Jessica Carlson

Jessica Carlson, M.S.

  • Position:
    Graduate Student - Masters

    University of California, Los Angeles (Los Angeles, CA)

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  • Degrees:
     
    M.S., Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles (Los Angeles, CA)
     
    M.S., Chemistry, California Institute of Technology (Pasadena, CA)
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  • Clinical Training:
     
    Internship, Inpatient ID consult service, Harbor-UCLA Medical Center
     
    Fellowship, Infectious Diseases, UCLA Medical Center and David Geffen School of Medicine, Clinical Microbiology Laboratory, Hospital Epidemiology program
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  • Past Advisors:
     
    Otoniel Martinez-Maza (as Graduate Student - Masters)
     
    Frederick A. Eiserling (as Graduate Student - Masters)
     
    Owen N. Witte (as Graduate Student - Masters)
     
    Ahmed H. Zewail (as Graduate Student - Masters)
     
    Robert Grubbs (as Graduate Student - Masters)
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  • Research:
    Immune Dysfunction and Cancer; AIDS Pathogenesis.

    Most of the work and research is to better understand the role of immune dysfunction in the genesis and growth of in human cancer. Solely focusing on better defining the role of HIV infection-associated immune dysfunction in the development and growth of AIDS-associated cancers. Our research work is directed at determining how immune system factors associated with B cell hyperactivation. Non-Hodgkin's B cell lymphoma (NHL) is a common cancer in HIV infection. Many NHL are thought to result from errors in class switch recombination and/or somatic hypermutation, processes that occur in germinal center B cells, and require the activity of activation induced cytidine deaminase (AID). Since NHL is a common cancer in HIV infection, and expression of AID could contribute to the development of NHL, we hypothesized that AID expression would be elevated in those who went on to develop AIDS-associated NHL (AIDS-NHL). AID mRNA levels were measured by TaqMan RT-PCR in peripheral blood mononuclear cells, obtained prior to AIDS-NHL diagnosis, from 16 HIV-infected subjects who developed AIDS-NHL, and from control subjects (AIDS but no NHL, and HIV-negative subjects). PBMC AID expression was markedly elevated in those who developed AIDS-NHL, when compared to AIDS and HIV-negative controls. Additionally, AID expression was seen to differ depending on NHL subtype, with the highest levels of expression seen in those who developed Burkitt's lymphoma.

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  • Other Experience:

    2004 Training and research in infectious diseases at UCLA Medical Center

    2004 NASA Jet Propulsion Laboratory

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  • Honors:

    2006-present Phi Beta Kappa

    2006-2007 Outstanding Achievement scholar

    2006-2007 AAI-Invitrogen Trainee Achievement Award

    2006-2007 Departmental Scholar Program (DSP)

    2005-2007 National Research Service Award (NIH F32)

Life Sciences
Health Sciences
Physical Sciences
Communities:

Jessica Carlson's Genealogy

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Jessica Carlson's Posters and Presentations (2)

  • Immune Dysfunction and AIDs Pathogensis (presentation)

    Jessica C.

    ASM and AAI, Annual meeting at Orange County Convention Center (Orlando, FL), Hynes Convention Center (Boston, MA); 05/2006
  • Mucosal Immune Dysfunction in AIDs Pathogensis (presentation)

    Jessica C.

    AAI; 04/2006

One Figure

One Figure for Jessica Carlson

burkitts_lymphoma_cells figure 1




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