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Journal ArticleDOI

Humoral rejection in cardiac transplantation: risk factors, hemodynamic consequences and relationship to transplant coronary artery disease.

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TLDR
Humoral rejection is a clinicopathologic entity with a high incidence in women and is associated with acute hemodynamic compromise, accelerated transplant coronary artery disease and death.
Abstract
Background Acute cellular rejection is the mechanism of most immune-related injury in cardiac transplant recipients. However, antibody-mediated humoral rejection (HR) has also been implicated as an important clinical entity following orthotopic heart transplantation. Humoral rejection has been reported to play a role in graft dysfunction in the early post-transplant period, and to be a risk factor for the development of transplant coronary artery disease. Some involved in transplantation pathology doubt the existence of clinically significant humoral rejection in cardiac allografts. Those who recognize its existence disagree on its possible role in graft dysfunction or graft coronary artery disease. In this study, we report clinical features of patients with the pathologic diagnosis of HR at our institution since July 1997, when we began systematic surveillance for humoral rejection. Methods We reviewed medical records of patients with the pathologic diagnosis of HR without concurrent cellular rejection between July 1997 and January 2001. Diagnosis was based on routine histology (“swollen cells” distending capillaries, interstitial edema and hemorrhage) and immunofluorescence (capillary deposition of immunoglobulin and complement with HLA-DR positivity), or immunoperoxidase staining of paraffin-embedded tissue (numerous CD68-positive macrophages and fewer swollen endothelial cells distending capillaries). Results A total of 44 patients (4 to 74 years old) showed evidence of HR without concurrent cellular rejection at autopsy or on one or more biopsies. Although females comprised only 26% of our transplant population, 23 patients (52%) with HR were female. A positive peri-operative flow cytometry T-cell crossmatch was observed in 32% of HR patients compared with 12% of controls ( p = 0.02). Hemodynamic compromise consisting of shock, hypotension, decreased cardiac output/index and/or a rise in capillary wedge or pulmonary artery pressure was observed in 47% of patients at the time of diagnosis of HR. Six patients (5 females) died (14% mortality) with evidence of HR at or just before autopsy, 6 days to 16 months after transplantation. The incidence of transplant coronary artery disease was 10% greater at 1 year, and 36% greater at 5 years, in patients with HR when compared with non-HR patients. Conclusion Humoral rejection was associated with acute hemodynamic compromise in 47% of patients, and was the direct cause of death in 6 patients (13%). Humoral rejection is a clinicopathologic entity with a high incidence in women and is associated with acute hemodynamic compromise, accelerated transplant coronary artery disease and death.

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Complement-independent mechanisms of antigraft antibodies in transplant arteriosclerosis and accommodation

TL;DR: Characterizing the response of endothelial and smooth muscle cells to antigraft antibodies and elucidating the signaling pathways have the potential to identify novel immunotherapies to promote cell survival while preventing transplant arteriosclerosis.
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Non-invasive cardiac allograft rejection surveillance: reliability and clinical value for prevention of heart failure

TL;DR: An overview of the current knowledge about the reliability and clinical value of non-invasive cardiac allograft AR surveillance is given to provide a theoretical and practical basis for those engaged in this particularly demanding up-to-date topic.
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Postoperative nursing care of the cardiac transplant recipient

TL;DR: This article provides an overview of the postoperative management of the cardiac transplant recipient while in the intensive care unit and the surgical techniques employed and the physiology related to cardiac denervation are presented.
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Successful Treatment of Hemodynamic Compromise Caused by Antibody-Mediated and Cellular Rejection in a Recipient 12 years After Heart Transplantation

TL;DR: A 16-year old patient with hemodynamic compromise caused by both cellular and antibody-mediated rejection 12 years after HTx was experienced, which was refractory to repeated steroid pulse treatment, intravenous immunoglobulin administration, and intensifying immunosuppression including addition of everolimus.
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Measurement of Human Erythrocyte C4d to Erythrocyte Complement Receptor 1 Ratio in Cardiac Transplant Recipients With Acute Symptomatic Allograft Failure

TL;DR: Measurement of the E-C4d/E-CR1 ratio may be a noninvasive method for detecting acute rejection after cardiac transplantation.
References
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Journal ArticleDOI

Cytomegalovirus Infection Is Associated With Cardiac Allograft Rejection and Atherosclerosis

TL;DR: It is demonstrated that CMV infection in cardiac transplant recipients is associated with more frequent rejection, graft atherosclerosis, and death.
Journal ArticleDOI

Transplantation of discordant xenografts: a review of progress.

TL;DR: In this paper, a model of hyperacute rejection was proposed and it was shown that if hyper-accurate rejection can be averted for a period after transplantation, prolonged xenograft survival is possible.
Journal ArticleDOI

Immunopathology of hyperacute xenograft rejection in a swine-to-primate model.

TL;DR: It is suggested that rhesus IgM contributes significantly to the development of hyperacute rejection in the swine to Rhesus model and that the fixation of complement is a critical factor in the recruitment of the coagulation cascade and platelet aggregation--and possibly in the adherence and infiltration of PMN.
Journal Article

Vascular (humoral) rejection in heart transplantation: pathologic observations and clinical implications.

TL;DR: It is concluded that immunofluorescence should be routinely done on all heart biopsies for the first month after transplantation, because patients with vascular (humoral) rejection cannot be reliably identified by any other means.
Journal ArticleDOI

Posttransplant therapy using high-dose human immunoglobulin (intravenous gammaglobulin) to control acute humoral rejection in renal and cardiac allograft recipients and potential mechanism of action

TL;DR: I.v.IG appears to be an effective therapy to control posttransplant AR episodes in heart and kidney transplant recipients, including patients who have had no success with conventional therapies.
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