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Local and Systemic Cell-Mediated Immunity after Immunization of Guinea Pigs with Live or Killed M. Tuberculosis by Various Routes

机译:通过各种途径对豚鼠进行活的或杀死的结核分枝杆菌免疫后的局部和全身细胞介导的免疫

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Recent studies have suggested that there is compartmentalization of the cell-mediated immune response, i.e., local (nasal) immunization with influenza virus vaccine is more effective in inducing local cell-mediated immunity (CMI) than is parenteral immunization, whereas parenteral immunization is more effective in inducing systemic immunity. This study was undertaken to investigate the development of local respiratory as compared to systemic CMI in response to both nasally and parenterally administered BCG or killed Mycobacterium tuberculosis H37Ra.CMI was tested with guinea pigs as the animal model and the inhibition of macrophage migration (IMM) technique at various intervals after immunization. Splenic lymphocytes were used as indicators of systemic immunity and pulmonary cells obtained by lung lavage were used to measure local immunity.The animals immunized via the respiratory tract with either H37Ra or BCG developed significantly greater local respiratory CMI (greater percentage of IMM) than did animals immunized subcutaneously although the parenterally immunized animals developed greater systemic immunity. This compartmentalization of CMI could be overcome partially with higher doses of H37Ra, i.e., both respiratory and systemic CMI resulted from high dose local or parenteral immunization.The response after BCG (live), as compared to H37Ra (killed organisms), was more prolonged: by 6 weeks after H37Ra immunization, by any route, there was no IMM; however, after BCG, high levels of IMM were present at 6 weeks. When guinea pigs were immunized i.v. with H37Ra, neither systemic nor respiratory CMI was stimulated. I.v. BCG stimulated systemic but not respiratory CMI.These results could not be explained on the basis of local immunization leading to local irritation and infiltration of lymphocytes into the lung, since cell counts and histologic studies revealed no difference between the animals immunized locally and systemically.These results may have implications with respect to immunization of humans against tuberculosis.
机译:最近的研究表明,细胞介导的免疫反应存在分隔性,即用流感病毒疫苗进行局部(鼻)免疫诱导的局部细胞介导的免疫(CMI)比肠胃外免疫更有效,而肠胃外免疫则更多有效诱导全身免疫。这项研究的目的是调查与鼻腔和胃肠外施用BCG或杀死的结核分枝杆菌H37Ra相比,全身性CMI较局部CMI的发展。以豚鼠为动物模型测试了CMI并抑制了巨噬细胞迁移在免疫后的不同间隔进行技术检查。脾淋巴细胞被用作全身免疫的指标,肺灌洗获得的肺细胞被用于测量局部免疫力。通过呼吸道用H37Ra或BCG进行免疫的动物比动物具有更大的局部呼吸CMI(IMM百分比更高)尽管经肠胃外免疫的动物表现出更大的全身免疫性,但皮下免疫。高剂量的H37Ra可以部分克服CMI的这种分隔,即高剂量的局部或肠胃外免疫可导致呼吸道和全身性CMI。与H37Ra(杀死的生物)相比,卡介苗(活)的反应更长:在H37Ra免疫后6周,无论通过哪种途径,都没有IMM;然而,卡介苗后6周IMM水平较高。当豚鼠经静脉免疫后。使用H37Ra,既不刺激全身性CMI,也不刺激呼吸CMI。 I.v.卡介苗刺激全身性而非呼吸性CMI,这些结果无法根据局部免疫导致局部刺激和淋巴细胞向肺部浸润的解释,因为细胞计数和组织学研究显示,局部免疫和全身免疫的动物之间没有差异。该结果可能对人类免疫结核病有影响。

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