白细胞介素2在正常受试者单次脊柱推拿治疗后调节体外抗体产生。

Julita A Teodorczyk-Injeyan, Marion McGregor, Richard Ruegg, H Stephen Injeyan
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引用次数: 15

摘要

背景:我们最近的研究表明,在上胸椎接受单一脊柱操纵治疗的受试者的细胞培养显示出关键免疫调节细胞因子白介素-2的产生能力增加。然而,尚未确定这些变化是否会影响免疫效应细胞的反应。因此,本研究的目的是确定,在相同的受试者中,脊柱操纵相关的体外白细胞介素-2合成的增强是否与白细胞介素-2依赖性和/或白细胞介素-2诱导的体液免疫反应(抗体合成)的调节有关。方法:对74名年龄和性别匹配的健康无症状受试者进行研究。受试者随机分为静脉穿刺对照组(n = 22)、无空化脊柱推拿治疗组(n = 25)和空化脊柱推拿治疗组(n = 27)。在治疗前(基线)和治疗后20分钟和2小时分别采集受试者的肝素化血样。用常规欧陆有丝分裂原或人重组白细胞介素-2诱导外周血单核细胞合成免疫球蛋白(抗体)。用特异性免疫分析法测定培养上清液中免疫球蛋白G和免疫球蛋白M的含量。结果:刺激美洲商陆有丝分裂原或人重组白细胞介素-2诱导的免疫球蛋白合成基线水平在所有组中具有可比性。在任何研究组中,治疗后未观察到美洲商陆有丝分裂原诱导的免疫球蛋白的产生有显著变化。与此相反,在脊髓操纵的培养物中,白细胞介素-2诱导的免疫球蛋白G和免疫球蛋白M的产生显著增加。在操作后20分钟,相对于单独进行空化操作和静脉穿刺的培养物,空化操作组免疫球蛋白G合成显著升高。在治疗后2小时,相对于静脉穿刺组,空化操作组的免疫球蛋白M合成明显升高。在研究的培养中,外周血B淋巴细胞和T淋巴细胞的数量没有变化。结论:脊柱推拿治疗不增加有丝分裂原激活的B细胞合成白细胞介素-2依赖性多克隆免疫球蛋白。然而,单独由白细胞介素-2诱导的抗体合成可以,至少暂时,在脊柱操作后增强。因此,在某些生理条件下,脊柱推拿治疗可能会影响白介素-2调节的生物反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interleukin 2-regulated in vitro antibody production following a single spinal manipulative treatment in normal subjects.

Interleukin 2-regulated in vitro antibody production following a single spinal manipulative treatment in normal subjects.

Interleukin 2-regulated in vitro antibody production following a single spinal manipulative treatment in normal subjects.

Background: Our recent investigations have demonstrated that cell cultures from subjects, who received a single spinal manipulative treatment in the upper thoracic spine, show increased capacity for the production of the key immunoregulatory cytokine, interleukin-2. However, it has not been determined if such changes influence the response of the immune effector cells. Thus, the purpose of the present study was to determine whether, in the same subjects, spinal manipulation-related augmentation of the in vitro interleukin-2 synthesis is associated with the modulation of interleukin 2-dependent and/or interleukin-2-induced humoral immune response (antibody synthesis).

Methods: A total of seventy-four age and sex-matched healthy asymptomatic subjects were studied. The subjects were assigned randomly to: venipuncture control (n = 22), spinal manipulative treatment without cavitation (n = 25) or spinal manipulative treatment associated with cavitation (n = 27) groups. Heparinized blood samples were obtained from the subjects before (baseline) and then at 20 minutes and 2 hours post-treatment. Immunoglobulin (antibody) synthesis was induced in cultures of peripheral blood mononuclear cells by stimulation with conventional pokeweed mitogen or by application of human recombinant interleukin-2. Determinations of the levels of immunoglobulin G and immunoglobulin M production in culture supernatants were performed by specific immunoassays.

Results: The baseline levels of immunoglobulin synthesis induced by pokeweed mitogen or human recombinant interleukin-2 stimulation were comparable in all groups. No significant changes in the production of pokeweed mitogen-induced immunoglobulins were observed during the post-treatment period in any of the study groups. In contrast, the production of interleukin-2 -induced immunoglobulin G and immunoglobulin M was significantly increased in cultures from subjects treated with spinal manipulation. At 20 min post-manipulation, immunoglobulin G synthesis was significantly elevated in subjects who received manipulation with cavitation, relative to that in cultures from subjects who received manipulation without cavitation and venipuncture alone. At 2 hr post-treatment, immunoglobulin M synthesis was significantly elevated in subjects who received manipulation with cavitation relative to the venipuncture group. There were no quantitative alterations within the population of peripheral blood B or T lymphocytes in the studied cultures.

Conclusion: Spinal manipulative treatment does not increase interleukin-2 -dependent polyclonal immunoglobulin synthesis by mitogen-activated B cells. However, antibody synthesis induced by interleukin-2 alone can be, at least temporarily, augmented following spinal manipulation. Thus, under certain physiological conditions spinal manipulative treatment might influence interleukin-2 -regulated biological responses.

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