Effects of cigarette smoke on the immune response. II. Chronic exposure to cigarette smoke inhibits surface immunoglobulin-mediated responses in B cells.

Effects of cigarette smoke on the immune response. II. Chronic exposure to cigarette smoke inhibits surface immunoglobulin-mediated responses in B cells.
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香烟烟雾对免疫反应的影响。

DOI:
10.1016/0041-008x(91)90256-e
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发表时间:
1991
影响因子:
3.8
通讯作者:
Sopori,ML
Sopori,ML
中科院分区:
医学3区
文献类型:
--
作者:
Savage,SM;Donaldson,LA;Cherian,S;Chilukuri,R;White,VA;Sopori,ML

文献摘要

被引文献

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我们以前曾报道,长期暴露在香烟烟雾中会抑制抗体形成细胞(AFC)对T依赖和T非依赖抗原的反应,并可能反映B细胞功能障碍。在这次交流中,我们扩展了这些研究,以表明长期吸烟暴露的大鼠(SM)的T细胞功能是正常的,根据它们对有丝分裂原和“名义”或同种异体抗原的反应来判断。虽然SM的B细胞对B细胞有丝分裂原脂多糖有显著的反应,但它们不能对抗μ抗体(抗-IgM)产生增殖反应,也不能对绵羊红细胞产生显著的AFC反应。根据三硝基苯化(TNP)马红细胞形成的花环数目,SM大鼠脾中TNP结合细胞(TNP-ABC)的频率与假手术对照组相当。而丹参能显著降低TNP-ABC对TNP-布鲁氏菌的增殖作用。SM B细胞反应的这些差异,即内毒素和抗μ/抗原之间的差异,可能与内毒素绕过部分膜信号转导通路的能力有关。这些结果表明,香烟烟雾影响抗原依赖的B细胞信号转导通路的早期步骤(S)。
We have previously reported that chronic exposure of rats to cigarette smoke inhibits the antibody-forming cell (AFC) response to both T-dependent and T-independent antigens and may reflect B cell dysfunction. In this communication we extend these studies to show that T cell functions are normal in chronically smoke-exposed rats (SM) as judged by their responses to mitogens and “nominal” or alloantigens. While B cells from SM respond significantly to the B cell mitogen lipopolysaccharide (LPS), they fail to proliferate in response to anti-IgM (anti-μ) or to produce significant AFC response to sheep red blood cells. On the basis of the number of rosettes formed with trinitrophenylated (TNP) horse red blood cells, the frequency of TNP-binding cells (TNP-ABC) in the spleens of SM is comparable to sham control rats. However, the proliferation of TNP-ABC to TNP-Brucella abortus is significantly decreased in SM. These differences in SM B cell responses, i.e., between LPS and anti-μ/antigen, may to be related to the ability of LPS to bypass a portion of the membrane signal transduction cascade. These results suggest that cigarette smoke affects an early step(s) in the antigen-dependent B cell signal transduction pathway.