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Chapter 5 Chapter 5 Immunoglobulin Immunoglobulin

Chapter 5 Immunoglobulin

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Chapter 5 Immunoglobulin. Contents. Introduction Section Ⅰ Molecular Structure of Ig SectionⅡ Characteristics and Functions of the 5 Classes of Ig Section Ⅲ Fc Receptors for Ab Molecules Section Ⅳ Biological Activity of Ab SectionⅤ Immunogenicity of Ig Section Ⅵ Artificial Ab. Concepts. - PowerPoint PPT Presentation

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Page 1: Chapter 5 Immunoglobulin

Chapter 5Chapter 5

ImmunoglobulinImmunoglobulin

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ContentsIntroductionSectionⅠ Molecular Structure of IgSectionⅡ Characteristics and Functions of the 5 Classes of IgSection Ⅲ Fc Receptors for Ab MoleculesSection Ⅳ Biological Activity of AbSectionⅤ Immunogenicity of IgSection Ⅵ Artificial Ab

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Concepts Antibody (Ab): Glycoprotein molecule

s that are produced by plasma cells and can combine with the corresponding Ag specifically are called Ab.

Ab is produced by B cells in the response to a stimulation of Ag.

Ab possesses a high degree of specificity and affinity

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• Immunoglobulin (Ig): It refers to all globulins that possess the activ

ity of Ab or show a similar structure to Ab

• Therefore, All Abs are Igs, but not all Igs possess the functions of Abs

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Other Concepts

γ- Globulin Antiserum Humoral Immunity sIg and mIg(BCR)

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SectionⅠ Molecular Structure of Ig

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Ⅰ. Basic structure Ig is composed of four polypeptide chains j

oined by S-S bonds. inter-chain disulfide bonds (S-S) intra-chain disulfide bonds (S-S)

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It shows “T” or “Y” shape.

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1. H and L chain:

. Heavy chains (H): 450 ~ 550 aa, 50 ~ 75 KD

. Light chains (L): 214 aa, 25 KD

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Two terminal ends for each peptide chain

“N” terminal end “C” terminal end

L chains attach to H chains from “N” end

“N”

“C”

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2. classes and types of Ig (1) According to the differences of H chains (amino acid composition, sequence) Igs can be divided into 5 classes • Five classes of H Chain: • Five classes of Igs: IgG IgA IgM IgD IgE

subclasses

IgG1~ IgG4 IgA1, IgA2

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(2) According to the differences of L chains:

Two types of L chain: ,

: 20:1 (in mice); 2:1 (in

human)

1~ 4

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3. Two regions of each peptide chain

(1) Constant region (C)

(3)(3) Hinge regionHinge region

(2) Variable(2) Variable regionregion (V) (V)

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(1) Constant region ( C )• CH: 3/4 or 4/5 (,) of H chain from the c

end

• CL: 1/2 of L chain from the c end

(2) Variable region ( V )• CH: 1/4 or 1/5 (,) of H chain from the N

end

• CL: 1/2 of L chain from the N end

3. Two regions of each peptide chain chain

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(2) Variable region ( V ):

Hypervariable region(HVR) There are three highly diversity

stretches within the V egion, they are called HVR.

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Framework region(FR): FR1-FR4

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Ag-binding sites

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Complementarity determining regions(CDR)

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(2) Variable region (V)

Complementarity determining regions(CDR) L: CDR1, CDR2, CDR3

H: CDR1, CDR2, CDR3

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Idiotype of Ig Igs produced by different B cells possess unique s

tructure respectively in hypervariable region (HVR), the unique structure of Ig is called idiotype or idiotypic determinant

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In fact: HVR CDR Idiotype are in the same sites of Ig

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(3) Hinge region:• Flexible and suitable for CDR of Ig bi

nding to antigenic determinants.• Sensitive to proteolytic enzyme• IgM, IgE

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Other structures of Ig • Joining chain(J) Secretory piece(SP)

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Joining chain(J ) :

Produced by plasma cells Functions:linker, to compose dimer 、

pentamer or polymer(IgA, IgM)

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Secretory piece( SP): . Produced by mucosa epithelial cells . Secretory IgA (sIgA) . Functions: protect sIgA, resist proteolys

is in extra secretory liquid.

IgA

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Ⅱ. Domains of Ig

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1. Domain :

Polypeptide chains of Ig are folded into a globul

ar structure by intra chain s-s bond within each 110aa region which is called a domain

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2. Domains of Ig

• L chain(2) : VL, CL• H chain(4~5): VH, CH1, CH2, CH3 CH4(in IgM,IgE) hinge region

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3. Function of each domain

• VH, VL: antigen-binding site• CH1, CL: allogeneic marker• CH2/CH3: complement-fixing site, permeate placenta(IgG) • CH3/CH4: cell-binding site Hinge region :flexible and suitable for CDR of I

g binding to antigenic determinants

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Ⅲ. Hydrolytic fragments of Ig

Ig can be digested by papain and pepsin

• Position • Fragments • Function

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1. Digested by papain• Position: near the S-S bonds of H inter-chains fromthe N end

Fragments: 2Fab:fragment antigen-binding Fc:fragment crystallizable

Function: Fab: recognize and bind Ag

Fc: (1) fix complement (2) crossing the placenta (3) bind to FcR in different cells

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2. Digested by pepsin• Position: near the S-S bond of H inter-chains from the C end

• Fragments and function : F(ab′)2: bind antigen(2 valence) pFc′: no function

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Significance

Elucidating the relationships between the structure and function of Igs

Decrease the immunogenicity of Ig for clinical treatment

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SectionⅡ Characteristics and Functions of the 5 Classes of Igs

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Ⅰ. IgG 1. Highest concentration in serum (75% of t

otal Ig)

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2. Four subclasses: IgG1, IgG2, IgG3, IgG4

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3. Unique Ig that can pass through placenta

4. Half-life is longer( 16-24 days )

5. Starts to be produced at 2-3 month after birth and reach the level of adult at 5 years old

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6. Functions of IgG:• Against bacteria and virus,neutralize toxin• Combine with the Fc receptor(FcγR)• Activate complement• Combine with SPA• Some belong to the auto-antibodies• Take part in type Ⅱ and Ⅲ hypersensitivi

ty

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Ⅱ. IgM 1. Highest MW : pentamer ( 90 KD ) ,10 valence

s

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2. Half-life is shorter(4~5 days)

3. The first Ig to be synthesized• Appear in the early stage after infection • Be produced during fetus• The first mIg of the B cells, act as the antigen recept

ors(BCR)

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4. Functions:• IgM is more effective in binding Ag and a

ctivating C, and play an important role in anti-infection

• Natural Ab for blood-type antigen • Auto-antibody: rheumatoid factor(RF)• Take part in type Ⅱ and Ⅲ hypersensiti

vity

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ⅢⅢ. . IgAIgA

1. Two types Serum type : monomer Secretary type ( sIgA ) : dimer , trimer or polymer

2. Two subclasses : IgA1 , IgA2

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3. To be produced at 4 months after birth

4. Exist in almost all body fluid

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6. Local mucosal immunity

• Immune barrier • Neutralize virus/toxin• Rich in colostrum • Activate C by alternative pathway• Take part in type Ⅲ hypersensitivity

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Ⅳ. IgD1. The concentration in serum is low and

sensitive to proteinase

2. Act as the antigen receptor on B cells (mIgD): Regulate the differentiation of B cells

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Ⅴ. IgE1.Concerntration of IgE in serum is the lo

west in normal individual, but is very high in some patients.

2.Related to typeⅠpersensitivity FcεRⅠ: mast cell, basophil

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Section Ⅲ Fc Receptors for Ab Molecules

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IgG---FcR: FcRⅠ(CD64)---phagocyte FcRⅡ(CD32)---immune complex FcRⅢ(CD16)---NK, MΦ,T cell

IgE---FcR: FcRⅠ--- mast cell, basophil FcRⅡ--- macrophage, B cell

IgA---FcαR(CD89)---phagocyte, neutrophil

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SectionⅣ Biological Activity of Ab

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1. Recognize and bind to antigen specifically 2. Fix complement3. Bind to Fc receptor on some cells 4. Transfer selectively : .Planceta transfer (IgG) .Mucosa transfer (sIgA)

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Affinity and Avidity

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Neutralization

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IgM,IgG1~3: classical pathway

IgA,IgG4,IgE:

alternative pathway

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MAC

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(1) Opsonization(IgG, IgM): Enhance the phagocytosis of MΦ

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(2) ADCC( antibody dependent cell mediated cytotoxicity)

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(3) Hypersensitivity typeⅠ - mast cell, basophil(FcRⅠ)

FcRI

degranulation

IgE

allergen

inflammationinflammation

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SectionⅤ Immunogenicity of Ig

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Isotype: CH, CL  

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Allotype: CH, CL

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Idiotype: VH, VL

Anti-idiotype antibody

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SectionⅥ Artificial Ab

Polyclonal Ab Monoclonal Ab Gene engineering Ab

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1. Polyclonal Ab A mixture Ab with different specifici

ties and affinities Generate in a natural response or ar

tificial immunization Cross reaction

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Cross-reactivity:if two antigens share an epitopean antibody recognizes an unrelated,but chemically similar, epitope

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2. Monoclonal Ab (mAb) Ab produced by single clone (or one hy

bridomas clone ) and having a single specificity

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mAb / McAb Prepared by hybridomas technique:

Immunized spleen cells(B) hybride with myeloma cells----hybridomas

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Artificial antibodies

Derived from different B Lymphocytes cell lines

POLYCLONAL. MONOCLONAL.

Derived from a single B cell clone

Batch to Batch variation affecting Ab reactivity &

titre

mAb offer Reproducible, Predictable & Potentially

inexhaustible supply of Ab with exquisite specificity

Enable the development of secure immunoassay systems.

NOT Powerful tools for clinical diagnostic tests

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3.Gene engineering Ab• Abs prepared by the method of gene r

ecombination

• Chimeric Ab:human Fc bind with mice Fab• Recombinant single chain Ab:VH-linker-VL

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Human-mouse chimeric Ab