BIOL 318: CH. 21 - IMMUNE SYSTEM: ADAPTIVE IMMUNITY

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175 Terms

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What line of defense is adaptive immunity?

Third line of defense with specificity and memory.

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What are the two main forms of adaptive immunity?

Cell-mediated (cellular) and antibody-mediated (humoral) immunity.

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What type of pathogens does cell-mediated immunity target?

Intracellular pathogens like viruses, certain bacteria, yeasts, protozoans, parasitic worms, cancer cells, and transplanted cells.

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Why can't antibodies handle intracellular pathogens?

Because the pathogens, like viruses, are inside the host cells.

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How do lymphocytes function in cell-mediated immunity?

They directly attack infected or abnormal cells.

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What else does cell-mediated immunity act against besides pathogens?

Parasitic worms, cancer cells, and transplanted tissue or organ cells.

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What type of pathogens does antibody-mediated immunity target?

Extracellular pathogens like bacteria, viruses, yeasts, protozoans, toxins, venoms, and allergens.

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How does antibody-mediated immunity handle foreign erythrocytes in a mismatched transfusion?

It destroys them as part of the immune response.

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How do antibodies affect pathogens in humoral immunity?

They tag pathogens for destruction but do not directly destroy them.

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Why might both humoral and cellular immunity be used against the same pathogen?

Because they may attack it in different ways or at different stages of its life cycle.

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What is active immunity?

Body produces antibodies or T cells against a pathogen.

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What is natural active immunity?

Production of own antibodies due to natural exposure to a pathogen.

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What is an example of natural active immunity?

Eating something with a pathogen in it.

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What is artificial active immunity?

Production of antibodies from vaccination.

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What types of vaccines provide artificial active immunity?

Dead, attenuated (weakened), or fragments of pathogens.

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Why are booster shots given?

To restimulate immune memory and maintain a high level of protection (e.g., tetanus boosters).

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What is passive immunity?

Receiving antibodies or serum from another person or animal already immune to the pathogen.

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How long does passive immunity typically last?

Only 2 or 3 weeks, until the acquired antibodies are degraded.

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What is natural passive immunity?

Temporary immunity from antibodies received from another person naturally.

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How does a fetus acquire natural passive immunity?

Through antibodies passed from the mother via the placenta.

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How does a baby acquire natural passive immunity after birth?

Through antibodies in breast milk.

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What is artificial passive immunity?

Temporary immunity from an injection of immune serum containing antibodies.

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What are examples of situations treated with artificial passive immunity?

Snakebites, botulism, tetanus, rabies.

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What is an antigen?

Any molecule that can bind an antibody.

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What are examples of free antigens?

Venoms, toxins, food-borne substances.

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What are examples of antigen components in organisms?

Plasma membranes and bacterial cell walls.

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What is the role of an antigen in the immune system?

Triggers an immune response.

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What size and complexity do typical antigens have?

Larger molecules with more complexity.

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How does molecular uniqueness affect immune response?

More uniqueness leads to fewer self-attacks.

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What types of molecules can act as antigens?

Proteins, polysaccharides, glycolipids.

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Where are antigens typically located?

Facing the extracellular fluid (ECF).

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What is agglutination?

Collection of red blood cells by antibodies.

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What part of an antigen stimulates immune responses?

Epitopes (antigenic determinants).

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What is a hapten?

A molecule too small to be antigenic on its own; considered an incomplete antigen.

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How can a hapten become antigenic?

By binding to a larger host molecule to form a complex that can bind to antibodies and stimulate an immune response.

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What are examples of common haptens?

Poison ivy, cat dander, penicillin.

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What is the most common drug allergy?

Penicillin allergy.

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How does penicillin cause an allergic reaction?

It binds to host proteins, forming a complex that activates mast cells and triggers the release of histamine and other inflammatory chemicals.

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What can a severe penicillin allergy lead to?

Anaphylactic shock, which can cause death.

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What are antibodies also known as?

Immunoglobulins (Igs).

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What type of globulins are antibodies and where are they produced?

Gamma globulins produced by plasma cells in the bloodstream.

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How many polypeptide chains make up an antibody?

Four polypeptides.

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What are the types of polypeptide chains in an antibody?

Two light chains (small) and two heavy chains (bent, give T or Y shape).

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What holds the polypeptide chains of an antibody together?

Disulfide bonds.

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What region is present in all antibody chains and what does it form?

Variable regions that form two antigen-binding sites.

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How many unique antibodies exist in the human body?

Approximately 10 billion to 1 trillion.

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What process creates diversity in antibodies through recombining DNA?

Somatic recombination.

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What is somatic recombination?

Mixing of nucleotide sequences to form new DNA combinations in somatic cells.

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What other process increases antibody diversity besides recombination?

High genetic mutation rate (somatic hypermutation).

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What is somatic hypermutation?

Creation of new DNA sequences through mutation, not just recombination.

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How many classes of antibodies are there?

Five classes.

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What are the five classes of antibodies?

IgA, IgD, IgE, IgG, IgM.

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Which antibody is important for newborn immunity and why?

IgG because it crosses the placenta easily.

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Which antibody is passed to infants through breast milk and colostrum?

IgA.

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How do antibody classes differ?

In location, structure, timing, and function.

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Where are antibodies found besides blood plasma?

Lymph, mucus, saliva, intestinal secretions, tears, and breast milk.

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Which immune cells have antibodies as integral membrane proteins?

Basophils, mast cells (innate immunity) and B lymphocytes (adaptive immunity).

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Where are T lymphocytes born?

Red bone marrow from hemopoietic stem cells.

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Where do T lymphocytes travel for training?

Thymus.

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Where in the thymus do T cells undergo their first test?

Cortex.

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What structure protects developing T cells in the cortex?

Blood-thymus barrier.

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Who gives the first test in the cortex and what kind of selection is it?

Epithelial cells; positive selection.

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What does the first test check for?

Capacity of T cells to respond to fragments of pathogens.

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What happens if a T cell has proper receptors during the first test?

Receives a life-sparing signal and becomes immunocompetent.

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What happens if a T cell lacks receptors during the first test?

Receives no signal and can retake the test.

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How can a T cell retake the first test?

Reshuffles its DNA for new receptors.

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What happens if the T cell fails again after retaking the test?

Dies by apoptosis and is phagocytized by cortical macrophages.

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Where do T cells go after passing the cortex test?

Medulla.

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Who gives the second test in the medulla and what kind of selection is it?

Macrophages and reticular cells; negative selection.

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What are T cells presented with in the medulla during the second test?

Self-antigens and binding proteins (MHC).

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What happens if a T cell responds to self-antigens?

Destroyed by macrophages.

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What does the second test ensure?

Self-tolerance so that T cells won’t attack the body’s own tissues.

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What percentage of T cells survive both tests?

2%.

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What is the result of passing both tests in the thymus?

Becomes part of the naïve lymphocyte pool.

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What does it mean to be a naïve T cell?

Has not yet encountered a foreign antigen.

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Where do naïve T cells go after leaving the thymus?

Travel by blood and lymph to lymphatic tissues and organs like the spleen.

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What do naïve T cells do once deployed?

Await activation by encountering their specific antigen.

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What do T cells require to recognize an antigen?

APCs (antigen-presenting cells).

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What are the types of antigen-presenting cells (APCs)?

Dendritic cells, macrophages, B cells.

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What do APCs depend on to present antigens?

MHC genes (proteins).

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What is the role of MHC I complexes in antigen presentation?

All cells can present antigens on MHC I complexes, serve as ID tags.

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How are antigens processed by APCs?

Ingested by endocytosis, broken into fragments, epitopes bound to MHC proteins.

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How do T cells interact with APCs?

Monitor APCs, test for antigen.

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What happens if an APC displays a self-antigen?

T cells disregard it.

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What happens if an APC displays a nonself-antigen?

Immune response against the foreign antigen.

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What is the primary function of T cells?

Directly attack infected/foreign cells and form memory.

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What do cytotoxic T cells (TC) do?

Carry out the attack on foreign cells.

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What is the role of helper T cells (TH)?

Promote the activity of TC cells and also contribute to humoral immunity.

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What is the function of regulatory T cells?

Inhibit multiplication and cytokine amplification by other T cells, reducing the response after attack.

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Why is the regulatory T cell function important?

Without it, TC cells would continue producing inflammatory cytokines, potentially causing long-term tissue damage.

  • It also reduces the risk of autoimmune diseases.

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What are memory T cells (TM) and how do they arise?

Memory T cells arise from TC cells and remain long-term after an infection.

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What are the three stages of both cellular and humoral immunity?

Recognition, attack, and memory.

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What do APCs do after migrating to lymph nodes?

What do APCs do after migrating to lymph nodes?
Present antigens to TC and TH cells.

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What proteins do TC cells respond to?

MHC-I proteins.

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Where are MHC-I proteins found?

All nucleated cells.

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What do MHC-I proteins present?

Internal peptides from within the cell.

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What happens if MHC-I peptides are normal self-antigens?

No T-cell response.

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What happens if MHC-I peptides are viral or abnormal antigens?

T-cell response → cell destruction.

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What proteins do TH cells respond to?

MHC-II proteins.

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What do MHC-II proteins present?

External antigens, phagocytosed foreign material.