Hélène Bazin-lee

Research Professor


Personal Summary

After completing a M.Sc. in Chemical Engineering at the ENSCCF (Clermont-Ferrand's Superior National School of Chemistry, France) with an emphasis in organic chemistry, Hélène received a Ph.D. in Organic Chemistry from the University of Lyon I (France) in 1994. During her postdoctorate at the University of Iowa under Professor Robert Linhardt, she developed synthetic methods for the synthesis of glycosaminoglycan building blocks and other sulfated carbohydrates. After working in industrial R&D involving carbohydrate modifications, she joined Corixa (acquired by GlaxoSmithKline in 2005) in Hamilton (MT) in 2002 and worked on developing new TLR agonists as vaccine adjuvants.  Dr Bazin-Lee left GSK in 2016 and joined the department of Biomedical and Pharmaceutical Sciences at the University of Montana in Missoula. Her current research interests include the design and synthesis of TLR agonists and antagonists as therapeutic immunomodulators, targeted delivery and drug conjugation.




M.S.: ENSCCF (Clermont-Ferrand's Superior National School of Chemistry, France), Chemical Engineering, 1991

Ph.D.: (summa cum laude) - University Claude Bernard - LYON I (France), Organic Chemsitry, 1994


Research Interests

The research focus of our group is the design, synthesis and development of new and safe vaccine adjuvants.

Vaccines have played a key role in the reduction of morbidity and mortality caused by infectious diseases since their introduction over 200 years ago. Many of the safest and most effective vaccines in use today employ killed or attenuated live viruses, as they mimic live infection without causing disease. However, it is not always practical or safe to use killed or attenuated viruses and much effort has been devoted to the development of subunit vaccines consisting of antigens purified from the pathogen or produced by recombinant technology. Unfortunately, these highly purified proteins are usually poorly immunogenic and often require the addition of adjuvants to enhance vaccine potency.

The discovery of toll-like receptors (TLRs) on cells of the immune system together with the identification of natural TLR ligands in the late 1990s has led to a great deal of interest in developing synthetic TLR agonists and antagonists to manipulate innate and adaptive immune responses. Toll-like receptors are a family of structurally related receptors that detect highly conserved microbial components common to large classes of pathogens and mobilize defense mechanisms aimed at eliminating these invading pathogens. Of the more than 10 known TLRs that have been identified in humans, five are associated with the recognition of bacterial components (TLRs 1, 2, 4, 5, 6) and four others (TLRs 3, 7, 8, 9) appear to be restricted to cytoplasmic compartments and are involved in the detection of viral RNA (TLRs 3, 7, 8) and unmethylated DNA (TLR9). Targeting TLR receptors and their cognate intracellular pathways could potentially lead to more effective vaccines and novel therapeutic approaches for the treatment of immune disorders.

Our adjuvant discovery approach is focused on the identification and lead optimization of a novel series of TLR7/8 agonist molecules, either alone or in synergistic combination with a TLR4-active agonist, that will enhance innate and adaptive immune responses in rapid-acting vaccines against viral agents. We are also investigating synthetic modifications to (i) improve the chemical and metabolic stability of these agonists and (ii) to optimize their physicochemical properties for specific formulation/delivery routes. Since TLR7 and TLR8 are located in endosomal/lysosomal compartments, cellular uptake is prerequisite for cellular activation by TLR7/8 ligands and we are also investigating strategies that will increase the penetration of the TLR7/8 ligand into DCs and other immune cells and reduce potential toxic effects. We are also exploring the synergy between TLR7/8 and TLR4 agonists and developing different types of TLR7/8-TLR4 conjugates. 


NIH/NIAID, HHSN272200900036C / N01-AI-90036

Innate Immune Receptors and Adjuvant Discovery: synthesis and evaluation of new adjuvants functioning via TLR-7 and TLR-8 receptors 

Field of Study

Medicinal chemistry with emphasis on carbohydrates, heterocycles and phospholipids synthesis

TLR agonists design and synthesis as vaccine adjuvants


Selected Publications

H.G. Bazin, Y. Li, J.K. Khalaf , S. Mwakwari, M.T. Livesay, J.T. Evans, D.A. Johnson, “Structural requirements for TLR7-selective signaling by 9-(4-piperidinylalkyl)-8-oxoadenine derivatives”,  Bioorg. Med. Chem. Lett., 25, 1318-1323, 2015

J. Khalaf, W. S. Bowen, H.G. Bazin , K.T. Ryter, M.T. Livesay, J.R. Ward, J.T. Evans, D.A. Johnson, “Characterization of TRIF selectivity in the AGP class of lipid A mimetics: Role of secondary lipid chains”, Bioorg. Med. Chem. Lett., 25, 547-533, 2015

H.G. Bazin, T.J. Murray, W.S. Bowen, A. Mozaffarian, S. Fling, L.S. Bess, M.T. Livesay, J.S. Arnold, C.L. Johnson, K.T. Ryter, C.W. Cluff, J.T. Evans, D.A. Johnson, “The ‘Ethereal’ nature of TLR4 agonism and  antagonism in the AGP class of lipid A mimetics”, Bioorg. Med. Chem. Lett., 18, 5350-5354, 2008

H.G. Bazin, L.S. Bess, M.T. Livesay, and D.A. Johnson, “New synthesis of the immunostimulant aminoethyl glucosaminide 4-phosphates RC-524 and RC-529”, Tetrahedron Lett., 47(13), 2087-2092, 2006

H.G. Bazin, M A. Marques, A.P. Owens III, R.J. Linhardt, and  K.A. Crutcher Inhibition of Apolipoprotein E-Related Neurotoxicity by Glycosaminoglycans and Their Oligosaccharides”, Biochemistry, 41(25), 8203-8211, 2002

A. Poveda, J.L. Asensio, T. Polat, H.G. Bazin, R.J. Linhardt, and J. Jiménez-Barbero, “Conformational behavior of C-glycosyl analogues of sialyl-a-(2→3)-galactose”, Eur. J. Org. Chem., 1805-1813, 2001

M.W. Wolff, H.G. Bazin, and R.J. Linhardt, “Analysis of fluorescently labeled oligosaccharides by electrospray ionization mass spectroscopy and capillary electrophoresis”, Biotechnology Techniques, 13, 797-801, 1999

H.G. Bazin, M.W. Wolff, and R.J. Linhardt, “Regio and stereoselective conversion of Delta4-uronate to L-ido-, D-gluco-, and L-altropyranosiduronic acids”, J. Org. Chem., 64, 144-152, 1999

H.G. Bazin, and R.J. Linhardt, “Regiospecific synthesis of new methyl sulfoglucopyranoside-based surfactants by nucleophilic displacement of a cyclic sulfate”, Synthesis, 4, 621-624, 1999

H.G. Bazin, I. Capila, and R.J. Linhardt, “Conformational study of D4-uronate derivatives of monosaccharide and disaccharide residues of glycosaminoglycans”, Carbohydr. Res., 309, 135-144, 1998

H.G. Bazin, T. Polat, and R.J. Linhardt, “Synthesis of sucrose-based surfactants through regioselective sulfonation of acyl sucrose and the nucleophilic opening of a sucrose cyclic sulfate”, Carbohydr. Res., 309, 189-205, 1998

H.G. Bazin, Y. Du, T. Polat, and R.J. Linhardt, “Synthesis of a versatile neuraminic acid C-disaccharide precursor for the synthesis of C-glycosides analogues of gangliosides”, J. Org. Chem., 64, 7254-7259, 1999

H.G. Bazin, R.J. Kerns, and R.J. Linhardt, “Regio and stereoselective synthesis of L-idopyranosiduronic acid and D-glucopyranosiduronic acid from Delta4-uronates”, Tet. Lett., 38, 923-926, 1997

T. Polat, H.G. Bazin, and R.J. Linhardt, “Enzyme catalyzed regioselective synthesis of sucrose fatty esters surfactants”, J. Carbohydr. Chem., 16, 1319-1325, 1997

H. Bazin, A. Bouchu, and G. Descotes, “Hydrolysis of cyanoethylated carbohydrates: synthesis of new carboxylic derivatives of sucrose, D-glucose and D-fructose”, J. Carbohydr. Chem., 14, 1187-1207, 1995

H. Bazin, A. Bouchu, G. Descotes, and M. Petit-Ramel, “Comparison of calcium complexation of some carboxylic acids derived from D-glucose and D-fructose”, Can. J. Chem., 73, 1338-1347, 1995

Book Chapters

H.G. Bazin, and R.J. Linhardt,, “Properties of Carbohydrates", in Glycoscience: Chemistry and Chemical Biology, B. Fraser-Reid, K. Tatsuta, J. Thiem, eds., Springer-Verlag, Heidelberg, ISBN 3-540-67764-X , 2001, 53-61

H.G. Bazin, and R.J. Linhardt,, “Separation and Purification of Carbohydrates”, in Glycoscience: Chemistry and Chemical Biology, B. Fraser-Reid, K. Tatsuta, J. Thiem, eds., Springer-Verlag, Heidelberg, ISBN 3-540-67764-X, 2001, 64-74.



PCT/IB2015/058774: "Adenine derivatives which are useful in the treatment of allergic diseases or other inflammatory conditions", 2015

US 8,802,684: “Adenine derivatives", 2014

US 8,575,340: “Purine derivatives and their pharmaceutical uses”, 2013

US 8,563,717: “Adenine derivatives”, 2013

US 7,816,105: “Method for preparing a fluid absorber “, 2010

US 7,288,640: “Processes for the production of aminoalkyl glucosaminide phosphate and disaccharide immunoeffectors, and intermediates therefore”, 2007 

US 7,232,900: “Processes for the production of aminoalkyl glucosaminide phosphate and disaccharide immunoeffectors, and intermediates therefore”, 2007

U.S 7,226,760: “Method for preparing a fluid absorber”, 2007

US 6,946,148: “Method for absorbing fluid”, 2005

US 6,245,902: “C-glycoside Analogs and methods for their preparation and use”, 2001

US 6,184,196: “Sucrose Based Surfactants and Method Thereof”, 2001

US 6,121,430: “Regiospecific synthesis of glucose based surfactants”, 2000


Professional Experience

1999-2000:           Research Scientist, Grain Processing Corporation (Muscatine, IA)

2000-2001:           Senior Scientist, ApoLogic, Inc. (Cincinnati, OH)

2001-2002:           Research Scientist, University of Iowa (Iowa City, IA)

2002-2005:           Research Scientist, Corixa (Hamilton, MT)

2005-2016:           Investigator, GSK (Hamilton, MT)