Download Free Medical Priniciples of Transplantation PowerPoint Presentation

Priniciples of Transplantation PowerPoint Presentation

DOWNLOAD MEDICAL POWERPOINT PRESENTATION

About This Presentation

Description : Check out this medical PowerPoint presentation titled "Priniciples of transplantation”.

This medical PowerPoint presentation is about organ transplantation.

HLA (Human Leukocyte Antigen) is a group of proteins that are found on the surface of cells and play a key role in the immune system. HLA is important in transplantation because it determines whether a donor organ or tissue is compatible with a recipients immune system.

Tags : Priniciples of transplantation, organ transplantation, HLA, Human Leukocyte Antigen, donor organ or tissue, Hematology, Hematology PowerPoint presentation

Published on : May 29, 2023 | Views : 1588 | Downloads : 1

Shareable Url :

Embed Code :

Comment

Transcript

Slide 1-

Principles of transplantation
Slide 2-

Goals and objectives Principal components Role of HLA in immunogenic response Understand the 3 signal pathway of T cell activation and its clinical significance
Slide 3-

Classification of grafts Autologous grafts Grafts transplanted from one part of the body to another in the same individual Syngeneic grafts (Isografts) Grafts transplanted between two genetically identical individuals of the same species Allogeneic grafts (Allografts) Grafts transplanted between two genetically different individuals of the same species Xenogeneic grafts (Xenografts) Grafts transplanted between individuals of different species
Slide 4-

2006-7year Immunology 4
Slide 5-

IMMUNE RESPONSES TO TRANSPLANTED TISSUES Transplant rejection caused by genetic differences between donor and recipient HLA and blood group antigens Alloantigens Antigens which vary between members of same species Alloreaction Immune response to an alloantigen Alloreactions in transplantation Host-versus-graft (transplant rejection) Graft-versus-host
Slide 6-

Figure 12-11
Slide 7-

Effectors of rejection Major players: T Cells B cells Antigen presenting cells MHC (Most important)
Slide 8-

T cells Arise in thymus from bone marrow derived precursors Each T-Cell has unique T Cell receptor (Clone) Selection Positive Negative Subtypes CD 4 T cells – Antigen specific immune response CD8 T cells - Precursors of CTL – Class I MHC
Slide 9-

B cells Arise and mature in bone marrow Negative selection Express BCRs on their surface When BCR is stimulated the B cell secrete antibodies of same specificity as their BCRs
Slide 10-

Antigen presenting cells Most important Activate T cells Endocytose antigen and display it on MHC molecules T cells recognize and interact with antigen MHC to become activated
Slide 11-

MHC complex Encode molecules crucial to the initiation and propagation of immune response The HLA complex on chromosome 6 contains over 200 genes, more than 40 of which encode leukocyte antigens The HLA genes that are involved in the immune response fall into two classes, I and II, which are structurally and functionally different
Slide 12-

Klein J and Sato A. N Engl J Med 2000;343:702-709 Location and Organization of the HLA Complex on Chromosome 6
Slide 13-

Types of MHC There are three classes of MHC molecules. Class I- encodes glycoproteins expressed on the surface of nearly all nucleated cell; the major function of the class I gene is presentation of peptide antigens to cytotoxic T-cells Class II- encodes glycoproteins expressed primarily on antigen-presenting cells, examples: macrophages, dendritic cells and B-cells, where they present processed antigenic peptides to T helper cells. Class III- encodes various secreted proteins that have immune function including components of the complement system; C2,C4, Factor B, &TNF, and molecules involved in inflammation.
Slide 14-

ppt slide no 14 content not found
Slide 15-

Function of MHC The function of both class I and class II molecules is the presentation of short, pathogen-derived peptides to T cells, a process that initiates the adaptive immune response Class I - Sample cytosolic proteins and detect foreign proteins that would indicate an intracellular pathogen such as virus or intracellular bacteria Recognised by CD 8 T cells and provide a surviellance mechanism to target infected cells for destruction
Slide 16-

Antigen Processing and Presentation
Slide 17-

Biological functions of Class I and Class II molecules Class I Present peptides derived from endogenously synthesized proteins Responding T cells express CD8+ http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/H/HLA.html#cd8
Slide 18-

Class II system is designated to sample extracellular proteins by extracellular proteins by specialized APC’s Class II are recognized by CD 4 helper T cells and allow for the generation of immune response to invading pathogens
Slide 19-

Antigen Processing and Presentation
Slide 20-

Biological functions of Class I and Class II molecules Class II Present peptides derived from exogenously synthesized proteins Responding T cells express CD4+ http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/H/HLA.html#class_II
Slide 21-

Class I The class I genes code for the polypeptide chain of the class I molecule; the ß chain of the class I molecule is encoded by a gene on chromosome 15, the beta2-microglobulin gene. There are some 20 class I genes in the HLA region; three of these, HLA-A, B, and C, the so-called classic, or class Ia genes, are the main actors in the immunologic theater
Slide 22-

Structure of Class I MHC Two polypeptide chains, a long α chain and a short β (β2 microglobulin) Four regions Cytoplasmic region containing sites for phosporylation and binding to cytoskeletal elements Transmembrane region containing hydrophobic amino acids
Slide 23-

Structure of Class I MHC Four regions A highly conserved α3 domain to which CD8 binds A highly polymorphic peptide binding region formed from the α1 and α2 domains Β2-microglobulin helps stabilize the conformation
Slide 24-

Klein J and Sato A. N Engl J Med 2000;343:702-709 Structure of HLA Class I and Class II Molecules
Slide 25-

ppt slide no 25 content not found
Slide 26-

Class II The class II genes code for the alpha and ß polypeptide chains of the class II molecules . The designation of their loci on chromosome 6 consists of three letters: the first (D) indicates the class, the second (M, O, P, Q, or R) the family, and the third (A or B) the chain ( or ß, respectively). HLA-DRB, for example, stands for class II genes of the R family coding for the ß chains.
Slide 27-

Structure of Class II MHC Two polypeptide chains,α and β, of roughly equal length Four regions Cytoplasmic region containing sites for phosporylation and binding to cytoskeletal elements
Slide 28-

Structure of Class II MHC Four regions Transmembrane region containing hydrophobic amino acids A highly conserved α2 and a highly conserved β2 domains to which CD4 binds A highly polymorphic peptide binding region formed from the α1 and β1 domains
Slide 29-

Klein J and Sato A. N Engl J Med 2000;343:702-709 Structure of HLA Class I and Class II Molecules
Slide 30-

ppt slide no 30 content not found
Slide 31-

Important aspects of MHC Normally, the proteins that undergo recycling are the organism's own, but in infected cells, proteins originating from the pathogen are also routed into the processing pathways. With the exception of jawed vertebrates, no organisms appear to make a distinction between peptides derived from their own (self) proteins and those derived from foreign (nonself) proteins. Jawed vertebrates, by contrast, use the peptides derived from foreign (usually microbial) proteins to mark infected cells for destruction
Slide 32-

Important aspects of MHC Protein processing and loading of peptides onto class I molecules are taking place all the time in most cells. There is always plenty of material to feed the processing machinery, because worn-out, damaged, and misfolded proteins are continuously being degraded and replaced by new ones. By contrast, the processing of exogenous proteins and the loading of peptides onto class II molecules are normally restricted to B cells, macrophages, and dendritic cells, which are very efficient in taking up material by endocytosis or phagocytosis.
Slide 33-

Important aspects of MHC The consequence of protein processing is that the surfaces of cells become adorned with peptide-laden HLA molecules, amounting on a per cell basis to roughly 100,000 to 300,000 class I or class II products of each of the highly expressed HLA loci. Since each HLA molecule has one peptide bound to it, each uninfected cell displays hundreds of thousands of self peptides on its surface. Each cell thus displays a heterogeneous collection of peptides, and the surface of a cell resembles rows of well-stocked stalls at a bazaar, with bargain hunters scrutinizing the wares. But if, in this metaphor, the vendors are the HLA molecules and the peptides the goods, who are the potential buyers? They are a group of lymphocytes reared in the thymus and then turned loose to roam the body — the T cells.
Slide 34-

Functions and Characteristics of HLA HLA’s are cell-surface proteins involved in the recognition of self and non-self by the immune system HLA’s present foreign antigens to the immune system – resistance to viral and bacterial pathogens HLA’s are codominantly expressed Highly polymorphic and polygenic
Slide 35-

HLA genes are co dominant: A protein from each parental gene is expresed on cell-surfaces
Slide 36-

Polymorphism and polygeny MHC genes are polymorphic: that is, there are large numbers of alleles for each gene MHC genes are polygenic: that is, there are a number of different MHC genes.
Slide 37-

Crossing overresults in new haplotypes
Slide 38-

Structure of Class I MHC Variability map of Class 1 MHC α Chain
Slide 39-

Class I polymorphism
Slide 40-

Structure of Class II MHC Variability map of Class2 MHC β Chain
Slide 41-

Class II polymorphism
Slide 42-

Why polymorphic? Multiple alleles of HLA in a population increases the likelihood that the population will survive a pathogen threat Unfortunately, it also cause histoincompatibility in organ and tissue transplants
Slide 43-

Important Aspects of MHC Primary HLA products that contribute to rejection are the most polymorphic including HLA- A, - B and DR Efforts are made to match HLA-A, - B and DR genes and proteins in kidney transplantation
Slide 44-

HLA profiles Tissue typing Cross matching test Panel reactive antibodies
Slide 45-

Tissue typing Helps to identify two alleles at each of the three loci One allele from mother and one from father Mother/Father: 25% chance of full match One Sibling: 25 % chance of full match Two Siblings: 44 % chance of full match HLA matching 3 year graft surivival 93 and 85% for HLA matched and mismatched live donors In cadaveric grafts 82 and 76% Most benefit with zero mismatches
Slide 46-

Cross matching test Serum of potential recipient is incubated with cells from possible donor If recipient has antidonor antibodies there is a strong likelihood that recipient would destroy transplant by antibody mediated rejection
Slide 47-

Panel reactive antibodies Anti HLA antibodies in the serum of a person can be assessed as PRAs Testing the serum of the patient against a panel of cells or antigens prepared from many different donors using cytotoxicity or flow cytometry Results are expressed as percentage of positive donors
Slide 48-

ppt slide no 48 content not found
Slide 49-

Response to antigenic stimulus
Slide 50-

ppt slide no 50 content not found
Slide 51-

ppt slide no 51 content not found
Slide 52-

T cell activation Activation of T cell is a crucial step in generation of immune response to specific antigens Naive T cells restricted to SLOs They interact with DCs that have migrated from the periphery in response to infection or injury Once naïve T cells encountered their cognate antigen presented on mature DCs, they become activated. Following activation CD 4 T cells help B cells to convert to plasma cells Plasma cells produce antibodies
Slide 53-

ppt slide no 53 content not found
Slide 54-

Generation of T cell effector function Alloreactive T cells can be found in both naive and memory T cells Naive T cells may be triggered by donor or recipient APCs to proliferate and develop effector functions in SLOs Memory cells can be activated in the same manner or by recognizing cells in allograft directly Reactions mediated by naïve T cells take longer to develop than those mediated by memory T cells
Slide 55-

ppt slide no 55 content not found
Slide 56-

Structure of the T cell Receptor Heterodimer with one α and one β chain of roughly equal length A short cytoplamic tail not capable of transducing an activation signal A transmembrane region with hydrophobic amino acids
Slide 57-

Structure of the T cell Receptor Both α and β chains have a variable (V) and constant (C) region V regions of the α and β chains contain hypervariable regions that determine the specificity for antigen
Slide 58-

Structure of the T cell Receptor Each T cell bears TCRs of only one specificity (allelic exclusion)
Slide 59-

TCR and CD3 Complex TCR is closely associated with a group of proteins collectively called the CD3 complex γ chain δ chain 2 ε chains 2 ξ chains CD3 proteins are invariant
Slide 60-

ppt slide no 60 content not found
Slide 61-

Role of CD3 Complex CD3 complex necessary for cell surface expression of TCR during T cell development CD3 complex transduces signals to the interior of the cells following interaction of Ag with the TCR
Slide 62-

The “Immunological Synapse” The interaction between the TCR and MHC molecules are not strong Accessory molecules stabilize the interaction CD4/Class II MHC or CD8/Class I MHC CD2/LFA-3 LFA-1/ICAM-1
Slide 63-

The “Immunological Synapse” Specificity for antigen resides solely in the TCR The accessory molecules are invariant Expression is increased in response to cytokines
Slide 64-

The “Immunological Synapse” Engagement of TCR and Ag/MHC is one signal needed for activation of T cells Second signal comes from costimulatory molecules CD28 on T cells interacting with B7-1 (CD80) or B7-2 (CD86) Others Costimulatory molecules are invariant “Immunological synapse”
Slide 65-

ppt slide no 65 content not found
Slide 66-

Costimulation is Necessary for T Cell Activation Engagement of TCR and Ag/MHC in the absence of costimulation can lead to anergy Engagement of costimulatory molecules in the absenece of TCR engagement results in no response Activation only occurs when both TCR and costimulatory molecules are engaged with their respective ligands Downregulation occurs if CTLA-4 interacts with B7 CTLA-4 send inhibitory signal
Slide 67-

Clonal expansion Signals 1 and 2 activate calcium calcineurin pathway, MAP kinase pathway and NF-Kb pathway These pathways activate transcription factors that trigger the expansion of many new molecules including IL-2, CD 154 and CD 25. IL-2 and other cytokines activate the TOR pathway to provide signal 3, the trigger for cell proliferation A subset of activated helper T cells migrate to the B region of lymph nodes located in the cortex and help to differentiate B cells while the remainder of the effector T cells leave the lymph node and proceeds the inflamed site
Slide 68-

The activated T cells rapidly accumulate in the interstitium of the allograft as the response mounts in the first few days. CD4 T cells are cytokine secreting cells that express IL-2 and alter a variety of cytokines CD4 cells help B cells to enhance their antibody production through CD40 ligand Alloantibody produced during rejection is mainly IG g and primarily participates in the destruction of vascular endothelium of the graft CD 8 T cells participate in rejection through DTH or cytotoxicty
Slide 69-

ppt slide no 69 content not found
Slide 70-

ppt slide no 70 content not found
Slide 71-

ppt slide no 71 content not found
Slide 72-

Key Steps in T cell Activation APC must process and present peptides to T cells T cells must receive a costimulatory signal Usually from CD28/B7 Accessory adhesion molecules help to stabilize binding of T cell and APC CD4/MHC-class II or CD8/MHC class I LFA-1/ICAM-1 CD2/LFA-3 Signal from cell surface is transmitted to nucleus Second messengers Cytokines produced to help drive cell division IL-2 and others
Slide 73-

Rejection
Slide 74-

1. Hyperacute rejection Occurrence time Occurs within minutes to hours after host blood vessels are anastomosed to graft vessels Pathology Thrombotic occlusion of the graft vasculature Ischemia, denaturation, necrosis
Slide 75-

ORIGINS OF ANTIBODIES TO HLA AND ABO ANTIGENS IN HYPERACUTE REJECTION Pregnancy Fetus is allograft in mothers body During birth, fetal cells can stimulate maternal immune response Blood transfusion HLA typing not performed for routine transfusion Leukocytes and platelets in whole blood Transplantation Persons with more than one transplant
Slide 76-

Figure 12-15
Slide 77-

Complement activation Endothelial cell damage Platelets activation Thrombosis, vascular occlusion, ischemic damage 2006-7year Immunology 77
Slide 78-

Hyperacute rejection of a kidney allograft with endothelial damage, platelet and thrombin thrombi, and early neutrophil infiltration in a glomerulus 78
Slide 79-

ppt slide no 79 content not found