Valla A
CTS des Alpes-Maritimes, Saint-Laurent-du-Var.
Rev Fr Transfus Hemobiol. 1993 Jun;36(3):281-91. doi: 10.1016/s1140-4639(05)80187-x.
HLA alloimmunization and subsequent refractoriness to platelet transfusions are frequent complications of transfusion therapy in patients with hematologic malignancies. Contaminating leukocytes in red cell and platelet concentrates are responsible for primary HLA alloimmunization. In many clinical trials, it has been demonstrated that the use of leukocyte-poor blood products prepared by filtration could reduce HLA-alloimmunization from 40% to 15%. The immunogenic level cannot be determined accurately, but the previous studies show that a residual contamination below 1.10(6) leukocytes was efficient to prevent primary alloimmunization. Leukocyte depletion does not avoid secondary responses in patients having an history of pregnancies or transfusions. The UV-B irradiation of platelet concentrates, in combination with filtration, should further reduce alloimmunization in these presensitized patients.
HLA同种免疫以及随后对血小板输注的难治性是血液系统恶性肿瘤患者输血治疗中常见的并发症。红细胞和血小板浓缩物中污染的白细胞是原发性HLA同种免疫的原因。在许多临床试验中,已经证明使用通过过滤制备的少白细胞血液制品可将HLA同种免疫从40%降低至15%。免疫原性水平无法准确测定,但先前的研究表明,残留污染低于1×10⁶白细胞可有效预防原发性同种免疫。白细胞去除不能避免有妊娠或输血史患者的二次反应。血小板浓缩物的UV-B照射与过滤相结合,应能进一步降低这些预先致敏患者的同种免疫。