Professor, Physiology and Immunology
Xiaolei.Tang@liu.edu
Education:
Ph.D., University of Arizona
M.Sc., Shanghai Medical College, Fudan University
M.D., Wannan Medical College
Specialties:
Regulatory T cells and adult stem cells
Dr. Tang holds an M.D. degree from Wannan Medical College, Wuhu, China, a Master's in Immunology from Shanghai Medical College, Fudan University, and a Ph.D. in Microbiology and Immunology from the University of Arizona.
Following medical school, Dr. Tang practiced medicine for two years as a radiologist at Huangshan City People's Hospital, Huangshan, Anhui Province, China. He then received a Master's degree in immunology in the Department of Immunology at Shanghai Medical College, Fudan University, where he continued as a lecturer for four years following graduation. Afterward, Dr. Tang obtained his Ph.D. in microbiology and immunology at the University of Arizona. He was then trained as a postdoctoral fellow in Dr. Vipin Kumar's research laboratory at Torrey Pines Institute for Molecular Studies in San Diego, California, where he remained for four years. Subsequently, he accepted a Research Fellow position in the laboratory of Dr. Harvey Cantor at the Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts. After 3.5 years at Harvard, Dr. Tang was a faculty member at the University of Texas, El Paso, Texas, for three years. Later, he decided to move to the Division of Regenerative Medicine, Department of Medicine, School of Medicine at Loma Linda University in California, first as an Assistant Research Professor and then as an Associate Research Professor for a total of 6 years. Dr. Tang joined the Long Island University College of Veterinary Medicine in September 2019.
Dr. Tang’s research interests focus on regulatory T cells and adult stem cells. His research has been funded by NIH, Department of Defense, National Multiple Sclerosis Society, the American Association of Immunologists, and industry. Dr. Tang is an editor of multiple scientific journals and a Morris Animal Health Advisory Council member. He often serves as an ad hoc member of grant review panels for the National Institute of Health (NIH), Department of Defense Congressional Directed Medical Research Programs (CDMRP), and Morris Animal Foundation. He is also an ad hoc grant application peer reviewer for UK Research and Innovation (UKRI).
One of Dr. Tang’s primary research interests is CD8+ Treg. He was the first to clone CD8alphaalpha+ Treg, which target pathogenic, autoreactive immune cells and are restricted by a nonclassical major histocompatibility complex (MHC) Ib molecule, Qa-1, whose human homologue is HLA-E. His laboratory also discovered that Qa-1-restricted CD8+ Treg can target tissue-specific antigens (e.g., myelin in the CNS) to suppress autoimmune diseases. In addition, his laboratory further developed technologies to uncover tissue-specific, regulatory Qa-1/HLA-E epitopes. The above discoveries and new technologies open the possibility that defining HLA-E epitopes in tissue-specific proteins can be harnessed to mobilize HLA-E-restricted, tissue-specific CD8+ Treg for treating autoimmune diseases, such as multiple sclerosis, type 1 diabetes, and others. This novel therapeutic concept, if successful, has several advantages. First, it does not depend on insight into the autoantigens recognized by pathogenic, autoreactive immune cells, which have been targeted for treating autoimmune diseases for many years but remain incompletely understood. Second, disease suppression does not compromise immune defense mechanisms, hence circumventing potential side effects associated with current therapies, such as infections and malignancies. Dr. Tang is currently collaborating with industry to commercialize this new therapeutic.
In addition to CD8+ Treg, Dr. Tang’s laboratory discovered that dendritic cells, engineered to de novo synthesize high concentrations of active vitamin D, can effectively stimulate CD4+ Treg and suppress immune-mediated diseases. A notable advantage of this technology is that it does not significantly raise blood calcium levels (hypercalcemia), which has been the roadblock in elevating vitamin D as a therapeutic agent for many diseases. His laboratory further investigates the potential to harness this finding to develop novel technologies to mobilize tissue- and antigen-specific CD4+ Treg for treating various immune-mediated diseases.
Dr. Tang’s laboratory has discovered that de novo synthesis of locally high concentrations of active vitamin D can promote the differentiation of Lgr5+ intestinal stem cells without compromising their stemness. His laboratory also investigates how the de novo synthesized locally high concentrations of active vitamin D may affect reserved intestinal stem cells. Moreover, his laboratory leverages this discovery to develop novel regenerative therapies for human and animal diseases.
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LIU is an EO/AA/ADA educator and employer and does not discriminate on the basis of race, color, national and ethnic origin, or religion, sex, sexual orientation, gender identity or expression, age, physical or mental disability, marital or veteran status in administration of its educational policies, admissions policies, scholarship and loan programs, and athletic and other school-administered programs. LIU admits students of any race, color, national, and ethnic origin to all the rights, privileges, programs and activities generally accorded or made available to its students.