1 / 17

Chapter 13 Immunological Tolerance (3)

Chapter 13 Immunological Tolerance (3). I. Introduction Concept Natural tolerance Acquired tolerance II. Factors Affecting Tolerogenicing of Antigen III. Mechanisms of Tolerance Induction IV. Clinical significance of immunologic tolerance.

percy
Download Presentation

Chapter 13 Immunological Tolerance (3)

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 13 Immunological Tolerance (3) I. Introduction Concept Natural tolerance Acquired tolerance II. Factors Affecting Tolerogenicing of Antigen III. Mechanisms of Tolerance Induction IV. Clinical significance of immunologic tolerance

  2. Concept Immunological tolerance is a state of unresponsiveness that is specific for a particular antigen; it is induced by prior exposure to that antigen.

  3. II. Factors Affecting Tolerogenicing of Ag 1. The structure of antigen 2. The antigen dosage 3. The route of administration

  4. Tolerance cells T cells T and B cells Speeds 24 hours slow ( 1-2 weeks) Time long (months) short (weeks) Antigens TD-Ag (low-dose) all Ag (high-dose) Low –zone tolerance High –zone tolerance

  5. Serum anti-BAS Response to secondary immunogenic dose of BSA% of control Immunity Control: signal Immunogenic Dose of BSA 100% Low-zone tolerance High-zone tolerance 10-12 10-9 10-6 10-3 1.0 Priming dose of BSA,g Experimental induction of tolerance at low and high doses of antigen

  6. III. Mechanisms of Tolerance Induction 1. Clonal deletion therapy Central thymic tolerance to self Ags-positive and negative selection. 2. Clonal anergy a.  Lack of signal of activation can cause unresponsiveness b. The blocking of immunocompetent cells c. Lack of helper cells 3. The Suppressant effect of various cells

  7. Mechanisms of Tolerance Induction • Clonal deletion: physically deleting cells from the repertoire at come stage during their lifespan. • Clonal anergy: downregulating the intrinsic mechaism of the immune response. • Suppression: inhibiting cellular activity through interaction with other cells, such as those producing inhibitory cytokines or idiotype-specific lymphocytes which recognize the antigen receptor itself.

  8. (A) (B) B B B B B B (C) Blocking of BCR

  9. IV. Clinical significance of immunologic tolerance 1. The induction and maintenance of immunologic tolerance 2. The elimination of immunologic tolerance

  10. Chapter14 Regulation of the Immune Response (4) Regulation by antigen Regulation by antibody Regulation by lymphocytes Idiotypic modulation of responses Neuroendocrine modulation of immune responses

  11. Regulation by antigen A decline in Ag levels ultimately results in diminished clonal proliferation and a decline in further homuoral or cell-mediated responses.

  12. Immune complexes BCR FcR B B APC suppress enhance Immune regulation by immune complexes

  13. TNF- IL-10R IL-2 IFN- IL-12 B7 IL-10 M TH1 TH2 IL-4 IL-5 IL-6 IL-10 IL-13 IFN- IFN-R Immune regulation by TH

  14. Idiotypic modulation of responses According to the network theory, a series (or network) of anti-idiotype antibodies are induced during an immune response; these anti--idiotype antibodies act to upregulate the immune response in some cases and to downregulate it in other cases.

  15. 2 Idiotypic modulation of responses Internal image group idiotype 1 Ag Anti-idiotype 3 1:ARC(antigen reaction cell) 2:ARC stimulate cells 4 3:ARC suppress cells 4:idiotype and ARC same cells Nonspecific parallel group

  16. Neuroendocrine modulation of immune responses It has long been known that stressful conditions may lead to a suppression of immune functions, for example, reducing the ability to recover from infection. There is considerable evidence demonstrating that the nervous, endocrine and immune systems are interconnected. Broadly, there are two main routes. a.  Most lymphoid tissues receive direct sympathetic innervation, both to the blood vessels passing through the tissues, and directly to the lymphocytes themselves. b. The nervous system directly or indirectly controls the output of various hormones, in particular, corticosteroids, growth hormone, thyroxine and adrenaline.

  17. hypothalamus Neuroendocrine modulation of immune responses anterior pituitary Groeth hormone adrenal interleukin-1 T cells catecholamines islets thyroid corticosteroids Sex hormones thymic hormones insulin thymus gonads Lymphoid tissue

More Related