Yano K, Nakabayashi T
Zentralbl Bakteriol Mikrobiol Hyg A. 1984 Mar;256(3):381-9.
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.
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。