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1
The interaction between CD8+ cytotoxic T cells and Leishmania-infected macrophages.CD8 + 细胞毒性T细胞与利什曼原虫感染的巨噬细胞之间的相互作用。
J Exp Med. 1991 Sep 1;174(3):499-505. doi: 10.1084/jem.174.3.499.
2
Murine cutaneous leishmaniasis: disease patterns in intact and nude mice of various genotypes and examination of some differences between normal and infected macrophages.小鼠皮肤利什曼病:不同基因型完整和裸鼠的疾病模式以及正常与感染巨噬细胞之间一些差异的研究
Aust J Exp Biol Med Sci. 1979 Feb;57(1):9-29. doi: 10.1038/icb.1979.2.
3
Leishmania mexicana promastigotes induce cytotoxic T lymphocytes in vivo that do not recognize infected macrophages.墨西哥利什曼原虫前鞭毛体在体内诱导出不识别受感染巨噬细胞的细胞毒性T淋巴细胞。
Eur J Immunol. 1993 Jan;23(1):217-23. doi: 10.1002/eji.1830230134.
4
CD8+ T cells from mice vaccinated against Toxoplasma gondii are cytotoxic for parasite-infected or antigen-pulsed host cells.用抗弓形虫疫苗接种的小鼠的CD8 + T细胞对寄生虫感染或抗原脉冲的宿主细胞具有细胞毒性。
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Murine cutaneous leishmaniasis: resistance correlates with the capacity to generate interferon-gamma in response to Leishmania antigens in vitro.小鼠皮肤利什曼病:抵抗力与体外对利什曼原虫抗原产生γ干扰素的能力相关。
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6
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Immunoregulatory pathways in murine leishmaniasis: different regulatory control during Leishmania mexicana mexicana and Leishmania major infections.小鼠利什曼病中的免疫调节途径:墨西哥利什曼原虫和硕大利什曼原虫感染期间的不同调节控制
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Roles of macrophages and neutrophils in the early host response to Bacillus anthracis spores in a mouse model of infection.巨噬细胞和中性粒细胞在小鼠感染炭疽芽孢杆菌孢子早期宿主反应中的作用。
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Perforin and gamma interferon are critical CD8+ T-cell-mediated responses in vaccine-induced immunity against Leishmania amazonensis infection.穿孔素和γ干扰素是疫苗诱导的抗亚马逊利什曼原虫感染免疫中关键的CD8 + T细胞介导的反应。
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本文引用的文献

1
Killing of intracellular Leishmania donovani by lymphokine-stimulated human mononuclear phagocytes. Evidence that interferon-gamma is the activating lymphokine.淋巴因子刺激的人单核吞噬细胞对细胞内杜氏利什曼原虫的杀伤作用。γ干扰素是激活淋巴因子的证据。
J Clin Invest. 1983 Oct;72(4):1506-10. doi: 10.1172/JCI111107.
2
Parasite antigens, their role in protection, diagnosis and escape: the leishmaniases.寄生虫抗原及其在保护、诊断和逃逸中的作用:利什曼病
Curr Top Microbiol Immunol. 1985;120:43-67. doi: 10.1007/978-3-662-09197-5_4.
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Immunological regulation and control of experimental leishmaniasis.实验性利什曼病的免疫调节与控制
Int Rev Exp Pathol. 1986;28:79-116.
4
The role of T cell--macrophage interactions in tuberculosis.T细胞与巨噬细胞相互作用在结核病中的作用。
Springer Semin Immunopathol. 1988;10(4):337-58. doi: 10.1007/BF02053845.
5
Gamma interferon, CD8+ T cells and antibodies required for immunity to malaria sporozoites.γ干扰素、CD8 + T细胞和抗体是对疟原虫免疫力所必需的。
Nature. 1987;330(6149):664-6. doi: 10.1038/330664a0.
6
A role for Lyt-2+ T cells in resistance to cutaneous leishmaniasis in immunized mice.Lyt-2⁺ T细胞在免疫小鼠抗皮肤利什曼病中的作用。
J Immunol. 1989 Mar 15;142(6):2052-6.
7
Monoclonal antibodies to murine gamma-interferon which differentially modulate macrophage activation and antiviral activity.针对小鼠γ干扰素的单克隆抗体,其可不同程度地调节巨噬细胞活化和抗病毒活性。
J Immunol. 1985 Mar;134(3):1609-18.
8
Elimination of CD4+ suppressor T cells from susceptible BALB/c mice releases CD8+ T lymphocytes to mediate protective immunity against Leishmania.从易感的BALB/c小鼠中清除CD4+抑制性T细胞可释放CD8+T淋巴细胞,以介导针对利什曼原虫的保护性免疫。
J Exp Med. 1989 May 1;169(5):1819-27. doi: 10.1084/jem.169.5.1819.
9
Cloned cytotoxic T cells recognize an epitope in the circumsporozoite protein and protect against malaria.克隆的细胞毒性T细胞识别环子孢子蛋白中的一个表位,并可预防疟疾。
Nature. 1989 Sep 28;341(6240):323-6. doi: 10.1038/341323a0.
10
Consequences of self-presentation of peptide antigen by cytolytic T lymphocytes.细胞毒性T淋巴细胞对肽抗原的自我呈递的后果。
J Immunol. 1989 Sep 1;143(5):1512-7.

CD8 + 细胞毒性T细胞与利什曼原虫感染的巨噬细胞之间的相互作用。

The interaction between CD8+ cytotoxic T cells and Leishmania-infected macrophages.

作者信息

Smith L E, Rodrigues M, Russell D G

机构信息

Department of Pathology, New York University Medical Center, New York 10016.

出版信息

J Exp Med. 1991 Sep 1;174(3):499-505. doi: 10.1084/jem.174.3.499.

DOI:10.1084/jem.174.3.499
PMID:1908507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2118943/
Abstract

Leishmania is resident within the macrophages of its vertebrate host. In any intramacrophage infection, where the pathogen is present in a form capable of mediating cell to cell transmission, the contribution of a cytotoxic T cell response to protective immunity is questionable. This study presents data from an in vitro model designed to elucidate the outcome of an interaction between CD8+, cytotoxic T cells and infected macrophages. Experiments were conducted with an H-2d-restricted, cytotoxic CD8+ T cell clone and Leishmania parasites present in mixed macrophage cultures, with the parasites confined to either histocompatible BALB/c macrophages, or incompatible CBA macrophages. Initial experiments indicated that the viability of Leishmania was unaffected by the lysis of its host macrophage by cytotoxic T cells. However, extended experiments showed that the parasites were killed between 24 and 72 h. The same results were obtained regardless of whether the parasites were resident in the target, BALB/c, macrophages or the bystander, CBA, macrophages. Addition of neutralizing, anti-IFN-g antibody to the cultures ablated most of the leishmanicidal behavior, indicating that parasite death was attributable to macrophage activation, resulting from cytokine secretion from the T cells following the initial recognition event.

摘要

利什曼原虫寄生于其脊椎动物宿主的巨噬细胞内。在任何巨噬细胞内感染中,若病原体以能够介导细胞间传播的形式存在,细胞毒性T细胞反应对保护性免疫的贡献就值得怀疑。本研究展示了来自体外模型的数据,该模型旨在阐明CD8 +细胞毒性T细胞与受感染巨噬细胞之间相互作用的结果。实验使用了一个H - 2d限制的细胞毒性CD8 + T细胞克隆以及混合巨噬细胞培养物中存在的利什曼原虫寄生虫,寄生虫被限制在组织相容性的BALB / c巨噬细胞或不相容的CBA巨噬细胞中。初步实验表明,细胞毒性T细胞对其宿主巨噬细胞的裂解并未影响利什曼原虫的活力。然而,进一步的实验表明,寄生虫在24至72小时内被杀死。无论寄生虫是存在于靶细胞BALB / c巨噬细胞还是旁观者CBA巨噬细胞中,都得到了相同的结果。向培养物中添加中和性抗IFN - g抗体消除了大部分杀利什曼原虫行为,表明寄生虫死亡归因于巨噬细胞活化,这是初始识别事件后T细胞分泌细胞因子所致。