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Pemphigus-specific T cell engagers for pemphigus targeted immunotherapy

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R43AI151635-01A1
Agency Tracking Number: R43AI151635
Amount: $280,352.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: NIAID
Solicitation Number: PA18-574
Timeline
Solicitation Year: 2018
Award Year: 2019
Award Start Date (Proposal Award Date): 2019-08-14
Award End Date (Contract End Date): 2020-07-31
Small Business Information
321 JONES BLVD, STE 300
Pottstown, PA 19464-3468
United States
DUNS: 962964990
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 HIEP TRAN
 (610) 990-7531
 tran@abzymetx.com
Business Contact
 ROLF SWOBODA
Phone: (610) 990-7531
Email: swoboda@abzymetx.com
Research Institution
N/A
Abstract

ABSTRACTPemphiguspemphigus vulgarisPVand pemphigus foliaceusPFis an acquired autoimmune disease in which IgG antibodies target the keratinocyte desmosomal cadherin proteins desmogleinand desmogleinresulting in intraepithelialmucocutaneous blisteringNearly all PV and PF patientsbut no unaffected individualsdemonstrate detectable anti DSGand anti DSGreactivityrespectivelyPV is a potentially fatal autoimmune disorder with a mortality rate ofon average without treatment with corticosteroidsCurrent methods for pemphigus treatment require general immune suppression to reduce overall antibody productionbut this approach impairs protective immune responseswhich can lead to potentially fatal infections and secondary cancersWe propose a novel approach for targeted immunotherapy of PV by directing patientandapos s T cells to specifically seek out and kill the pemphigus specific B cellswhile sparing the beneficial immune cells that protect from infectionAs a proof of principlein phase IMulti specific T cell Engagers or MuTEIgG like recombinant proteins consisting of a well characterized anti CDantibody OKTwith mutated human IgGFcand human desmogleinand desmogleinextracellular domains will be producedThe T cell mediated target elimination of anti desmoglein specific B cells by MuTE will be validated in cell based assays and in mouse modelsPhase II work will focus on scale up of biologics productionobtaining the preclinical in vivo pharmacodynamicspharmacokinetics and toxicity data in animal models necessary for submission of an IND NARRATIVEPemphigus vulgaris is a potentially fatal autoimmune diseaseCurrent methods for pemphigus treatment impair protective immune responseswhich can lead to potentially fatal infections and secondary cancersOur novel targeted immunotherapy for PV is designed to direct patientandapos s T cells to specifically seek out and kill the pemphigus specific B cellswhile sparing the immune cells that protect from infection

* Information listed above is at the time of submission. *

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