Translating research into novel immunotherapies delivers scientific and economic gains for the pharmaceutical/biotechnology sector in drug discovery
Submitting Institution
University of BristolUnit of Assessment
Clinical MedicineSummary Impact Type
TechnologicalResearch Subject Area(s)
Medical and Health Sciences: Immunology
Summary of the impact
    Research into novel immunotherapies has given rise to a novel drug
      (EtxB), which is now in Phase
      II clinical trials, and to a profitable contract research company
      partnering with the pharmaceutical
      industry to develop their compounds. Trident Pharmaceuticals was formed
      around patents filed by
      the University of Bristol, has received investment of [text removed
       for publication], successfully
      completed Phase I trials (2011) and is in the midst of Phase IIa trials in
      humans with inflammatory
      disease (2013). KWS BioTest arose as a result of the underpinning research
      and experience
      gained from developing EtxB, and is now a leading contract research
      organisation working with
      pharmaceutical and biotechnology companies developing novel treatments for
      human disease.
      KWS has directly contributed to the development of therapies at more than
      75 different companies,
      employs 28 people, has exported [text removed for publication] and
      was 2012 winner of a
      Biomedical iNet Award for outstanding business achievement.
    Underpinning research
    Research in Infection and Immunology has long been a major strength
      within Bristol, which was
      also one of the first Universities in the UK to organise its support for
      entrepreneurial activities. Neil
      Williams (appointment at the University of Bristol initially as a Lecturer
      in 1991, now as a
      Professor) collaborated with Hirst (then at University of Kent, but
      subsequently at the University of
      Bristol 1996-2003) in seeking to understand the unusual ability of a
      bacterial protein (EtxB) to
      stimulate mucosal antibodies (Nashar, PNAS 1992; cited 114 times,
      6.71/year). This basic
      immunological finding had little obvious translational value by itself.
      However, Williams followed
      these findings up with studies to determine the effects of EtxB on
      populations of immune cells. He
      established a range of cellular assays showing that EtxB caused the
      activation of B lymphocytes,
      triggered apoptosis in CD8+ T-cells and modulated CD4+ T-cell activation
      (Nashar, Int Immunol
      1996; Immunol 1997). Looking at this range of effects, Williams
      hypothesised that it may be
      possible to harness this protein as a novel treatment for human
      inflammatory diseases.
    A combination of cell biology studies and in vivo experiments
      validated the hypothesis, culminating
      in the ground-breaking discovery that EtxB could completely block the
      development of disease in
      the gold standard rodent model of rheumatoid arthritis.[1] The potential
      to use EtxB as a therapy
      was patented[12] and a key review foresaw its potential in a range of
      diseases.[2] Peer-reviewed
      grant funding directly aimed at determining the therapeutic potential of
      EtxB and to identify its
      mechanism of action drove the programme forwards over the following ten
      years (£2.66m from the
      MRC, Wellcome Trust, Arthritis Research UK, CRUK and others[7-11]).
      Further patents were
      subsequently filed covering the use of EtxB as a treatment for allergic
      disease[13] and as a
      modulator for use in a vaccine.[14] Peer-reviewed publications
      corroborated this potential.[3-6]
    Investigations of the potential of EtxB as a novel therapy led the
      Williams laboratory to establish
      key translational models of human diseases, including type 1 diabetes
      (Ola, Immunol 2006), colitis
      and asthma,[6] and to use state-of-the-art techniques to characterise the
      effects of EtxB on a range
      of immune parameters underlying disease pathogenesis in these conditions
      (Plant EJI, 2003; [5]).
      The research established that EtxB was able to modulate the activity of T
      regulatory cells following
      its delivery. Demonstrating this required the development of a range of
      assay systems, enabling
      the activation and differentiation of T-cells to be tracked in vivo
      in rodents, and necessitated their
      application to diseased animals. These tools were not only critical to
      uncovering the mechanism of
      action of EtxB, but also established the Williams laboratory as a centre
      for the study of immune
      modulating therapies. The data generated from these endeavours and the
      resulting reputation of
      the laboratory provided the springboard for the formation by Williams of
      KWS BioTest Ltd, which
      offers these and other models developed following its formation to
      pharmaceutical and
      biotechnology companies around the world in support of their drug
      discovery programmes.
    References to the research
    Peer reviewed journal publications
    30 original articles and 7 refereed reviews since 1992 from the
        Williams lab relating to the use of
        EtxB as an immune modulating agent, including:
    
[1] Williams, N.A., Stasuik, L., Nashar, T.O., Richards, C.M., Lang,
      A.K., Day, M.J. & Hirst, T.R.
      (1997). Prevention of autoimmune disease due to lymphocyte modulation by
      the B-subunit of
      Escherichia coli heat-labile enterotoxin. Proc Natl Acad Sci U
        S A. 94:5290-5295 [cited 53 times,
        3.31/year] PMID: 9144230
     
[2] Williams, N.A., Hirst, T.R. & Nashar, T.O. (1999). Immune
      modulation by the cholera-like
      enterotoxins: from adjuvant to immunotherapeutic. Immunol Today 20:95-101
      [cited 172 times,
        12.29/year]. PMID: 10098329
     
[3] Richards, C.M., Aman, T., Hirst, T.R., Hill, T.J. & Williams,
      N.A. (2001) Protective mucosal
      immunity to ocular herpes simplex virus type-1 infection in mice using Escherichia
        coli heat-labile
      enterotoxin B-subunit as an adjuvant. J Virol 75:1664-1671
      PMID: 11160664
     
[4] Luross, J.A., Heaton, C.P.E., Hirst, T.R., Day, M.J. & Williams,
      N.A. (2002) Escherichia coli
      heat-labile enterotoxin B-subunit prevents autoimmune arthritis through
      the induction of regulatory
      CD4+ T cells. Arthritis Rheum 46:1671-1682 PMID: 12115200
     
[5] Donaldson DS, Tong KK, Williams NA. (2011) Mucosal administration of
      the B subunit of E. coli
      heat-labile enterotoxin promotes the development of Foxp3-expressing
      regulatory T cells. Mucosal
        Immunol 4(2):227-238 PMID: 20944556
     
[6] Donaldson, DS, Apostolaki M, Bone HK, Richards CM, Williams NA.(2013)
      The Escherichia coli
      heat-labile enterotoxin B subunit protects from allergic airway disease
      development by inducing
      CD4+ regulatory T cells. Mucosal Immunol 6:535-546. PMID:
      23032791
     
Peer reviewed grants
    £2.66m peer-reviewed and £1.91m industry funding since 1992 to the
        Williams laboratory relating
        to investigations into the use of EtxB as an immune modulating agent,
        including:
    [7] The Wellcome Trust — £280,492 "Receptor mediated effects on molecular
      and cellular
      mechanisms in antigen presentation, processing and the generation of
      immunological memory
      responses by Escherichia coli enterotoxin B-subunits (EtxB)" March
      1997-July 2001.
    [8] The Medical Research Council — £307,544 "A generic carrier for
      targeted delivery into both
      class I and class II processing and presentation pathways" Jun 1999-May
      2002.
    [9] The Wellcome Trust — £275,917 "Cell signals underlying the
      immunomodulatory properties of E.
        coli heat-labile enterotoxin" January 1999-December 2002.
    [10] The Wellcome Trust — £275,762 "Control of ocular HSV-1 infection
      using mucosal vaccination
      strategies which stimulate Th1 or Th2 dominated immune responses" May
      2000-April 2003.
    [11] Cancer Research Technology (CRUK) — £236,519 EtxB; a novel approach
      to cancer
      vaccinations and therapy July 2007-June 2009.
    Patents arising, licensed to Trident Pharmaceuticals Inc.
    [12] Therapeutic agents and autoimmune diseases; Priority date: 5
      July 1995 (UK)
      Owner: University of Bristol, PCT Number: PCT/GB96/01614
      Inventors: Williams, N.A., Hirst, T.R. & Nashar, T.O.
      Status: Granted Australia, Austria, Belgium, Canada, China, Czech
      Republic, Denmark, European
      Patent Convention, Finland, France, Germany, Greece, Hungary, Ireland,
      Italy, Luxembourg,
      Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Russian
      Federation, Singapore,
      Spain, Sweden, Switzerland, United Kingdom, United States
    [13] Agent for treating allergic and hypersensitivity condition; Priority
        date: 9 January 1998 (UK)
      Owner: University of Bristol, PCT Number: PCT/GB99/00070
      Inventors: Williams, N.A., Hirst, T.R. & Bienenstock, J.
      Status: Granted Australia, Austria, Belgium, Canada, Cyprus,
      Denmark, European Patent
      Convention, Finland, France, Germany, Greece, Ireland, Italy, Luxembourg,
      Monaco, Netherlands,
      New Zealand, Portugal, Spain, Sweden, Switzerland, United Kingdom
    [14] Vaccination; Priority date: 8 May 1998 (UK), Owner:
      University of Bristol
      PCT Number: PCT/GB99/01461
      Inventors: Williams, N.A. & Hirst, T.R. (Morgan, A.J., Wilson,
      A.D. & Bird, L.)
      Status: Granted Czech Republic, Eurasian Patent Organisation,
      Israel, Japan, Mexico, US.
    Details of the impact
    EtxB is a first in class disease-modifying therapy, with potential
      utility across a range of human
      diseases in which there is a unmet need: 125 million people suffer from
      psoriasis worldwide[a];
      approximately 5.5 million people in the UK are being treated for
      asthma;[b] and rheumatoid arthritis
      affects approximately 0.5-1.0% of the population.[c] These and other
      inflammatory diseases are
      currently treated with chronically administered non-specific drugs, which
      primarily control damage
      rather than impacting on the underlying drivers of disease. In contrast, a
      short course of EtxB can
      turn off these processes for long periods,[1,4,6] resetting the balance
      between inflammation and
      normal physiology.[4,5] This is a novel and exciting new paradigm for
      treatment.
    Williams spun out the EtxB patent portfolio (1999), subsequently rolled
      into the formation of Trident
      Pharmaceuticals Inc,[d] established in 2006 to bring EtxB (company code
      HF1020) through Phase
      II trials before seeking a large pharmaceutical partner. Williams remains
      an integral part of the
      team and KWS (see below) has performed all the preclinical work on EtxB.
      All 11 substantiating
      papers cited on the Trident website were published by Williams. Trident
      generated GMP material
      (2008-2011) and tested this in formal GLP acute and repeat dose toxicology
      studies in rodents and
      primates (completed in 2011). It was found to be safe and in 2011 the MHRA
      approved a clinical
      trials application (CTA) for a Phase 1a study in healthy volunteers.
      Following completion of Phase
      Ia, in 2013 the MHRA approved a CTA for a Phase II study [text removed
        for publication]. As with
      all new drugs, the process of getting them to market takes years, but EtxB
      has already passed
      many of the major hurdles. Press coverage of its potential impact included
      articles in international
      newspapers, television and radio.[e] Other companies including Hunter
      Immunology are
      developing approaches to mimic the effects of EtxB using novel peptides
      that target the same
      receptor.[f]
    The underlying research and the experience gained by Williams of
      developing EtxB directly gave
      rise to the formation of KWS BioTest Ltd. Coverage of his work on EtxB
      established him as a
      leader in disease efficacy and mechanism of action studies, and repeated
      requests for work came
      in from companies wanting to access these models:
    
      - Williams formed KWS BioTest in 2004,[g] with Professor Day (veterinary
        pathology).
 
      - KWS received £200k of investment from a Government Challenge Fund[h]
        to employ
        scientists and commercial management and respond to these requests.
 
      - KWS is now a leading partner for high quality drug discovery and
        efficacy in Europe, an
        achievement that was recognised by the award of the 2012 South West
        Biomedical iNet
        award for outstanding business achievement.[i] KWS runs validated in
          vitro and in vivo
        models of human disease in inflammation, autoimmunity, pain and
        infection, all of which are
        founded on the academic work of the Williams laboratory and other groups
        within Bristol.
 
    
    The success of KWS is based on offering in-depth scientific expertise and
      analysis of the sort that
      is lacking in large contract research organisations, while providing
      service and data quality that are
      lacking from academia (ISO9001 accredited, GLP led). These activities have
      generated substantial
      commercial impact directly within KWS and for partner companies, and have
      contributed to the
      discovery of new drugs now in clinical trials and development (details of
      which are confidential).
    Since 2004, KWS has carried out experimental studies for more than 75
      different companies (39%
      UK, 44% EU, 12% US, 5% rest-of-the-world; 57% small, 24% medium and 19%
      large pharma).[j]
      In the case of small companies, this work has been absolutely critical as
      they typically lack
      expertise and facilities to carry out pharmacology testing. In the case of
      medium and large pharma,
      partners want the expertise that it can offer, recognising that
      outsourcing is a more cost-effective
      and ethical approach to drug discovery.[k]
    Dr Sean Mason (Senior Group Leader at UCB) stated "KWS have provided
        excellent, high quality
        scientific support for several projects, covering a range of diverse
        activities including complex
        immune cell-based assays and imaging studies, which together with their
        prompt and detailed
        feedback has benefited several of our projects". The ability of KWS
      to provide in vivo efficacy
      models that are validated with control drugs, and which are run regularly,
      has a clear 3Rs impact.
    Since its formation, KWS has expanded and grown as evidenced by:
    
      - Increased turnover from [text removed for publication].[j].
 
      - Profits have grown from [text removed for publication].
 
      - KWS employs [text removed for publication], and during 2012
        contributed [text removed for
          publication] of income to the University of Bristol.
 
      - KWS has become a significant exporter (over [text removed for
          publication] in the last three
        years).
 
      - Strategic partnership with Quotient Bioresearch facilitating further
        exports from these
        companies.
 
    
    Sources to corroborate the impact 
    [a] National Psoriasis Foundation http://www.psoriasis.org/learn_statistics.
      Corroborates the
        prevalence of psoriasis worldwide.
    [b] Asthma UK http://www.asthma.org.uk/news-centre/facts-for-journalists/.
      Corroborates the
        prevalence and health impact of asthma on the UK population.
    [c] Center for Disease Control (US) http://www.cdc.gov/arthritis/basics/rheumatoid.htm#5.
      Corroborates the global prevalence and health impact of arthritis.
    [d] Trident Pharmaceuticals Inc. http://www.tridentpharma.com/index.html.
      Main company website
        for Trident highlighting the current status of the therapy underlining
        the impact case and
        demonstrating that this is the sole focus for the company.
    [e] Television and radio: ITN National News (30 November
      1999); Radio 4 `Science Now' (January
      2000); Portuguese National Radio (September 2003); Dutch
        National Radio (Sept 2003); BBC
        Radio 5 Live (September 2003). Print media: The Daily Mail
      (1 December 1999); New
        Scientist (4 December 1999); The Times (4 February 2000); Vogue
      (March 2000). Provide
        evidence of impact in raising public awareness of the health issues and
        of potential new
        approaches to developing therapies for human disease.
    [f] Patent licensed by Hunter Immunology, now Bioxyne. Evidence that
        the technology pioneered in
        Bristol has led other companies to adopt similar approaches (commercial
        impact and impact
        amongst peers).
    [g] KWS BioTest http://www.kwsbiotest.co.uk.
      Evidence of the current scope of the activities of the
        spin-out arising from the research and vehicle for the impact.
    [h] Wyvern Investment Fund http://www.wyvernfund.com/.
      Evidence that KWS received investment
        from and remains part of the portfolio of companies within the Wyvern
        Government Challenge
        Fund (economic impact).
    [i] Outstanding business award (http://www.inets-sw.co.uk/;
      Drug discovery Impact 1.pdf).
      Evidence of peer recognition of the Economic and Business Impact of KWS
        BioTest.
    [j] KWS Operating Plan summary 2012 (Confidential document that can be
      provided for audit
      purposes). Evidence of the economic impact of KWS BioTest
        (CONFIDENTIAL).
    [k] Clark DE (2011) Outsourcing lead optimisation: the eye of the storm.
      Drug Discovery Today
      16:147-157. DOI: 10.1016/j.drudis.2010.11.012. Evidence of the growing
        business and
        economic need for the services of KWS Biotest from Biotech and
        Pharmaceutical Companies.
      PMID: 21145413.