Introduction To The Immune System

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Introduction to the immune system

dr. Dita Kartika Sari,M.Biomed


Terminology
• Immunity is defined as resistance to disease specifically
infectious disease
• Immune system : collection of cells, tissue and molecules
that mediate resistance to infections
• Immune response : reaction of these cells and molecules
to infectious microbes
• Immunology is the study of the immune system and its
responses to invading pathogens
The Importance of the Immune System
Role of the immune system Implications
Defense against infections Deficient immunity results in increased
susceptibility to infections; exemplified
by AIDS
Vaccination boosts immune defenses
and protects against infections

The immune system recognizes and Immune responses are important


responds to tissue grafts and newly barriers to transplantation and gene
introduced proteins therapy

Defense against tumors Potential for immunotherapy of cancer


Antibodies are highly specific reagents Immunologic approaches for laboratory
for detecting any class of molecules testing are widely used in clinical
medicine and research
Immune Mediated Diseases

• Hypersensitivity
• Autoimmune
• Immune deficiency
• Infection
• Tumor
• Graft Rejection
• Inflammation
General properties of immune
response
The immune system

Infectious or inflammatory trigger

Innate or natural Acquired or adaptive


response response
Innate and adaptive immunity
Adaptive (acquired) immunity
• Defence against specific pathogenic agents expressing
specific antigens (proteins inducing an immune response)
• Lymphocytes (T and B cells) respond selectively to antigens,
leading to specific memory that may last a lifetime
Humoral Immunity

Mechanisms in Rheumatology ©2001


Propertie of Adaptive Immune Responses

Property Significance for immunity to microbes

Specificity Ability to recognize and respond to


many different microbes
Memory Enhanced responses to recurrent or
persistent infections
Specialization Responses to distinct microbes are
optimized for defense against these
microbes
Non reactivity to Prevent injurious immune responses
selfantigens againsthost cells and tissue
Cells and tissue of the immune system
Anatomy and functions of lymphoid tissues

• Generative ( primary ) lymphoid organs :


- bone marrow, where all the circulating blood cells
(including lymphocytes) arises and the site of B cells
maturation
- thymus, where T cells mature and reach a state of
functional competence

• Peripheral ( secondary ) lymphoid organs, where


lymphocyte responses to foreign antigens are initiated
and develop : lymph nodes, the spleen, the mucosal
and cutaneous immune systems
Hematopoiesis
Maturation of lymphocyte
Overview of
immune responses
Summary (1)

• Immune response is mediated by innate and adaptive immunity


(AI). Innate immunity is stimulated by structures shared by groups
of microbes. AI is specific for different antigen and is increased by
repeated exposures to antigen.

• Humoral immunity is mediated by B cells and their secreted


products, antibodies, defence against extracellular microbes. CMI is
mediated by T cells and acrivated macrophages and their products,
such as cytokines, defence against intracellular microbes.

• The immune system possesses several properties : specificity for


different antigens, a diverse repertoire capable of recognizing a wide
variety of antigens, memory for antigen exposure, specialized
responses to different microbes, self-limitation, and self tolerance .
Summary (2)

• Lymphocytes are the only cells capable of specifically recognizing


antigen, the principal cells of adaptive immunity (AI).

• Specialized APC capture microbial antigen and display these antigen for
recognition by lymphocytes.

• The AI response is initiated by the recognition of foreign antigen by


specific lymphocytes. Lymphocytes respond by proliferating and by
differentiating into effector cells.

• The effector phase of AI requires the participation of various defence


mechanisms, including the complement system and phagocytes. These
mechanisms neutralize and eliminate the microbes and antigen that
elicited the response.
Summary (3)
• The adaptive immune response depends on Ag-specific lymphocytes,
APCs required for lymphocytes activation, and effector cells that
eliminate antigens

• B and T cells express highly diverse with specific Ag receptors and are
cells responsible for the specifity and memory of AI responses. NK cells
function in innate immune response

• After maturing, B and T ( naive ) cells leave the bone marrow and
thymus, enter the circulation, and populate peripheral lymphoid
organs

• When naive B and T cells encounter Ag they differentiate into effector


cells ( B cells : plasma cells and T cells : CD4+ helper T cells and CD8+
CTLs ) and memory cells.
Summary (4)
• The organs of the immune system may be divided into the generative
organs , where lymphocytes mature and the peripheral organs, where
naive B and T lymphocytes are activated by antigens
• Lymphocyte recirculation is the process by which lymphocytes
continuously move between sites throughout the body through blood
and lymphatic vessels
• Naive T cells normally recirculate among the various peripheral
lymphoid organs. Efector T cells are recruited to sites of
inflammation. Memory T cells may enter either lymphoid organs or
peripheral tissue
• The process of lymphocyte recirculation is regulated by adhesion
molecules on lymphocytes ( homing receptors ), and their ligands on
vascular endotheial cells ( addressins )
Antibody

• Produced after stimulation of B lymphocyte by


antigens / microbe in peripheral lymphoid organs

• Use their antigen-binding (Fab) region to bind to and


block the harmful effect of microbes and toxin

• Use their Fc regions to activate diverse effector


mechanisms that eliminate these microbes

• Heavy chain class (isotype) switching and affinity


maturation enhanche the protective function
Antibody isotype : specific effector function
• Ig G : Neutralization, Opsonization
Activation of classical pathway of complement
ADCC mediated by NK cells
Neonatal immunity
• IgM : Activation of classical pathway of complement
• Ig A : Mucosal immunity
• Ig E : ADCC mediated by eosinophils
Mast cell degranulation

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