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T helper cells

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Anatomy and Physiology I

Definition

T helper cells, also known as CD4+ T cells, are a type of lymphocyte that play a crucial role in the adaptive immune response. They coordinate and enhance the activities of other immune cells, such as B-lymphocytes and cytotoxic T cells, to mount an effective immune response against pathogens.

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5 Must Know Facts For Your Next Test

  1. T helper cells express the CD4 surface protein, which allows them to recognize and bind to antigen-presenting cells, such as dendritic cells and macrophages.
  2. T helper cells secrete a variety of cytokines, which are signaling molecules that regulate and coordinate the activities of other immune cells.
  3. There are two main subsets of T helper cells: Th1 cells, which promote cell-mediated immunity, and Th2 cells, which enhance humoral immunity and antibody production.
  4. T helper cells play a crucial role in activating and supporting the function of B-lymphocytes, which produce antibodies to neutralize or eliminate pathogens.
  5. Dysfunction or depletion of T helper cells, as seen in HIV/AIDS, can lead to a weakened immune system and increased susceptibility to opportunistic infections.

Review Questions

  • Explain the role of T helper cells in the adaptive immune response, specifically in relation to B-lymphocytes and antibody production.
    • T helper cells play a central role in the adaptive immune response by coordinating and enhancing the activities of other immune cells, such as B-lymphocytes. When a B-lymphocyte encounters an antigen, it requires the help of a T helper cell to become fully activated and begin producing antibodies. T helper cells secrete cytokines that stimulate B-lymphocytes to proliferate and differentiate into antibody-producing plasma cells. This collaboration between T helper cells and B-lymphocytes is crucial for the humoral immune response, which involves the production of antibodies to neutralize or eliminate pathogens.
  • Describe the different subsets of T helper cells and their respective functions in the context of the adaptive immune response.
    • There are two main subsets of T helper cells: Th1 cells and Th2 cells. Th1 cells promote cell-mediated immunity, which involves the activation of cytotoxic T cells and macrophages to directly attack and eliminate intracellular pathogens, such as viruses and some bacteria. Th1 cells secrete cytokines like interferon-gamma (IFN-γ) and tumor necrosis factor-alpha (TNF-α) to enhance the function of these effector cells. In contrast, Th2 cells enhance humoral immunity and antibody production by B-lymphocytes. Th2 cells secrete cytokines like interleukin-4 (IL-4) and interleukin-5 (IL-5) that stimulate B-lymphocytes to proliferate and differentiate into antibody-producing plasma cells. The balance between Th1 and Th2 responses is crucial for maintaining a well-coordinated and effective adaptive immune response.
  • Analyze the consequences of T helper cell dysfunction or depletion, as seen in HIV/AIDS, and explain how this can lead to a weakened immune system and increased susceptibility to opportunistic infections.
    • T helper cells, specifically the CD4+ T cell subset, play a central role in coordinating and regulating the adaptive immune response. In the case of HIV/AIDS, the human immunodeficiency virus (HIV) targets and destroys CD4+ T helper cells, leading to a progressive depletion of this crucial cell population. As T helper cells are depleted, the immune system becomes increasingly compromised, and the body loses its ability to mount effective responses against a wide range of pathogens. This weakened state leaves the individual susceptible to opportunistic infections, which are typically harmless to individuals with a healthy immune system but can become life-threatening in the context of HIV/AIDS. The loss of T helper cell function and the resulting immunodeficiency is a hallmark of the progression of HIV/AIDS, highlighting the critical importance of these cells in maintaining a robust and coordinated adaptive immune response.

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