The present invention relates to transgene expression systems, related compositions comprising the transgene expression systems, and methods of making and using them. Preferred systems employ an adenovirus transgene expression vector comprising DNA encoding a transgene which codes for a desired product operably linked to expression control sequence, and at least a portion of the adenovirus E3 region and certain portions of the E4 region. The E4 portions comprise the open reading frame sequence known as E40RF3 and at least one other portion of E4. Preferably the E4 portion of the vector (or âE4 cassetteâ) includes E40RF3 and at least one other portion selected from E40RF4, E40RF6/7 and E40RF3/4. The invention has a number of important features including improving persistency of transgene expression in a desired host cell. The transgene expression systems of the present invention are useful for a variety of applications including providing persistent cellular expression of the transgene in vitro and in vivo.
The present invention relates to transgene expression systems, related compositions comprising the transgene expression systems, and methods of making and using them. Preferred systems employ an adenovirus transgene expression vector comprising DNA encoding a transgene which codes for a desired product operably linked to expression control sequence, and at least a portion of the adenovirus E3 region and certain portions of the E4 region. The E4 portions comprise the open reading frame sequence known as E4ORF3 and at least one other portion of E4. Preferably the E4 portion of the vector (or âE4 cassetteâ) includes E4ORF3 and at least one other portion selected from E4ORF4, E4ORF6/7 and E4ORF3/4. The invention has a number of important features including improving persistency of transgene expression in a desired host cell. The transgene expression systems of the present invention are useful for a variety of applications including providing persistent cellular expression of the transgene in vitro and in vivo.
Antibodies Specific For Cystic Fibrosis Transmembrane Conductance Regulator And Uses Therefor
Seng H. Cheng - Bosaton MA John Marshall - Milford MA Richard J. Gregory - Ayer MA Patrick W. Rafter - Natick MA
Assignee:
Genzyme Corporation - Cambridge MA
International Classification:
C07K 1628 C12N 518
US Classification:
5303882
Abstract:
Antibodies for binding epitopes of cystic fibrosis transmembrane conductance regulator (CFTR) and hybridomas which produce such antibodies are described. The antibodies of the present invention can be used in a method for detecting CFTR in a biological sample and/or in a method for purifying CFTR from an impure solution. In addition, the present invention includes a method for detecting CFTR in a biological sample from a nonhuman cystic fibrosis knockout animal wherein the the nonhuman cystic fibrosis knockout animal has been subjected to human CFTR replacement therapy. Another aspect of the present invention is a method for determining the orientation of CFTR in the membrane of a lipid vesicle. Yet another aspect of the invention is a kit for detecting CFTR in a biological sample.
Johanne Kaplan - Sherborn MA Donna Armentano - Belmont MA Richard J. Gregory - Westford MA
Assignee:
Genzyme Corporation - Cambridge MA
International Classification:
C12N 1586 C07J 900
US Classification:
4353201
Abstract:
The present invention relates to transgene expression systems, related pharmaceutical compositions, and methods of making and using them. Preferred systems employ an adenovirus transgene expression vector comprising DNA sequence encoding a transgene which codes for a desired product, expressibly contained within an adenovirus vector containing at least a portion of the E3 region and certain portions of the E4 region. The E4 portions comprise the open reading frame sequence known as E4ORF3 and at least one other portion of E4. Preferably the E4 portion of the vector (or "E4 cassette") includes E4ORF3 and at least one other portion selected from E4ORF4, E4ORF6/7 and E4ORF3/4. The invention has a number of important features including improving persistency of transgene expression in a desired host cell. The transgene expression systems of the present invention are useful for a variety of applications including providing persistent cellular expression of the transgene in vitro and in vivo.
Organ-Specific Targeting Of Cationic Amphiphile / Dna Complexes For Gene Therapy
Ronald K. Scheule - Hopkinton MA Rebecca G. Bagley - Natick MA Simon J. Eastman - Hudson MA Seng H. Cheng - Wellesley MA John Marshall - Hopedale MA David J. Harris - Lexington MA Edward R. Lee - Natick MA Craig S. Siegel - Woburn MA S. Catherine Hubbard - Belmont MA Duane E. Johnson - Encinitas CA Daniel C. Maneval - San Diego CA H. Michael Shepard - Rancho Santa Fe CA Richard J. Gregory - Westford MA
Assignee:
Genzyme Corporation - Framingham MA
International Classification:
A61K 4800 C12N 1588 C12N 1563
US Classification:
514 44
Abstract:
Novel cationic amphiphiles are provided that facilitate transport of biologically active (therapeutic) molecules into cells. The amphiphiles contain lipophilic groups derived from steroids, from mono or dialkylamines, or from alkyl or acyl groups; and cationic groups, protonatable at physiological pH, derived from amines, alkylamines or polyalkylamines. There are provided also therapeutic compositions prepared typically by contacting a dispersion of one or more cationic amphiphiles with the therapeutic molecules. Therapeutic molecules that can be delivered into cells according to the practice of the invention include DNA, RNA, and polypeptides. Representative uses of the therapeutic compositions of the invention include providing gene therapy, and delivery of antisense polynucleotides or biologically active polypeptides to cells. With respect to therapeutic compositions for gene therapy, the DNA is provided typically in the form of a plasmid for complexing with the cationic amphiphile. Novel and highly effective plasmid constructs are also disclosed, including those that are particularly effective at providing gene therapy for clinical conditions complicated by inflammation.
- Paris, FR Kevin Brower - Holliston MA, US Patrick Finn - Franklin MA, US Richard C. Gregory - Framingham MA, US Rao Koduri - Shrewsbury MA, US Feng Liu - San Diego CA, US Natalia Malkova - Needham MA, US Parminder Mankoo - Foster City CA, US Jack R. Pollard - Acton MA, US Huawei Qiu - Westborough MA, US Joachim Theilhaber - Cambridge MA, US Christopher Winter - Swampscott MA, US Marcella Yu - Fremont CA, US
The invention provides an improved pan-TGF-β antibody for treatment of conditions that are mediated by TGF-β, including autoimmune diseases, fibrotic conditions, and cancers. Also provided are methods and uses of the antibody in conjunction with other immunomodulatory agents such as an anti-PD-1 antibody.
- Paris, FR Kevin Brower - Holliston MA, US Patrick Finn - Franklin MA, US Richard C. Gregory - Framingham MA, US Rao Koduri - Shrewsbury MA, US Feng Liu - San Diego CA, US Natalia Malkova - Needham MA, US Parminder Mankoo - Foster City CA, US Jack R. Pollard - Acton MA, US Huawei Qiu - Westborough MA, US Joachim Theilhaber - Cambridge MA, US Christopher Winter - Swampscott MA, US Marcella Yu - Fremont CA, US
The invention provides an improved pan-TGF-β antibody for treatment of conditions that are mediated by TGF-β, including autoimmune diseases, fibrotic conditions, and cancers. Also provided are methods and uses of the antibody in conjunction with other immunomodulatory agents such as an anti-PD-1 antibody.
Compositions And Methods To Treating Hemoglobinopathies
- Boston MA, US David A. WILLIAMS - Dover MA, US Richard GREGORY - Brookline MA, US
Assignee:
THE CHILDREN'S MEDICAL CENTER CORPORATION - Boston MA
International Classification:
C12N 15/113 A61K 35/28 C12N 7/00
Abstract:
Embodiments herein provide specially designed synthetic BCL11A-targeting microRNAs for RNA polymerase II expression, and methods of use to treat hemoglobinopathies such as sickle cell disease or thalassemia by increasing the expression levels of fetal hemoglobin levels.
License Records
Richard E Gregory
License #:
20857 - Active
Category:
Dual Towing Operator(IM)/VSF Employee
Expiration Date:
Jul 15, 2017
Name / Title
Company / Classification
Phones & Addresses
Richard Gregory
B C Packers Ltd Nelson Bros Fisheries Ltd Packing & Crating Service
Po Box 5000 Stn Terminal, Vancouver, BC V6B 8N8 6042772212, 6042778122
Neurological Associates Of St Paul PAHealtheast Neurosurgery Clinic 17 Exchange St W STE 850, Saint Paul, MN 55102 6512323900 (phone), 6512323956 (fax)
Education:
Medical School University of Minnesota Medical School at Minneapolis Graduated: 1968
Procedures:
Craniotomy Spinal Cord Surgery Spinal Fusion Spinal Surgery
Conditions:
Intervertebral Disc Degeneration
Languages:
English
Description:
Dr. Gregory graduated from the University of Minnesota Medical School at Minneapolis in 1968. He works in Saint Paul, MN and specializes in Surgery , Neurological. Dr. Gregory is affiliated with Healtheast St Josephs Hospital.
Institute Of Aesthetic Surgery 400 Celebration Pl STE A320, Kissimmee, FL 34747 4074098000 (phone), 8667607840 (fax)
Education:
Medical School Indiana University School of Medicine Graduated: 1971
Conditions:
Abdominal Hernia Breast Disorders Cholelethiasis or Cholecystitis Malignant Neoplasm of Female Breast
Languages:
English
Description:
Dr. Gregory graduated from the Indiana University School of Medicine in 1971. He works in Kissimmee, FL and specializes in Plastic Surgery. Dr. Gregory is affiliated with Florida Hospital Celebration Health and Florida Hospital Orlando.