Miniero R, Busca A, Roncarolo M G, Saitta M, Iavarone A, Timeus F, Biondi A, Amoroso A, Perugini L, Ciuti E
Department of Pediatrics, University of Turin, Italy.
Bone Marrow Transplant. 1995 Aug;16(2):229-40.
Growing attention has been focused on cord blood as a source of transplantable hematopoietic stem cells. However, clinical experience is rather limited. In this study we describe a child with advanced acute lymphoblastic leukemia who received an HLA-haploidentical cord blood transplant. The patient was transplanted in third complete remission after conditioning with fractionated total body irradiation, thiotepa and cyclophosphamide. Forty-one milliliters of cryopreserved umbilical cord blood, containing 0.15 x 10(8) nucleated cells/kg and 0.25 x 10(4) CFU-GM/kg, were infused. Cyclosporine and prednisone were administered for graft-versus-host disease (GVHD) prophylaxis. The patient received G-CSF from day +1 to day +35, but no improvement in granulocyte counts was observed. Therefore, administration of GM-CSF was started on day +36 to day +59, which resulted in a significant increase in white blood cells and granulocyte counts. Sustained myeloid engraftment was evidenced by a granulocyte count > 0.5 x 10(9)/l by day +41. The presence of donor-derived cells could be documented in the peripheral blood and bone marrow of the patient by cytogenetic analysis, HLA phenotyping and DNA studies. Forty-one days after transplant, clonogenic bone marrow assays showed the presence of low frequencies of primitive hematopoietic progenitor cells (BFU-E = 19/10(5) and CFU-GM = 8/10(5)). The chimerism was complete and no host-derived cells could be detected. However, the engraftment was restricted to the myeloid lineage whereas lymphoid and megakaryocytic engraftments were inadequate. The immunophenotype of the patient's peripheral blood showed the presence of T lymphocytes expressing an immature phenotype (CD2+ CD3-) at day +21.(ABSTRACT TRUNCATED AT 250 WORDS)
越来越多的关注聚焦于脐带血,将其作为可移植造血干细胞的来源。然而,临床经验相当有限。在本研究中,我们描述了一名患有晚期急性淋巴细胞白血病的儿童,他接受了HLA半相合脐带血移植。患者在接受分次全身照射、噻替哌和环磷酰胺预处理后,于第三次完全缓解期接受移植。输注了41毫升冷冻保存的脐带血,其中含有0.15×10⁸有核细胞/千克和0.25×10⁴集落形成单位-粒细胞巨噬细胞/千克。给予环孢素和泼尼松预防移植物抗宿主病(GVHD)。患者从第+1天至第+35天接受粒细胞集落刺激因子(G-CSF)治疗,但粒细胞计数未见改善。因此于第+36天至第+59天开始给予粒细胞-巨噬细胞集落刺激因子(GM-CSF),这导致白细胞和粒细胞计数显著增加。到第+41天时,粒细胞计数>0.5×10⁹/升,证明有持续的髓系植入。通过细胞遗传学分析、HLA分型和DNA研究,可在患者的外周血和骨髓中证实供体来源细胞的存在。移植后41天,克隆形成骨髓分析显示存在低频的原始造血祖细胞(爆式红系集落形成单位=19/10⁵,集落形成单位-粒细胞巨噬细胞=8/10⁵)。嵌合是完全的,未检测到宿主来源的细胞。然而,植入仅限于髓系谱系,而淋巴系和巨核系植入不足。患者外周血的免疫表型显示在第+21天时存在表达不成熟表型(CD2⁺CD3⁻)的T淋巴细胞。(摘要截短于250字)