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[一种用于诊断获得性弓形虫病发育阶段的新型凝集反应]

[A new agglutination reaction for the diagnosis of the developmental stage of acquired toxoplasmosis].

作者信息

Thulliez P, Remington J S, Santoro F, Ovlaque G, Sharma S, Desmonts G

出版信息

Pathol Biol (Paris). 1986 Mar;34(3):173-7.

PMID:3517786
Abstract

Agglutination of acetone treated toxoplasma (AC) is different from that one of formalin fixed parasites (HS). Sera from patients with a recently acquired ("acute") infection agglutinate both HS and AC parasites suspensions as well; contrary to sera from patients with past infection ("chronic stage") in which high titers of HS agglutination are often present, while the titres of AC agglutination are lower even negative. This is markedly observed in patients with local lesions (relapsing chorioretinitis, patients with AIDS and brain abscesses). The reason might be that different membrane toxoplasma antigens may induce the synthesis of agglutinating IgG. For example, antigens 35 KD and 27 KD described by E. Handman et al. The antibody specific for 27 KD is apparently present mainly during acute infection, contrary to the antibody specific for 35 KD which might be responsible of the high HS agglutination titre in sera from patients with chronic infection. Even if these hypotheses were not confirmed in the future, comparison of the titre in the HS and AC agglutination test might actually be helpful for practical diagnosis of the stage of toxoplasma infection.

摘要

丙酮处理的弓形虫(AC)的凝集反应与福尔马林固定寄生虫(HS)的凝集反应不同。近期获得性(“急性”)感染患者的血清也能凝集HS和AC寄生虫悬液;而既往感染(“慢性期”)患者的血清则相反,其中HS凝集反应的滴度往往较高,而AC凝集反应的滴度较低甚至为阴性。在有局部病变的患者(复发性脉络膜视网膜炎、艾滋病患者和脑脓肿患者)中可明显观察到这种情况。原因可能是不同的弓形虫膜抗原可诱导凝集性IgG的合成。例如,E. Handman等人描述的35 KD和27 KD抗原。与可能导致慢性感染患者血清中HS凝集滴度高的35 KD特异性抗体相反,27 KD特异性抗体显然主要在急性感染期间出现。即使这些假设将来未得到证实,但HS和AC凝集试验中滴度的比较实际上可能有助于弓形虫感染阶段的实际诊断。

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