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20.3D: Lymphocytes

A lymphocyte is a type of white blood cell in the vertebrate immune system.

 

LEARNING OBJECTIVES

 

Describe the role of lymphocytes

 

KEY TAKEAWAYS

Key Points

 

  • The main types of T cells are helper T cells, cytotoxic T cells, memory T cells, and regulatory T cells.
  • The main types of B cells are plasma cells, plasmablasts, memory B cells, and regulatory B cells.
  • T cells are involved in cell-mediated immunity, whereas B cells are primarily responsible for humoral ( antibody -related) immunity.
  • If an antigen is detected again after the initial adaptive immune response, memory T cells create new helper and cytotoxic T cells, while memory B cells create new antibodies.
  • Regulatory T and B cells suppress immune responses at the end of an infection and suppress T and B cells involved in autoimmunity.

 

Key Terms

 

  • Memory T cells: A type of T cell that rapidly differentiates into helper and cytotoxic T cells if its associated antigen is detected.
  • Plasma Cell: A type of B cell that produces most of the antibodies during development of adaptive immune response.

A lymphocyte is a type of white blood cell in the immune system, including both the B and T cells of the adaptive immune system and natural killer (NK) cells of the innate immune system.

B and T cells and their various subdivisions perform many adaptive immune functions.

 

T Cells

 

T cells mature in the thymus and contain T cell receptors (TCRs) that allow them to bind to antigens on MHC complexes. T cells are a major component in cell-mediated adaptive immunity because they provide a pathway for the direct killing of pathogens. There are two main types of T cells that express either CD4 or CD8 depending on signals that occur during T cell maturation, as well as less common types:

  • Helper T cells (CD4s) facilitate the organization of immune responses, and can bind to MHC class II. Subtype 2 helper T cells present antigens to B cells. Subtype 1 helper T cells produce cytokines that guide cytotoxic T cells to pathogens and activate macrophages.
  • Cytotoxic T cells (CD8s) destroy pathogens associated with an
    antigen. They function similarly to NK cells by binding to
    MHC class I and releasing perforin, granzymes, and proteases to induce apoptosis in a pathogen. They are different from NK cells because they only bind to
    cells that express their specific antigen, and are not large or granular like NK cells.
  • Suppressor T cells (T-reg cells) retain some of their ability to bind to self-cells. They have an immunosuppressive effect that inhibits cell-mediated immunity at the end of a response and destroys autoimmune T cells that aren’t filtered out by negative selection in the thymus.
  • Memory T cells are created after an adaptive immune response subsides, retaining the presented antigen. They rapidly proliferate and differentiate into helper and cytotoxic T cells that are specific to that antigen should it be detected in the body again.

While these are the main categories of T lymphocytes, there are other subtypes within these categories as well as additional categories that are not fully understood.

 

B Cells

 

image

Lymphocyte: A scanning electron microscope (SEM) image of a single human lymphocyte.

B cells are involved in humoral adaptive immunity, producing the antibodies that circulate through the plasma. They are produced and mature in bone marrow tissues and contain B cell receptors (BCRs) that bind to antigens. While in the bone marrow, B cells are sorted through positive and negative selection in a manner somewhat similiar to T cell maturation in the thymus, with the same process of killing B cells that are nonreactive to antigens or reactive to self-antigens. Instead of apoptosis, though, defective B cells are killed through other mechanisms such as clonal deletion. Mature B cells leave the thymus and travel to secondary lymphoid tissue such as the lymph nodes.

During antigen presentation, antigen-presenting cells first present antigens to T cells. Then mature helper T cells bind their antigen to naive B cells through BCRs. After antigen presentation, the naive B cells migrate together to germinal centers within the lymphoid tissue, where they undergo extensive proliferation and differentiation into different types of mature B cells. Some of the major categories of B cells that arise include:

  • Plasma cell and long-lived B cells that are the main source of antibodies. They do not have the ability to proliferate and are considered terminally-differentiated.
  • Plasmablasts are short-lived B cells produced early in an infection. Their antibodies have a weaker binding affinity than those of plasma cells.
  • Regulatory B cells (B reg cells) are immunosuppresive B cells that secrete anti-inflammatory cytokines (such as IL-10) to inhibit autoimmune lymphocytes.
  • Memory B cells are dormant B cells with the same BCR as the B cell from which they differentiated. They are specific to the antigen presented to that BCR and rapidly secrete large amounts of antigen-specific antibodies to prevent reinfection if that antigen is detected again.

Besides antibody production, B cells may also function in antigen presentation, though not to the degree of macrophages or dendritic cells. B cells are important to adaptive immune function but can cause problems as well. Autoreactive B cells may cause autoimmune disease that involves antibody-induced damage and inflammation. Certain B cells may undergo malignant tranformation into cancer cells such as lymphoma, in which they continually divide and form solid tumors.