AQUILA BIOPHARMACEUTICALS INC
DEFA14A, 1997-05-05
IN VITRO & IN VIVO DIAGNOSTIC SUBSTANCES
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                    SECURITIES AND EXCHANGE COMMISSION

                          Washington, D.C.  20549

                                 __________

                                SCHEDULE 14A
                  Proxy Statement Pursuant to Section 14(a) 
                   of the Securities Exchange Act of 1934
                                 __________


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                      AQUILA BIOPHARMACEUTICALS, INC.
              (Name of Registrant as Specified In Its Charter)

 (Name of Person(s) Filing Proxy Statement, if Other than the Registrant)

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    _______________________________________________________________________

       The following letter was sent to shareholders with the proxy
       solicitation materials on April 18, 1997.






        April 18, 1997

        Dear Shareholder,

        In 1996 Aquila Biopharmaceuticals emerged as a new biotechnology
        company, creating and commercializing products which modulate the
        immune system to treat or prevent infectious diseases and cancer.
        Aquila's technology is focused on the proprietary Stimulon  family
        of adjuvants and our capabilities for producing antigens through
        recombinant methods.  Our goal is to develop safe, effective and
        marketable products through our own efforts and in collaboration
        with our corporate partners.

        We have made significant progress over the last few years, and
        recently achieved several milestones.  We anticipate that we will
        report to you several new important accomplishments over the next
        one to two years.  Our lead human health product, Quilimmune-P 
        for preventing pneumococcal infections is in Phase I clinical
        trials.  If the product meets the clinical end points in this
        trial, we expect to move into Phase II clinical testing this year.
        Quilvax-M  for preventing bovine mastitis is in animal trials.  We
        have completed feasibility testing in cows and have research
        challenge trials underway to demonstrate efficacy.  We expect to
        complete the research studies this year and initiate final
        efficacy and safety licensing trials in 1998.

        The company's six corporate partners and academic collaborators
        have completed 14 clinical trials with products incorporating
        QS-21, our lead Stimulon  adjuvant.  An additional 22 trials are
        underway targeting a number of different diseases, including
        influenza, malaria, hepatitis, herpes and certain cancers.  

        The strength of the company and its technology is a direct result
        of the expertise and outstanding commitment of our employees.  We
        thank them for their efforts.  We also thank you, our
        shareholders, for your support.

        Welcome to Aquila Biopharmaceuticals.

        Yours sincerely,


        /s/ Alison Taunton-Rigby

        Alison Taunton-Rigby, Ph.D.
        President and Chief Executive Officer


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