Title: Acquired Immunity
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2Peter Medawar
3Immunologic Basis of Graft Rejection
The Behavior and Fate of Skin Autografts and
Skin Homografts in Rabbits
(A report to the War Wounds Committee of the
Medical Research Council)
By P.B. Medawar,From the Department of Zoology
and Comparative Anatomy University of Oxford
- Inducibility
- Memory
- Specificity
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5First Set Rejection
Rejection 7-8 Days
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7Second Set Rejection (Memory)
First Graft
Rejection 3-4 Days
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9Specificity
Rejection 3-4 Days
Rejection 7-8 Days
Third Party Graft
10Terminology
Autograft - One site to another on the same
individual
Isograft - between two genetically identical
individuals
11Terminology (cont.)
Allograft - between genetically distinct
individuals of the same species
Xenograft - between different species
12Beginning of Rejection
13Rejected Mouse Skin Graft
14Rejection is mediated by T cells
15Role of CD4 and CD8 Cells
16Laws of Transplantation
- Tx between individuals of the same inbred strain
will succeed. - Tx between inbred strains are rejected.
- Tx parent to F1 will succeed, but the reverse
will fail. -
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18Parent to F2
B
B
A
B
A
A
AA
AB
AB
AB
F2
F1
A
B
AB
AB
BA
BB
Survival Probability 0.75 For 2 Loci (0.75) x
(0.75)
Graft Survival (P to F2) (0.75)n
n Number of histocompatibility loci
19The Human MHC
Class I
Class III
Class II
DP
DQ
DR
C4
C2
Bf
B
C
E
A
G
F
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22Mixed Leukocyte Reaction
Spleen
5 Days
2000 RADS
Add 3H-Thymidine
18-24 Hours
Spleen
Determine Incorporation
23Acute Rejection
- Primary Cellular
- Massive infiltration of macrophages and
lymphocytes - Decreased graft function
- Clinically appears at gt10 days post-tx and can
occur anytime thereafter.
24Acute Rejection Grade 1a
25Acute Rejection - Grade 3a
26Chronic Rejection
- Slow steady decline of graft function and
progressive occlusion of of vessels/passageways. - Result of cellular and humoral mechanisms
27Chronic Rejection
28Hyperacute Rejection
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31Clinical Transplantation
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36Objectives of Immunosuppression
- Facilitate acceptance of the allograft
- Specific
- Low toxicity
37Basic Strategies of Immunosuppression
- High dose initial immunospression
- Facilitate graft acceptance
- Minimize early rejection
- Favor induction of tolerance
- Maintenance therapy for chronic acceptance
- Augmentation to reverse acute rejection.
38Major Immunosuppressants
- Cyclosporine A
- Tacrolimus (FK-506)
- Sirolimus (Rapamycin)
- Steroids
- Azathioprine
- Mycophenylate Mofetil
39Medical Issues and Immunosuppression
- Selected Side Effects of Cyclosporine
- Gingival Hyperplasia
- Infection
- Nephrotoxicity
- Hypertension
- Tremors, Nightmares, Insomnia
- Hirsutism
- Fibrous Breast Tissue
40Infections
- Prophylactic Antibiotics for procedures with
potential to cause bacteremia. - Metabolism of some drugs may be altered,
especially for liver transplant patients (e.g.
acetominophin, lidocain, procain ampicillin etc).
41Graft Rejection
- Highly dependent on T cell activation and
proliferation. - Signaling pathways and control points for entry
into cell cycle are appropriate targets for
immunsuppression.
42Broad Mechanisms of Immunosuppression
- Inhibition of T cell activation.
- Block antigen binding.
- Block accessory molecules.
- Inhibition of IL-2 production.
- Inhibition of T cell proliferation.
- T cell depletion.
- Inhibition of B cell proliferation.
43Major Immunosuppressants
- Cyclosporine A
- Tacrolimus (FK-506)
- Sirolimus (Rapamycin)
- Steroids
- Azathioprine
- Mycophenylate Mofetil
44Inhibitors of T cell Receptor Signaling
45T cell Receptor Signaling Pathway
46T cell Signaling Calcineurin
Calcineurin
47Immunosuppressants
- Monoclonal/Polyclonal Antibodies
- Antithymocyte Globulin
- CD3 (OKT3)
- CD25 (
- Inhibitors of Cytokine Transcription
- Corticosteroids
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49Antiproliferative Agents
- Azathioprine
- Mycophenylate mofetil
50Inhibition of Clonal Expansion
51Corticosteroids
- Mechanism
- Binds intracytoplasmic receptors
- Steroid/receptor complex migrates to nucleus
- Binds to gene promoters and NFAT
- Therefore impairs gene transcription of
regulatory cytokines.
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53Summary
- Immunosuppressive properties related to effects
on T cell activation and proliferation. - Inhibition of T cell activation and proliferation
are associated with the most successful
immunosuppression.