Sergio A. Jimenez, MD

Professor
Co-Director, Jefferson Institute of Molecular Medicine
Director, Division of Connective Tissue Diseases
Director, The Scleroderma Center
Professor of Biochemistry and Molecular Biology (Secondary Appointment)

Sergio Jimenez

Contact

233 South Tenth Street
Bluemle Life Sciences Building, Room 509
Philadelphia, PA 19107

Email Sergio A. Jimenez

215-503-5042
215-923-4649 fax

Sergio A. Jimenez, MD

Professor
Co-Director, Jefferson Institute of Molecular Medicine
Director, Division of Connective Tissue Diseases
Director, The Scleroderma Center
Professor of Biochemistry and Molecular Biology (Secondary Appointment)

Education

Medical School

MD Magna Cum Laude, National University of San Marcos, School of Medicine, Lima, Peru - 1964
MS Honoris Cause, University of Pennsylvania, Philadelphia, PA - 1984

Residency

Mayo Medical Center, Rochester MN
Philadelphia General Hospital

Fellowship

Hospital of University of Pennsylvania (HUP)

Most Recent Peer-Reviewed Publications

Board Certification

Internal Medicine

Hospital Appointment

Thomas Jefferson University Hospital

Expertise & Research Interests

Dr. Jimenez's research activities have focused on the application of biochemical, molecular biological, and genetic approaches to the study of Scleroderma, fibrotic disorders, and Osteoarthritis. His major contributions have been the identification of mechanisms of cytokine regulation of collagen gene expression and of the interactions between inflammatory cells and fibroblasts, the study of the role of transforming growth factor in tissue fibrosis, the identification of cartilage gene mutations in Osteoarthritis, and the demonstration of microchimeric fetal cells in affected tissues from Scleroderma patients supporting the hypothesis that fetal cell transfer across the placenta during pregnancy may cause the disease.

The goals of Dr. Jimenez's current research interests are to unravel the early events responsible for the initiation of the fibrotic process in systemic sclerosis, focusing on the role of two novel proteins, allograft inflammatory factor-1 and caveolin-1, and to study the role of macrophages as initiators of this process through their interactions with environmental or infectious agents.