Kwon Lab

Principal Investigator: Douglas S. Kwon, M.D. Ph.D., Instructor in Medicine
Lab staff: 2 postdoctoral fellows, 1 M.D. Ph.D. student, 2 medical students, 1 technician, 1 study coordinator
Contact: phone (617) 724-7370 / dkwon@partners.org

Currently hiring for the following positions:
Research Technologist - Job Code 2219266 description (doc)
Research Technician - Job Code 2223966 description (doc)
  how to apply
Current News:
Kwon Awarded 2011 Burroughs Wellcome Career Award for Medical Scientists
Burroughs Wellcome Award for Medical Scientists funds technologies to prevent HIV infection in women read more

   
 
 

The focus of the Kwon lab is the application of new technologies to the study of immune responses against HIV at mucosal surfaces.

Mucosal surfaces represent both the primary site of HIV transmission and the largest reservoir of viral replication. Despite this, the immune response to HIV has largely been studied in the peripheral blood, which contains just 2-3% of all lymphocytes- a small minority relative to the 60-90% of the body’s T and B cells that reside at mucosal sites. One of the greatest barriers to a more detailed understanding of these responses is the inherently small amount of material that can be obtained from mucosal sampling. We are therefore employing new technologies, developed in conjunction with our collaborators at the Massachusetts Institute of Technology, to simultaneously capture multiple measures of HIV-specific immune responses using small numbers of cells. Using these methodologies we have begun to map mucosal immune responses in gut associated lymphoid tissue (GALT) and the female reproductive tract at a level of resolution that has not been possible employing standard assays. This work is being performed using the large, well characterized patient cohorts available at the Ragon Institute to better understand resistance to HIV acquisition and spontaneous control of chronic HIV infection.

Dr. Douglas Kwon is a physician scientist at the Ragon Institute of MGH, MIT and Harvard with a clinical practice in the division of Infectious Diseases at Brigham and Women’s Hospital. He received his M.D. Ph.D. degrees from New York University and then underwent Internal Medicine training at the University of California, San Francisco and New York Hospital/Weill Cornell Medical Center. He then completed his training in the combined Massachusetts General Hospital and Brigham and Women’s Hospital Infectious Disease fellowship program.

  3D rendering of immunofluorescent staining of pancreatic islet
 
  Studies of Mucosal Immune Responses Against HIV
 
 
Present Areas of Investigation:
Employing novel technologies to further our understanding of mucosal adaptive immune responses in gut associated lymphoid tissue (GALT) and the female reproductive tract
Determining viral dynamics in mucosal and peripheral compartments in chronic HIV infection
Characterizing the role of immunoregulatory pathways in mucosal T cell responses in chronic HIV infection
Assessing the effects of the microbiome on mucosal immune responses in controlled versus chronic HIV infection

 

Published Works:

1. Geijtenbeek TB, Kwon DS, Torensma R, van Vliet SJ, van Duijnhoven GC, Middel J, Cornelissen IL, Nottet HS, KewalRamani VN, Littman DR, Figdor CG, van Kooyk Y. (2000) DC-SIGN, a dendritic cell-specific HIV-1-binding protein that enhances trans-infection of T cells. Cell. 100(5):587-97.
2. Kwon DS, Greggario G, Bitton N, Hendrickson WA, and Littman DR. (2002) DC-SIGN mediated internalization of HIV is required for trans-enhancement of T cell infection. Immunity. 16(1):135-44.
3. Brockman MA*, Kwon DS*, Tighe DP, Pavlik DF, Addo MM, Kavanagh DG, Walker BD, and Kaufmann DE. (2009) IL-10 acts as a reversible suppressor of T cell function during viremic HIV infection and is upregulated by multiple cell types. Blood. 114(2):7641-8. *equally contributed.
4. Quigley M, Pereyra F, Nilsson B, Porichis F, Fonseca C, Eichbaum Q, Julg B, Jesneck JL, Brosnahan K, Imam S, Russell K, Toth I, Piechocka-Trocha A,Dolfi D, Angelosanto J, Crawford A, Shin H, Kwon DS, Zupkosky J, Francisco L, Freeman GJ, Wherry EJ, Kaufmann DE, Walker BD, Ebert B, and Haining WH. (2010) Integrative genomic analysis of HIV-specific CD8+ T cells reveals that PD-1 inhibits T cell function by upregulating BATF. Nat Med. Accepted.
5. Streeck H*, Kwon DS*, Pyo A, Flanders M, Chevalier M, Law K, Anahtar MN, Julg B, Trocha K, Jolin JS, Lian J, Toth I, Brumme Z, Chang J, Caron T, Rodig SJ, Milner DA, Kaufmann DE, Walker BD, Altfeld M. Epithelial adhesion molecules inhibit HIV-1-specific CD8+ T cell functions. Submitted. *equally contributed.
6. Varadarajan N*, Kwon DS*, Law KM, Ogunniyi A, Anahtar MN, Richter J, Walker BD, and Love JC. Efficient cloning of functional, HIV-specific CD8+ T-cells targeting multiple epitopes enabled by microengraving. Proceedings of the National Academy of Sciences of the United States of America 2012;109:3885-90. * equally contributed.
7. Kwon DS, Angin M, Hongo T, Law K, Streeck H, Pavlik DP, Tighe DP, Addo MA, Walker BD, Kaufmann DE. The role of CD4+ CD25+ regulatory T cells in the control of IL-10 mediated T cell impairment in chronic HIV infection. Manuscript in preparation.

 

  Kwon Lab Members