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Strain-specific antibody therapy prevents cytomegalovirus reactivation after transplantation

机译:应变特异性抗体疗法可防止移植后巨细胞病毒重新激活

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摘要

Cytomegalovirus infection is a frequent and life-threatening complication that significantly limits positive transplantation outcomes. We developed preclinical mouse models of cytomegalovirus reactivation after transplantation and found that humoral immunity is essential for preventing viral recrudescence. Preexisting antiviral antibodies decreased after transplant in the presence of graft-versus-host disease and were not replaced, owing to poor reconstitution of donor B cells and elimination of recipient plasma cells. Viral reactivation was prevented by the transfer of immune serum, without a need to identify and target specific antigenic determinants. Notably, serotherapy afforded complete protection, provided that the serum was matched to the infecting viral strain. Thus, we define the mechanisms for cytomegalovirus reactivation after transplantation and identify a readily translatable strategy of exceptional potency, which avoids the constraints of cellular therapies.
机译:巨细胞病毒感染是一种常见的威胁生命的并发症,严重限制了积极的移植结果。我们开发了移植后巨细胞病毒重新激活的临床前小鼠模型,发现体液免疫对于预防病毒复发至关重要。在移植物抗宿主病的存在下,移植后已有的抗病毒抗体减少,并且由于供体B细胞的重组不良和受体浆细胞的清除而没有被替代。免疫血清的转移阻止了病毒的再激活,而无需鉴定和靶向特定的抗原决定簇。值得注意的是,只要血清与感染的病毒株相匹配,血清疗法即可提供完全的保护。因此,我们定义了移植后巨细胞病毒重新激活的机制,并确定了一种具有极强效用的易于翻译的策略,从而避免了细胞疗法的局限性。

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  • 来源
    《Science》 |2019年第6424期|288-293|共6页
  • 作者单位

    QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia|Univ Queensland, Sch Med, Brisbane, Qld, Australia;

    Univ Western Australia, Immunol & Virol Program, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia|Lions Eye Inst, Ctr Expt Immunol, Perth, WA, Australia|Monash Univ, Biomed Discovery Inst, Infect & Immun Program, Clayton, Vic, Australia|Monash Univ, Dept Microbiol, Infect & Immun Program, Clayton, Vic, Australia;

    Univ Western Australia, Immunol & Virol Program, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia|Lions Eye Inst, Ctr Expt Immunol, Perth, WA, Australia;

    QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia;

    Univ Western Australia, Immunol & Virol Program, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia|Lions Eye Inst, Ctr Expt Immunol, Perth, WA, Australia|Monash Univ, Biomed Discovery Inst, Infect & Immun Program, Clayton, Vic, Australia|Monash Univ, Dept Microbiol, Infect & Immun Program, Clayton, Vic, Australia;

    Univ Western Australia, Immunol & Virol Program, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia|Lions Eye Inst, Ctr Expt Immunol, Perth, WA, Australia;

    Univ Western Australia, Immunol & Virol Program, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia|Lions Eye Inst, Ctr Expt Immunol, Perth, WA, Australia;

    QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia;

    QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia;

    Univ Western Australia, Immunol & Virol Program, Ctr Ophthalmol & Visual Sci, Perth, WA, Australia|Lions Eye Inst, Ctr Expt Immunol, Perth, WA, Australia|Monash Univ, Biomed Discovery Inst, Infect & Immun Program, Clayton, Vic, Australia|Monash Univ, Dept Microbiol, Infect & Immun Program, Clayton, Vic, Australia;

    QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia|Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA|Univ Washington, Div Med Oncol, Seattle, WA 98195 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 04:10:14

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