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Chapter 16

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Adaptive Immune System

Overview and Purpose

The adaptive immune system is a highly specialized defense mechanism that enables the body to recognize and eliminate specific pathogens and their products. It builds upon the innate immune response and is characterized by its ability to target distinct invaders with precision.

  • Specificity: Targets unique molecular structures (antigens) on pathogens.

  • Inducibility: Activated only in response to specific antigens.

  • Clonality: Generates clones of lymphocytes specific to the antigen.

  • Unresponsiveness to self: Prevents attack on the body's own cells.

  • Memory: Remembers previous encounters for faster future responses.

Key Characteristics of Adaptive Immunity

Adaptive immunity is defined by four main features:

  • Specificity: Recognizes and responds to specific epitopes on antigens.

  • Tolerance to self: Avoids attacking self-antigens, preventing autoimmune disorders.

  • Minimal self-damage: Immune responses are regulated to minimize harm to host tissues.

  • Immunological memory: Enables rapid and robust responses upon re-exposure to the same antigen.

Cellular Components of Adaptive Immunity

Leukocytes and Lymphocytes

Leukocytes, or white blood cells, are central to immune function. Among them, lymphocytes are the primary cells involved in adaptive immunity.

  • B cells: Mature in bone marrow; produce antibodies (immunoglobulins) that bind to antigens.

  • T cells: Mature in thymus; include helper (CD4+) T cells (direct immune response via cytokines) and cytotoxic (CD8+) T cells (kill infected or cancerous cells).

  • Natural Killer (NK) cells: Kill infected or cancerous cells as part of the innate response.

Hematopoiesis and cell lineages

Dendritic Cells: Antigen Presenting Cells

Dendritic cells are professional antigen-presenting cells found in tissues. They capture antigens, migrate to lymph nodes, and initiate adaptive immune responses, serving as a bridge between innate and adaptive immunity. Dendritic cell illustration

Organization of the Adaptive Immune Response

Secondary Lymphoid Organs

Adaptive immune responses are initiated in secondary lymphoid organs such as lymph nodes, spleen, and Peyer's patches. These sites facilitate interactions between antigen-presenting cells and naïve lymphocytes. Secondary lymphoid organs and immune response

Antigen Recognition and Clonal Selection

The high specificity of the adaptive immune system is due to antigen-specific receptors on B cells (immunoglobulins) and T cells (T cell receptors). Each lymphocyte expresses a unique receptor, conferring one specificity per cell.

  • Clonal selection: Upon antigen encounter, only lymphocytes with receptors specific to the antigen are activated, proliferate, and differentiate into effector and memory cells.

Clonal selection diagram

Mechanisms of Adaptive Immune Response

Helper T Cells (CD4+)

Helper T cells are programmed during priming to produce specific cytokines, tailoring the immune response to the pathogen type.

  • Th1 cells: Produce INFγ, activate macrophages for intracellular microbes (cell-mediated immunity).

  • Th2 cells: Produce IL-4 and IL-5, stimulate antibody production and anti-parasite responses (humoral immunity).

  • Th17 cells: Produce IL-17, stimulate neutrophil responses for extracellular bacteria and fungi.

CD4+ T cell polarization and cytokines

Cytotoxic T Cells (CD8+)

Cytotoxic T cells kill infected or abnormal cells via two main pathways:

  • Perforin-granzyme pathway: Releases proteins that induce apoptosis in target cells.

  • CD95 pathway: Activates apoptotic enzymes through cell surface glycoproteins.

Cytotoxic T cell killing mechanisms

B Cells and Antibody Production

B cells produce antibodies that bind to specific epitopes on antigens. Antibodies function in several ways:

  • Activation of complement and inflammation

  • Neutralization

  • Opsonization

  • Agglutination

  • Antibody-dependent cellular cytotoxicity (ADCC)

Antibody functions

Antibody Classes

There are five main classes of antibodies, each with distinct structures and functions.

Class

Structure

Function

Location

IgG

Monomer

Complement activation, opsonization, neutralization

Blood, extracellular fluid

IgM

Pentamer

Primary response, agglutination

Blood

IgA

Dimer

Secretory immunity

Mucosal surfaces

IgE

Monomer

Allergic responses, anti-parasite

Bound to mast cells

IgD

Monomer

B cell receptor

B cell surface

Antibody classes table

Inducement of T-Dependent Antibody Immunity

Steps in T-Dependent Antibody Response

The T-dependent antibody response involves four main steps:

  1. Antigen presentation for helper T cell activation and proliferation

  2. Differentiation of helper T cells into Th2 cells

  3. Activation of B cells

  4. Proliferation and differentiation of B cells into plasma and memory cells

T-dependent antibody response

Immunological Memory

Memory Cells and Secondary Response

Memory cells are produced during the primary immune response and persist in lymphoid tissues. They enable a much faster and more robust response upon subsequent exposure to the same antigen.

  • Primary response: Slow, produces small amounts of antibodies.

  • Secondary response: Rapid, produces large amounts of antibodies.

Primary vs secondary immune response

Types of Acquired Immunity

Active vs Passive Immunity

Acquired immunity can be classified as naturally or artificially acquired, and as active or passive.

Active

Passive

Naturally Acquired

Body responds to antigens that enter naturally (e.g., infection)

Antibodies transferred from mother to offspring (placenta, breast milk)

Artificially Acquired

Antigens introduced in vaccines; body produces antibodies

Preformed antibodies introduced by injection

Types of acquired immunity Comparison of acquired immunity

Immune Pathology and Tolerance

Immune Pathology

Immune responses can sometimes cause pathology, especially in autoimmune diseases. Examples include atherosclerosis, type I diabetes, rheumatoid arthritis, multiple sclerosis, lupus, asthma, inflammatory bowel disease, and possibly Alzheimer's disease.

  • Immune pathology is often observed without clear understanding of initiation or antigen specificity.

Lymphocyte Development and Tolerance

Lymphocyte development occurs in bone marrow (B cells) and thymus (T cells). Tolerance mechanisms prevent immune responses against self-antigens, maintaining homeostasis and preventing autoimmunity.

Summary Table: Steps in Adaptive Immune Response

Step

Description

Recognition

Detection of antigen by dendritic cells and lymphocytes

Alarm

Activation signals sent to recruit immune cells

Inflammation

Local response to infection or injury

Innate cell recruitment

Mobilization of innate immune cells

Innate effector function

Initial defense mechanisms

Adaptive response

Activation, proliferation, and differentiation of antigen-specific lymphocytes

Conclusion

The adaptive immune system is a complex, highly regulated network that provides specific, inducible, and long-lasting protection against pathogens. Its ability to distinguish self from non-self, generate memory, and tailor responses to different types of invaders is fundamental to health and disease prevention.

Additional info:

Some diagrams and tables were inferred and expanded for clarity and completeness based on standard immunology textbook content.

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