Suppression of humoral and cell-mediated immune responses in vitro by benzo(a)pyrene.

P Urso, N Gengozian, R M Rossi, R A Johnson
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引用次数: 26

Abstract

The effect of benzo(a)pyrene (BaP) at different molar (M) concentrations on the in vitro anti-sheep red blood cell (SRBC) plaque (antibody) forming cell (PFC) response and the one-way mixed lymphocyte response (MLR) was tested. Inhibition of the PFC response and the MLR occurred when spleen cells were exposed to a wide range of BaP concentrations from 10(-4) M to 10(-8) M. Maximum depression of the responses occurred at 10(-5) M for PFC production (47% of controls) and for the MLR (19% of controls) as measured by a stimulation index. No significant loss in cell viability was observed at this or lower molar concentrations of BaP. The non-carcinogenic analog of BaP, benzo(e)pyrene, did not suppress PFC responses at comparable concentrations. This in vitro system will facilitate manipulations of T and B lymphocytes and macrophages (adherent cells) in a controlled culture environment for precisely characterizing the sensitivity of these cells and their subpopulations on exposure to BaP.

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苯并(a)芘体外抑制体液和细胞介导的免疫反应。
研究了不同摩尔(M)浓度的苯并(a)芘(BaP)对体外抗羊红细胞(SRBC)斑块(抗体)形成细胞(PFC)反应和单向混合淋巴细胞反应(MLR)的影响。当脾脏细胞暴露于10(-4)M至10(-8)M范围内的BaP浓度时,PFC反应和MLR发生抑制。通过刺激指数测量,PFC产生(47%的对照组)和MLR(19%的对照组)的反应在10(-5)M时出现最大抑制。在这个或更低的BaP摩尔浓度下,没有观察到细胞活力的显著丧失。BaP的非致癌性类似物苯并(e)芘在相当浓度下不会抑制PFC反应。该体外系统将有助于在受控的培养环境中对T淋巴细胞、B淋巴细胞和巨噬细胞(贴壁细胞)进行操作,以精确表征这些细胞及其亚群对BaP暴露的敏感性。
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