Minimal evidence of platelet and endothelial cell reactive antibodies in thrombotic thrombocytopenic purpura

Thrombotic thrombocytopenic purpura (TTP) is a syndrome characterized by microvascular thrombosis with thrombocytopenia and end‐organ injury. Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunog...

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Veröffentlicht in:American journal of hematology 1999-10, Vol.62 (2), p.82-87
Hauptverfasser: Raife, Thomas J., Atkinson, Bonnie, Aster, Richard H., McFarland, Janice G., Gottschall, Jerome L.
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container_issue 2
container_start_page 82
container_title American journal of hematology
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creator Raife, Thomas J.
Atkinson, Bonnie
Aster, Richard H.
McFarland, Janice G.
Gottschall, Jerome L.
description Thrombotic thrombocytopenic purpura (TTP) is a syndrome characterized by microvascular thrombosis with thrombocytopenia and end‐organ injury. Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. Six of 48 (13%) patient plasma samples contained antibodies that bound to human umbilical vein endothelial cells activated with γ‐interferon and tumor necrosis factor‐α. Of twenty samples that were reactive in one or more platelet or endothelial cell assay, eight contained human leukocyte antigen antibodies reactive in microlymphocytotoxicity. These studies demonstrate that antibodies reactive against platelet or endothelial cell antigens are not prevalent in TTP, and that more than a third of antibodies detected are human leukocyte antigen alloantibodies. Our findings suggest that autoantibodies against platelets or endothelial cells are not important in the pathogenesis of this syndrome. Am. J. Hematol. 62:82–87, 1999. © 1999 Wiley‐Liss, Inc.
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Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. Six of 48 (13%) patient plasma samples contained antibodies that bound to human umbilical vein endothelial cells activated with γ‐interferon and tumor necrosis factor‐α. Of twenty samples that were reactive in one or more platelet or endothelial cell assay, eight contained human leukocyte antigen antibodies reactive in microlymphocytotoxicity. These studies demonstrate that antibodies reactive against platelet or endothelial cell antigens are not prevalent in TTP, and that more than a third of antibodies detected are human leukocyte antigen alloantibodies. Our findings suggest that autoantibodies against platelets or endothelial cells are not important in the pathogenesis of this syndrome. Am. J. 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Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. Six of 48 (13%) patient plasma samples contained antibodies that bound to human umbilical vein endothelial cells activated with γ‐interferon and tumor necrosis factor‐α. Of twenty samples that were reactive in one or more platelet or endothelial cell assay, eight contained human leukocyte antigen antibodies reactive in microlymphocytotoxicity. These studies demonstrate that antibodies reactive against platelet or endothelial cell antigens are not prevalent in TTP, and that more than a third of antibodies detected are human leukocyte antigen alloantibodies. Our findings suggest that autoantibodies against platelets or endothelial cells are not important in the pathogenesis of this syndrome. Am. J. 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Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. 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subjects antibody
Autoantibodies - blood
Biological and medical sciences
Blood Platelets - immunology
Cells, Cultured
Cytotoxicity, Immunologic
endothelial cell
Endothelium, Vascular - immunology
Enzyme-Linked Immunosorbent Assay
Flow Cytometry
Hematologic and hematopoietic diseases
Humans
Immunoglobulin G - immunology
Immunoglobulin M - immunology
Medical sciences
platelet
Platelet diseases and coagulopathies
Platelet Membrane Glycoproteins - immunology
Purpura, Thrombotic Thrombocytopenic - blood
Purpura, Thrombotic Thrombocytopenic - immunology
thrombotic thrombocytopenic purpura
Umbilical Veins
title Minimal evidence of platelet and endothelial cell reactive antibodies in thrombotic thrombocytopenic purpura
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