Ana Carrizosa Anderson | |
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Born | |
Alma mater | Harvard University University of Miami |
Scientific career | |
Institutions | Harvard University |
Thesis | T cell cross-reactivity in the selection and expansion of the autoreactive T cell repertoire (1999) |
Website | Ana Anderson Lab |
Ana Carrizosa Anderson is a Colombian-American microbiologist who is a professor at the Harvard Medical School. Her research combines transcriptomics and systems biology to understand T-cell response to chronic disease.
Anderson was born in Bogotá.[1] She grew up in Miami, and eventually attended the University of Miami. Anderson studied microbiology and immunology as an undergraduate degree.[2] She moved to Harvard University for her doctoral research, where she studied T cell cross reactivity.[3][4]
Anderson looks to understand the pathways that are involved with T cell response to chronic disease. She has explored the role of regulatory T cells in cancer, and the specific effector T cells in tumor tissue.[5] Her research combines mass cytometry, transcriptomics, and genome editing. Checkpoint receptors regulate the activation, differentiation and function of T-cells. They are up-regulated (e.g. increases response) on activated T cells to mitigate for uncontrolled inflammation. Immune checkpoint receptors are hijacked in cancer, where their high rates of expression on tumor T cells hampers the anti-tumor response. Anderson has investigated TIM-3, an immune checkpoint receptor that is involved with immunity to tumors.[2] The blockade of immune checkpoint receptors is a recognized form of cancer treatment. Anderson is interested in how TIM-3 is involved with regulating tumor tissue immune cells, and understanding how the blockade impacts immune cell function in the tumor microenvironment.[3]
Anderson uses transcriptomics technologies and systems biology to understand dysfunctional T-cells.[citation needed]
Anderson looks to understand the function of Treg in tumor tissue. CD4+FoxP3+ Treg are immunosuppressive cells that suppress anti-tumor immunity. Inside tumor cells, Treg cells up-regulate checkpoint receptors and are major suppressors of anti-tumor immunity. The Treg cells that infiltrate tumor tissue up-regulate immune checkpoint receptors and have a highly suppressive phenotype.[citation needed]