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通过转移培养的脾细胞抑制大鼠佐剂性关节炎。

Suppression of adjuvant arthritis in rats by transfer of cultured spleen cells.

作者信息

Ogawa H, Tsunematsu T

出版信息

Clin Exp Immunol. 1986 Apr;64(1):88-93.

PMID:2942324
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1542152/
Abstract

We studied the in vivo effect of transfer of nonspecific suppressor spleen cells into syngeneic Lewis rats. The rats were immunized with Freund's adjuvant on day 0, and then given 5 X 10(7) cells on days--7, 0 and 7. These cells had been incubated for 3 days, with or without mitogenic stimulation. Transfer of the cultured cells markedly diminished the severity of adjuvant arthritis (AA). On the contrary, transfer of concanavalin A (Con A)-stimulated cells led to no suppressive activity. These results differed from findings in a prior in vitro experiment, in which the suppressive influence of previously cultured cells on T and B lymphocytes proliferation rates was examined and significant suppressive activity was detected in Con A-stimulated cells but not in cultured cells. Suppressor activity by transfer of solely cultured cells was identified in T cell fractions. Transfer of 5 X 10(7) spleen cells proved to be the optimal dose for suppressing AA, and transfer of less than 2 X 10(7) cells had no significant effect. The number and time of transfer were also important factors in the suppression. Each group of transfer on days--7, 0 and 7, days--7 and 0, and days 0 and 7 led to a similar reduction in the severity of AA, and was less prominent in the group injected on days 7 and 14. A single injection on days--7, 0, or 7 revealed minimal or no effects. These observations indicate that the transfer of in vitro cultured spleen cells nonspecifically modified the course of rat AA in vivo, thereby differing from the results of the suppressor activity seen in vitro. The transfer of cultured cells, as a potential tool for the treatment of clinical diseases warrants further attention.

摘要

我们研究了将非特异性抑制性脾细胞转移至同基因Lewis大鼠体内的效应。在第0天用弗氏佐剂对大鼠进行免疫,然后在第 -7、0和7天给予5×10⁷个细胞。这些细胞已培养3天,有无丝裂原刺激。转移培养细胞显著减轻了佐剂性关节炎(AA)的严重程度。相反,转移伴刀豆球蛋白A(Con A)刺激的细胞则无抑制活性。这些结果与之前的体外实验结果不同,在体外实验中检测了先前培养的细胞对T和B淋巴细胞增殖率的抑制影响,发现Con A刺激的细胞有显著抑制活性,而培养细胞则没有。在T细胞组分中鉴定出仅通过转移培养细胞产生的抑制活性。转移5×10⁷个脾细胞被证明是抑制AA的最佳剂量,转移少于2×10⁷个细胞则无显著效果。转移的数量和时间也是抑制中的重要因素。在第 -7、0和7天、第 -7和0天以及第0和7天进行的每组转移都导致AA严重程度有类似程度的降低,而在第7和14天注射的组中这种降低不太明显。在第 -7、0或7天单次注射显示效果极小或无效果。这些观察结果表明,体外培养的脾细胞转移在体内非特异性地改变了大鼠AA的病程,从而与体外所见的抑制活性结果不同。作为治疗临床疾病的潜在工具,培养细胞的转移值得进一步关注。

相似文献

1
Suppression of adjuvant arthritis in rats by transfer of cultured spleen cells.通过转移培养的脾细胞抑制大鼠佐剂性关节炎。
Clin Exp Immunol. 1986 Apr;64(1):88-93.
2
Transfer of spleen cells expanded by T cell growth factor suppresses arthritis induced in rats.经T细胞生长因子扩增的脾细胞转移可抑制大鼠诱发的关节炎。
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3
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Clin Exp Immunol. 1988 Jun;72(3):476-80.
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Restoration of diminished splenic responses to phytohemagglutinin and concanavalin A in adjuvant-induced disease by virazole: possible pathogenetic role of a virus and suppressor cells.病毒唑对佐剂诱导疾病中脾脏对植物血凝素和刀豆球蛋白A反应减弱的恢复作用:病毒和抑制细胞可能的致病作用
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In vitro X-ray irradiation of human peripheral blood T lymphocytes enhances suppressor function.对人外周血T淋巴细胞进行体外X射线照射可增强抑制功能。
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引用本文的文献

1
Transfer of spleen cells expanded by T cell growth factor suppresses arthritis induced in rats.经T细胞生长因子扩增的脾细胞转移可抑制大鼠诱发的关节炎。
Clin Exp Immunol. 1987 Jan;67(1):176-81.
2
Participation of suppressor-inducer cells in the suppression of adjuvant arthritis by transfer of spleen cells expanded by T cell growth factor.抑制诱导细胞通过转移经T细胞生长因子扩增的脾细胞参与佐剂性关节炎的抑制作用。
Clin Exp Immunol. 1988 Jun;72(3):476-80.

本文引用的文献

1
Carrageenin-induced edema in hind paw of the rat as an assay for antiiflammatory drugs.角叉菜胶诱导大鼠后爪水肿作为抗炎药物的一种测定方法。
Proc Soc Exp Biol Med. 1962 Dec;111:544-7. doi: 10.3181/00379727-111-27849.
2
Total lymphoid and local joint irradiation in the treatment of adjuvant arthritis.全淋巴照射与局部关节照射治疗佐剂性关节炎
Arthritis Rheum. 1981 Jan;24(1):38-44. doi: 10.1002/art.1780240106.
3
Adoptive transfer of suppression of experimental allergic orchitis with lymphoid cells from antigen-pretreated guinea pigs.采用来自抗原预处理豚鼠的淋巴细胞进行实验性变应性睾丸炎抑制作用的过继转移。
Clin Immunol Immunopathol. 1984 Feb;30(2):202-13. doi: 10.1016/0090-1229(84)90055-2.
4
In vitro X-ray irradiation of human peripheral blood T lymphocytes enhances suppressor function.对人外周血T淋巴细胞进行体外X射线照射可增强抑制功能。
Clin Exp Immunol. 1983 Aug;53(2):444-50.
5
Role of T lymphocytes in the pathogenesis of experimental autoimmune encephalomyelitis.T淋巴细胞在实验性自身免疫性脑脊髓炎发病机制中的作用。
Eur J Immunol. 1973 Apr;3(4):243-5. doi: 10.1002/eji.1830030413.
6
Suppression of collagen type II-induced arthritis by transfer of lymphoid cells from rats immunized with collagen.通过转移用胶原蛋白免疫的大鼠的淋巴细胞来抑制II型胶原诱导的关节炎。
Clin Exp Immunol. 1985 Aug;61(2):368-72.
7
T lymphocyte clones illuminate pathogenesis and affect therapy of experimental arthritis.T淋巴细胞克隆阐明了实验性关节炎的发病机制并影响其治疗。
Arthritis Rheum. 1985 Aug;28(8):841-5. doi: 10.1002/art.1780280802.
8
Modulation of autoimmunity in NZB mice by cyclophosphamide-induced, nonspecific suppressor cells.环磷酰胺诱导的非特异性抑制细胞对新西兰黑小鼠自身免疫的调节作用。
J Immunol. 1985 Feb;134(2):847-51.
9
Control of human B lymphocyte responsiveness: enhanced suppressor T cell activity after in vitro incubation.人类B淋巴细胞反应性的控制:体外培养后抑制性T细胞活性增强
J Immunol. 1978 Mar;120(3):902-10.
10
Ontogeny of culture-generated suppressor cells.由文化产生的抑制细胞的个体发生。
J Exp Med. 1979 Dec 1;150(6):1359-66. doi: 10.1084/jem.150.6.1359.