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通过滤膜免疫斑试验测定单纯疱疹病毒诱导的分泌α干扰素的人血白细胞。

Determination of herpes simplex virus-induced alpha interferon-secreting human blood leucocytes by a filter immuno-plaque assay.

作者信息

Rönnblom L, Cederblad B, Sandberg K, Alm G V

机构信息

Department of Medicine, Central Hospital, Boden, Sweden.

出版信息

Scand J Immunol. 1988 Feb;27(2):165-70. doi: 10.1111/j.1365-3083.1988.tb02335.x.

Abstract

A filter immuno-plaque assay was developed which detects alpha interferon (INF-alpha)-secreting human peripheral blood leucocytes (PBL). Polyclonal anti-IFN-alpha antibodies were fixed to the nitrocellulose membrane bottoms of 96-well Millititer plates, which also contained monolayers of glutaraldehyde-fixed human WISH amnion cells infected by Herpes simplex virus type 1 (HSV). Such cells are potent IFN inducers and during a 16 h cocultivation with PBL, IFN-alpha was absorbed by the membrane-bound polyclonal antibodies around IFN-alpha-secreting cells. This IFN-alpha was detected with murine monoclonal antibodies against IFN-alpha and peroxidase-labelled antibodies against murine immunoglobulin, using diaminobenzidine as substrate. Distinctly stained plaques were seen, the frequency of which gave a minimal estimate of approximately 10 IFN-alpha-producing cells in 10(4) PBL (range in 12 blood donors 2.95-25.1). Fewer plaques than expected were seen at low PBL numbers per culture, one explanation being that cell interactions then limit the IFN-alpha response. The immuno-plaque assay should be useful in further studies of the cellular basis of the IFN-alpha response.

摘要

开发了一种滤膜免疫斑试验,用于检测分泌α干扰素(IFN-α)的人外周血白细胞(PBL)。将多克隆抗IFN-α抗体固定在96孔Millititer板的硝酸纤维素膜底部,该板中还含有经戊二醛固定、被1型单纯疱疹病毒(HSV)感染的人WISH羊膜细胞单层。此类细胞是有效的IFN诱导剂,在与PBL共培养16小时期间,IFN-α被IFN-α分泌细胞周围与膜结合的多克隆抗体吸收。使用抗IFN-α的鼠单克隆抗体和抗鼠免疫球蛋白的过氧化物酶标记抗体,以二氨基联苯胺为底物检测这种IFN-α。可见明显染色的斑块,其频率给出了在10⁴个PBL中约10个产生IFN-α细胞的最低估计值(12名献血者的范围为2.95 - 25.1)。在每个培养物中PBL数量较低时,观察到的斑块比预期的少,一种解释是细胞间相互作用会限制IFN-α反应。这种免疫斑试验在进一步研究IFN-α反应的细胞基础方面应会有用。

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