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Antigens Where we’re going- Immunogenicity vs antigenicity

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Presentation on theme: "Antigens Where we’re going- Immunogenicity vs antigenicity"— Presentation transcript:

1 Antigens Where we’re going- Immunogenicity vs antigenicity
What makes for a good immunogen Haptens Pattern recognition receptors

2 Aulanni’am Biochemistry Laboratory Faculty of Sciences_UB
Antigens Aulanni’am Biochemistry Laboratory Faculty of Sciences_UB

3 Some definitions: Immunogenicity
Immunogen, for practical purposes= antigen Antigenicity- ability to react with antibodies or Tcells; all immunogens are antigens, but haptens have antigenicity but not immunogenicity.

4 Immunogen’s contribution- usually think “protein”
Foreignness- Size- > 100 kDa better, < 10 kDa worse, especially for proteins Complexity- homopolymers poor, heteropolymers better Easily processed better than poorly processed; adding L-amino acids to a D-polymer increases its immunogenicity.

5 Genetics- mouse studies- responders and non-responder mice.
Dosage and route of administration- the pneumococcal polysaccharide story. Route determines which lymph tissues meet the antigen- e.g., spleen vs local lymph nodes.

6 contribution- adjuvants
Something that stimulates the immune response to the antigen. Alum- ppt’s, prolongs persistence Inflammatory- dead Mycobacterium Non-specific proliferation of cells- LPS,

7 Epitopes, or Ag determinants
Our cells don’t react to the whole molecule, but to parts- epitopes B cells react to differently to epitopes than do T cells. Remember- interaction is specific!

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9 How B cells do it An epitope can be non-sequential and can be brought together spatially, producing a single epitope. B cell eptitopes tend to be on the surface,.

10 How T cells do it The binding is ternary- three components- MHCII, TCR, antigen. Only parts are displayed. No MHC binding= no antigenicity B cell eptitopes tend to be on the surface, but T cells can be from the interior of the molecule.

11 Haptens Haptens aren’t immunogenic alone.
BUT- when bound to a carrier, Ab’s are produced that DO bind to the unbound hapten

12 Toll-like Receptors Recognize bacterial patterns. The response:
Attraction of phagocytic and Antigen-presenting cells- better at stimulating T cells Activation of macrophages Induction of interferon Induces secretion of several cytokines

13 Summary… Terms: Immunogen(icity), antigen(icity), hapten
What makes a good antigen? Adjuvants and what they might do B-cell epitopes and T cell epitopes- differences and why Haptens, and practical applications Toll-like receptors- examples of what they recognize, types of response.


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