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体内辅助性T淋巴细胞和抑制性T淋巴细胞耗竭对伤口愈合的影响。

The effect of in vivo T helper and T suppressor lymphocyte depletion on wound healing.

作者信息

Barbul A, Breslin R J, Woodyard J P, Wasserkrug H L, Efron G

机构信息

Department of Surgery, Sinai Hospital of Baltimore, Maryland 21215.

出版信息

Ann Surg. 1989 Apr;209(4):479-83. doi: 10.1097/00000658-198904000-00015.

DOI:10.1097/00000658-198904000-00015
PMID:2522759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1493975/
Abstract

The role of T lymphocytes in wound healing is still not well-defined. Because it had been previously shown that in vivo depletion of T cells leads to impaired wound healing, the effect of depleting T cell subsets on subsequent fibroplasia was studied. T helper/effector cells were depleted by the use of the monoclonal antibody GK1.5, reactive against the L3T4 antigen (CD4). T suppressor/cytotoxic lymphocytes were depleted by using the 2.43 monoclonal antibody reactive against the Lyt 2 antigen (CD8). In the first experiment, Balb/c mice were treated with the antibodies starting at 24 hours before wounding was performed, and weekly thereafter. Depletion of the T helper/effector cells had no effect on wound-breaking strength or hydroxyproline deposition in sponge granulomas, whereas depletion of T suppressor/cytotoxic cells significantly enhanced both of these healing parameters. In a second experiment, T cell subset depletion was started on Days 0, 3, 7, 10, and 14 postwounding, and treatments were continued weekly thereafter. Once again, depletion of T helper/effector cells had no effect on wound healing, whereas depletion of T suppressor/cytotoxic cells markedly increased both wound-breaking strength and collagen synthesis. In conclusion, the data show that T suppressor/cytotoxic cells have a counter-regulatory role in wound healing, whereas the T cell subset responsible for up-regulating wound healing remains to be identified.

摘要

T淋巴细胞在伤口愈合中的作用仍未明确界定。由于先前已有研究表明体内T细胞耗竭会导致伤口愈合受损,因此研究了耗竭T细胞亚群对后续纤维增生的影响。通过使用针对L3T4抗原(CD4)的单克隆抗体GK1.5来耗竭T辅助/效应细胞。通过使用针对Lyt 2抗原(CD8)的2.43单克隆抗体来耗竭T抑制/细胞毒性淋巴细胞。在第一个实验中,Balb/c小鼠在受伤前24小时开始用抗体治疗,此后每周一次。耗竭T辅助/效应细胞对伤口抗张强度或海绵肉芽肿中的羟脯氨酸沉积没有影响,而耗竭T抑制/细胞毒性细胞则显著提高了这两个愈合参数。在第二个实验中,在受伤后第0、3、7、10和14天开始耗竭T细胞亚群,此后每周继续治疗。同样,耗竭T辅助/效应细胞对伤口愈合没有影响,而耗竭T抑制/细胞毒性细胞则显著提高了伤口抗张强度和胶原蛋白合成。总之,数据表明T抑制/细胞毒性细胞在伤口愈合中具有反调节作用,而负责上调伤口愈合的T细胞亚群仍有待确定。

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Ann Surg. 1989 Apr;209(4):479-83. doi: 10.1097/00000658-198904000-00015.
2
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本文引用的文献

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The determination of hydroxyproline in tissue and protein samples containing small proportions of this imino acid.对含有少量这种亚氨基酸的组织和蛋白质样品中羟脯氨酸的测定。
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Evidence implicating L3T4 in class II MHC antigen reactivity; monoclonal antibody GK1.5 (anti-L3T4a) blocks class II MHC antigen-specific proliferation, release of lymphokines, and binding by cloned murine helper T lymphocyte lines.有证据表明L3T4参与II类主要组织相容性复合体(MHC)抗原反应;单克隆抗体GK1.5(抗L3T4a)可阻断II类MHC抗原特异性增殖、淋巴因子释放以及克隆化小鼠辅助性T淋巴细胞系的结合。
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Characterization of the murine antigenic determinant, designated L3T4a, recognized by monoclonal antibody GK1.5: expression of L3T4a by functional T cell clones appears to correlate primarily with class II MHC antigen-reactivity.被单克隆抗体GK1.5识别的、命名为L3T4a的鼠类抗原决定簇的特性:功能性T细胞克隆对L3T4a的表达似乎主要与II类主要组织相容性复合体(MHC)抗原反应性相关。
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Cloned T lymphocytes and monoclonal antibodies as probes for cell surface molecules active in T cell-mediated cytolysis.克隆的T淋巴细胞和单克隆抗体作为探测T细胞介导的细胞溶解中起作用的细胞表面分子的探针。
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Stimulation of the chemotactic migration of human fibroblasts by transforming growth factor beta.转化生长因子β对人成纤维细胞趋化性迁移的刺激作用。
J Exp Med. 1987 Jan 1;165(1):251-6. doi: 10.1084/jem.165.1.251.
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