Gadol N, Johnson J E, Waldman R H
Infect Immun. 1974 May;9(5):858-62. doi: 10.1128/iai.9.5.858-862.1974.
A secondary local and splenic cell-mediated immune response was observed and compared to the primary response. Previous studies have demonstrated cell-mediated immunity (CMI) by lymphocytes from bronchopulmonary washings and have shown that its appearance is to a large extent inedpendent of splenic CMI. This study evaluated the secondary as compared to the primary response, with respect to both cellular and humoral immune responses. Guinea pigs were immunized with influenza virus vaccine either nasally or parenterally, booster immunizations were given by the same route, and animals were killed at various times after immunization or booster. The inhibition of macrophage migration was used to assess CMI. As in previous studies, local application of antigen led to mainly local appearance of CMI, whereas parenteral immunization led to mainly systemic CMI. Both pulmonary and splenic lymphocytes showed an inhibition of macrophage migration that appeared 2 to 3 days sooner after the booster, as compared to the primary immunization. There was no evidence, however, for the earlier production or increased amount of antibody in the bronchial secretions in the boosted animals. The results suggest that pulmonary as well as splenic T lymphocytes exhibit memory, but that pulmonary B lymphocytes do not.
观察到了次级局部和脾脏细胞介导的免疫反应,并将其与初级反应进行了比较。先前的研究已经证明支气管肺灌洗淋巴细胞介导的细胞免疫(CMI),并表明其出现很大程度上独立于脾脏CMI。本研究评估了次级反应与初级反应相比在细胞免疫和体液免疫反应方面的情况。用流感病毒疫苗经鼻或经胃肠外途径免疫豚鼠,通过相同途径进行加强免疫,并在免疫或加强免疫后的不同时间处死动物。采用巨噬细胞游走抑制试验评估CMI。与先前的研究一样,局部应用抗原主要导致CMI的局部出现,而胃肠外免疫主要导致全身CMI。与初次免疫相比,加强免疫后2至3天,肺和脾脏淋巴细胞均出现巨噬细胞游走抑制。然而,没有证据表明加强免疫的动物支气管分泌物中抗体产生更早或量增加。结果表明,肺和脾脏的T淋巴细胞均表现出记忆,但肺B淋巴细胞则不然。