1957
DOI: 10.1111/j.1423-0410.1957.tb03700.x
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Élimination de certains chocs transfusionnels par l'utilisation de sang appauvri en leucocytes*

Abstract: Résumé Chez une malade dans le sérum de laquelle existait une puissante leuco‐agglutinine et qui présentait à chaque transfusion des chocs violents ont été entreprises des expériences de transfusion des diffé‐rents éléments du sang. Aucun choc n'a suivi I'injection du plasma, du plasma riche en plaquettes, du sang appauvri en leucocytes. Un choc a été observé chaque fois que les leucocytes en nombre suffisant ont été injectés. Ces résultats ont conduit à n'utiliser chez cette malade que du sang préalablement… Show more

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Cited by 30 publications
(6 citation statements)
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“…(c) Transfusion reactions. As with leucocyte antibodies [5, 11,261 it is probable that a great number of transfusion reactions are due t o a reaction between platelets transfused and platelets agglutinins present in the patient's plasma. We have investigated a typical case.…”
Section: (11) Correlation With the Clinical Picturementioning
confidence: 99%
“…(c) Transfusion reactions. As with leucocyte antibodies [5, 11,261 it is probable that a great number of transfusion reactions are due t o a reaction between platelets transfused and platelets agglutinins present in the patient's plasma. We have investigated a typical case.…”
Section: (11) Correlation With the Clinical Picturementioning
confidence: 99%
“…(4) Weakly positive results: these varied for different sera from 3 yo to 12 yo. (5) The optimum temperature was found to be 37" C. The reaction was weaker a t 22" C. and negative a t 4" C. (6) Variation in the p H from 6 to 8 had no definite influence on the agglutination reaction. (7) Freezing the sera to -20" C. during several months caused no decrease in titre.…”
Section: Other Characteristicsmentioning
confidence: 85%
“…Inhibitors of Factor IX.-Some patients with haemophilia B develop inhibitors following repeated transfusion with plasma in the same way as do patients with classical haemophilia (18,24,25,(63)(64)(65). Dausset (18) was of the opinion that patients with haemophilia B were more likely to develop inhibitors than those with haemophilia A.…”
Section: Acquired Inhibitors Of Coagulation Factors Other Than Factormentioning
confidence: 97%
“…In one of these the plasma is totally deficient in protein bearing any immunological relationship to the missing factor and such patients might be expected to develop an inhibitor following treatment. In the other group, the defect, possibly caused by the substitution of a particular amino acid in the protein structure, in analogy with abnormal haemoglobins, gives rise to a deficiency of function in the coagulation mech anism, but the immunological specificity of the protein is unaffected, and the normal version of the coagulation factor would not then be antigenic (18,(20)(21)(22)(23). Patients belonging to the same family should have the same type of defect, and therefore a similar tendency to develop inhibitors.…”
mentioning
confidence: 97%
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