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在人类 HLA 同型干细胞移植后,供体 CD4+ 或 CD8+ T 细胞上 CD25 的表达与移植物抗宿主病风险增加相关。

CD25 expression on donor CD4+ or CD8+ T cells is associated with an increased risk for graft-versus-host disease after HLA-identical stem cell transplantation in humans.

作者信息

Stanzani Marta, Martins Sergio L R, Saliba Rima M, St John Lisa S, Bryan Susan, Couriel Daniel, McMannis John, Champlin Richard E, Molldrem Jeffrey J, Komanduri Krishna V

机构信息

Transplant Immunology Laboratory, MD Anderson Cancer Center, SCRB 3.3019, 7455 Fannin St, Houston, TX 77030, USA.

出版信息

Blood. 2004 Feb 1;103(3):1140-6. doi: 10.1182/blood-2003-06-2085. Epub 2003 Aug 7.

DOI:10.1182/blood-2003-06-2085
PMID:12907445
Abstract

Graft-versus-host disease (GVHD) occurs in an unpredictable fashion after 30% to 50% of matched-related transplantations. The presence of increased frequencies of CD4(+)CD25(+) regulatory T cells in donor grafts has been shown to ameliorate GVHD after allogeneic transplantation in murine models. To determine whether a similar relationship exists in humans, we quantitated the coexpression of CD25 on CD4(+) and CD8(+) T cells within 60 donor grafts infused into matched siblings and examined GVHD incidence in the respective recipients. Recipients in whom GVHD developed received donor grafts containing significantly higher frequencies of CD4(+) T cells coexpressing CD25 than those who did not (median, 9.26% vs 2.22%; P =.004). Frequencies of donor graft CD8(+) T cells coexpressing CD25 were also higher (0.65% vs 0.14%; P =.002). Furthermore, transplant recipients who received grafts containing fewer CD4(+)CD25(+) and CD8(+)CD25(+) T cells were less likely to acquire acute GVHD, even though these donor-recipient pairs were similar to others with respect to relevant clinical variables. These data suggest that the coexpression of CD4 and CD25 may be insufficient to identify regulatory T cells in humans and that increased frequencies and numbers of CD25(+) T cells in donor grafts is associated with GVHD in transplant recipients.

摘要

移植物抗宿主病(GVHD)在30%至50%的匹配相关移植术后以不可预测的方式发生。在小鼠模型中,已证明供体移植物中CD4(+)CD25(+)调节性T细胞频率增加可改善异基因移植后的GVHD。为了确定人类是否存在类似关系,我们对注入匹配同胞体内的60份供体移植物中CD4(+)和CD8(+)T细胞上CD25的共表达进行了定量,并检查了相应受者的GVHD发生率。发生GVHD的受者所接受的供体移植物中,共表达CD25的CD4(+)T细胞频率显著高于未发生GVHD的受者(中位数分别为9.26%和2.22%;P = 0.004)。供体移植物中共表达CD25的CD8(+)T细胞频率也更高(0.65%对0.14%;P = 0.002)。此外,接受含较少CD4(+)CD25(+)和CD8(+)CD25(+)T细胞移植物的移植受者发生急性GVHD的可能性较小,尽管这些供体-受者对在相关临床变量方面与其他供体-受者对相似。这些数据表明,CD4和CD25的共表达可能不足以识别人类中的调节性T细胞,并且供体移植物中CD25(+)T细胞频率和数量的增加与移植受者的GVHD相关。

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CD25 expression on donor CD4+ or CD8+ T cells is associated with an increased risk for graft-versus-host disease after HLA-identical stem cell transplantation in humans.在人类 HLA 同型干细胞移植后,供体 CD4+ 或 CD8+ T 细胞上 CD25 的表达与移植物抗宿主病风险增加相关。
Blood. 2004 Feb 1;103(3):1140-6. doi: 10.1182/blood-2003-06-2085. Epub 2003 Aug 7.
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CD4+CD25+ regulatory T cells preserve graft-versus-tumor activity while inhibiting graft-versus-host disease after bone marrow transplantation.CD4+CD25+调节性T细胞在骨髓移植后保留移植物抗肿瘤活性,同时抑制移植物抗宿主病。
Nat Med. 2003 Sep;9(9):1144-50. doi: 10.1038/nm915. Epub 2003 Aug 17.
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CD4 Donor Lymphocyte Infusion Can Cause Conversion of Chimerism Without GVHD by Inducing Immune Responses Targeting Minor Histocompatibility Antigens in HLA Class II.CD4 供者淋巴细胞输注可通过诱导针对 HLA II 类中次要组织相容性抗原的免疫反应,在无移植物抗宿主病的情况下引起嵌合状态的转换。
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