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B 细胞在脐血移植受者免疫抑制反应中的潜在作用。

A potential role for B cells in suppressed immune responses in cord blood transplant recipients.

机构信息

Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL, USA.

出版信息

Bone Marrow Transplant. 2013 Jan;48(1):85-93. doi: 10.1038/bmt.2012.104. Epub 2012 Jun 25.

DOI:10.1038/bmt.2012.104
PMID:22732699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3985415/
Abstract

We evaluated immune reconstitution in 58 adults who received hematopoietic SCTs from allogeneic siblings (allosib), matched unrelated donors (MUD) or cord blood (CB) at 90-day intervals for 1 year post transplant. CB recipients had a higher incidence of infections in the first 100 days compared with allosib and MUD recipients. The number of circulating T cells was lower in CB recipients compared with MUD recipients at 90 days and compared with allosib recipients at 180 days. Spectratype analysis of the TCR Vβ complementarity determining region 3 (CDR3) of patient lymphocytes revealed that the TCR repertoire remained poorly diversified even at 360 days in nearly all patients. In contrast, the number of circulating B cells was significantly elevated in CB recipients compared with allosib recipients throughout the first year post transplant and compared with MUD recipients at 9-12 months. Spectratype analysis of the B-cell receptor V(H) CDR3 showed that the B-cell repertoire was diversified in most patients by 90 days. CD5(pos) B cells from assayed CB recipients expressed intracellular IL-10 early post transplant. Our data suggest that B cells, in addition to T cells, may have a role in impaired immune responses in CB transplant patients.

摘要

我们评估了 58 位成年人的免疫重建情况,这些成年人在接受异基因兄弟姐妹(allosib)、匹配的无关供体(MUD)或脐带血(CB)造血干细胞移植后,在移植后 1 年内每隔 90 天进行一次随访。CB 受者在前 100 天的感染发生率高于 alloSib 和 MUD 受者。与 MUD 受者相比,CB 受者在 90 天时循环 T 细胞数量较低,在 180 天时循环 T 细胞数量与 alloSib 受者相比也较低。患者淋巴细胞 TCR Vβ 互补决定区 3(CDR3)的谱型分析表明,TCR 受体库在几乎所有患者中甚至在 360 天时仍然多样性较差。相比之下,在移植后 1 年内,CB 受者的循环 B 细胞数量明显高于 alloSib 受者,在 9-12 个月时也高于 MUD 受者。B 细胞受体 V(H)CDR3 的谱型分析表明,在大多数患者中,B 细胞受体库在 90 天时就具有多样性。从检测到的 CB 受者中分离出的 CD5(pos)B 细胞在移植后早期表达细胞内 IL-10。我们的数据表明,B 细胞除了 T 细胞外,在 CB 移植患者的免疫应答受损中可能也有一定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/e83b8348f5f5/nihms-376431-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/ec263bfcaf7e/nihms-376431-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/e83b8348f5f5/nihms-376431-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/ec263bfcaf7e/nihms-376431-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/046f69a8e991/nihms-376431-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/2df92afdae6a/nihms-376431-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/70ab1dd48a98/nihms-376431-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/39dd7aeb4829/nihms-376431-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/3985415/e83b8348f5f5/nihms-376431-f0006.jpg

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本文引用的文献

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IL-10 produced by activated human B cells regulates CD4(+) T-cell activation in vitro.活化的人 B 细胞产生的白细胞介素-10 可调节体外 CD4(+)T 细胞的活化。
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