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用抗CD3/TCR单克隆抗体治疗异基因骨髓移植后类固醇难治性移植物抗宿主病。

Treatment of steroid-resistant graft-versus-host disease after allogeneic bone marrow transplantation with anti-CD3/TCR monoclonal antibodies.

作者信息

Hebart H, Ehninger G, Schmidt H, Berner B, Reuss-Borst M, Waller H D, Müller C A, Einsele H

机构信息

Medizinische Universitätsklinik Tübingen, Abteilung II, Germany.

出版信息

Bone Marrow Transplant. 1995 Jun;15(6):891-4.

PMID:7581087
Abstract

Acute graft-versus host disease (GVHD), one of the major complications of allogeneic bone marrow transplantation (BMT), occurs in 30-50% of all patients transplanted from HLA-identical sibling donors and in 50-80% of all patients transplanted from an unrelated or HLA-mismatched family donor, despite GVHD prophylaxis with methotrexate and cyclosporin. We report our experience with OKT3/BMA031 treatment in 14 patients with severe steroid-resistant GVHD following allogeneic BMT. Three of 5 patients treated in the early post-transplant period with OKT3 remitted and 2 of 3 became long-term survivors. Two patients treated for extensive chronic GVHD showed only minor responses. Five of 7 patients treated with BMA031 showed a partial remission; no complete remission was seen after treatment with this antibody. Shortly after the introduction of OKT3 or BMA031 therapy a rapid decline of the lymphocyte count, especially the CD3+ subset, was observed coinciding with a relative increase of CD56+ lymphocytes and of gamma/delta TCR+ T cells. Increasing numbers of CD3+ lymphocytes preceded recurrence of acute GVHD in three patients. In contrast, persisting CD3-lymphocytopenia was associated with complete clearance of acute GVHD. The incidence of infectious complications following OKT3 or BMA031 therapy was high (42%). Thus, to improve treatment results of severe acute GVHD, prophylactic or pre-emptive strategies are required to reduce the rate of fatal viral and fungal infections.

摘要

急性移植物抗宿主病(GVHD)是同种异体骨髓移植(BMT)的主要并发症之一,在接受 HLA 相同的同胞供体移植的所有患者中,有 30% - 50%会发生,而在接受无关或 HLA 不匹配的家族供体移植的所有患者中,有 50% - 80%会发生,尽管使用了甲氨蝶呤和环孢素进行 GVHD 预防。我们报告了我们对 14 例同种异体 BMT 后发生严重类固醇抵抗性 GVHD 的患者进行 OKT3/BMA031 治疗的经验。在移植后早期接受 OKT3 治疗的 5 例患者中,有 3 例缓解,3 例中有 2 例成为长期存活者。2 例接受广泛慢性 GVHD 治疗的患者仅表现出轻微反应。接受 BMA031 治疗的 7 例患者中有 5 例部分缓解;用该抗体治疗后未见完全缓解。在引入 OKT3 或 BMA031 治疗后不久,观察到淋巴细胞计数迅速下降,尤其是 CD3 + 亚群,同时 CD56 + 淋巴细胞和γ/δTCR + T 细胞相对增加。3 例患者急性 GVHD 复发前 CD3 + 淋巴细胞数量增加。相反,持续的 CD3 - 淋巴细胞减少与急性 GVHD 的完全清除相关。OKT3 或 BMA031 治疗后感染并发症的发生率很高(42%)。因此,为了改善严重急性 GVHD 的治疗效果,需要采取预防或先发制人的策略来降低致命病毒和真菌感染的发生率。

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