Worcester Office 55 Lake Ave N, Worcester, MA 01655 5083341000 (Phone), 5088566902 (Fax)
Certifications:
Internal Medicine, 1971
Awards:
Healthgrades Honor Roll
Languages:
English
Hospitals:
Worcester Office 55 Lake Ave N, Worcester, MA 01655
UMass Memorial Medical Center - University Campus 55 Lake Avenue North, Worcester, MA 01655
Education:
Medical School Tufts University Graduated: 1964 Medical School SUNY Syracuse Hosp Graduated: 1964 Medical School Boston Va Hosp Graduated: 1964 Medical School New York Hosp Graduated: 1964 Medical School Cornell and The New York Hospital Graduated: 1964 Medical School Ntnl Institute Of Health MD Graduated: 1964
Dr. Francis Ennis, Greenwich CT - MD (Doctor of Medicine)
Medical School Duke University School of Medicine Graduated: 1999
Procedures:
Hip Replacement Hip/Femur Fractures and Dislocations Knee Replacement Arthrocentesis Knee Arthroscopy Lower Leg/Ankle Fractures and Dislocations Occupational Therapy Evaluation
Conditions:
Osteoarthritis Fractures, Dislocations, Derangement, and Sprains Internal Derangement of Knee Internal Derangement of Knee Cartilage Internal Derangement of Knee Ligaments
Languages:
English Spanish
Description:
Dr. Ennis graduated from the Duke University School of Medicine in 1999. She works in Greenwich, CT and specializes in Orthopaedic Surgery. Dr. Ennis is affiliated with Greenwich Hospital.
University of Massachusetts Medical Center - Worcester MA
International Classification:
A61K 4900
US Classification:
435 724, 424 92, 435 6
Abstract:
The present invention relates to an in vitro method for determining the ability of a vaccine composition which comprises one or more antigens or a nucleic acid molecule which encodes one or more antigens to stimulate a T cell response. In one embodiment, the method comprises the steps of: (1) contacting antigen presenting cells in culture with a vaccine composition selected from among the group of vaccine compositions, thereby, if one or more of the antigens or nucleic acid molecules can be taken up and processed by the antigen presenting cells, producing one or more processed antigens; (2) contacting the antigen presenting cells with T cells under conditions sufficient for the T cells to respond to one or more of the processed antigens; (3) determining whether the T cells respond to one or more of the processed antigens; whereby if the T cells respond to one or more of the processed antigens, then the vaccine composition stimulates a T cell response; and (4) repeating steps (1), (2) and (3) with each vaccine composition in the group, thereby identifying vaccine compositions which stimulate a T cell response; and, if one or more of the vaccine compositions stimulates a T cell response, (5) selecting at least one vaccine composition which stimulates a T cell response for assessment in one or more animals and/or human subjects.
University of Massachusetts Medical Center - Worcester MA
International Classification:
C12N015/00
US Classification:
435 724, 424 92, 4241991, 4242001, 435 6
Abstract:
The present invention relates to an in vitro method for determining the ability of a vaccine composition which comprises one or more antigens or a nucleic acid molecule which encodes one or more antigens to stimulate a T cell response. In one embodiment, the method comprises the steps of: (1) contacting antigen presenting cells in culture with a vaccine composition selected from among the group of vaccine compositions, thereby, if one or more of the antigens or nucleic acid molecules can be taken up and processed by the antigen presenting cells, producing one or more processed antigens; (2) contacting the antigen presenting cells with T cells under conditions sufficient for the T cells to respond to one or more of the processed antigens; (3) determining whether the T cells respond to one or more of the processed antigens; whereby if the T cells respond to one or more of the processed antigens, then the vaccine composition stimulates a T cell response; and (4) repeating steps (1), (2) and (3) with each vaccine composition in the group, thereby identifying vaccine compositions which stimulate a T cell response; and, if one or more of the vaccine compositions stimulates a T cell response, (5) selecting at least one vaccine composition which stimulates a T cell response for assessment in one or more animals and/or human subjects.
Identification Of Gene Sequences And Proteins Involved In Vaccinia Virus Dominant T Cell Epitopes
The present invention relates to the identification of gene sequences and proteins involved in vaccinia virus dominant T cell epitopes. Two vaccinia virus CD8 T cell epitopes restricted by the most common human MHC class I allele, HLA-A0201 have been identified. Both epitopes are highly conserved in vaccinia and variola viruses. The induction of the T cell responses following primary vaccination is demonstrated by the kinetics of epitope specific CD8 T cells in 3 HLA-A0201 individuals. This information will be useful for the design and analyses of the immunogenicity of experimental vaccinia vaccines, and for basic studies of human T cell memory.
University of Massachusetts Medical Center - Worcester MA
International Classification:
A61K 39/00 G01N 33/53
US Classification:
435 724, 424 92, 4241841
Abstract:
The present invention relates to an in vitro method for determining the ability of a vaccine composition which comprises one or more antigens or a nucleic acid molecule which encodes one or more antigens to stimulate a T cell response. In one embodiment, the method comprises the steps of: (1) contacting antigen presenting cells in culture with a vaccine composition selected from among the group of vaccine compositions, thereby, if one or more of the antigens or nucleic acid molecules can be taken up and processed by the antigen presenting cells, producing one or more processed antigens; (2) contacting the antigen presenting cells with T cells under conditions sufficient for the T cells to respond to one or more of the processed antigens; (3) determining whether the T cells respond to one or more of the processed antigens; whereby if the T cells respond to one or more of the processed antigens, then the vaccine composition stimulates a T cell response; and (4) repeating steps (1), (2) and (3) with each vaccine composition in the group, thereby identifying vaccine compositions which stimulate a T cell response; and, if one or more of the vaccine compositions stimulates a T cell response, (5) selecting at least one vaccine composition which stimulates a T cell response for assessment in one or more animals and/or human subjects.
Identification Of Gene Sequences And Proteins Involved In Vaccinia Virus Dominant T Cell Epitopes
The present invention relates to the identification of gene sequences and proteins involved in vaccinia virus dominant T cell epitopes. Two vaccinia virus CD8 T cell epitopes restricted by the most common human MHC class I allele, HLA-A0201 have been identified. Both epitopes are highly conserved in vaccinia and variola viruses. The induction of the T cell responses following primary vaccination is demonstrated by the kinetics of epitope specific CD8 T cells in 3 HLA-A0201 individuals. This information will be useful for the design and analyses of the immunogenicity of experimental vaccinia vaccines, and for basic studies of human T cell memory.
Identification Of Gene Sequences And Proteins Involved In Vaccinia Virus Dominant T Cell Epitopes
Masanori Terajima - Holden MA, US John Cruz - Shrewbury MA, US Francis A. Ennis - Shrewsbury MA, US
Assignee:
The University of Massachusetts - Boston MA
International Classification:
A61K 38/08 A61K 39/285
US Classification:
530328, 4242321
Abstract:
The present invention relates to the identification of gene sequences and proteins involved in vaccinia virus dominant T cell epitopes. Three vaccinia virus CD8 T cell epitopes restricted by the most common human M. C. class I allele, HLA-A0201, were identified. Each of these epitopes is highly conserved in vaccinia and variola viruses. In addition, the induction of the T cell responses following primary vaccination with two of these epitopes is demonstrated by the kinetics of epitope specific CD8 T cells in 3 HLA-A0201 individuals. Two vaccinia virus CD8 T cell epitopes restricted by another common human M. C. class I allele, HLA-B7, also were identified. Both epitopes are highly conserved in vaccinia and variola viruses. This information will be useful for the design and analysis of the immunogenicity of experimental vaccinia vaccines, and for basic studies of human T cell memory.
University of Massachusetts Medical Center - Worcester MA
International Classification:
C12Q 1/02
US Classification:
435 29
Abstract:
The present invention relates to an in vitro method for determining the ability of a vaccine composition which comprises one or more antigens or a nucleic acid molecule which encodes one or more antigens to stimulate a T cell response. In one embodiment, the method comprises the steps of: (1) contacting antigen presenting cells in culture with a vaccine composition selected from among the group of vaccine compositions, thereby, if one or more of the antigens or nucleic acid molecules can be taken up and processed by the antigen presenting cells, producing one or more processed antigens; (2) contacting the antigen presenting cells with T cells under conditions sufficient for the T cells to respond to one or more of the processed antigens; (3) determining whether the T cells respond to one or more of the processed antigens; whereby if the T cells respond to one or more of the processed antigens, then the vaccine composition stimulates a T cell response; and (4) repeating steps (1), (2) and (3) with each vaccine composition in the group, thereby identifying vaccine compositions which stimulate a T cell response; and, if one or more of the vaccine compositions stimulates a T cell response, (5) selecting at least one vaccine composition which stimulates a T cell response for assessment in one or more animals and/or human subjects.
University of Massachusetts Medical Center - Worcester MA
International Classification:
A61K 3912 A61K 39145 A61K 3900 A61K 3938
US Classification:
4242061
Abstract:
This disclosure relates to methods and compositions for stimulating in an individual an influenza A virus protective response which is subtype cross-protective. Influenza A virus NS1 protein, or a T cell epitope thereof, is administered to the individual in an amount sufficient to stimulate the virus protective response.
Name / Title
Company / Classification
Phones & Addresses
Francis A. Ennis Medical Doctor
ORTHOPAEDIC & NEUROSURGERY SPECIALISTS, PC Medical Doctor's Office · Orthopedic & Neurosurgery Physicians' Office · Neurosurgeon · Spine Doctor · Emergency Medicine · Orthopedics · Family Doctor · Internist
6 Greenwich Office Park, Greenwich, CT 06831 6 Greenwich Office Park Vly Dr, Greenwich, CT 06831 2038691145, 2038692170
Resumes
Professor Of Medicine And Molecular Genetics And Microbiology