Viruses, bacteria, parasits, fungi, toxins, foreign cells (transplantation, grafts, transfusions), foreign molecules

(pills, food....), tumorous cells– threats

exogenous or endogenous

FOREIGN AGENSES, MOLECULES,

CELLS

1.2

barrieres

innated mechanisms

adaptive

3 DEFENSIVE LINES

immune mechanisms

1.2

- Isolation- Disruption

- Engulfment and killing

Microorganisms are prevented from spreading and growing by killing through:1. Mechanical, 2. biological, 3. chemical bariéres, 4. formation of granulomes, 5. phagocytosis,

ELIMINATION OF THREATS BY IMMUNITY SYSTEM

and combination

1.6

6. appoptosis, 7. complement, 8. antibodies, 9. natural killers, 10. specific lymphocytes, 11. cytokins production

The ability to induce humoral and/or cell-mediated immune responses.

The ability of antigen to elicit immune response is called "immunogenicity."

Property of a substance to induce a response in the animal or human body: Antigen

Antigens that do provoke the immune response are immunogens.

IMMUNOGENICITY

Immunogen or antigen:

* A foreign substance, when introduced into human body, stimulate formation of

specific antibodies or sensitized lymphocytes

* Antigens have the ability to combine

specifically with antibodies produced or sensitized T-lymphocytes induced

IMMUNOGENS OR ANTIGENS

molecules, organisms or parts of molecules recognised by immune system

simple, complex, proteins, carbohydrates, synthetic

Epitope, Immunogen, Hapten

ANTIGENS2.4

Exogenous Antigens

1- Bacterial antigens:

a- Antigens related to bacterial cells - Somatic antigen (O): part of cell wall gm –ve bacteria. - Capsular antigen: usually polysaccharide - Flagellar Ag (H) : a protein made of flagellin - Fimbrial Ag: surface antigens in fimbriated bacilli

b- Antigen secreted by bacteria: - Exotoxins - Enzymes

2- Viral antigens: a- protein coat viral antigens b- Soluble antigens (soluble nucleoproteins as in influenza)

TYPES OF ANTIGENS

Endogenous antigens

Human tissue antigens: a- Blood group antigens: A, B and Rh antigens b- Histocompatibility antigens: Glycoprotein molecules on all nucleotide cells: - Major histocompatibility complex antigens (MHC) - Human leucocyte antigen (HLA)

TYPES OF ANTIGENS

* MHC has an important function in presentation of antigens to T-cells

* Helper T-cells recognize foreign antigens on surface of APCs, only when these antigens are presented in the groove of MHC II molecule * Cytotoxic T-cells will only recognize antigens, on the surfaces of virus infected cells or tumor cells only when these antigens are presented in the groove of Class I molecule (MHC restriction)

MAJOR HISTOCOMPATIBILITY COMPLEX ANTIGENS

(MHC)

A typical antigen-antibody reaction: antibodies bind to specific chemical groups or structures, called epitopes or antigenic determinants

Antigens are recognized by and bind to:1) B-cell receptors (BCR) : - These are membrane-bound immunoglobulins (IgM and IgD) on B-cells - BCRs can be secreted in plasma as antibodies

2) T-cell receptors (TCR) - α and β chains anchored to T-cells - There is a groove which binds small peptides presented by MHC on surface of APCs

3) MHC molecules They are essential for presentation of peptides so

that they can be recognized and bind to TCRs

ANTIGEN BINDING AND RECOGNITION MOLECULES

Epitope – the smallest identifiable part of antigen that can be bound to the receptor–

antigenic determinant

ANTIGENS AND RECEPTORS 2.3

1. contain epitopes, thats induce immune reaction and are the target immune reaction

2. not every antigen is immunogenic

3. Antigen is a molecule recognised by immune system

4. non-immunogenic molecules (haptens) can be bound on immunogen (called carrier)

IMMUNOGEN

•small, not immunogenic molecules, commonly not of biological ethiology (synthetic epitopes)

•are antigens able to bind on immunity receptors and not able to induce immunity reaction, not immunogenic

•Hapten + immunogen (carrier) = immunity reaction against both. These substances not immunogenic by itself

- If couple to a larger carrier molecule (albumin, globulins), they become immunogenic

- Examples :• simple chemicals and drugs: • penicillin, sulphonamid, aspirin, cosmetic, tranquillizers, neomycin skin ointment

HAPTEN

1. Engagement of receptors is the event, that leads to different activities, acc. to the type of ligand, molecule or cell, that the receptor will bind

2. bind molecules and induce generation of signals by which cells communicate

3. recognise particals from environment and detect invaders

4. watch environment (neighbours), to be sure that they are part of self and do not represent the threat

RECEPTORS

•present as part of innate immunity

•enable rapid reaction

1. PRR – on soluble molecules and host cells

2. TLR – present on host cells

3. KAR – on NK cells

4. KIR – on NK cells

5. CR – on soluble molecules, phagocytes, on B cells

6. FcR – on phagocyting cells

PREFORMED RECEPTORS

1. They activate multiple clones of T-lymphocytes

2. Bacterial toxins:

• Staph. aureus toxic shock syndrome toxin (TSST) and enterotoxins

• Strpt. pyogenes pyrogenic toxin A

3. They have the ability to bind both class II MHC molecules and TCR β chain

4. They act as a clamp between the two, providing a signal for T-cell activation

SUPERANTIGENS (SAGS)

1. * They are active at very low concentration causing release of large amounts of cytokines

2. * The massive T-cell activation and release of large amounts of cytokines cause systemic toxicity

3. * This method of stimulation is not specific for the pathogen

4. * It does not lead to acquired immunity i.e no memory

SUPERANTIGENS (SAGS)

1-Foreigness : Foreign substances are immunogenic

2- Molecular size: High molecular weight increase immunogenicity

3- Chemical structure complexity: High complexity increase immunogenicty

4- Route of administration: Parenteral routes are more immunogenic to oral route

FACTORS INFLUENCING IMMUNOGENICTY

5- Method of administration: a- Antigen dose: Appropriate dose optimum antigenicty Low dose low- zone tolerance High dose high-zone tolerance

b- Adjuvant: Substance when injected with an antigen enhance immunogenicity

FACTORS INFLUENCING IMMUNOGENICTY