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肾病治疗患者血清对梅森-辉瑞病毒的中和作用。

Neutralization of Mason-Pfizer virus by sera from patients treated for renal disease.

作者信息

Thiry L, Sprecher-Goldberger S, Bossens M, Cogniaux-Le Clerc J, Vereerstraeten P

出版信息

J Gen Virol. 1978 Dec;41(3):587-97. doi: 10.1099/0022-1317-41-3-587.

Abstract

Sera from 67 patients treated for renal diseases were assayed by as many as three different tests for activities against Mason-Pfizer virus (M-P V) antigens. Firstly, in patients studied before kidney transplantation, neutralizing activity against syncytium-forming units of M-P V was found in 50% of 24 cases of chronic glomerulonephritis but in only 10% of 20 cases with other diseases (P less than 0.01). These proportions were higher after treatments accompanying transplantation since, of the 19 patients without antibodies before graft, 53% showed a sero-conversion after this treatment. The incidence of M-P V antibodies did not correlate with the number of transfusions received by the patients. Neither did these antibodies correlate with the presence of antibodies to antigens associated with baboon endogenous virus or simian sarcoma virus; antibodies to the latter two viruses were found in 6 to 21% of the sera, with no specific distribution among the sera. Secondly, pseudotypes of vesicular stomatitis virus with M-P V antigens in their envelope were prepared; they were inactivated by 90% of the sera which neutralized M-P V syncytium forming units and by none of the negative sera. Thirdly, specific complement-dependent cytotoxic antibodies to HeLa cells producing M-P V were also found in 61% of the sera with neutralizing activity to M-P V and only in 12% of the sera which did not neutralize M-P V. Absorption experiments indicated that the serum activities against M-P V associated antigens were not due to anticellular antibodies directed against normal constituents of human cells. However, no evidence has been provided that the M-P V associated antigens reacting with the human sera were virus coded.

摘要

对67例接受肾脏疾病治疗的患者血清进行了多达三种不同的检测,以检测其针对梅森 - 辉瑞病毒(M-P V)抗原的活性。首先,在肾移植前研究的患者中,24例慢性肾小球肾炎患者中有50%的血清对M-P V的合胞体形成单位具有中和活性,而20例患有其他疾病的患者中只有10%具有该活性(P小于0.01)。移植后的治疗后这些比例更高,因为在移植前没有抗体的19例患者中,53%在治疗后出现了血清转化。M-P V抗体的发生率与患者接受输血的次数无关。这些抗体也与针对狒狒内源性病毒或猿猴肉瘤病毒相关抗原的抗体的存在无关;后两种病毒的抗体在6%至21%的血清中被发现,在血清中没有特定分布。其次,制备了包膜中带有M-P V抗原的水泡性口炎病毒假型;90%能中和M-P V合胞体形成单位的血清使其失活,而阴性血清则不能。第三,在61%对M-P V具有中和活性的血清中也发现了针对产生M-P V的HeLa细胞的特异性补体依赖性细胞毒性抗体,而在不中和M-P V的血清中只有12%发现了该抗体。吸收实验表明,血清针对M-P V相关抗原的活性不是由于针对人类细胞正常成分的抗细胞抗体。然而,没有证据表明与人类血清反应的M-P V相关抗原是病毒编码的。

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