Theodos C M, Shankar A, Glasebrook A L, Roeder W D, Titus R G
Department of Tropical Public Health, Harvard School of Public Health, Boston, MA 02115.
Parasite Immunol. 1994 Nov;16(11):571-7. doi: 10.1111/j.1365-3024.1994.tb00312.x.
To assess the role of interleukin-1 (IL-1) in cutaneous leishmaniasis, Leishmania major-infected mice were treated with an anti-IL-1 receptor monoclonal antibody, LA-15.6. MoAb LA-15.6 prevents binding of IL-1 to both the T cell and B cell/macrophage forms of the IL-1 receptor. We found that treating with LA 15.6 inhibited the development of cutaneous lesions of L. major in both genetically-susceptible and resistant mice. Interestingly, this treatment had little or no effect on parasite numbers in the lesions or on the cytokines (interferon-gamma, interleukin-4) that the animals produced in response to infection with the parasite. These results suggest that although IL-1 plays a detrimental role in cutaneous leishmaniasis, it does not mediate this effect by altering the parasite-specific T cell response.
为评估白细胞介素-1(IL-1)在皮肤利什曼病中的作用,用抗IL-1受体单克隆抗体LA-15.6处理感染硕大利什曼原虫的小鼠。单克隆抗体LA-15.6可阻止IL-1与T细胞以及B细胞/巨噬细胞形式的IL-1受体结合。我们发现,用LA-15.6处理可抑制硕大利什曼原虫在遗传易感性和抗性小鼠皮肤病变的发展。有趣的是,这种处理对病变中的寄生虫数量或动物感染寄生虫后产生的细胞因子(干扰素-γ、白细胞介素-4)几乎没有影响。这些结果表明,尽管IL-1在皮肤利什曼病中起有害作用,但它并非通过改变寄生虫特异性T细胞反应来介导这种作用。