Intrathymic administration of B cells induces prolonged survival of fully allogeneic cardiac grafts without prolonged deletion of donor-specific thymocytes
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作者:
Niimi, M
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机构:Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
Niimi, M
Jones, ND
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机构:Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
Jones, ND
Pajaro, OB
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机构:Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
Pajaro, OB
Morris, PJ
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机构:Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
Morris, PJ
Wood, KJ
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机构:Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
Wood, KJ
机构:
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
[2] Johns Hopkins Hosp, Div Cardiac Surg, Baltimore, MD 21287 USA
Intrathymic (IT) injection of alloantigen has been shown to induce unresponsiveness to allografts although the exact mechanisms of tolerance induction remains unclear. C57BL/10 (H2(b)) cardiac allografts were accepted in C3H/He (H2(k)) mice pretreated with IT inoculation of donor splenocytes (1 x 10(6)) in combination with a depleting anti-CD4 monoclonal antibody 27 days before cardiac transplantation. To investigate which cell types were responsible for tolerance induction by IT injection of alloantigen, resting B (rB) cells or dendritic cells were used as the thymic inoculum instead of whole splenocytes. IT injection of rB cells induced indefinite graft prolongation in all recipients while only 20% of mice that had received IT injection of dendritic cells accepted grafts for over 100 days. In contrast, IT injection of dendritic cells resulted in significant deletion of donor-specific thymocytes whereas rB cells were relatively ineffective. IT deletion is not essential for the induction of tolerance by IT injection of rB cells; nondeletional mechanisms can be involved.
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA
GOSS, JA
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NAKAFUSA, Y
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA
NAKAFUSA, Y
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YU, S
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA
YU, S
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FLYE, MW
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA
GOSS, JA
;
NAKAFUSA, Y
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA
NAKAFUSA, Y
;
YU, S
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA
YU, S
;
FLYE, MW
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WASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USAWASHINGTON UNIV, SCH MED,DEPT SURG,1 BARNES HOSP PLAZA,SUITE 5108, ST LOUIS, MO 63110 USA