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Judith Shizuru

Academic Appointments

Contact Information

  • Clinical Offices
    Blood and Marrow Transplantation 875 Blake Wilbur Dr Clinic E Stanford, CA 94305-5820
    Tel Work (650) 723-0822 Fax (650) 725-8950

Professional Snapshot

Clinical Focus

  • Bone Marrow Transplant
  • Blood and Marrow Transplantation
  • Hematology

Professional Education

Fellowship: Stanford University Medical Center, CA (1997)
Residency: UCSF Medical Center, CA (1994)
Internship: UCSF Medical Center, CA USA (1993)
Medical Education: Stanford University School of Medicine, CA (1992)

Postdoctoral Advisees

Rose Ko

Scientific Focus

Current Research Interests

The research interests are to understand the cellular and molecular basis of resistance to engraftment of transplanted allogeneic bone marrow (BM) cells and to understand the way in which BM grafts modify immune responses. This research complements our interest in clinical BM transplantation and aspects of these studies are aimed at solving some of the major problems of BM transplantation which include graft-vs-host disease and BM engraftment failure. Conventional BM transplantation involves the transfer of heterogeneous populations of cells composed of rare hematopoietic stem cells (HSCs) and differentiated blood cell types. To study these issues our approach has been to transplant phenotypically purified cells under defined conditions. The specific projects in my laboratory include:

1) Identification of the cells and molecules responsible for resistance to engraftment of purified allogeneic HSCs. We and others have shown that cells with NK determinants constitute a significant barrier to allogeneic HSC engraftment, and that transplanted whole BM contains a population that facilitates engraftment. In these experiments our approach to identify the cell population(s) and mechanism by which HSC engraftment is resisted is to use recipient mice from strains that lack defined immune functions. We are studying the cells in BM and spleen that are bound and/or depleted by a-ASGMI, and in this way identify the candidate barrier populations.

2) Use of transplants of purified HSCs to induce tolerance to allo- and autoantigens, and study of the mechanisms by which such tolerance is induced. We continue to develop preclinical models for organ tolerance induction and treatment of autoimmune disease by using cell specific therapy. One goal is to decrease the morbidity of the recipient preparative regimen and to determine the lowest level of chimerism needed to induce immune tolerance. We propose to test donor/host strain combinations most relevant to human...

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