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Section 21.1: Adaptive Immune Defenses - Overview

  • Page ID
    144221
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    Learning Objectives
    • Define memory, primary response, secondary response, and specificity
    • Distinguish between humoral and cellular immunity
    • Differentiate between antigens, epitopes, and haptens
    • Describe the structure and function of antibodies and distinguish between the different classes of antibodies

    Adaptive immunity is defined by two important characteristics: specificity and memory. Specificity refers to the adaptive immune system’s ability to target specific pathogens, and memory refers to its ability to quickly respond to pathogens to which it has previously been exposed. For example, when an individual recovers from chickenpox, the body develops a memory of the infection that will specifically protect it from the causative agent, the varicella-zoster virus, if it is exposed to the virus again later.

    Specificity and memory are achieved by essentially programming certain cells involved in the immune response to respond rapidly to subsequent exposures of the pathogen. This programming occurs as a result of the first exposure to a pathogen or vaccine, which triggers a primary response. Subsequent exposures result in a secondary response that is faster and stronger as a result of the body’s memory of the first exposure (Figure \(\PageIndex{1}\)). This secondary response, however, is specific to the pathogen in question. For example, exposure to one virus (e.g., varicella-zoster virus) will not provide protection against other viral diseases (e.g., measles, mumps, or polio).

    Adaptive specific immunity involves the actions of two distinct cell types: B lymphocytes (B cells) and T lymphocytes (T cells). Although B cells and T cells arise from a common hematopoietic stem cell differentiation pathway, their sites of maturation and their roles in adaptive immunity are very different.

    B cells mature in the bone marrow and are responsible for the production of glycoproteins called antibodies, or immunoglobulins. Antibodies are involved in the body’s defense against pathogens and toxins in the extracellular environment. Mechanisms of adaptive specific immunity that involve B cells and antibody production are referred to as humoral immunity. The maturation of T cells occurs in the thymus. T cells function as the central orchestrator of both innate and adaptive immune responses. They are also responsible for destruction of cells infected with intracellular pathogens. The targeting and destruction of intracellular pathogens by T cells is called cell-mediated immunity, or cellular immunity.

    A graph with time on the X axis and concentration of antibody on the Y axis. The concentration is near 0 at the initial exposure and increases during the primary immune response. The concentration then drop back down but remains above the level at initial exposure. The secondary exposure increases the concentration of antibody to higher levels than the primary response. And even after dropping back down this count remains relatively high.
    Figure \(\PageIndex{1}\): This graph illustrates the primary and secondary immune responses related to antibody production after an initial and secondary exposure to an antigen. Notice that the secondary response is faster and provides a much higher concentration of antibody.
    Exercise \(\PageIndex{2}\)
    1. List the two defining characteristics of adaptive immunity.
    2. Explain the difference between a primary and secondary immune response.
    3. How do humoral and cellular immunity differ?

    Key Concepts and Summary

    • Adaptive immunity is an acquired defense against foreign pathogens that is characterized by specificity and memory. The first exposure to an antigen stimulates a primary response, and subsequent exposures stimulate a faster and strong secondary response.
    • Adaptive immunity is a dual system involving humoral immunity (antibodies produced by B cells) and cellular immunity (T cells directed against intracellular pathogens).
    • Antigens, also called immunogens, are molecules that activate adaptive immunity. A single antigen possesses smaller epitopes, each capable of inducing a specific adaptive immune response.
    • An antigen’s ability to stimulate an immune response depends on several factors, including its molecular class, molecular complexity, and size.
    • Antibodies (immunoglobulins) are Y-shaped glycoproteins with two Fab sites for binding antigens and an Fc portion involved in complement activation and opsonization.
    • The five classes of antibody are IgM, IgG, IgA, IgE, and IgD, each differing in size, arrangement, location within the body, and function. The five primary functions of antibodies are neutralization, opsonization, agglutination, complement activation, and antibody-dependent cell-mediated cytotoxicity (ADCC).

    This page titled Section 21.1: Adaptive Immune Defenses - Overview is shared under a CC BY 4.0 license and was authored, remixed, and/or curated by Ying Liu via source content that was edited to the style and standards of the LibreTexts platform.