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Journal ArticleDOI

Leukocyte antigens in renal transplantation. 1. The paradox of blood transfusions in renal transplantation.

Peter J. Morris, +2 more
- 14 Dec 1968 - 
- Vol. 2, Iss: 24, pp 1088-1090
TLDR
This work is not able to show evidence of sensitization of recipients of renal allografts by whole-blood transfusions, thus providing the paradox alluded to in the title.
Abstract: 
PATIENTS in terminal renal failure who are awaiting renal transplantation are generally maintained on frequent bremodialysis. This period of maintenance may last for several months, during which time the patient may receive a number of whole blood transfusions, depending on the type of machine used for dialysis. This ranges from no transfusions to as many as 100 transfusions in the months immediately before transplantation. As it is known that leukocytes carry transplantation antigens (Medawar, 1946; Friedman et alii, 1961; Rapaport et alii, 1964), it might be expected that these frequent transfusions of whole blood (with leukocytes) would lead commonly to sensitization of potential recipients against a subsequent renal allograft. In fact, because of this theoretical risk of sensitization, many transplantation units use only leukocyte-free blood for transfusions. If this risk is real, it should be possible to demonstrate that renal allografts have a stormier early course, as judged by rejection crises, when the recipient has received a large number of transfusions before grafting. As just the opposite is suggested to be the case by two other units (Dossetor et alii, 1967; Michielsen, 1966), we have examined our own experience in this regard. We, too, are not able to show evidence of sensitization of recipients of renal allografts by whole-blood transfusions, thus providing the paradox alluded to in the title. The implications of the results to be described will be discussed at some length.

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Citations
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Pretransplant blood transfusion without additional immunotherapy generates CD25+CD4+ regulatory T cells: a potential explanation for the blood-transfusion effect.

TL;DR: It is demonstrated that pretreatment with multiple DSTs generates CD25+CD4+ T cells that are as effective as those that result from blood transfusion under anti-CD4 antibody cover, and these cells also develop following multiple transfusions of unrelated (random) blood.
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Pretransplant administration of a single donor class I major histocompatibility complex molecule is sufficient for the indefinite survival of fully allogeneic cardiac allografts: evidence for linked epitope suppression.

TL;DR: These data provide clear evidence for linked epitope suppression in the induction of operational tolerance in vivo and indicate that the allografts bearing Kb could tolerize recipients to other alloantigens expressed by the transplanted heart.
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Immunologic effects of blood transfusion upon renal transplantation, tumor operations, and bacterial infections.

TL;DR: In the absence of any satisfactory substitute, blood transfusion remains an essential therapeutic modality in the management of surgical patients and it seems reasonable to avoid the administration of small-volume transfusions whenever possible and encourage the use of autodonated blood for elective surgery.
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Current Research on the Immunomodulatory Effect of Allogeneic Blood Transfusion

TL;DR: This review summarizes three aspects of current research on the immunomodulatory effect of allogeneic transfusion, and the potential clinical impact of increased infection and tumor recurrence resulting from transfusion‐induced Immunomodulation is assessed.
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Both self and non-inherited maternal HLA antigens influence the immune response

TL;DR: Evidence that three HLA haplotypes, those inherited from the parents plus NIMA, shape the immune response is discussed, which could influence tolerance of organ grafts and disease susceptibility.
References
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Journal ArticleDOI

Serotyping for homotransplantation. XII. Occurrence of cytotoxic antibodies following kidney transplantation in man.

TL;DR: It appears that humoral cytotoxic antibodies are associated with kidney transplant rejections and that they either act directly on the transplant or serve as indicators of a state of presensitization.
Journal ArticleDOI

Cadaver kidney transplants.

TL;DR: The experience obtained from 59 renal transplantations is presented and there was a significant difference whereby those with more hemodialysis prior to transplantation showed less evidence of rejection activity, and this finding is discussed.
Journal ArticleDOI

Tolerance of skin homografts induced in adult mice by multiple injections of homologous spleen cells.

TL;DR: Adult mice of the Z(C3H) strain have been made tolerant of skin homo-grafts of the(A X Z) F1 hybrid strain by repeated intravenous and intraperitoneal injections of homologous spleen cells.
Journal ArticleDOI

Cadaveric renal transplantation

TL;DR: Cadaveric renal transplantation at present seems to offer a more practical solution to the treatment of chronic renal failure than recurrent haemodialysis.
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