CYTOKINES, SURFACE MOLECULES, ANTIBODIES Jan Novák

CYTOKINES, SURFACE MOLECULES, ANTIBODIES

Jan Novák

The Immune System is the Third Line of Defense Against

Infection

Clonal Selection of B Cells is Caused by Antigenic

Stimulation

• Humoral Immunity - apoptosis

Programmed cell death (“Falling away”). Human body makes 100 million lymphocytes

every day. If an equivalent number doesn’t die, will develop leukemia.

B cells that do not encounter stimulating antigen will self-destruct and send signals to phagocytes to dispose of their remains.

Many virus infected cells will undergo apoptosis, to help prevent spread of the infection.

• Immunological Memory– Antibody Titer: The amount of antibody in the

serum.– Pattern of Antibody Levels During Infection– Primary Response: After initial exposure to antigen, no antibodies

are found in serum for several days. A gradual increase in titer, first of IgM and then

of IgG is observed. Most B cells become plasma cells, but some B

cells become long living memory cells. Gradual decline of antibodies follows.

Monomer: A flexible Y-shaped molecule with four protein chains: 2 identical light chains 2 identical heavy chains

Variable Regions: Two sections at the end of Y’s arms. Contain the antigen binding sites (Fab). Identical on the same antibody, but vary from one antibody to another.

Constant Regions: Stem of monomer and lower parts of Y arms.

Fc region: Stem of monomer only. Important because they can bind to complement or cells.

•Antibody Structure

Antibodies are Proteins that Recognize Specific Antigens

• Consequences of Antigen-Antibody

Binding– 1. Agglutination: Antibodies cause antigens

(microbes) to clump together. IgM (decavalent) is more effective that IgG (bivalent). Hemagglutination: Agglutination of red blood cells.

Used to determine ABO blood types and to detect influenza and measles viruses.

2. Opsonization: Antigen (microbe) is covered with antibodies that enhances its ingestion and lysis by phagocytic cells.

• Humoral Immunity• 3. Neutralization: IgG inactivates viruses by

binding to their surface and neutralize toxins by blocking their active sites.– 4. Antibody-dependent cell-mediated

cytotoxicity: Used to destroy large organisms (e.g.: worms). Target organism is coated with antibodies and bombarded with chemicals from nonspecific immune cells.

– 5. Complement Activation: Both IgG and IgM trigger the complement system which results in cell lysis and inflammation.

Consequences of Antibody Binding

• Immunoglobulin Classes• I. IgG Structure: Monomer Percentage serum antibodies: 80% Location: Blood, lymph, intestine Half-life in serum: 23 days Complement Fixation: Yes Placental Transfer: Yes Known Functions: Enhances phagocytosis, neutralizes toxins

and viruses, protects fetus and newborn.

• Immunoglobulin Classes• II. IgM Structure: Pentamer Percentage serum antibodies: 5-10% Location: Blood, lymph, B cell surface (monomer) Half-life in serum: 5 days Complement Fixation: Yes Placental Transfer: No Known Functions: First antibodies produced during an

infection. Effective against microbes and agglutinating antigens.

• Immunoglobulin Classes• III. IgA Structure: Dimer Percentage serum antibodies: 10-15% Location: Secretions (tears, saliva, intestine, milk), blood and

lymph. Half-life in serum: 6 days Complement Fixation: No Placental Transfer: No Known Functions: Localized protection of mucosal surfaces.

Provides immunity to infant digestive tract.

• Immunoglobulin Classes• IV. IgD Structure: Monomer Percentage serum antibodies: 0.2% Location: B-cell surface, blood, and lymph Half-life in serum: 3 days Complement Fixation: No Placental Transfer: No Known Functions: In serum function is unknown. On B cell

surface, initiate immune response.

• Immunoglobulin Classes• V. IgE Structure: Monomer Percentage serum antibodies: 0.002% Location: Bound to mast cells and basophils throughout

body. Blood. Half-life in serum: 2 days Complement Fixation: No Placental Transfer: No Known Functions: Allergic reactions. Possibly lysis of

worms.

CYTOKINES

a diverse group of non-antibody proteins released by cells that act as intercellular mediators, especially in immune processes

Low molecular weight soluble proteins (polypeptides) produced in response to microbes and other antigens

They act via cell surface receptors to mediate and regulate the amplitude and duration of the immune-inflammatory responses, through activation of macrophages, controlling growth and differentiation of T and B cells

CYTOKINES

Naming of Cytokines

1. Monokines - produced by mononuclear phagocytes (monocytes)

2. Lymphokines - produced by activated T cells, primarily helper T cells

3. Interleukins - cytokines made by one leukocyte and acting on other leukocytes 4.Chemokines-cytokines with chemotactic activities

Classification of Cytokines Interleukins - cytokines made by one leukocyte and

acting on other leukocytes Chemokines - cytokines with chemotactic activities Interferons – tissue antiviral cytokines Transforming growth factors – growth, regulation Colony stimulating factors – growth, stimulation Tumor necrosis factors – induction of apoptosis

Properties 1.Produced by cells involved in both natural and specific

immunity 2. Mediate and regulate immune and inflammatory

responses 3. Secretion is brief and limited not stored as pre-formed

molecules. Synthesis is initiated by new short-lived gene transcription mRNA is short-lived

5. Redundancy -similar functions can be stimulated by different cytokines. Receptors for cytokines are heterodimers (sometimes heterotrimers) that can be grouped into families in which one subunit is common to all members of a given family. (hard clinical diagnostics)

6. Often influence the synthesis of other cytokines. They can produce cascades, or enhance or suppress production of other cytokines. They exert positive or negative regulatory mechanisms for immune inflammatory responses

7. Often influence the action of other cytokines. antagonistic -cytokines causing opposing activities additive synergistic -two or more cytokines acting together (greater than

additive)

Properties

8. Bind to specific receptors on target cells with high affinity.. 9. Cellular responses to cytokines are generally slow (hours),

require new mRNA and protein synthesis

Properties

Cytokine action can be

Functional Categories of Cytokines1) Proinflammatory cytokines

- Produced by activated microphages and NK cells in response to microbial infection

- chemotaxis- killing- IL1, IL-6, IL-8, IL-12, IL-18, TNF-a

Functional Categories of Cytokines2) Anti-inflammatory cytokines

- Produced mainly by T cells- IL1Ra, IL-4, IL-10, TGF-b

Functional Categories of Cytokines3) Growth factors

- IL2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-9, IL-11, IL-14, IL-15, G-CSF, EPO…

Functional Categories of Cytokines4) Cytokines of humoral immunity

- IL-4, IL-5, IL-9, IL-13

Functional Categories of Cytokines5) Cytokines of cellular immunity

- IL-2, IL-12, IFN-g

Functional Categories of Cytokines6) Cytokines with antiviral potential

- IFN-a,b,g,

Cytokine Receptors

Divided into several families based on their structure and activities

Hematopoietin family receptors are dimers or trimers conserved cysteines in their extracellular

domains and a conserved Trp-Ser-X-Trp-Ser sequence.

Examples are receptors for IL-2 through IL-7 and GM-CSF.

Interferon family receptors have the conserved cysteine

residues but not the Trp-Ser-X-Trp-Ser sequence,

Eg. the receptors for IFNa, IFNb, and IFNg.

Tumor Necrosis Factor family receptors have four extracellular domains;

they include receptors for soluble TNFa and TNFb as well as membrane-bound CD40 (important for B cell and macrophage activation) and Fas (which signals the cell to undergo apoptosis).

Chemokine family receptors have seven transmembrane helices

and interact with G protein. This family includes receptors for IL-8, MIP-1 and RANTES.

Chemokine receptors CCR5 and CXCR4 are used by HIV to preferentially enter either macrophages or T cells.

Therapeutic Uses of Cytokines1) Interferon in treatment of viral diseases, cancer

2) Several cytokines are used to enhance T-cell activation in immunofideficincy diseases, e.g. IL-2, IFN-,TNF-

3) IL-2 and lymphokine activating killer cells (LAK) in treatment of cancer

4) GM-CSF induces increase in white cell count, it is used: a- To restore leukocytic count after cytotoxic chemotherapy induced neutropenia b- After bon marrow transplantation C- To correct AIDS-associated leukopenia

5) Anti-cytokines antibodies in management of

autoimmune diseases and transplant rejection:

a- Anti-TNF in treatment rheumatoid arthritis

b- Anti-IL2R to reduce graft rejection

c- Anti-TNF antibodies in treating septic shock

d- Anti-IL-2R in treating adult T-cell leukemia

e- Anti-IL-4 is under trial for treatment of allergies

Adhesive molecules

Adhesion of cells Signal transduction

Groups of adhesive molecules Integrins

Structures of intercellular matrix Formed by two subunites (a and b) Quiscent and activated conformation LFA-1, VLA-1-5, CR3, CR4

Groups of adhesive molecules Molecules of immunoglobulin structure

ICAM, CD80/86, CD2

Groups of adhesive molecules Selectins and Lectins

L (leucotytes) E (endothelial) P (platelet) Interactions between leukocytes and endothelium Receptors of NK cells (Lektins of C type)

Groups of adhesive molecules Mucins

CD43 Supression of interlekcocyte contact

FC receptors

Bind FC parts of immunoglobulins Divided according to the class of antibody

they bind CD16, CD32, CD64

Complement receptors

Phagocytosis of opsonized particles (CR3,4) Clearance of immunocomplexes Receptors for chemotaxis (C3aR, C5aR)

CD – cluster of differentiation system was intended for the classification of

the many  monoclonal antibodies generated by different laboratories around the world against epitopes on the surface molecules of leukocytes

proposed surface molecule is assigned a CD number once two specific monoclonal antibodies are shown to bind to the molecule

 +/- or hi, mid or low (alternatively bright, mid or dim

CD – cluster of differentiation CD1, CD2, CD3, CD4, CD5, CD8, CD11,

CD14, CD16, CD19, CD20, CD25, CD28, CD34, CD38, CD45, CD56, CD69, CD96, CD161