Gratama J W, van den Bergh R L, Naipal A, D'Amaro J, Zwaan F E, Jansen J, de Gast G C
Exp Hematol. 1986 Feb;14(2):133-7.
In eight recipients of allogeneic bone marrow grafts who had sex-mismatched donors, the reduction and subsequent repopulation of T4+ and T8+ T-lymphocytes of recipient origin were studied. The origin of the donor-recipient T4+ and T8+ T cells was studied using quinacrine staining of Y chromatin combined with T-cell typing for T4 and T8. Following chemoradiotherapy and bone marrow transplantation (BMT), T cells reached their nadir at a median of five (range 1-8) days after BMT. T8+ T cells decreased at a faster rate from the peripheral blood than T4+ T cells. The first T cells that appeared in the circulation at day 12 were predominantly T4+, and a large number of them were of recipient origin. Thereafter, they gradually decreased, and the numbers of T cells of donor origin increased. In the patients who had no or only minor complications, T4+ and T8+ T cells of donor origin repopulated the blood at similar rates. This pattern, however, was modified by severe graft-versus-host disease or by cytomegalovirus infection.
在8名接受了供体性别不匹配的同种异体骨髓移植的受者中,对源自受者的T4+和T8+ T淋巴细胞的减少及随后的重新增殖情况进行了研究。采用Y染色体的喹吖因染色结合T4和T8的T细胞分型来研究供体-受者T4+和T8+ T细胞的来源。在进行化疗放疗和骨髓移植(BMT)后,T细胞在BMT后中位时间为5天(范围1 - 8天)时降至最低点。T8+ T细胞从外周血中减少的速度比T4+ T细胞更快。在第12天出现在循环中的首批T细胞主要是T4+,且其中大量是源自受者的。此后,它们逐渐减少,而源自供体的T细胞数量增加。在没有或仅有轻微并发症的患者中,源自供体的T4+和T8+ T细胞以相似的速率重新填充血液。然而,这种模式会因严重的移植物抗宿主病或巨细胞病毒感染而改变。