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一种武装抗免疫球蛋白轻链纳米抗体可保护小鼠免受甲型和乙型流感感染。

An armed anti-immunoglobulin light chain nanobody protects mice against influenza A and B infections.

机构信息

Program in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.

CBS2 University of Montpellier, 163 rue Auguste Broussonnet, 34090 Montpellier, France.

出版信息

Sci Immunol. 2023 Jun 23;8(84):eadg9459. doi: 10.1126/sciimmunol.adg9459.

Abstract

The immune system eliminates pathogen intruders such as viruses and bacteria. To recruit immune effectors to virus-infected cells, we conjugated a small molecule, the influenza neuraminidase inhibitor zanamivir, to a nanobody that recognizes the kappa light chains of mouse immunoglobulins. This adduct was designed to achieve half-life extension of zanamivir through complex formation with the much-larger immunoglobulins in the circulation. The zanamivir moiety targets the adduct to virus-infected cells, whereas the anti-kappa component simultaneously delivers polyclonal immunoglobulins of indeterminate specificity and all isotypes. Activation of antibody-dependent cell-mediated cytotoxicity and complement-dependent cytotoxicity promoted elimination of influenza neuraminidase-positive cells. A single dose of the conjugate protected mice against influenza A or B viruses and was effective even when given several days after infection with a lethal dose of virus. In the absence of circulating immunoglobulins, we observed no in vivo protection from the adduct. The type of conjugates described here may thus find application for both anti-influenza prophylaxis and therapy.

摘要

免疫系统会清除病毒和细菌等病原体入侵者。为了将免疫效应器招募到病毒感染的细胞中,我们将一种小分子流感神经氨酸酶抑制剂扎那米韦与一种能够识别小鼠免疫球蛋白 κ 轻链的纳米抗体偶联。这种加合物的设计目的是通过与循环中更大的免疫球蛋白形成复合物来延长扎那米韦的半衰期。扎那米韦部分将加合物靶向病毒感染的细胞,而抗 κ 部分则同时递送不确定特异性和所有同种型的多克隆免疫球蛋白。抗体依赖性细胞介导的细胞毒性和补体依赖性细胞毒性的激活促进了流感神经氨酸酶阳性细胞的清除。单次给予该缀合物即可保护小鼠免受甲型或乙型流感病毒的侵害,即使在感染致死剂量病毒几天后给予该缀合物也有效。在没有循环免疫球蛋白的情况下,我们没有观察到该加合物在体内的保护作用。因此,这里描述的缀合物类型可能适用于抗流感的预防和治疗。

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