Rose Hendrix
Emory University
15 Papers
631 Citations
Rose Hendrix is an academic researcher from Emory University. The author has contributed to research in topics: T cell & Transplantation. The author has an hindex of 13, co-authored 15 publications.
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Papers
Development of a Chimeric Anti-CD40 Monoclonal Antibody That Synergizes with LEA29Y to Prolong Islet Allograft Survival
Andrew B. Adams,Nozomu Shirasugi,Thomas R. Jones,Megan M. Durham,Elizabeth Strobert,Shannon R. Cowan,Phyllis Rees,Rose Hendrix,Karen Price,Norma S. Kenyon,David Hagerty,Robert M. Townsend,Dianne Hollenbaugh,Dianne Hollenbaugh,Thomas C. Pearson,Christian P. Larsen +15 more
TL;DR: It is found that the effects of Chi220 treatment were not mediated solely through deletion of CD20-bearing cells and that the combined therapy did not significantly impair established antiviral immunity.
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Gene expression analysis in human renal allograft biopsy samples using high-density oligoarray technology.
Enver Akalin,Rose Hendrix,Rathna Giri Polavarapu,Thomas C. Pearson,John F. Neylan,Christian P. Larsen,Christian P. Larsen,Fadi G. Lakkis,Fadi G. Lakkis +8 more
TL;DR: High-density oligoarray technology is useful for screening gene expression in transplanted tissues undergoing acute rejection and is likely to yield novel insights into the mechanisms and diagnosis of rejection.
141
CTLA4-Ig plus bone marrow induces long-term allograft survival and donor specific unresponsiveness in the murine model. Evidence for hematopoietic chimerism.
Thomas C. Pearson,Diane Z. Alexander,Rose Hendrix,Eric T. Elwood,Peter S. Linsley,Kevin J. Winn,Christian P. Larsen +6 more
TL;DR: The results suggest that there may be a donor-derived radiosensitive element that enhances allograft survival in this model and imply that complex mechanisms may be important for the induction and maintenance of transplantation tolerance in the CTLA4-Ig plus bone marrow murine cardiac allografted model.
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Vigorous Allograft Rejection in the Absence of Danger
Adam W. Bingaman,Jongwon Ha,Seung Yeun Waitze,Megan M. Durham,Hong Rae Cho,Carol Tucker-Burden,Rose Hendrix,Shannon R. Cowan,Thomas C. Pearson,Christian P. Larsen +9 more
TL;DR: It is reported that skin and cardiac allografts without evidence of inflammation are vigorously rejected by transferred T cells or when recipients are reconstituted with T cells at a physiologic rate by nude bone graft transplantation, suggesting that in the absence of central deletional tolerance, peripheral tolerance mechanisms are not sufficient to inhibit alloimmune responses even in the presence of inflammation or danger.
Fas-mediated cytotoxicity. An immunoeffector or immunoregulatory pathway in T cell-mediated immune responses?
TL;DR: It is observed that Fas transcripts are constitutively expressed in syngeneic and allogeneic murine cardiac transplants, while Fas ligand (FasL) is up-regulated only in rejecting allografts, suggesting that the Fas pathway may be principally involved in the regulation of clonal expansion and subsequent contraction of T cell populations during immune responses.
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