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急性与慢性曼氏血吸虫病患者体内细胞因子的产生:γ干扰素和白细胞介素-10在调节外周血单个核细胞和脾细胞对寄生虫抗原反应中的交叉调节作用

Cytokine production in acute versus chronic human Schistosomiasis mansoni: the cross-regulatory role of interferon-gamma and interleukin-10 in the responses of peripheral blood mononuclear cells and splenocytes to parasite antigens.

作者信息

Montenegro S M, Miranda P, Mahanty S, Abath F G, Teixeira K M, Coutinho E M, Brinkman J, Gonçalves I, Domingues L A, Domingues A L, Sher A, Wynn T A

机构信息

Department de Imunologia, Centro de Pesquisas Aggeu Magalhaes-FIOCRUZ, Cidade Universitaria, 7472, 50670-420 Recife-PE, Brazil.

出版信息

J Infect Dis. 1999 Jun;179(6):1502-14. doi: 10.1086/314748.

Abstract

The contribution of interleukin (IL)-10 and interferon (IFN)-gamma to the regulation of type 1 and type 2 cytokine responses was investigated in Brazilians with different clinical forms of schistosomiasis mansoni. Cells from members of a family with acute intestinal schistosomiasis responded to schistosomal soluble egg antigen (SEA) or soluble adult worm antigen preparation (SWAP) with greater amounts of IFN-gamma than did cells from several patients with chronic intestinal schistosomiasis; IL-10 levels were similar. Neutralization of IL-10 had no effect on the SEA-specific IFN-gamma response in patients with acute infection, whereas SWAP-induced IFN-gamma was increased in both groups. Anti-IL-10 also up-regulated SEA-specific IFN-gamma protein and mRNA responses in most splenocyte cultures from hepatosplenic schistosomiasis patients but had no effect on antigen-specific IL-4 or IL-5 production. Neutralization of IFN-gamma resulted in a comparable increase in SWAP-specific IL-10 and IL-5, while IL-4 was not affected. These studies demonstrate that early disease in schistosomiasis is associated with a significant IFN-gamma response and that IL-10 contributes to the suppression of that response during both early and chronic infection.

摘要

在患有不同临床类型曼氏血吸虫病的巴西人中,研究了白细胞介素(IL)-10和干扰素(IFN)-γ对1型和2型细胞因子反应调节的作用。来自一个患有急性肠道血吸虫病家庭的成员的细胞,对血吸虫可溶性虫卵抗原(SEA)或可溶性成虫抗原制剂(SWAP)产生的IFN-γ量,比来自几名慢性肠道血吸虫病患者的细胞更多;IL-10水平相似。在急性感染患者中,中和IL-10对SEA特异性IFN-γ反应没有影响,而在两组中SWAP诱导的IFN-γ均增加。抗IL-10在大多数肝脾型血吸虫病患者的脾细胞培养物中也上调了SEA特异性IFN-γ蛋白和mRNA反应,但对抗原特异性IL-4或IL-5的产生没有影响。中和IFN-γ导致SWAP特异性IL-10和IL-5有类似的增加,而IL-4不受影响。这些研究表明,血吸虫病早期疾病与显著的IFN-γ反应相关,并且IL-10在早期和慢性感染期间都有助于抑制该反应。

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