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在缺乏 artemis 的小鼠中,使用抗自然杀伤细胞抗体和光化学处理致敏供体 T 细胞,非匹配造血干细胞移植而无需烷化剂治疗即可重建 T 细胞和 B 细胞免疫。

T cell and B Cell immunity can be reconstituted with mismatched hematopoietic stem cell transplantation without alkylator therapy in artemis-deficient mice using anti-natural killer cell antibody and photochemically treated sensitized donor T cells.

机构信息

Blood and Marrow Transplant Division, Department of Pediatrics, University of California San Francisco Benioff Children's Hospital, 505 Parnassus Avenue, San Francisco, CA 94143-1278, USA.

出版信息

Biol Blood Marrow Transplant. 2012 Feb;18(2):200-9. doi: 10.1016/j.bbmt.2011.10.017. Epub 2011 Oct 19.

Abstract

Children with Artemis-deficient T(-)B(-)NK(+) severe combined immunodeficiency are at high risk for graft rejection from natural killer (NK) cells and toxicity from increased sensitivity to the alkylating agents used in mismatched hematopoietic stem cell transplantation (HSCT). We evaluated the use of a nonalkylating agent regimen before HSCT in Artemis-deficient (mArt(-/-)) C57Bl/6 (B6) mice to open marrow niches and achieve long-term multilineage engraftment with full T cell and B cell immune reconstitution. We found that partial depletion of both recipient NK cells using anti-NK1.1 monoclonal antibody and donor T cells sensitized to recipient splenocytes was necessary. BALB/c-sensitized T cells (STCs) were photochemically treated (PCT) with psoralen and UVA light to inhibit proliferation, reduce the risk of graft-versus-host disease (GVHD), and target host hematopoietic stem cells (HSCs). A dose of 4 × 10(5) PCT STCs coinjected with 1 × 10(5) lineage-depleted c-kit(+) BALB/c HSCs resulted in 43.9% ± 3.3% CD4(+) and 10.9% ± 1.2% CD8(+) donor T cells in blood, 29% ± 7.8% and 21.7% ± 4.0 donor B220(+) IgM(+) in spleen and bone marrow, and 15.0% ± 3.6% donor Gran-1(+) cells in bone marrow at 6 months post-HSCT versus 0.02% ± 0.01%, 0.13% ± 0.10%, 0.53% ± 0.16%, 0.49% ± 0.09%, and 0.20% ± 0.06%, respectively, in controls who did not receive PCT STCs. We found that STCs target host HSCs and that PCT STCs are detectable only up to 24 hours after infusion, in contrast to non-photochemically treated STCs, which proliferate resulting in fatal GVHD. Increased mortality in the groups receiving 4-6 × 10(5) PCT STCs was associated with evidence of GVHD, particularly in the recipients of 6 × 10(5) cells. These results demonstrate that blocking NK cell-mediated resistance and making niches in bone marrow are both essential to achieving multilineage engraftment of mismatched donor cells and T cell and B cell reconstitution, even though GVHD is not completely eliminated.

摘要

患有 Artemis 缺陷的 T(-)B(-)NK(+)严重联合免疫缺陷的儿童由于自然杀伤 (NK) 细胞的移植物排斥反应和对用于不匹配造血干细胞移植 (HSCT) 的烷化剂敏感性增加的毒性而面临高风险。我们评估了在 Artemis 缺陷 (mArt(-/-)) C57Bl/6 (B6) 小鼠进行 HSCT 前使用非烷化剂方案的效果,以开放骨髓龛并实现具有完全 T 细胞和 B 细胞免疫重建的长期多谱系植入。我们发现,使用抗 NK1.1 单克隆抗体部分耗尽受体 NK 细胞和对受体脾细胞敏感的供体 T 细胞是必要的。BALB/c 致敏 T 细胞 (STC) 用补骨脂素和 UVA 光进行光化学处理 (PCT) 以抑制增殖,降低移植物抗宿主病 (GVHD) 的风险,并靶向宿主造血干细胞 (HSC)。4×10(5)个 PCT STC 与 1×10(5)个谱系耗竭的 c-kit(+)BALB/c HSC 共注射导致 43.9%±3.3%的供体 CD4(+)和 10.9%±1.2%的 CD8(+)T 细胞在血液中,29%±7.8%和 21.7%±4.0%的供体 B220(+)IgM(+)在脾脏和骨髓中,以及 15.0%±3.6%的供体 Gran-1(+)细胞在骨髓中,而对照组未接受 PCT STC 的分别为 0.02%±0.01%、0.13%±0.10%、0.53%±0.16%、0.49%±0.09%和 0.20%±0.06%。我们发现 STC 靶向宿主 HSC,并且与非光化学处理的 STC 不同,PCT STC 仅在输注后 24 小时内可检测到,而非光化学处理的 STC 增殖导致致命的 GVHD。接受 4-6×10(5)个 PCT STC 的组的死亡率增加与 GVHD 的证据有关,特别是在接受 6×10(5)个细胞的组中。这些结果表明,阻断 NK 细胞介导的抵抗并在骨髓中形成龛位对于实现不匹配供体细胞和 T 细胞和 B 细胞重建的多谱系植入都是至关重要的,尽管 GVHD 并未完全消除。

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