Theodos C M, Povinelli L, Molina R, Sherry B, Titus R G
Department of Tropical Public Health, Harvard School of Public Health, Boston, Massachusetts 02115.
Infect Immun. 1991 Aug;59(8):2839-42. doi: 10.1128/iai.59.8.2839-2842.1991.
Recombinant human tumor necrosis factor (TNF) and purified murine TNF were both able to activate macrophages to destroy intracellular Leishmania major in vitro. In addition, parasitizing macrophages with L. major markedly increased the ability of the cells to produce TNF. Finally, when mice were vaccinated with an avirulent form of L. major, the animals produced large amounts of TNF but no gamma interferon in response to infection with virulent L. major. Treating these mice with a neutralizing anti-TNF antibody led to partial but not complete inhibition of the resistant state, which suggests that factors other than TNF and gamma interferon contribute to resistance to L. major.
重组人肿瘤坏死因子(TNF)和纯化的鼠TNF均能够在体外激活巨噬细胞以破坏细胞内的硕大利什曼原虫。此外,用硕大利什曼原虫感染巨噬细胞显著增强了细胞产生TNF的能力。最后,当用无毒形式的硕大利什曼原虫对小鼠进行免疫接种时,这些动物在受到有毒力的硕大利什曼原虫感染后会产生大量TNF,但不产生γ干扰素。用中和性抗TNF抗体处理这些小鼠会导致抗性状态受到部分但非完全抑制,这表明除了TNF和γ干扰素之外的其他因素也有助于对硕大利什曼原虫的抗性。