601 Jones Ferry Rd, Carrboro, NC 27510 • (919)9675969
601 Jones Ferry Rd #HY607, Carrboro, NC 27510 • (919)8970476
3202 N Country Club Rd #72, Tucson, AZ 85716
2201 Cedar Grove Dr, Durham, NC 27703 • (919)4052585 • (919)9675969
Work
Company:
Argos therapeutics
Jan 2008
Position:
Director, manufacturing & process development
Education
Degree:
MS
School / High School:
North Carolina State University
1996 to 1999
Specialities:
Biological Engineering
Skills
Biotechnology • Biopharmaceuticals • Gmp • Technology Transfer • U.s. Food and Drug Administration • Process Simulation • Standard Operating Procedure • Validation
Industries
Biotechnology
Resumes
Vice President, Process And Analytical Development
Argos Therapeutics since Jan 2008
Director, Manufacturing & Process Development
Argos Therapeutics Apr 2007 - Jan 2008
Director, Process Development and Project Management, Oncology
Argos Therapeutics Aug 2002 - Apr 2007
Process Development (Director, Sr. Manager, Manager, Supervisor, Sr. Engineer)
Argos Therapeutics Feb 2002 - Jul 2002
Production Engineer
Biolex Jan 1999 - Feb 2002
Sr. Process Design Engineer / Process Design Engineer
Education:
North Carolina State University 1996 - 1999
MS, Biological Engineering
University of Arizona 1989 - 1994
BS, Chemical Engineering
Skills:
Biotechnology Biopharmaceuticals Gmp Technology Transfer U.s. Food and Drug Administration Process Simulation Standard Operating Procedure Validation
Tamara Monesmith - Durham NC, US Irina Tcherepanova - Rougemont NC, US Lois Dinterman - Kearneysville WV, US
Assignee:
Argos Therapeutics, Inc. - Durham NC
International Classification:
C12N 5/07
US Classification:
435325
Abstract:
Methods are provided for the production of dendritic cells from monocytes that have been incubated at a temperature of 1 C. -34 C. for a period of approximately 6 to 96 hours from the time they are isolated from a subject. After the incubation period, the monocytes can then be induced to differentiate into dendritic cells. Mature dendritic cells made by the methods of the invention have increased levels of one or more of CD80, CD83, CD86, MHC class I molecules, or MHC class II molecules as compared to mature dendritic cells prepared from monocytes that have not been held at 1 C. -34 C. for at least 6 hours from the time they were isolated from a subject. Dendritic cells made by the methods of the invention are useful for the preparation of vaccines and for the stimulation of T cells.
Tamara Monesmith - Durham NC, US Irina Tcherepanova - Rougemont NC, US Lois Dinterman - Kearneysville WV, US
International Classification:
A61K 39/00 C12N 5/08 A61P 31/00
US Classification:
4241841, 435372
Abstract:
Methods are provided for the production of dendritic cells from monocytes that have been incubated at a temperature of 1 C.-34 C. for a period of approximately 6 to 96 hours from the time they are isolated from a subject. After the incubation period, the monocytes can then be induced to differentiate into dendritic cells. Mature dendritic cells made by the methods of the invention have increased levels of one or more of CD80, CD83, CD86, MHC class I molecules, or MHC class II molecules as compared to mature dendritic cells prepared from monocytes that have not been held at 1 C.-34 C. for at least 6 hours from the time they were isolated from a subject. Dendritic cells made by the methods of the invention are useful for the preparation of vaccines and for the stimulation of T cells.
Tamara Monesmith - Durham NC, US Irina Tcherepanova - Rougemont NC, US Lois Dinterman - Kearneysville WV, US
International Classification:
C12N 5/0784
US Classification:
435372, 435377
Abstract:
Methods are provided for the production of dendritic cells from monocytes that have been incubated at a temperature of 1 C.-34 C. for a period of approximately 6 to 96 hours from the time they are isolated from a subject. After the incubation period, the monocytes can then be induced to differentiate into dendritic cells. Mature dendritic cells made by the methods of the invention have increased levels of one or more of CD80, CD83, CD86, MHC class I molecules, or MHC class II molecules as compared to mature dendritic cells prepared from monocytes that have not been held at 1 C.-34 C. for at least 6 hours from the time they were isolated from a subject. Dendritic cells made by the methods of the invention are useful for the preparation of vaccines and for the stimulation of T cells.
- Durham NC, US Mark DEBENEDETTE - Durham NC, US Joseph HORVATINOVICH - Raleigh NC, US Alex DUSEK - Chapel Hill NC, US Tamara MONESMITH - Cambridge MA, US
International Classification:
A61K 35/15 A61K 39/00 G01N 33/50
Abstract:
This invention provides methods of evaluating immune system parameters to identify and treat patients who are likely to experience more favorable treatment outcomes. This invention also provides methods for treating a human patient with a dendritic cell therapy by obtaining at least one value or measurement of the level and/or amount of a particular type of treatment indicator in the patient, confirming that said value or measurement exceeds or is less than the treatment threshold value for that value or measurement, and administering said dendritic cell therapy to the patient.
- Durham NC, US Tamara Monesmith - Durham NC, US Irina Tcherepanova - Rougemont NC, US Lois Dinterman - Oxford NC, US
International Classification:
C12N 5/0784
Abstract:
Methods are provided for the production of dendritic cells from monocytes that have been incubated at a temperature of 1 C.-34 C. for a period of approximately 6 to 96 hours from the time they are isolated from a subject. After the incubation period, the monocytes can then be induced to differentiate into dendritic cells. Mature dendritic cells made by the methods of the invention have increased levels of one or more of CD80, CD83, CD86, MHC class I molecules, or MHC class II molecules as compared to mature dendritic cells prepared from monocytes that have not been held at 1 C.-34 C. for at least 6 hours from the time they were isolated from a subject. Dendritic cells made by the methods of the invention are useful for the preparation of vaccines and for the stimulation of T cells.
- Durham NC, US Tamara Monesmith - Durham NC, US Irina Tcherepanova - Rougemont NC, US Lois Dinterman - Oxford NC, US
International Classification:
C12N 5/0784
US Classification:
435347, 435377, 435372
Abstract:
Methods are provided for the production of dendritic cells from monocytes that have been incubated at a temperature of 1 C.-34 C. for a period of approximately 6 to 96 hours from the time they are isolated from a subject. After the incubation period, the monocytes can then be induced to differentiate into dendritic cells. Mature dendritic cells made by the methods of the invention have increased levels of one or more of CD80, CD83, CD86, MHC class I molecules, or MHC class II molecules as compared to mature dendritic cells prepared from monocytes that have not been held at 1 C.-34 C. for at least 6 hours from the time they were isolated from a subject. Dendritic cells made by the methods of the invention are useful for the preparation of vaccines and for the stimulation of T cells.
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