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人外周血淋巴细胞重建的重症联合免疫缺陷小鼠对刚地弓形虫抗原的抗体反应重现了淋巴细胞供体的免疫状态。

Antibody responses to Toxoplasma gondii antigen in human peripheral blood lymphocyte-reconstituted severe-combined immunodeficient mice reproduce the immunological status of the lymphocyte donor.

作者信息

Walker W, Roberts C W, Brewer J M, Alexander J

机构信息

Department of Immunology, University of Strathclyde, Glasgow, Scotland.

出版信息

Eur J Immunol. 1995 May;25(5):1426-30. doi: 10.1002/eji.1830250543.

DOI:10.1002/eji.1830250543
PMID:7774646
Abstract

These studies describe the production of specific antibodies in human peripheral blood lymphocyte-reconstituted severe-combined immunodeficient (PBL-SCID) mice following vaccination with antigen from the protozoan parasite Toxoplasma gondii. To determine the effect of previous exposure of the lymphocyte donor to antigen, human-PBL-SCID animals were created by transferring peripheral blood lymphocytes from either a single T. gondii-seronegative or a single seropositive donor. These reconstituted animals were subsequently inoculated with T. gondii soluble tachyzoite antigen (STAg) entrapped within non-ionic surfactant vesicles as an immunological adjuvant. Animals were bled at pre-determined time points post-vaccination and the expression of human anti-STAg antibodies in the plasma determined by enzyme-linked immunosorbent assay. Human antibodies specific for STAg were readily inducible in both groups of reconstituted animals, although the pattern of isotype production differed markedly between groups. The response in animals reconstituted with lymphocytes from the T. gondii-seronegative donor consisted primarily of IgM and subsequently of IgG (predominantly IgG1). In animals reconstituted with lymphocytes from the seropositive donor, no parasite-specific IgM could be demonstrated. The detectable response to STAg consisted entirely of human antibodies of the IgG isotype (IgG1), indicative of a memory-type response. These results mimicked exactly the antibody responses that would be expected had the lymphocyte donors been directly challenged with either the antigen or the live infectious agent, demonstrating that the immune system within these animals is functional and reproducible with regard to both the primary and secondary responses of the human donors.

摘要

这些研究描述了在用来自原生动物寄生虫刚地弓形虫的抗原进行疫苗接种后,人外周血淋巴细胞重建的严重联合免疫缺陷(PBL - SCID)小鼠中特异性抗体的产生。为了确定淋巴细胞供体先前暴露于抗原的影响,通过转移来自单个刚地弓形虫血清阴性或单个血清阳性供体的外周血淋巴细胞来创建人 - PBL - SCID动物。随后,将包埋在非离子表面活性剂囊泡中的刚地弓形虫可溶性速殖子抗原(STAg)作为免疫佐剂接种给这些重建动物。在疫苗接种后的预定时间点采集动物血液,并通过酶联免疫吸附测定法测定血浆中人抗STAg抗体的表达。两组重建动物中均可轻易诱导出对STAg特异的人抗体,尽管两组之间同种型产生模式明显不同。用来自刚地弓形虫血清阴性供体的淋巴细胞重建的动物中的反应主要由IgM组成,随后是IgG(主要是IgG1)。在用来自血清阳性供体的淋巴细胞重建的动物中,未检测到寄生虫特异性IgM。对STAg的可检测反应完全由IgG同种型(IgG1)的人抗体组成,表明是记忆型反应。这些结果与淋巴细胞供体直接受到抗原或活感染因子攻击时预期的抗体反应完全一致,表明这些动物体内的免疫系统在人类供体的初次和二次反应方面是有功能且可重复的。

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引用本文的文献

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J Exp Med. 2000 May 15;191(10):1777-88. doi: 10.1084/jem.191.10.1777.
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Transfer of human CD4(+) T lymphocytes producing beta interferon in Hu-PBL-SCID mice controls human immunodeficiency virus infection.在人外周血淋巴细胞-严重联合免疫缺陷(Hu-PBL-SCID)小鼠中产生β干扰素的人CD4(+) T淋巴细胞的转移可控制人类免疫缺陷病毒感染。
J Virol. 1999 Dec;73(12):10281-8. doi: 10.1128/JVI.73.12.10281-10288.1999.
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Innate immunity to Toxoplasma gondii is influenced by gender and is associated with differences in interleukin-12 and gamma interferon production.
对刚地弓形虫的先天免疫受性别影响,并与白细胞介素-12和γ干扰素产生的差异相关。
Infect Immun. 1997 Mar;65(3):1119-21. doi: 10.1128/IAI.65.3.1119-1121.1997.
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T-cell dysfunctions in hu-PBL-SCID mice infected with human immunodeficiency virus (HIV) shortly after reconstitution: in vivo effects of HIV on highly activated human immune cells.重建后不久感染人类免疫缺陷病毒(HIV)的人外周血淋巴细胞-重症联合免疫缺陷(hu-PBL-SCID)小鼠中的T细胞功能障碍:HIV对高度活化的人类免疫细胞的体内影响
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