Ben-Smith A, Lammas D A, Behnke J M
Karonga Prevention Study, PO Box 46, Chilumba, Malawi.
J Helminthol. 2003 Jun;77(2):133-46. doi: 10.1079/JOH2003173.
T helper cell (Th1 and Th2) associated responses were examined following a primary infection with the gastrointestinal nematode Heligmosomoides polygyrus in five inbred strains of mice with different resistance phenotypes. Levels of (i) mast cell protease, (ii) specific IgE, (iii) nitric oxide and (iv) specific IgG2a, as markers of Th2 and Th1 associated responses, respectively, were determined in sera and intestinal fluids and correlated with worm burdens. The "fast" responder (resistant) strains SWR and SJL produced strong Th2 and Th1 associated responses respectively in a mutually exclusive fashion. The F1 hybrid (SWRxSJL) F1, showed rapid expulsion of the parasite and expressed both intense Th1 and Th2 responses, suggesting synergism between Th1 and Th2 activity in these mice. The results indicate that both Th2 and Th1 responses operate in mice following a primary infection with H. polygyrus and that each Th response may be involved to a greater or lesser degree within certain strains. Resistance to H. polygyrus was found to correlate only to the intensity of either the gut-associated mastocytosis or nitric oxide production in these strains but not to either specific IgE or IgG2a titres. Chronic infections in the "slow" response phenotype mouse strains CBA and C57BL/10, were associated with both poor Th2 and poor Th1-associated responses attributed to a general parasite-mediated immunosuppression of the host immune response to infection.
在用胃肠道线虫多房棘球绦虫对五种具有不同抗性表型的近交系小鼠进行初次感染后,检测了辅助性T细胞(Th1和Th2)相关反应。分别在血清和肠液中测定了(i)肥大细胞蛋白酶、(ii)特异性IgE、(iii)一氧化氮和(iv)特异性IgG2a的水平,作为Th2和Th1相关反应的标志物,并将其与虫负荷相关联。“快速”反应(抗性)品系SWR和SJL分别以相互排斥的方式产生强烈的Th2和Th1相关反应。F1杂种(SWRxSJL)F1显示出对寄生虫的快速驱除,并表达了强烈的Th1和Th2反应,表明这些小鼠中Th1和Th2活性之间存在协同作用。结果表明,在用多房棘球绦虫进行初次感染后,Th2和Th1反应在小鼠中均起作用,并且每种Th反应在某些品系中可能或多或少地参与其中。发现对多房棘球绦虫的抗性仅与这些品系中肠道相关肥大细胞增多症或一氧化氮产生的强度相关,而与特异性IgE或IgG2a滴度无关。“缓慢”反应表型小鼠品系CBA和C57BL/10中的慢性感染与Th2反应不良和Th1相关反应不良均有关,这归因于寄生虫对宿主感染免疫反应的一般免疫抑制。