Bone marrow aplasia induced by passenger leukocytes from heart allografts.

Standard

Bone marrow aplasia induced by passenger leukocytes from heart allografts. / Ko, S; Dahlke, M H; Lauth, O; Jäger, M D; Deiwick, A; Dinkel, A; Tsui, Tung Yu; Wonigeit, K; Schlitt, H J.

in: EXP HEMATOL, Jahrgang 29, Nr. 3, 3, 2001, S. 339-344.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Ko, S, Dahlke, MH, Lauth, O, Jäger, MD, Deiwick, A, Dinkel, A, Tsui, TY, Wonigeit, K & Schlitt, HJ 2001, 'Bone marrow aplasia induced by passenger leukocytes from heart allografts.', EXP HEMATOL, Jg. 29, Nr. 3, 3, S. 339-344. <http://www.ncbi.nlm.nih.gov/pubmed/11274762?dopt=Citation>

APA

Ko, S., Dahlke, M. H., Lauth, O., Jäger, M. D., Deiwick, A., Dinkel, A., Tsui, T. Y., Wonigeit, K., & Schlitt, H. J. (2001). Bone marrow aplasia induced by passenger leukocytes from heart allografts. EXP HEMATOL, 29(3), 339-344. [3]. http://www.ncbi.nlm.nih.gov/pubmed/11274762?dopt=Citation

Vancouver

Ko S, Dahlke MH, Lauth O, Jäger MD, Deiwick A, Dinkel A et al. Bone marrow aplasia induced by passenger leukocytes from heart allografts. EXP HEMATOL. 2001;29(3):339-344. 3.

Bibtex

@article{3110435a1f8649ffb87ce990fcddd71d,
title = "Bone marrow aplasia induced by passenger leukocytes from heart allografts.",
abstract = "OBJECTIVE: Organ allografts contain passenger leukocytes that are transferred to the recipient with the transplantation, but their functional relevance to the recipient's immune system is still controversial. MATERIALS AND METHODS: To clarify the functional capacity of passenger leukocytes, we attempted to enhance their effect in rat heart allograft recipients by selective depletion of recipient leukocytes using a monoclonal antibody (mAb) against a recipient-specific allotype of CD45 (RT7(a)). RESULTS: Although antibody treatment of the recipient alone led to profound lymphopenia and reversible myelosuppression, additional transplantation of an major histocompatibility complex-incompatible heart graft from an RT7(b) donor led to lethal aplastic anemia in the recipients. This lethal effect was completely abrogated by postoperative anti-CD3 treatment of the recipient and was partially abrogated or delayed by depletion of passenger leukocytes through additional anti-RT7(b) antibody treatment of the recipient or gamma-irradiation of the graft. CONCLUSIONS: The results suggest a role for both donor and recipient-type T cells for the induction of aplastic anemia in this model. The study shows that, under defined conditions, allogeneic passenger leukocytes in a heart graft can have a profound effect on the recipient's immune system and bone marrow.",
author = "S Ko and Dahlke, {M H} and O Lauth and J{\"a}ger, {M D} and A Deiwick and A Dinkel and Tsui, {Tung Yu} and K Wonigeit and Schlitt, {H J}",
year = "2001",
language = "Deutsch",
volume = "29",
pages = "339--344",
journal = "EXP HEMATOL",
issn = "0301-472X",
publisher = "Elsevier Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Bone marrow aplasia induced by passenger leukocytes from heart allografts.

AU - Ko, S

AU - Dahlke, M H

AU - Lauth, O

AU - Jäger, M D

AU - Deiwick, A

AU - Dinkel, A

AU - Tsui, Tung Yu

AU - Wonigeit, K

AU - Schlitt, H J

PY - 2001

Y1 - 2001

N2 - OBJECTIVE: Organ allografts contain passenger leukocytes that are transferred to the recipient with the transplantation, but their functional relevance to the recipient's immune system is still controversial. MATERIALS AND METHODS: To clarify the functional capacity of passenger leukocytes, we attempted to enhance their effect in rat heart allograft recipients by selective depletion of recipient leukocytes using a monoclonal antibody (mAb) against a recipient-specific allotype of CD45 (RT7(a)). RESULTS: Although antibody treatment of the recipient alone led to profound lymphopenia and reversible myelosuppression, additional transplantation of an major histocompatibility complex-incompatible heart graft from an RT7(b) donor led to lethal aplastic anemia in the recipients. This lethal effect was completely abrogated by postoperative anti-CD3 treatment of the recipient and was partially abrogated or delayed by depletion of passenger leukocytes through additional anti-RT7(b) antibody treatment of the recipient or gamma-irradiation of the graft. CONCLUSIONS: The results suggest a role for both donor and recipient-type T cells for the induction of aplastic anemia in this model. The study shows that, under defined conditions, allogeneic passenger leukocytes in a heart graft can have a profound effect on the recipient's immune system and bone marrow.

AB - OBJECTIVE: Organ allografts contain passenger leukocytes that are transferred to the recipient with the transplantation, but their functional relevance to the recipient's immune system is still controversial. MATERIALS AND METHODS: To clarify the functional capacity of passenger leukocytes, we attempted to enhance their effect in rat heart allograft recipients by selective depletion of recipient leukocytes using a monoclonal antibody (mAb) against a recipient-specific allotype of CD45 (RT7(a)). RESULTS: Although antibody treatment of the recipient alone led to profound lymphopenia and reversible myelosuppression, additional transplantation of an major histocompatibility complex-incompatible heart graft from an RT7(b) donor led to lethal aplastic anemia in the recipients. This lethal effect was completely abrogated by postoperative anti-CD3 treatment of the recipient and was partially abrogated or delayed by depletion of passenger leukocytes through additional anti-RT7(b) antibody treatment of the recipient or gamma-irradiation of the graft. CONCLUSIONS: The results suggest a role for both donor and recipient-type T cells for the induction of aplastic anemia in this model. The study shows that, under defined conditions, allogeneic passenger leukocytes in a heart graft can have a profound effect on the recipient's immune system and bone marrow.

M3 - SCORING: Zeitschriftenaufsatz

VL - 29

SP - 339

EP - 344

JO - EXP HEMATOL

JF - EXP HEMATOL

SN - 0301-472X

IS - 3

M1 - 3

ER -