Naylor P H, Naylor C W, Hendrix S, Leveque F G
Department of Internal Medicine, Wayne State University School of Medicine, Harper Hospital, Detroit, MI 48201, USA.
J Interferon Cytokine Res. 1999 Aug;19(8):953-9. doi: 10.1089/107999099313505.
Although administration of interferon-alpha (IFN-alpha) via the oral-mucosal route has shown efficacy in a variety of human and animal diseases, the mechanism of action of orally administered IFN is not clearly understood. To assess the possibility that IFN-alpha given via a lozenge alters the local mucosal immune system, immunoglobulins (Ig) and cytokines were measured in salivary secretions. Volunteers were given low doses of IFN-alpha and saliva was collected over a 24-h period. IgA and precursor IgM were measured by sandwich enzyme-linked immunosorbent assay (ELISA). Salivary concentrations of interleukin-5 (IL-5), the T helper cytokine primarily responsible for the switch from IgM to IgA, were also determined. After oral administration of IFN-alpha, there was an initial decline in IgM and IgA followed by a return to baseline levels by 8-24 h. This change in Ig concentration was associated with a gradual increase in IL-5, consistent with the return of Ig to baseline as a result of modulation by Ig-mediating cytokines.
尽管通过口腔黏膜途径给予α-干扰素(IFN-α)已在多种人类和动物疾病中显示出疗效,但口服IFN的作用机制尚不清楚。为了评估通过含片给予IFN-α是否会改变局部黏膜免疫系统,对唾液分泌物中的免疫球蛋白(Ig)和细胞因子进行了检测。志愿者接受低剂量的IFN-α,并在24小时内收集唾液。通过夹心酶联免疫吸附测定(ELISA)测量IgA和前体IgM。还测定了唾液中白细胞介素-5(IL-5)的浓度,IL-5是主要负责从IgM转换为IgA的辅助性T细胞细胞因子。口服IFN-α后,IgM和IgA最初下降,随后在8至24小时恢复到基线水平。Ig浓度的这种变化与IL-5的逐渐增加有关,这与Ig介导的细胞因子调节导致Ig恢复到基线一致。