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用弓形虫抗原免疫小鼠后的迟发性二次免疫反应及其对抵抗刚地弓形虫感染的保护作用。

Delayed secondary immune response in mice immunized with Toxoplasma antigens and its effect for protection against Toxoplasma gondii.

作者信息

Yano K, Nakabayashi T

出版信息

Zentralbl Bakteriol Mikrobiol Hyg A. 1984 Mar;256(3):381-9.

PMID:6730784
Abstract

Primary immune response by mice immunized with Toxoplasma peritoneal exudate (PE) was produced slowly at a low level. To induce high Toxoplasma antibodies, mice should be boostered after the primary immune response reached the peak in 4 weeks or later. Immunization of mice with PE alone in 4 weeks could suppress the growth of Toxoplasma but could not accomplish protection. Two of 9 mice immunized with PE in complete Freund's adjuvant (CFA), and 16 of 27 mice immunized with PE containing Toxoplasma ( ToxoPE ) in CFA were protected against a challenge of 1 X 10(3) Toxoplasma, RH strain. The mice surviving to the challenge showed complete protection against a rechallenge of higher dose, 1 X 10(6) RH strain. Their ascites were very high in LA titer and would be a great source for obtaining high titer antibodies to Toxoplasma without contamination of host serum components. Biological characters of Toxoplasma, RH strain, in chronic infection of mice are discussed.

摘要

用弓形虫腹腔渗出液(PE)免疫的小鼠产生的初次免疫反应缓慢且水平较低。为诱导产生高滴度的弓形虫抗体,应在初次免疫反应4周或更晚达到峰值后对小鼠进行加强免疫。4周时仅用PE免疫小鼠可抑制弓形虫生长,但无法实现保护作用。9只用完全弗氏佐剂(CFA)中PE免疫的小鼠中有2只,27只用CFA中含弓形虫的PE(ToxoPE)免疫的小鼠中有16只受到保护,免受1×10³个弓形虫RH株的攻击。存活至攻击的小鼠对更高剂量(1×10⁶个RH株)的再次攻击显示出完全保护。它们腹水中的LA滴度非常高,将是获得高滴度抗弓形虫抗体且不被宿主血清成分污染的重要来源。本文讨论了弓形虫RH株在小鼠慢性感染中的生物学特性。

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