Projects per year
Personal profile
Area of Expertise
Dr. Mathew is one of the pioneers who identified, cloned, and characterized several receptors expressed on human NK cells including 2B4 (CD244, SLAMF4), CS1 (CD319, SLAMF7) and LLT1 (CLEC-2D). Research in his laboratory has identified their ligands, elucidated the signaling pathways, and also determined the transcriptional regulation of these genes in health and disease conditions. Dr. Mathew has shown that anti-CS1 antibody activates NK cell cytotoxicity against various cancer cells. The FDA has approved a humanized anti-CS1 mAb, Empliciti, as a breakthrough drug for multiple myeloma treatment. Thus, his research has led to the development of novel NK cell based immunotherapy for cancer. Current focus is identification of markers for cancer stem cells (CSCs) and targeting CSCs to NK cell mediated killing.
Education/Academic qualification
BS in Physics, University of Kerala
MS in Biochemistry, University of Poona
PhD in Biochemistry, University of Poona
Fingerprint
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Projects
- 17 Finished
-
Emerging role of tumor-derived
Chaudhary, P. (PI), Mathew, P. (CoI) & Nandy, R. (CoI)
NCI: National Cancer Institute
1/08/23 → 31/07/25
Project: Research
-
Exosomal-Annexin A2 Promotes Metastasis in Triple-negative Breast Cancer
Chaudhary, P. (PI) & Mathew, P. (CoI)
1/06/17 → 30/11/18
Project: Research
-
Molecular Characterization of NKp44 Ligand on Astrocytes
Mathew, P. (PI)
National Institute of Neurological Disorders and Stroke
1/02/17 → 31/01/20
Project: Research
-
Molecular Characterization of NKp44 Ligand on Astrocytes
Mathew, P. (PI)
1/02/17 → 31/01/20
Project: Research
-
Molecular Characterization of NKp44 Ligand on Astrocytes
Mathew, P. (PI) & Mathew, S. (CoI)
NINDS: Neurological Disorders & Stroke
1/02/17 → 31/01/20
Project: Research
-
2B4, a new member of the immunoglobulin gene superfamily, is expressed on murine dendritic epidermal T cells and plays a functional role in their killing of skin tumors
Schuhmachers, G., Ariizumi, K., Mathew, P. A., Bennett, M., Kumar, V. & Takashima, A., 1995, In: Journal of Investigative Dermatology. 105, 4, p. 592-596 5 p.Research output: Contribution to journal › Article › peer-review
-
Regulation of IFN-γ production following 2B4 activation in human NK cells
Johnson, L. A., Goldfarb, R. H. & Mathew, P. A., 2000, In: In Vivo. 14, 5, p. 625-629 5 p.Research output: Contribution to journal › Article › peer-review
-
Blocking LLT1 (CLEC2D, OCIL)-NKRP1A (CD161) interaction enhances natural killer cell mediated lysis of triple-negative breast cancer cells
Marrufo, A. M., Mathew, S., Chaudhary, P., Malaer, J., Vishwanatha, J. & Mathew, P., 2018, In: American Journal of Cancer Research. 8, 6, p. 1050-1063 14 p.Research output: Contribution to journal › Article › peer-review
-
Prospective Molecular Targets for Natural Killer Cell Immunotherapy against Glioblastoma Multiforme
Cooksey, L. C., Friesen, D. C., Mangan, E. D. & Mathew, P. A., Sep 2024, In: Cells. 13, 18, 1567.Research output: Contribution to journal › Review article › peer-review
-
Altered expression of signalling lymphocyte activation molecule (SLAM) family receptors CS1 (CD319) and 2B4 (CD244) in patients with systemic lupus erythematosus
Kim, J. R., Mathew, S. O., Patel, R. K., Pertusi, R. M. & Mathew, P. A., Jun 2010, In: Clinical and Experimental Immunology. 160, 3, p. 348-358 11 p.Research output: Contribution to journal › Article › peer-review