2005
DOI: 10.1111/j.1423-0410.2005.00586.x
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Heterogeneity of platelet responsiveness to anti‐CD36 in plasma associated with adverse transfusion reactions

Abstract: Plasma containing anti-CD36, implicated in the development of NHTRs, exhibited a platelet-activating capability. Additionally, platelets from healthy human subjects exhibited a considerable degree of heterogeneity in their responsiveness to this plasma. The heterogeneity of these responses may determine the occurrence of anti-CD36-related NHTRs.

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Cited by 15 publications
(9 citation statements)
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“…These CD36 antibodies exhibited PLT‐activating capability mediated though FcγRIIa, and, interestingly, PLTs from healthy human subjects exhibited a considerable degree of heterogeneity in their responsiveness to this plasma. The PLT surface expression levels of CD36 and FcγRIIa and their degree of binding to these antibodies were apparently associated with the profound differences in PLT responsiveness to this plasma (Wakamoto et al , ).…”
Section: Patient Factors Other Than Allergens and Antibodiesmentioning
confidence: 99%
“…These CD36 antibodies exhibited PLT‐activating capability mediated though FcγRIIa, and, interestingly, PLTs from healthy human subjects exhibited a considerable degree of heterogeneity in their responsiveness to this plasma. The PLT surface expression levels of CD36 and FcγRIIa and their degree of binding to these antibodies were apparently associated with the profound differences in PLT responsiveness to this plasma (Wakamoto et al , ).…”
Section: Patient Factors Other Than Allergens and Antibodiesmentioning
confidence: 99%
“…The other suggested the involvement of a mediator, such as RANTES released from activated PLTs 19 . It should be stressed that we found that S.S. plasma could induce the aggregation of PLTs derived from some (but not all) healthy adults and release of RANTES 20 . Thus, we speculated that the patient's PLT could also be activated by the S.S. plasma.…”
Section: Resultsmentioning
confidence: 72%
“…19 It should be stressed that we found that S.S. plasma could induce the aggregation of PLTs derived from some (but not all) healthy adults and release of RANTES. 20 Thus, we speculated that the patient's PLT could also be activated by the S.S. plasma. In other words, the serious adverse effects including hypotension might be caused by the aggregation of PLTs in the circulation induced by the anti-CD36 isoantibody in the S.S. plasma, resulting in the release of various mediators.…”
Section: Resultsmentioning
confidence: 99%
“…(2003) reported that TRALI‐related antibodies could activate monocytes as well and induce increased cytoplasmic expression of interleukin‐1, tumour necrosis factor‐α and tissue factor. In addition, platelet antibodies and associated platelet activation have also been described in nonhaemolytic transfusion reactions (Taylor et al ., 2000; Wakamoto et al ., 2005). Therefore, it is important to clarify whether antibodies in a blood product can bind on blood cells of a patient when transfused.…”
Section: Discussionmentioning
confidence: 99%