scispace - formally typeset
T

Tatsuo Kawai

Researcher at Harvard University

Publications -  271
Citations -  12138

Tatsuo Kawai is an academic researcher from Harvard University. The author has contributed to research in topics: Transplantation & Kidney transplantation. The author has an hindex of 49, co-authored 254 publications receiving 10467 citations. Previous affiliations of Tatsuo Kawai include Aristotle University of Thessaloniki & University of California, San Francisco.

Papers
More filters
Journal ArticleDOI

HLA-Mismatched Renal Transplantation without Maintenance Immunosuppression

TL;DR: Five patients with end-stage renal disease received combined bone marrow and kidney transplants from HLA single-haplotype mismatched living related donors, with the use of a nonmyeloablative preparative regimen, and it was possible to discontinue all immunosuppressive therapy 9 to 14 months after the transplantation.
Journal ArticleDOI

Strategies to improve long-term outcomes after renal transplantation.

TL;DR: Current antirejection therapy, including calcineurin blockers such as cyclosporine and tacrolimus, the interleukin-2 signal-transduction inhibitor sirolimus and the purine-synthesis inhibitor mycophenolate mofetil are discussed, which inhibits the proliferation of T cells and B cells.
Journal ArticleDOI

Angiotensin II Signal Transduction: An Update on Mechanisms of Physiology and Pathophysiology.

TL;DR: It is expected that rigorous translational research of the ANG II signaling pathways including those in large animals and humans will contribute to establishing effective new therapies against various diseases.
Journal ArticleDOI

Thromboembolic complications after treatment with monoclonal antibody against CD40 ligand.

TL;DR: In this article, the authors report that they developed thromboembolic complications after treatment with monoclonal antibody against CD40 ligand and showed that the antibody was ineffective.
Journal ArticleDOI

Mixed allogeneic chimerism and renal allograft tolerance in cynomolgus monkeys.

TL;DR: At least transient engraftment of DBM appears to be essential for induction of donor specific tolerance in this monkey model of MHC-disparate nonhuman primates.