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Adaptive Immunity: B Lymphocytes and Antibodies

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Adaptive Immunity

B Lymphocytes (B Cells) and Antibodies

Adaptive immunity is a highly specific defense mechanism that develops in response to exposure to antigens. B lymphocytes (B cells) are a central component of this system, primarily responsible for the production of antibodies. These cells are found mainly in the spleen, lymph nodes, and mucosa-associated lymphoid tissue (MALT), with a smaller proportion circulating in the blood.

  • Major Function: Secretion of antibodies that bind specifically to antigens.

  • Location: Spleen, lymph nodes, MALT, and blood.

B Cell Receptor (BCR) Specificity

Each B lymphocyte expresses multiple copies of a unique B cell receptor (BCR) on its surface. The BCR is designed to recognize a specific epitope, which is a distinct part of an antigen. The diversity of BCRs in the body allows recognition of millions of different epitopes, but each individual B cell is specific for only one epitope.

  • Antigen-Binding Sites: Formed by two variable regions of the BCR.

  • Specificity: Each B cell recognizes only one epitope.

  • Diversity: The total BCR repertoire can recognize millions of epitopes.

Structure of B cell receptor (BCR) showing antigen-binding sites, variable regions, and membrane anchoring

Antibody Structure and Secretion

Antibodies, also known as immunoglobulins, are secreted by activated B cells called plasma cells. The structure of an antibody is similar to that of the BCR, with antigen-binding sites and specificity identical to the BCR of the activated B cell.

  • Antigen-Binding Sites: Identical to those of the BCR from which the plasma cell originated.

  • Secretion: By plasma cells derived from B lymphocytes.

Antibody structure showing variable and constant regions, heavy and light chains

Antibody Functions

Antibodies perform several critical functions in the immune response by binding to antigens. Their antigen-binding sites are complementary to specific epitopes, enabling a range of immune activities:

  • Activation of Complement: Especially by IgM antibodies, leading to pathogen lysis.

  • Inflammation: IgE antibodies bind to mast cells/eosinophils, triggering release of inflammatory chemicals.

  • Neutralization: Antibodies block the activity of toxins or prevent pathogens from attaching to host cells.

  • Opsonization: IgG antibodies enhance phagocytosis by marking pathogens for ingestion.

  • Agglutination: Antibodies cause pathogens to clump together, facilitating removal.

  • Antibody-Dependent Cellular Cytotoxicity (ADCC): Antibodies recruit natural killer (NK) cells to destroy target cells.

Diagram showing antibody functions: neutralization, opsonization, agglutination, and ADCC

Classes of Antibodies

There are five main classes of antibodies, each with distinct roles in the immune response. The class involved depends on the type of antigen, the portal of entry, and the required immune function.

  • IgM: First antibody produced; effective in complement activation and agglutination.

  • IgG: Most common and longest-lasting antibody in the blood; provides the majority of antibody-based immunity.

  • IgA: Associated with mucosal surfaces and bodily secretions (e.g., saliva, tears, breast milk).

  • IgE: Involved in responses to parasitic infections and allergic reactions.

  • IgD: Function not fully understood; found on B cell surfaces.

Class

Structure

Functions

Locations

IgM

Pentamer

Complement activation, agglutination, first antibody produced

Blood, B cell surface

IgG

Monomer

Most abundant, crosses placenta, opsonization, neutralization

Blood, extracellular fluid

IgA

Dimer (secretory)

Secretions, mucosal immunity

Secretions (saliva, tears, mucus)

IgE

Monomer

Allergic reactions, defense against parasites

Bound to mast cells, basophils

IgD

Monomer

Unclear, B cell receptor

B cell surface

Table summarizing the five classes of antibodies and their characteristics

Clonal Deletion of B Cells

Clonal deletion is a process that ensures self-tolerance by eliminating or inactivating B cells that react against self-antigens. This process occurs in the bone marrow and is similar to the deletion of self-reactive T cells. Some self-reactive B cells may become inactive (anergic) or alter their BCRs instead of undergoing apoptosis.

  • Location: Bone marrow.

  • Outcome: Apoptosis, anergy, or receptor editing for self-reactive B cells.

Diagram of clonal deletion of B cells in the bone marrow

Immune Response Cytokines

Cytokines are soluble regulatory proteins that serve as intercellular signals in the immune system. They are secreted by various leukocytes and form a complex network of communication among immune cells. Different types of cytokines have specialized roles:

  • Interleukins (ILs): Mediate communication between leukocytes.

  • Interferons (IFNs): Antiviral proteins that can also act as cytokines.

  • Growth Factors: Stimulate stem cell division and differentiation.

  • Tumor Necrosis Factor (TNF): Regulates immune responses, inflammation, and can induce apoptosis in tumor cells.

  • Chemokines: Direct the movement of immune cells (chemotaxis).

Representative Cytokines and Their Actions

Cytokine

Source

Target

Action

Interleukin 2 (IL-2)

Th1 cell, Tc cell

Tc cell

Cloning of Tc cell

Interleukin 4 (IL-4)

Th2 cell

B cell

B cell differentiates into plasma cell

Interleukin 12 (IL-12)

Dendritic cell

Th cell

Th cell differentiates into Th1 cell

Gamma interferon (IFN-γ)

Th1 cell

Macrophage

Increases phagocytosis

Tumor necrosis factor (TNF)

Macrophages, T cells

Body tissues

Triggers inflammation or apoptosis

Key Concepts Review

  • The antibody-binding site of an antibody is made up of: The variable regions of both the heavy and light chains.

  • The most prevalent antibody class in the blood is: IgG.

  • A single B lymphocyte can recognize multiple antigenic determinants: False. Each B lymphocyte recognizes only one antigenic determinant (epitope).

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