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一种针对小鼠疟疾T细胞免疫的体外检测方法。

An in vitro assay for T cell immunity to malaria in mice.

作者信息

Weinbaum F I, Evans C B, Tigelaar R E

出版信息

J Immunol. 1976 May;116(5):1280-3.

PMID:774978
Abstract

After infection with a nonlethal strain of murine malaria (17XNL Plasmodium berghei yoelli), BALB/c mice are then resistant to a lethal strain (17XL P.b. yoelli). BALB/c mice were infected with 17XNL, anc challenged 3 weeks later, after clearing their parasitemias, with 17XL. Three weeks thereafter, spleen cells from such immune animals were used to define an early peaking T-dependent (anti-theta sensitive) antigen-specific proliferative response when incubated in vitro with 17XL infected RBC, or a saline soluble 17XL antigen preparation. T dependent responsiveness of spleen cells from uninoculated control animals to the 17XL antigen preparation was also observed, but demonstrated a much different (delayed) kinetics from that observed with immune cells.

摘要

用非致死性鼠疟原虫株(17XNL伯氏疟原虫约氏亚种)感染BALB/c小鼠后,这些小鼠随后对致死性毒株(17XL伯氏疟原虫约氏亚种)具有抗性。将BALB/c小鼠用17XNL感染,在清除寄生虫血症3周后,再用17XL进行攻击。此后3周,将来自此类免疫动物的脾细胞用于确定当在体外与17XL感染的红细胞或盐溶性17XL抗原制剂一起孵育时,早期达到峰值的T细胞依赖性(抗θ敏感)抗原特异性增殖反应。未接种的对照动物的脾细胞对17XL抗原制剂的T细胞依赖性反应性也被观察到,但显示出与免疫细胞观察到的非常不同(延迟)的动力学。

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