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Elizabeth Burke

Researcher at Columbia University

Publications -  29
Citations -  1747

Elizabeth Burke is an academic researcher from Columbia University. The author has contributed to research in topics: Transplantation & Heart transplantation. The author has an hindex of 17, co-authored 28 publications receiving 1687 citations.

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Journal ArticleDOI

Use of Rapamycin Slows Progression of Cardiac Transplantation Vasculopathy

TL;DR: In this patient cohort with cardiac vasculopathy, treatment with rapamycin slowed disease progression probably by its antiproliferative and antimigratory effects.
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Prevention of rejection in cardiac transplantation by blockade of the interleukin-2 receptor with a monoclonal antibody.

TL;DR: Induction therapy with daclizumab safely reduces the frequency and severity of cardiac-allograft rejection during the induction period and no significant differences between the groups in the incidence of infection or cancer during follow-up.
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Activation-induced T-cell death and immune dysfunction after implantation of left-ventricular assist de vice

TL;DR: LVAD implantation results in an aberrant state of T-cell activation, heightened susceptibility of CD4 T cells to activation-induced cell death, progressive defects in cellular immunity, and increased risk of opportunistic infection.
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Preformed IgG antibodies against major histocompatibility complex class II antigens are major risk factors for high-grade cellular rejection in recipients of heart transplantation

TL;DR: The results emphasize the importance of specifically screening heart transplantation candidates for the presence of IgG antibodies directed against MHC class II molecules and suggest that strategies aimed at their reduction may have an impact on the onset and frequency of high-grade cellular rejections after transplantation.
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Intravenous immunoglobulin reduces anti-HLA alloreactivity and shortens waiting time to cardiac transplantation in highly sensitized left ventricular assist device recipients.

TL;DR: Results indicate that IVIg is an effective and safe modality for sensitized recipients awaiting cardiac transplantation, reducing serum anti-HLA alloreactivity and shortening the duration to transplantation.