| 词条 | Harrington–Hollingsworth experiment |
| 释义 |
The Harrington–Hollingsworth experiment was an experiment that established the autoimmune nature of the blood disorder immune thrombocytopenic purpura.[1][2] It was performed in 1950 by the academic staff of Barnes-Jewish Hospital in St. Louis, Missouri.[2] ExperimentThe experiment was undertaken in 1950 by William J. Harrington and James W. Hollingsworth, who postulated that in patients with idiopathic thrombocytopenic purpura (ITP), it was a blood factor that caused the destruction of platelets.[2] To test this hypothesis, Harrington received 500 ml of blood from a patient with ITP.[2] Within three hours, his platelets dropped to dangerously low levels and he experienced a seizure.[2] His platelet count remained extremely low for four days, finally returning to normal levels by the fifth day.[2] Bone marrow biopsy from Harrington's sternum demonstrated normal megakaryocytes, the cells necessary for platelet production.[2] Subsequently the experiment was repeated on all suitable staff members at the Barnes-Jewish Hospital. All subjects developed low platelet counts within three hours, and all recovered after a period of several days.[2] ImplicationsSchwartz notes that the Harrington–Hollingsworth experiment was a turning point in the understanding of ITP's pathophysiology: {{quote|The Harrington–Hollingsworth experiment changed the meaning of the "I" in ITP from idiopathic to immune, but "immune" in this case means "autoimmune," because the antibodies bind to and cause the destruction of the patient's own platelets.[2]}}The experiment was the first to demonstrate that infusion of an ITP patient's plasma into a normal patient caused a precipitous drop in platelet count.[2] This suggested that low platelet counts (thrombocytopenia) in patients with ITP was caused by a circulating factor found in the blood.[2] Many studies performed since then have demonstrated that this circulating factor is in fact a collection of immunoglobulins.[3][4] Many physician-scientists believe the findings had a major influence on the field of autoimmunity, which was not universally accepted at the time as a mechanism of human disease. References1. ^{{cite journal |vauthors=Harrington WJ, Minnich V, Hollingsworth JW, Moore CV |title=Demonstration of a thrombocytopenic factor in the blood of patients with thrombocytopenic purpura |journal=J. Lab. Clin. Med. |volume=38 |issue=1 |pages=1–10 |date=July 1951 |pmid=14850832 |doi= |url=}} {{DEFAULTSORT:Harrington-Hollingsworth experiment}}2. ^1 2 3 4 5 6 7 8 9 10 {{cite journal |author=Schwartz RS |title=Immune thrombocytopenic purpura--from agony to agonist |journal=N. Engl. J. Med. |volume=357 |issue=22 |pages=2299–301 |year=2007 |pmid=18046034 |doi=10.1056/NEJMe0707126}} 3. ^{{cite journal |vauthors=Tomer A, Koziol J, McMillan R |title=Autoimmune thrombocytopenia: flow cytometric determination of platelet-associated autoantibodies against platelet-specific receptors |journal=J. Thromb. Haemost. |volume=3 |issue=1 |pages=74–8 |date=January 2005 |pmid=15634268 |doi=10.1111/j.1538-7836.2004.01052.x}} 4. ^{{cite journal |vauthors=Li J, Yang C, Xia Y, etal |title=Thrombocytopenia caused by the development of antibodies to thrombopoietin |journal=Blood |volume=98 |issue=12 |pages=3241–8 |date=December 2001 |pmid=11719360 |doi= 10.1182/blood.V98.12.3241|url=http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=11719360}} 1 : Hematology |
| 随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识，基本涵盖了大多数领域的百科知识，是一部内容自由、开放的电子版国际百科全书。