yes, because no viral peptide:MHC class I complexes would form to activate CD8 T cells. No, because dendritic cells would take up infected cells and cross-present viral peptides to activate CD8 T cells. No, because some presentation of MHC class I complexes with viral peptides would occur before the virus could down-regulate all the surface MHC class I protein. Yes, because this immune evasion strategy would also function in dendritic cells, even if the virus doesn’t replicate in dendritic cells. No, because the type I interferon response induced by the virus infection will up-regulate MHC class I expression and override the…arrow_forwardWhat are the components of innate immunity?arrow_forwardT-cell receptors concentrate diversity in the third hypervariable region. For alpha:beta T-cell receptors, sequence diversity is heavily concentrated at the junctions formed by the rearrangement of gene segments during the generation of the expressed Va and Vb regions. The result of this organization is to position the most variable part of the T-cell receptor over a certain region of the ligand recognized by this receptor. Which region (outlined in red in figure below) indicates this part of the ligand recognized by the T-cell receptor?arrow_forward
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