1. Serum hypoalbuminemia predicts late mortality on the liver transplant waiting list.

    Transplantation 99(1):158 (2015) PMID 25050469

    The reduction of liver transplant wait list mortality remains a priority for transplant programs and depends on the accurate stratification of patients by mortality risk. Although estimation of 90-day mortality by Model for End-Stage Liver Disease (MELD) score has improved wait list survival, it...
  2. Serum hypoalbuminemia predicts late mortality on the liver transplant waiting list.

    Transplantation 99(1):158 (2015) PMID 25050469

    The reduction of liver transplant wait list mortality remains a priority for transplant programs and depends on the accurate stratification of patients by mortality risk. Although estimation of 90-day mortality by Model for End-Stage Liver Disease (MELD) score has improved wait list survival, it...
  3. Serum hypoalbuminemia predicts late mortality on the liver transplant waiting list.

    Transplantation 99(1):158 (2015) PMID 25050469

    The reduction of liver transplant wait list mortality remains a priority for transplant programs and depends on the accurate stratification of patients by mortality risk. Although estimation of 90-day mortality by Model for End-Stage Liver Disease (MELD) score has improved wait list survival, it...
  4. Regulatory T cells occupy an isolated niche in the intestine that is antigen independent.

    Cell Reports 9(5):1567 (2014) PMID 25482559

    Regulatory T cells (Tregs) are CD4(+) T cells that maintain immune homeostasis and prevent autoimmunity. Like all CD4(+) T cells, Tregs require antigen-specific signals via T cell receptor-major histocompatibility complex class II (TCR-MHCII) interactions for their development. However, the requ...
  5. Regulatory T Cells Occupy an Isolated Niche in the Intestine that Is Antigen Independent

    Cell Reports 9(5):1567 (2014)

    Regulatory T cells (Tregs) are CD4+ T cells that maintain immune homeostasis and prevent autoimmunity. Like all CD4+ T cells, Tregs require antigen-specific signals via T cell receptor-major histocompatibility complex class II (TCR-MHCII) interactions for their development. However, th...
  6. Regulatory T Cells Occupy an Isolated Niche in the Intestine that Is Antigen Independent.

    Cell Reports 9(5):1567 (2014) PMID 25482559

    Regulatory T cells (Tregs) are CD4(+) T cells that maintain immune homeostasis and prevent autoimmunity. Like all CD4(+) T cells, Tregs require antigen-specific signals via T cell receptor-major histocompatibility complex class II (TCR-MHCII) interactions for their development. However, the requ...
  7. Immunosuppression: trends and tolerance?

    Clinics in Liver Disease 18(3):687 (2014) PMID 25017084

    Advances in pharmacologic immunosuppression are responsible for the excellent outcomes experienced by recipients of liver transplants. However, long-term follow-up of these patients reveals an increasing burden of morbidity and mortality that is attributable to these drugs. The authors summarize...
  8. Regulatory T Cells Occupy an Isolated Niche in the Intestine that Is Antigen Independent

    Cell Reports (2013)

    Regulatory T cells (Tregs) are CD4+ T cells that maintain immune homeostasis and prevent autoimmunity. Like all CD4+ T cells, Tregs require antigen-specific signals via T cell receptor-major histocompatibility complex class II (TCR-MHCII) interactions for their development. However, th...
  9. Regulatory T Cells Occupy an Isolated Niche in the Intestine that Is Antigen Independent

    Cell Reports (2013)

    Regulatory T cells (Tregs) are CD4+ T cells that maintain immune homeostasis and prevent autoimmunity. Like all CD4+ T cells, Tregs require antigen-specific signals via T cell receptor-major histocompatibility complex class II (TCR-MHCII) interactions for their development. However, th...
  10. Regulatory T Cells Occupy an Isolated Niche in the Intestine that Is Antigen Independent

    Cell Reports (2013)

    Regulatory T cells (Tregs) are CD4+ T cells that maintain immune homeostasis and prevent autoimmunity. Like all CD4+ T cells, Tregs require antigen-specific signals via T cell receptor-major histocompatibility complex class II (TCR-MHCII) interactions for their development. However, th...
  11. Donor assessment scores: relevance and complete irrelevance.

    Liver Transplantation and Surgery 18 Suppl 2:S25 (2012) PMID 22767426

    1. Donor assessment scores can be used to prognosticate recipient outcomes but are often not clinically relevant. 2. The donor risk index, the survival outcomes following liver transplantation score, and the Donor Model for End-Stage Liver Disease score have specific advantages and disadvantages...
  12. Innate immunity in transplant tolerance and rejection.

    Immunological Reviews 241(1):39 (2011) PMID 21488888

    Historically, research on transplant rejection and tolerance has focused on cells of the adaptive immune system, especially T cells. Anti-graft effector T cells are necessary and sufficient for the rejection of most allografts, while regulatory T cells, either arising naturally or as a result of...
  13. Late surgical complications following liver transplantation.

    Liver Transplantation and Surgery 15 Suppl 2:S12 (2009) PMID 19877292

    1. Biliary strictures and incisional hernias are the most common surgical complications encountered late after liver transplantation. 2. Anastomotic biliary strictures are amenable to endoscopic intervention and rarely need surgical intervention. 3. The presence of a biliary stricture mandates a...
  14. Kidney transplantation at the University of Pennsylvania: 1998-2008.

    Clinical transplants :143 (2009) PMID 20527069

    Kidney transplantation at the University of Pennsylvania has grown substantially over the past 11 years. Although our transplant volume has increased primarily as a consequence of multiorgan transplants as well as the utilization of historically "marginal" allografts, our post-transplantation ou...
  15. Migratory and Lymphoid-Resident Dendritic Cells Cooperate to Efficiently Prime Naive CD4 T cells

    Immunity 29(5):795 (2008)

    To initiate an adaptive immune response, rare antigen-specific naive CD4+ T cells must interact with equally rare dendritic cells (DCs) bearing cognate peptide-major histocompatibility complex (MHC) complexes. Lymph nodes (LNs) draining the site of antigen entry are populated by lympho...
  16. Migratory and lymphoid-resident dendritic cells cooperate to efficiently prime naive CD4 T cells.

    Immunity 29(5):795 (2008) PMID 18951047 PMCID PMC2746692

    To initiate an adaptive immune response, rare antigen-specific naive CD4(+) T cells must interact with equally rare dendritic cells (DCs) bearing cognate peptide-major histocompatibility complex (MHC) complexes. Lymph nodes (LNs) draining the site of antigen entry are populated by lymphoid-resid...
  17. Mechanisms underlying blockade of allograft acceptance by TLR ligands.

    Journal of Immunology 181(3):1692 (2008) PMID 18641305 PMCID PMC2840047

    Immune activation via TLRs is known to prevent transplantation tolerance in multiple animal models. To investigate the mechanisms underlying this barrier to tolerance induction, we used complementary murine models of skin and cardiac transplantation in which prolonged allograft acceptance is eit...
  18. Interleukins 27 and 6 induce STAT3-mediated T cell production of interleukin 10.

    Nature Immunology 8(12):1363 (2007) PMID 17994025

    Interleukin 10 (IL-10) has a prominent function in regulating the balance between protective and pathological T cell responses. Consistent with that activity, many sources of this cytokine are found in vivo, including from myeloid cells and a variety of T cell subsets. However, although there ar...
  19. Deacetylase inhibition promotes the generation and function of regulatory T cells.

    Nature Medicine 13(11):1299 (2007) PMID 17922010

    Histone/protein deacetylases (HDACs) regulate chromatin remodeling and gene expression as well as the functions of more than 50 transcription factors and nonhistone proteins. We found that administration of an HDAC inhibitor (HDACi) in vivo increased Foxp3 gene expression, as well as the product...
  20. Availability of suitable islet donors in the United States.

    Transplantation 84(2):280 (2007) PMID 17667824

    We characterize donor utilization for islet transplantation and estimate the number of recipients who could achieve normoglycemia through islet transplantation if the current donor pool were used. Potential islet donors from all United Network for Organ Sharing donors (1/00-5/04) were identified...