20.3A: Overview of Adaptive Immunity

The adaptive immune system is composed of highly-specialized systemic cells and processes that rule out or prevent infective growth .
Learning Objectives

  • Describe adaptive immunity

Key Points

  • The adaptive immune response provides the vertebrate immune system with the ability to recognize and remember specific pathogens to generate immunity, and mount stronger attacks each time the pathogen is encountered.
  • The cells of the adaptive immune system are a type of leukocyte called a lymphocyte. B cells and T cells are the major types of lymphocytes involved in adaptive immunity.
  • B and T cells can create memory cells to defend against future attacks by the same pathogen by mounting a stronger and faster adaptive immune response against that pathogen before it can even cause symptoms of infection.
  • Antigen -presenting cells present captured antigens to immature lymphocytes, which then mature to be specific to that antigen and work to destroy pathogens that express that antigen.
  • Hypersensitivity disorders (allergies) may occur when an adaptive immune response forms against antigens that aren’t associated with pathogens, such as pollen. More complex hypersensitivity disorders may involve cytotoxic T cells and cause chronic inflammation and damage to the body’s own tissues.

Key Terms

  • antigen: A substance that induces an immune response, usually a molecule found on a pathogen such as a toxin or molecule expressed by the pathogen or pathogen-infected cells.
  • hypersensitivity: A disorder in which an adaptive immune response forms memory cells specific to antigens that aren’t associated with pathogens.
  • antigen presenting cell: A cell that presents captured antigens to immature T-cells. Dendritic cells and macrophages are the best examples, but several other cells can present antigens as well.

The adaptive immune system, besides known as the specific immune system, is composed of highly-specialized systemic cells and processes that excrete or prevent infective growth. The adaptive immune organization works to protect and heal the body when the unconditioned immune system fails. It provides the body with the ability to recognize and remember specific pathogens through their antigens. This mechanism allows the immune system to mount stronger attacks each time the pathogen is encountered, therefore preparing itself for future challenges and preventing reinfection by the same pathogen .

Functions of the Adaptive Immune System

The adaptive immune arrangement starts to work after the natural immune organization is activated. If an infection progresses despite the excitement, fever, natural killer whale ( NK ) cellular telephone and phagocyte activity of the unconditioned immune system, a more coordinate answer is required in holy order to destroy the pathogen. The adaptive immune answer occurs a few days after the natural immune answer is initiated. The major functions of the adaptive immune system include :

  • The recognition of specific “non-self” antigens in the presence of “self” during the process of antigen presentation
  • The generation of responses that are tailored to maximally eliminate specific pathogens or pathogen-infected cells
  • The development of immunological memory in which each pathogen is “remembered” by a signature antibody, which can then be called upon to quickly eliminate a pathogen should subsequent infections occur.

Formation of Adaptive Immunity

adaptive immunity is triggered when a pathogen evades the natural immune system for long enough to generate a threshold level of an antigen. An antigen is any molecule that induces an immune response, such as a toxin or molecular component of a pathogen cell membrane, and is unique to each species of pathogen. A typical adaptive immune reaction includes several steps :

  1. The antigen for the pathogen is taken up by an antigen-presenting cell (APC), such as a dendritic cell or macrophage, through phagocytosis.
  2. The APC travels to a part of the body that contains immature T and B cells, such as a lymph node.
  3. The antigen is processed by the APC and bound to MHC class II receptors and MHC class I receptors on the cell membrane of the APC.
  4. The antigen is presented to immature helper T cells and cytotoxic T cells through binding the MHC II (helper T) or MHC I (cytotoxic T) to T-cell receptors.
  5. These T lymphocytes mature and proliferate. Helper T cells activate B cells, which proliferate and produce antibodies specific to the antigen, while cytotoxic T cells destroy pathogens that bear the antigen that was presented to them by the APCs.
  6. Memory B and T cells are formed after the infection ends.

Antigen Presentation : Antigen presentation stimulates T cells to become either “ cytotoxic ” CD8+ cells or “ assistant ” CD4+ cells. Cytotoxic cells immediately attack cells carrying certain foreign or abnormal molecules on their surfaces. Helper T cells, or Th cells, coordinate immune responses by communicating with other cells. In most cases, T cells alone recognize an antigen if it is carried on the surface of a cell by one of the body ’ s own MHC, or major histocompatibility complex, molecules .

Immunological Memory

When B cells and T cells are activated, some become memory cells. Throughout the life of an animal, these memory cells form a database of effective B and T lymphocytes. Upon interaction with a previously-encountered antigen, the appropriate memory cells are selected and activated. In this manner, the second and subsequent exposures to an antigen produce a stronger and faster immune response. This is “ adaptive ” because the soundbox ’ s immune system prepares itself for future challenges, which can stop an contagion by the like pathogen before it can even cause symptoms .

Antibody : An antibody is made up of two heavy chains and two light chains. The unique variable region allows an antibody to recognize its pit antigen
immunological memory can either be in the shape of passive short-run memory or active long-run memory. passive memory is normally short-run, lasting between a few days and respective months, and is particularly crucial for newborn infants, who are given passive memory from maternal antibodies and immune cells before birth. active immunity is generally long-run and can be acquired by infection followed by B cells and T cells activation, or artificially acquired by vaccines in a serve called immunization .
The memory system does have a few flaws. Pathogens that undergo mutation much have different antigens than those known by memory B and T cells, meaning that different strains of the same pathogen can avoid the memory-enhanced immune answer. additionally, the memory cell serve enables the development of hypersensitivity disorders, such as allergies and many chronic diseases ( like multiple sclerosis or myasthenia gravis ). In these cases, memory cells form for an antigen that elicits an immune response without actually being caused by a pathogen, which leads to immune system mediated-damage to the consistency from mast cell, antibody, or T-cell mediated activities and inflammation .

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