Olsson J, Poles M, Spetz A L, Elliott J, Hultin L, Giorgi J, Andersson J, Anton P
Division of Infectious Diseases F82, Huddinge University Hospital, 141 86 Huddinge, Sweden.
J Infect Dis. 2000 Dec;182(6):1625-35. doi: 10.1086/317625. Epub 2000 Oct 23.
Mucosal inflammation is characterized by increased expression of proinflammatory cytokines and chemoattractant chemokines, resulting in infiltration of immunocompetent cells. This study compared the degree of mucosal inflammation in human immunodeficiency virus type 1 (HIV-1)-infected gut mucosa with that in tissue samples from subjects with inflammatory bowel disease (IBD) and from healthy seronegative control subjects. Gut mucosal biopsy specimens were immunohistochemically stained and were evaluated by in situ imaging. There was significantly increased expression of HIV-1 coreceptors CCR5 and CXCR4, beta-chemokine RANTES, and macrophage inflammatory protein (MIP)-1alpha and MIP-1beta, as well as increased numbers of T cells in lamina propria of HIV-1-infected patients. The results were similar in patients with IBD and in HIV-1-infected patients, suggesting increased inflammation in the colon of HIV-1-infected patients. To further investigate the effect of inflammation in HIV-1-infected lamina propria, treatments that reduce immune activation in lamina propria must be evaluated.
黏膜炎症的特征是促炎细胞因子和趋化因子趋化因子的表达增加,导致免疫活性细胞浸润。本研究比较了1型人类免疫缺陷病毒(HIV-1)感染的肠道黏膜与炎症性肠病(IBD)患者及健康血清阴性对照受试者组织样本中的黏膜炎症程度。对肠道黏膜活检标本进行免疫组织化学染色,并通过原位成像进行评估。在HIV-1感染患者的固有层中,HIV-1共受体CCR5和CXCR4、β趋化因子调节激活正常T细胞表达和分泌的因子(RANTES)、巨噬细胞炎性蛋白(MIP)-1α和MIP-1β的表达显著增加,T细胞数量也增加。IBD患者和HIV-1感染患者的结果相似,提示HIV-1感染患者结肠炎症增加。为了进一步研究HIV-1感染固有层中炎症的影响,必须评估降低固有层免疫激活的治疗方法。