immune system

Immune System Overview

  • Adaptive Defenses: Specialized responses that recognize specific antigens.

    • Specific: Targets specific antigens (example: flu virus).

    • Systemic: Responses are not limited to the site of initial infection.

    • Memory: Strengthened responses upon re-exposure to known antigens.

Types of Adaptive Immunity

  • Humoral Immunity: Mediated by antibodies in the blood.

    • Involves B cells producing antibodies that bind to pathogens.

  • Cellular Immunity: Involves T cells.

    • Directly kills infected cells or marks them for destruction.

    • Involves a respiratory burst, generating reactive oxygen species.

    • Marks target cells for destruction by phagocytes.

  • Antigens: Substances that provoke immune responses.

    • Targets adaptive immunity; usually large, complex, and nonself molecules.

Antigenic Determinants

  • Antigenic Determinants: Unique parts of antigens that trigger immune responses.

    • Natural antigens can activate multiple lymphocyte populations.

    • Large, simple molecules have low immunogenicity.

    • Almost any protein is recognized by antibodies.

Antibody Structure

  • Antibody regions include recognition sites for specific antigens.

Antibodies and Allergies

  • Normal immunoglobulin levels:

    • High IgM, IgG; low IgE.

  • Allergic Reactions: High levels of IgE associated with allergies.

    • Sequence from B cell activation to plasma cells producing IgE leading to allergic responses.

Major Histocompatibility Complex (MHC)

  • MHC Role: Essential for T cell education and immune function.

    • Presents foreign proteins on cell surfaces to be recognized by T cells.

    • Mutations can cause T cells to attack the body’s cells.

  • MHC Proteins: Self-antigens crucial for distinguishing self from nonself.

    • Unique to the individual, important for organ transplant compatibility.

Types of Cells in Adaptive Immunity

  1. B Lymphocytes (B Cells): Humoral immunity, produce antibodies upon activation.

  2. T Lymphocytes (T Cells): Cell-mediated immunity.

  3. Antigen Presenting Cells (APCs):

    • Essential for presenting antigens to T cells.

    • Include dendritic cells and macrophages.

T Cell Development and Education

  • T Cell Education: Occurs in the thymus; involves negative and positive selection.

    • Positive selection ensures T cells recognize self-MHC.

    • Negative selection eliminates self-reactive T cells.

Naive Lymphocytes

  • Naive B and T cells are immunocompetent but not yet exposed to antigens.

  • Once exposed, they undergo clonal selection and activation.

Clonal Selection and Activation

  • Clonal Selection: Naive lymphocyte's first antigen encounter results in activation.

  • Proliferation and Differentiation: Activated lymphocytes become effector cells or memory cells.

    • Memory cells circulate to respond more quickly upon re-exposure.

Antigen-Presenting Cells (APCs)

  • APCs engulf antigens and present fragments to T cells for recognition.

    • Major types include dendritic cells, macrophages, and B cells.

Cell-Mediated Immune Response

  • Differentiation into CD4+ (helper) and CD8+ (cytotoxic) T cells.

    • Helper T cells activate B cells, T cells, and macrophages.

    • Cytotoxic T cells kill infected cells, foreign cells, and tumor cells.

Activation of CD8+ T Cells

  • Requires APC presentation and assistance from helper T cells.

  • Cytotoxic Mechanisms:

    1. Release of perforins to create pores in target cell membranes.

    2. Induction of apoptosis in infected or abnormal cells.

Vaccination and Immune Memory

  • Vaccines activate adaptive immune responses and create memory T and B cells.

    • Can contain dead, living, or engineered viruses for immune stimulation.

    • Example: Cowpox utilized by Edward Jenner for smallpox vaccination.

Influenza Overview

  • High incidence of severe cases each year, requires annual vaccine updates based on viral mutations.

COVID-19 Vaccination

  • mRNA technology used to induce immune response and memory formation.

  • Concerns regarding adjuvants enhancing immune responsiveness.

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