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首页> 外文期刊>Infection and immunity >Immune response to lactate dehydrogenase-elevating virus: serologically specific rabbit neutralizing antibody to the virus.
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Immune response to lactate dehydrogenase-elevating virus: serologically specific rabbit neutralizing antibody to the virus.

机译:对乳酸脱氢酶升高病毒的免疫反应:对该病毒的血清学特异性兔中和抗体。

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A rabbit was immunized with large amounts of the lactate dehydrogenase-elevating virus (LDV) over a 9-month period. The plasma from this rabbit possessed an anti-LDV IgG titer of 1:80,000 as measured by the enzyme-linked immunosorbent assay (ELISA) method and a neutralizing titer of 1:1,000 for the homologous strain of LDV. LDV neutralization at 4 degrees C followed single-hit kinetics. In contrast, mouse anti-LDV IgG in plasma of chronically LDV-infected mice failed to neutralize LDV at 4 degrees C and neutralization at 37 degrees C was slow, biphasic, and inefficient compared with the neutralization caused by rabbit anti-LDV IgG, even though high levels of anti-LDV IgG were detectable in mouse plasma by the ELISA method. Rabbit anti-LDV IgG neutralized one heterologous strain of LDV as rapidly as it did the homologous strain, but failed to significantly neutralize five other strains of LDV, all of which were originally isolated from different mouse strains bearing transplantable tumors. The results indicate clear serological differences between LDV strains. Cross-reactions between the strains, however, were observed by ELISA, using the antibody induced during persistent infection of mice with each LDV strain. Immunoglobulin M (IgM) from mice infected for 15 days with the various strains bound equally to our LDV strain. IgG obtained from 2-month-infected mice also cross-reacted, but to a varying extent which partly correlated with the specificity detected by neutralization. Both rabbit and mouse anti-LDV IgG enhanced the infectivity of LDV at a low multiplicity of infection for primary cultures of peritoneal mouse macrophages.
机译:在9个月内用大量乳酸脱氢酶升高病毒(LDV)免疫兔子。通过酶联免疫吸附测定(ELISA)方法测得,来自该兔子的血浆具有1:80,000的抗LDV IgG效价和对于LDV的同源菌株的中和效价为1:1,000。在4摄氏度下LDV中和遵循单发动力学。相反,与LDV IgG引起的中和作用相比,慢性LDV感染的小鼠血浆中的小鼠抗LDV IgG未能在4℃下中和LDV,而在37℃下的中和作用缓慢,两相且效率低下。尽管通过ELISA方法可在小鼠血浆中检测到高水平的抗LDV IgG。兔抗-LDV IgG与其中一株LDV一样快地中和了LDV,但未能显着中和其他五株LDV,它们最初都是从带有可移植肿瘤的不同小鼠株中分离得到的。结果表明LDV菌株之间明显的血清学差异。然而,通过ELISA,使用在每种LDV菌株持续感染小鼠期间诱导的抗体,通过ELISA观察到了菌株之间的交叉反应。来自感染了15天的各种菌株的小鼠的免疫球蛋白M(IgM)与我们的LDV菌株均等结合。从感染2个月的小鼠获得的IgG也发生交叉反应,但程度不同,部分与通过中和检测到的特异性相关。对于腹膜小鼠巨噬细胞的原代培养,兔和小鼠抗LDV IgG均可在低感染复数下提高LDV的感染力。

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