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Antibody Class Switching.
Presentation by: Gidwani Manish N.
Roll No.: 147905.
1CHARLIE.
What Is Ab Class Switching?
• a biological mechanism that changes a B cell's production
of immunoglobulin (antibodies) from one class to another,
such as from the isotype IgM to the isotype IgG.
• the constant-region portion of the antibody heavy chain is
changed, but the variable region of the heavy chain stays the
same.
• the variable region does not change, class switching does not
affect antigen specificity. Instead, the antibody
retains affinity for the same antigens, but can interact with
different effector molecules.
CHARLIE 2
Antibody Gene Arrangement.
CHARLIE 3
“Switching” to these classes requires
DNA recombination and is distinct from
V(D)J recombination.
Ab Gene Arrangement (Contd.)
CHARLIE 4
Mechanism of Class Switching by Gene
Rearrangement.
CHARLIE 5
Ab Class Switch in B-Cell by Cytokine
mediated Response.
CHARLIE 6
(from CD4 T cells)
Processing of Genes Re-arranged.
• Double-stranded breaks are generated in DNA at conserved nucleotide motifs,
called switch (S) regions, which are upstream from gene segments that encode the
constant regions of antibody heavy chains; these occur adjacent to all heavy chain
constant region genes with the exception of the δ-chain.
• DNA is nicked and broken at two selected S-regions by the activity of a series
of enzymes, including Activation-Induced (Cytidine) Deaminase (AID), uracil DNA
glycosylase and apyrimidic/apurinic (AP)-endonucleases. The intervening DNA
between the S-regions is subsequently deleted from the chromosome, removing
unwanted μ or δ heavy chain constant region exons and allowing substitution of a
γ, α or ε constant region gene segment.
• The free ends of the DNA are rejoined by a process called non-homologous end
joining (NHEJ) to link the variable domain exon to the desired downstream
constant domain exon of the antibody heavy chain. In the absence of non-
homologous end joining, free ends of DNA may be rejoined by an alternative
pathway biased toward microhomology joins. With the exception of the μ and δ
genes, only one antibody class is expressed by a B cell at any point in time.
CHARLIE 7
Summary.
CHARLIE 8
References.
• Janeway CA Jr., Travers P, Walport M, Shlomchik MJ
(2001). Immunobiology. (5th ed.). Garland Publishing.(via
NCBI Bookshelf)
• Stavnezer J, Amemiya CT (2004): Evolution of isotype
switching. Semin. Immunol. 16 pg: 257–75.
• Eleonora Market, F. Nina Papavasiliou (2003): V(D)J
Recombination and the Evolution of the Adaptive Immune
System . PLoS Biology.
CHARLIE 9
Thank You.
CHARLIE 10

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Antibody class switch ppt

  • 1. Antibody Class Switching. Presentation by: Gidwani Manish N. Roll No.: 147905. 1CHARLIE.
  • 2. What Is Ab Class Switching? • a biological mechanism that changes a B cell's production of immunoglobulin (antibodies) from one class to another, such as from the isotype IgM to the isotype IgG. • the constant-region portion of the antibody heavy chain is changed, but the variable region of the heavy chain stays the same. • the variable region does not change, class switching does not affect antigen specificity. Instead, the antibody retains affinity for the same antigens, but can interact with different effector molecules. CHARLIE 2
  • 3. Antibody Gene Arrangement. CHARLIE 3 “Switching” to these classes requires DNA recombination and is distinct from V(D)J recombination.
  • 4. Ab Gene Arrangement (Contd.) CHARLIE 4
  • 5. Mechanism of Class Switching by Gene Rearrangement. CHARLIE 5
  • 6. Ab Class Switch in B-Cell by Cytokine mediated Response. CHARLIE 6 (from CD4 T cells)
  • 7. Processing of Genes Re-arranged. • Double-stranded breaks are generated in DNA at conserved nucleotide motifs, called switch (S) regions, which are upstream from gene segments that encode the constant regions of antibody heavy chains; these occur adjacent to all heavy chain constant region genes with the exception of the δ-chain. • DNA is nicked and broken at two selected S-regions by the activity of a series of enzymes, including Activation-Induced (Cytidine) Deaminase (AID), uracil DNA glycosylase and apyrimidic/apurinic (AP)-endonucleases. The intervening DNA between the S-regions is subsequently deleted from the chromosome, removing unwanted μ or δ heavy chain constant region exons and allowing substitution of a γ, α or ε constant region gene segment. • The free ends of the DNA are rejoined by a process called non-homologous end joining (NHEJ) to link the variable domain exon to the desired downstream constant domain exon of the antibody heavy chain. In the absence of non- homologous end joining, free ends of DNA may be rejoined by an alternative pathway biased toward microhomology joins. With the exception of the μ and δ genes, only one antibody class is expressed by a B cell at any point in time. CHARLIE 7
  • 9. References. • Janeway CA Jr., Travers P, Walport M, Shlomchik MJ (2001). Immunobiology. (5th ed.). Garland Publishing.(via NCBI Bookshelf) • Stavnezer J, Amemiya CT (2004): Evolution of isotype switching. Semin. Immunol. 16 pg: 257–75. • Eleonora Market, F. Nina Papavasiliou (2003): V(D)J Recombination and the Evolution of the Adaptive Immune System . PLoS Biology. CHARLIE 9

Notas do Editor

  1. Immunoglobulin class switching, also known as isotype switching, isotypic commutation or class-switch recombination (CSR), is a biological mechanism that changes a B cell's production of immunoglobulin (antibodies) from one class to another, such as from the isotype IgM to the isotype IgG. During this process, the constant-region portion of the antibody heavy chain is changed, but the variable region of the heavy chain stays the same (the terms "variable" and "constant" refer to changes or lack thereof between antibodies that target different epitopes). Since the variable region does not change, class switching does not affect antigen specificity. Instead, the antibody retains affinity for the same antigens, but can interact with differenteffector molecules.
  2. Joining can occur anywhere within the large, repetitive S-regions. There is no obvious conserved sequence motif. Unlike V(D)J recombination, this gene splicing occurs between, rather than within, coding sequences. Like V(D)J recombination, targeting of elements for rearrangement is correlated with prior “sterile transcription”
  3. Recombination is targeted by DNA "accessibility" that is controlled by sterile transcription starting at the I-region. I region transcription is regulated by short and long range cytokines provided mainly by T cells. The specificity of the cytokines determines the H-chain class to be used, and hence, the effector function. Like V(D)J recombination, class switch recombination is regulated by 1) expression of a recombination machine 2) targeted “accessibility” mediated by nearby enhancers and promoters