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dc.contributor.advisorWolchok, Jedd
dc.contributor.authorMalandro, Nicole
dc.date.accessioned2019-03-26T18:53:05Z
dc.date.available2019-03-27T06:01:16Z
dc.date.issued2016
dc.identifier.urihttps://hdl.handle.net/1813/64692
dc.description.abstractMany of the current approaches to cancer immunotherapy aim to exploit and enhance the natural T cell response against cancer. However, these treatment modalities may fall short of their potential due to the elimination of self-tumor antigen specific T cells from the immune repertoire to guard against autoimmunity. To investigate how the precursory frequency of self-antigen specific T cells shapes therapeutic outcome, our lab developed a model system in which the precursor number of T cells specific for a self/melanoma antigen could be manipulated in mice bearing melanoma tumors through the adoptive transfer of tumor specific T cells. Using this model we had previously determined that bringing the frequency of CD8+ T cells within or slightly above a normal physiologic range favored proliferation and generation of polyfunctional effector T cells and anti-tumor immunity, while dramatically exceeding this threshold resulted in intraclonal competition and an impaired immune response. We adapted this model to investigate CD4+ T cells specific for the tumor-self antigen TRP-1 and demonstrated that clonal abundance dictates the development of CD4+ T cell mediated anti-tumor immunity as well. Tumor specific CD4+ T cells operate within the constraints imposed by intraclonal competition, despite ubiquitous expression of cognate antigen. Unlike CD8+ T cells, the defects in activation and proliferation are uncoupled from the development of effector function. Low physiologic precursor frequencies of self-antigen specific T cells support rapid expansion of the population at the expense of the generation of effector function due to onset of irreversible T cell exhaustion. Despite decreased expansion at high precursor frequencies, tumor specific effector CD4+ T cells accumulate in the periphery and tumor in greater numbers, with a lower proportion of TRP-1 specific Foxp3+ regulatory T cells within the population. Through a mechanism of population-induced positive feedback involving paracrine IFN? sharing and traditional T cell help, we observe intraclonal cooperation resulting in strong Th1 differentiation, increased T cell cytotoxicity, and potent anti-tumor responses. These findings assert that the differential effects of T cell clonal abundance on phenotypic outcome should be considered during the design of adoptive T cell therapies, including the use of engineered T cells.
dc.language.isoen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCD4
dc.subjectclonal abundance
dc.subjectexhaustion
dc.subjectprecursor frequency
dc.subjectT cell
dc.titleThe Effect Of Self-Antigen Specific Cd4+ T Cell Precursor Frequency On The Anti-Tumor Immune Response
dc.typedissertation or thesis
thesis.degree.disciplineImmunology & Microbial Pathogenesis
thesis.degree.grantorWeill Cornell Graduate School of Medical Sciences
thesis.degree.levelDoctor of Philosophy


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