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+ T cell MHC/self-peptide MHC/Vβ Induction of + T H 1 mediated autoimmunity: A paradigm for the pathogenesis of rheumatoid arthritis, multiple sclerosis and type I diabetes APC Activated autoreactive + TH1 cell (1) expansion of +, autoreactive TH1 cells specific for autoantigens (2) migration and infiltration of these self reactive + TH1 cells into tissues and induction of inflammation and autoimmunity (3) induction of regulatory cells and cytokines which control the growth and activation of the pathogenic autoreactive + T cells 1 Rheumatoid Arthritis: Genetics Twin and other genetic studies have demonstrated that a major genetic contribution to disease predisposition resides in the MHC class II HLA-DR locus. Females are about 2-3 times more susceptible than males. More than 80% of caucasian rheumatoid patients express DR1 or DR4 subtypes which share an epitope mapping to amino acids 70-74 of the DRβ chain, in the polymorphic region lining the peptide binding groove. There is recent evidence that the genetically susceptible HLA-DR4 (e.g., DR0401) alleles bind different peptides in their peptide binding groove than the non-susceptible (e.g., DR0402) alleles. Susceptible alleles bind a negatively charged amino acid at the p4 pocket of the binding groove. Mutation analysis revealed that position 71 of the DRβ chain in particular correlates with the genetic linkage of RA susceptibility 4 Rheumatoid Arthritis: Definition Amino acid sequences in the β chain HLA-DRB*0401 molecules dictate susceptibility to RA Rheumatoid arthritis is characterized by a chronic inflammation of the synovial joints and infiltration by blood-derived cells, chiefly T cells, macrophages, and plasma cells, all of which show signs of activation. This leads in most cases to progressive destruction of cartilage and bone, which occurs after invasion of these tissues by the cellular synovial tissue and is believed to be mainly mediated by cytokine induction of destructive enzymes, including matrix metalloproteinases. There is also prominent development of new vessels and evidence of systemic inflammation, for example, upregulated acute phase proteins. In more severe cases there is involvement of vessels and other organs. 48 46 44 55 53 85-89 59 57 35 28 11 78 14 C C 75 75 9 66 69 70 15 76 77 80 14 11 Shared epitope in RA 12 37 13 38 28 61 67 71 40 70 26 66 65 63 2 17 47 64 5 Requirements in the Development of an Autoimmune Disease Amino Acids in the Shared Epitope 0401 0404 0101 0402 67 70 71 74 RA Association Leu Gln Lys+ Ala ++ Arg+ ++ Arg+ ++ Ile Asp- Glu- None 3 6 1

Clinical Manifestations of Rheumatoid Arthritis Extra-Articular manifestations of RA (1) Arthritis (a) Symmetrical involvement of the small joints of the hands and feet, particularly the proximal interphalangeal (PIP), metatarsophalangeal (MTP), and metacarpophalangeal (MCP) joints, but involvement of wrists, ankles, knees, elbows, and hips is also common. (b) When the disease involves the axial skeleton, it is most frequently in the cervical region. 7 10 Clinical Manifestations of Rheumatoid Arthritis (3) Associated Syndromes (a) Sjögren s syndrome-salivary gland inflammation and keratoconjunctivitis (b) Felty s syndrome-profound neutropenia, thrombocytopenia and splenomegaly (C) Amyloidosis-type II 8 11 Clinical Manifestations of Rheumatoid Arthritis Clinical Manifestations of Sjögren s syndrome (2) Extra-Articular (a) Constitutional -normochromic and normocytic anemia, fever, malaise and weight loss (b) Subcutaneous nodules (rheumatoid nodules) (c) Pulmonary involvement-(pleuritis, interstitial pneumonitis, alveolitis and intrapulmonary rheumatoid nodules) (d) Cardiac involvement-pericarditis (e) Ocular disease-keratoconjunctivitis, granulomatous scleritis (e) Other common vasculitic manifestations-skin ulcerations, palpable purpura, ischemic ulceration of GI tract, mononeuritis multiplex 9 12 2

Pathogenesis of Rheumatoid Arthritis. Initiating Event in Rheumatoid Arthritis α,β α,β DR4/peptide Fc Receptor T cell Macrophage/ dendritic cell/b cell 13 16 The Initiating Event in Rheumatoid Arthritis APC BCR or FcR RA auto antigen ER Golgi endos DR4/CLIP ome HLA- DM &DO DR4/ peptide α,β DR4/ InvChain CD80 (B7.1) 8 T cell 14 The putative RA inducing protein binds antigen specific SmIg on B or phagocytic receptors on dendritic cells cells and is internalized and digested into peptides in endosomes and bound to the MHC class II molecule (DR4). The DR4/peptide complex triggers the on antigen specific T cells leading to T cell activation. 17 Normal synovium Villous Synovitis RA auto-antigenic peptide DR4, DR1 Rheumatoid Synovium (Pannus) Pannus Invading and Destroying cartilage and Bone 15 18 3

+ T Cells Differentiate into Distinct T H 1 and T H 2 Subsets Final Phases of B cell Differentiation are Mediated by Contact T cell signals (L/) and Lymphokines 3 Th1 IL-12 IFN-γ Th0 IL-10/ IL-4 IL-4 Th2 Negative Feedback Loops Cytokine Profile Functions IL-2, IFN-γ T cell-macrophage interactions DTH responses Intracellular pathogens IL4, IL-5, IL-6 IL-10, IL-13 T cell-b cell interactions Antibody responses Extracellular pathogens BCR Activated B cell L IL-4, IL-5, IL-6, IFN-γ, TGF-β Activated T cell IgG IgA IgE IL-4, IL-10 suppress emergence of T H 1 clones IFN-γ suppresses emergence of T H 2 clones 19 Plasma Cell 22 Consequences of L/ interactions on Dendritic cell function Activated T cell L 8 MHC class II/ autopeptide B7 B7 MHC class II (1) Induction of cytokines (IL-8, IL-12, TNF-α, MIP-1) (2) Stimulation of B7-1 and B7-2 expression and co-stimulatory function with activation of T cell growth (3) Augmentation of antigen-presenting function 20 Dendritic cell/ APC + Cell (T H 2 ) Immunopathophysiology of Rheumatoid Arthritis DR4/RA peptide + Cell (TH0 ) IL-12 α,β, IFN-γ IL-4 Sm Ig Inflammation RA antigen B Cell Synovial fibroblast Rheumatoid Plasma Cell factor (RF) (1) Synthesis of PGE 2, Collagenase, IL-1 (2) Synovial cell Vasculitis proliferation L Fc R IL-1, TNF-α, TGF-β Activated T H 1 + T Cell RF Macrophage PGE 2, collagenase chemokines Endothelial cell hypothalamus Fever Osteoclast activation Bone and cartilage destruction 23 T cell-macrophage Interactions Induce Synovial Cell Proliferation and Activation α,β, DR4/peptide Fc Receptor + T H 1 Cell L Macrophage Rheumatoid factor (RF) IL-1, TNF-α, TGF-β BONE RESORBTION Synthesis of PGE 2, Collagenase, IL-1 Inflammation Synovial Cell Proliferation 21 24 4

(1) Characteristics of RFs Rheumatoid Factors Rheumatoid Factors and Immune Complexes Augment the Activation of Macrophages (a) RFs are autoantibodies with specificity for the Fc region of self-igg (b) Most RFs are IgM but IgG and IgA RFs are also observed (2) Biologic Occurrence and Disease Associations (a) RFs are the major autoantibodies observed in RA (b) RFs can be induced in experimental animals by injection of either denatured IgG or by immunization with bacteria. (c) High titer RF is seen in chronic inflammatory conditions such as rheumatoid arthritis, other rheumatic conditions, TB and SBE (3) Biologic and Pathologic Functions of RF's (a) RFs may play a role in augmenting the phagocytosis of opsonized particles and in the clearance of immune complexes. (b) RF bound to IgG or to immune complexes can precipitate in vessel walls and induce vasculitis. High titer RF is associated with systemic vasculitis in RA (c) Rheumatoid factors can bind to Fcγ receptors on macrophages and augment the release of monokines, including IL-1 and and TNF-α 25 + T H 1 Cell IFN-γ IL-1 L DR4/peptide α,β, Activated Macrophage Macrophage Rheumatoid factor (RF) Fc Receptor Rheumatoid factor (RF) or Immune complexes Increased synthesis of IL-1, TNF-α, TGF-β, IL-6, PGE 2 and Collagenase 28 TNF, IL-1 and RANK-L activate osteoclasts to induce bone resorbtion Activated + T Cell α,β, Macrophage or dendritic cell Soluble RANK Receptor Precursor Osteoclast RANK-L Soluble RANK-L RANK TNF TNF-R B7 TNF-α IL-1 PGE 2 MHC class II 26 Activated Osteoclast Bone Resorbtion 29 Mechanisms of action of drugs used to treat RA (a) Block T cell-apc interaction antibodies to MHC class II, or the TNF IL-1 (b) Decrease T cell activation cyclosporine, anti-, anti-8, anti-cd80 (B7), anti- L, CTLA-4 agonist (e) Inhibit products of T cells and macrophages NSAIDs, TNF receptor inhibitors, IL-1 receptor inhibitors (c) Prevent T cell, B cell or synovial cell proliferation Methotrexate, Imuran, Cytoxan (d) Inhibit T cell or APC function steroids, gold, penicillamine 27 30 5

31 32 New Surface Molecules are Expressed after T cell Activation γ δ ε ζ ζ ηη 8 α β 5RA T Cell Activation γ δ ε ζ ζ ηη IL-2R L CTLA-4 8 α β 5 RA 5 RO MHC Class II FAS-L VLA-1 33 6