Alessandra Pernis, MD

Education

MD, College of Physicians & Surgeons, Columbia University, New York 1986

Internship

Presbyterian Hospital, Internal Medicine, New York 1986-1987

Residency

Presbyterian Hospital, Internal Medicine, New York 1987-1989

Fellowship

Allergy/Immunology - Presbyterian Hospital, Internal Medicine, New York 1991-1995

Certification

Internal Medicine

Selected Publications

Gupta S., M. Jiang, A. Anthony, and A. Pernis (1999) Lineage-specific modulation of IL-4 signaling by IRF-4. Journal of Experimental Medicine, 190; 1837-1848

Fanzo, J.C., C.M. Hu., S.Y. Jang and A. B. Pernis (2003) Regulation of Lymphocyte Apoptosis by Interferon Regulatory Factor 4 (IRF-4). Journal of Experimental Medicine, 197; 303-314

Gupta S., J. C. Fanzo, C. Hu, D. Cox, S.Y. Jang, A.E. Lee, S. Greenberg and A. B. Pernis (2003) T cell receptor engagement leads to the recruitment of IBP, a novel guanine nucleotide exchange factor, to the immunological synapse. Journal of Biological Chemistry, 278; 43541-9

Fanzo J. C., W. Yang, S. Jang, S. Gupta, Q. Chen, A. Siddiq, S. Greenberg and A. B. Pernis (2006) Lack of IBP leads to the spontaneous development of systemic autoimmunity. Journal of Clinical Investigation, 116; 703-14

A. B. Pernis (2007) Estrogen and CD4+ T cells. Curr. Op. Rheum. 19; 414-420

Chen Q., W. Yang, S. Gupta, P. Biswas, P. Smith, G. Bhagat, and A. B. Pernis (2008) IBP inhibits IL-17 and IL-21 production by controlling IRF-4 function. Immunity, 29:899-911

Chen Q., S. Gupta and A. B. Pernis (2009) Regulation of TLR4-mediated signaling by IBP/Def6, a novel activator of Rho GTPases. Journal of Leukocyte Biology, 85; 539-43

A. B. Pernis (2009) Th17 cells in Rheumatoid Arthritis and Systemic Lupus Erythematosus. Journal of Internal Medicine, 265; 644-52

Biswas, P., Bhagat G., and A. B. Pernis (2010) IRF4 and its regulators: evolving insights into the pathogenesis of inflammatory arthritis? Immunological Reviews; 233; 79-96

Partha S. Biswas, Sanjay Gupta, Emily Chang, Li Song, James K. Liao, Govind Bhagat, and A. B. Pernis (2010) Phosphorylation of IRF4 by ROCK2 regulates IL-17 and IL-21 production and the development of autoimmunity in mice. Journal of Clinical Investigation; In Press

For more publications, please see the PubMed listing.

Research Description

Molecular Mechanisms of T Cell Dysfunction in Autoimmunity

Effective immune responses require the appropriate activation and differentiation of peripheral CD4+ T cells. These processes need to be followed by the timely elimination of the responding T cells in order to restore T cell homeostasis. Defects in the appropriate regulation of T cell activation, expansion, and survival underlie the pathogenesis of many autoimmune disorders including Systemic Lupus Erythematosus (SLE) and Rheumatoid Arthritis (RA). The molecular machinery employed by T cells to properly control these processes and prevent the onset of autoimmunity has not been fully elucidated.

Our laboratory has had a longstanding interest in understanding the molecular mechanisms employed by lymphocytes to accurately respond to the signals that guide them along specific pathways. Our initial work focused on IRF4, a transcription factor that is highly expressed in the immune system. Absence of IRF4 leads to profound defects in the function and homeostasis of mature T and B cells. Our early studies demonstrated that IRF4 is upregulated in response to lymphocyte activation and that it controls crucial processes like cytokine production and apoptosis supporting the idea that IRF4 plays a central role in lymphocyte biology. This notion has been further corroborated by recent studies by our group as well as others, which have demonstrated that IRF4 is a critical regulator of TH-17 differentiation and that it is absolutely required for the production of IL-17 and IL-21, two cytokines that have recently been implicated in the pathogenesis of multiple autoimmune disorders including SLE and RA.

During studies aimed at isolating proteins interacting with IRF4, we cloned a novel protein that we termed IBP (IRF4 Binding Protein). The current official name of the gene is Def6, a terminology that we have now adopted. Def6 exhibits significant homology to only one other protein, SWAP-70, a novel activator of Rho GTPases. Rho GTPases (which include Rac, Cdc42, and RhoA) are molecular switches that regulate both cytoskeletal dynamics and cell signaling. We have previously shown that, upon TCR engagement, Def6 is recruited to the immunological synapse and activates Rac and Cdc42. Def6 is also present in the nucleus where it interacts with IRF4. Def6 exerts an important immunoregulatory role in vivo as demonstrated by the finding that Def6-deficient mice can spontaneously develop either a lupus-like syndrome or, when crossed with mice carrying a specific TCR transgene, RA-like arthritis and vasculitis. The pathophysiology observed in the absence of Def6 is accompanied by three major abnormalities within the peripheral CD4+ T cell compartment: hyperresponsiveness to low-levels of stimulation, inappropriate acquisition of TH effector functions marked by deregulated production of IL-17 and IL-21, and impaired elimination of activated CD4+ T cells. At a molecular level, Def6-deficient T cells exhibit defective Rac activation as well as enhanced binding of IRF4 to the IL-17 and IL-21 promoters. Interestingly, we have recently found that Def6 employs a dual mechanism to control the function of IRF4. It physically sequesters IRF4 and it also prevents IRF4 phosphorylation by the serine-threonine kinase, ROCK2. Taken all together, these findings have led us to propose that Def6 is a novel regulator of T cell activation and homeostasis that is critical for the prevention of autoimmune pathophysiology.

We are presently studying the function of Def6 to gain a mechanistic understanding of the signaling pathways that control both physiologic and pathologic T cell responses. The long-term goals of the laboratory are to employ both murine models and translational approaches to further delineate the molecular networks responsible for lymphocyte dysfunction in autoimmune diseases. A detailed understanding of these mechanisms will enable us to gain a better understanding of the pathogenesis of autoimmune diseases like SLE and RA and provide important information for the development of novel therapeutic regimens for the treatment of SLE and RA.

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Contact Information

Office Locations

Caspary Research Building
541 East 71st Street
New York, NY 10021

Tel: 212.606.1612

email: PernisA@HSS.EDU

Mailing Address

Hospital for Special Surgery
535 East 70th Street
New York, New York 10021