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Abatacept (hCTLA4-Ig) For the Treatment of Rheumatoid Arthritis:. Product Attributes and Mechanism of Action Joy Williams, Ph.D. Arthritis Advisory Committee September 6, 2005. Abatacept BLA. Continuous Marketing Application (Rolling submission of BLA) Unit: Date of
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Abatacept (hCTLA4-Ig) For the Treatment of Rheumatoid Arthritis: Product Attributes and Mechanism of Action Joy Williams, Ph.D. Arthritis Advisory Committee September 6, 2005
Abatacept BLA Continuous Marketing Application (Rolling submission of BLA) Unit: Date of submission: Pharmacology and Toxicology reviewable unit 11/15/04 Clinical pharmacology and biopharmaceutics Full clinical reviewable unit 12/20/04 Chemistry, Manufacturing and Controls (CMC) reviewable unit 3/31/05 PDUFA action date for BLA 125118 (Abatacept): 12/31/05
Review team Statisticians: Kyung Lee-stat reviewer Boguang Zhen-stat team leader Facilities reviewer: Ann deMarco DSI/BiMo: Dianne Tesch DDMAC: Catherine Gray DDRE: Hyon Kwon Regulatory Project manager: Erik Laughner Product reviewers: Joy Williams, chair Elizabeth Shores Susan Kirshner Ennan Guan Edward Max Barbara Rellahan Clinical reviewers: Keith Hull – Chair, clinical reviewer Jeffrey Siegel –Team leader Mark Walton-Director Pharm/Tox: Anita O'Connor-toxicology reviewer Anil Rajpal-Pharm reviewer Hannan Guan
Abatacept (CTLA4-Ig) homodimer CTLA-4 domain: Extracellular sequence of human CTLA-4 IgG1 Fc domain: Hinge, CH2 and CH3 regions of human IgG1 Fc sequence
Abatacept manufacturing process Abatacept is produced as a secreted protein in large scale culture of Chinese hamster ovary cell line Series of purification/viral clearance steps Final formulation Abatacept for Injection, 250 mg/vial sterile, non-pyrogenic lyophile for intravenous administration following reconstitution with Sterile Water for Injection; supplied with non-siliconized syringe Excipients: maltose monohydrate, sodium phosphate monobasic, Sodium chloride, hydrochloric acid, sodium hydroxide
T cell activation requires signals from TCR and costimulatory molecules B7 CD28 TCR MHC + peptide activated T cell Antigen presenting cell
CD28 B7 CTLA4 TCR MHC + peptide CTLA4 – a CD28 homologue that binds to B7 with higher affinity than CD28 Antigen presenting cell T cell
CTLA4 extracellular domain (B7-binding domain) is fused to IgG1 Fc to create soluble CTLA4-Ig B7 CTLA4 IgG1 Fc CTLA4 extracellular domain CTLA4-Ig
CTLA4-Ig binds to B7 molecules and inhibits CD28-B7 interactions; suppresses T cell response CD28 B7 TCR MHC + peptide Antigen presenting cell T cell
B7 engaged by CTLA4-Ig directly signals to dendritic cells Suppresses T cell response Additional possible mechanisms of action to consider: INF-g tryptophan B7 IDO IDO kynurenine IDO Grohmann et al. Nat Immunol. 3:1097-101 Mellor et al. JI 171:1652-5 Boasso et al. Blood 105: 1574-81 Munn et al. JI 172: 4100-10 T cell proliferation is inhibited
Additional possible mechanisms of action to consider: Potential functions of the IgG1 Fc portion of abatacept Resulting in elimination of B7-expressing cells and suppression of T cell response B7 expressing cell ? Antibody-dependent Cellular cytoxicity (ADCC) CTLA4 ? IgG1 Fc Phagocytosis/clearance of opsonized cells Binding to Fc receptors
The paradox: CTLA4-Ig may disrupt critical pathways required for maintenance of immune tolerance
T regulatory cells are critical components in the maintenance of peripheral tolerance to tissue-specific self-antigens T regulatory cell Effector T cell B7-CTLA4 Self-antigen Antigen presenting cell In both humans and mice, absence of T regulatory cells is associated with aggressive autoimmunity
CD28-B7 interactions are essential for both thymic development of Tregs and for their peripheral homeostasis Decrease in Tregs (CD4+CD25+) cells in lymph nodesofwildtype mice treated with CTLA4Ig for 10 days Decreased development of Tregs In the thymus in B7 knockout mice 4 3 2 % CD4+CD25+ thymocytes 1 0 wildtype B7 knockout Williams et al. (not published) Tang et al. JI 171: 3348-52 In certain inbred mouse strains, autoimmune disease is exacerbated in the absence of B7 or CD28 due to loss of Tregs Implications for development of fetal immune system during gestation?
Activated T cells express CTLA4: CTLA4 transduces a negative signal to T cells and functions to attenuate the immune response B7 CD28 CTLA4 TCR MHC + peptide Antigen presenting cell T cell
Activated T cells express CTLA4: CTLA4 transduces a negative signal to T cells and functions to attenuate the immune response; CTLA4-Ig may interfere with this process B7 CD28 CTLA4 TCR MHC + peptide Antigen presenting cell T cell
Abatacept (CTLA4-Ig) Mechanism of Action Summary Mechanisms of action that may function to ameliorate RA: Blocking CD28 costimulation Induction of suppressor antigen-presenting cells (via IDO) Depletion of B7-expressing cells Mechanisms of action that may exacerbate autoimmunity: Inhibition of T regulatory (CD4+CD25+) cell maintenance/development Inhibition of endogenous CTLA4 signals