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James E. Galen, PhD

Academic Title:

Adjunct Professor

Primary Appointment:

Medicine

Location:

HSF II, S-359

Phone (Primary):

(410) 706-6995

Fax:

(410) 706-6205

Education and Training

University of Virginia, B.A., Biochemistry, 1979

University of Maryland School of Medicine, Ph.D., Microbiology & Immunology, 1991

Biosketch

For over 15 years, Dr. Galen has focused on the construction of attenuated bacterial vaccines and their use as live vectors to deliver foreign antigens to the immune system. His work has had broad applications to the development and pre-clinical testing of a variety of live vaccines against both eukaryotic and prokaryotic pathogens, including the etiological agents for malaria, SARS, plague, anthrax, tetanus, enteric fever, and most recently infections caused by Clostridium difficile.

Dr. Galen has been involved in instrumental research on the development of plasmid-based expression systems for delivery of foreign antigens from both prokaryotic and eukaryotic organisms.

He has invented two novel systems:

  • Antigen transport system for export of antigens out to the surface of attenuated S. Typhi.
  • Plasmid stabilization and selection system that removes the need for plasmid selection using antibiotics and guarantees plasmid retention in vivo after introduction into live vector strains.

Dr. Galen’s work has resulted in multiple patents issued in both the United States and abroad.

Recent efforts have focused on the design and development of novel vaccines and therapeutic treatments against enteric disease caused by Clostridium difficile. On the vaccine side, Dr. Galen has worked on the development of a live oral vaccine designed to elicit toxin neutralizing antibodies against the three known toxins of C. difficile: Toxin A (TcdA), toxin B (TcdB), and binary toxin (CDT). On the therapeutic treatment side, he is collaborating on a unique project to engineer a probiotic strain of yeast called Saccharomyces boulardii to efficiently and stably deliver in situ therapeutically relevant levels of a novel tetravalent neutralizing antibody against CDI enterotoxins TcdA and TcdB, to interrupt recurrent disease.

Research/Clinical Keywords

Attenuated bacterial vaccines, live oral vaccines, malaria, SARS, plague, anthrax, tetanus, enteric fever, enteric disease, plasmid-based expression systems, Clostridium difficile, Acinetobacter baumannii.

Highlighted Publications

Galen JE, Buskirk AD, Tennant SM, Pasetti MF. Live attenuated human salmonella vaccine candidates: tracking the pathogen in natural infection and stimulation of host immunity. EcoSal Plus. In press.

Galen JE, Wang JY, Carrasco JA, Lloyd SA, Mellado-Sanchez G, Diaz-McNair J, Franco O, Buskirk AD, Nataro JP, Pasetti MF. A bivalent typhoid live vector vaccine expressing both chromosome- and plasmid-encoded Yersinia pestis antigens fully protects against murine lethal pulmonary plague infection. Infection and Immunity. 2015; 83(1):161-72.

Galen JE and Curtiss R 3rd. The delicate balance in genetically engineering live vaccines. Vaccine. 2014; 32(35):4376-85.

Wang JY, Harley RH, Galen JE. Novel methods for expression of foreign antigens in live vector vaccines. Hum Vaccin Immunother. 2013; 9(7):1558-64.

Galen JE, Wang JY, Chinchilla M, Vindurampulle C, Vogel JE, Levy H, Blackwelder WC, Pasetti MF, Levine MM. A new generation of stable, non-antibiotic, low copy number plasmids improve immune responses to foreign antigens in Salmonella enterica serovar Typhi live vectors. Infection and Immunity. 2013; 78(1):337-47.

Additional Publication Citations

Research Interests

Grants and Contracts

Patents

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