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恒河猴感染猴免疫缺陷病毒(SHIV)后诱导产生的针对 HIV-1 的中和抗体与新生儿免疫相关。

Neonatal immunity associated with heterologous HIV-1 neutralizing antibody induction in SHIV-infected Rhesus Macaques.

机构信息

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, USA.

Departments of Medicine and Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Nat Commun. 2024 Nov 27;15(1):10302. doi: 10.1038/s41467-024-54753-6.

DOI:10.1038/s41467-024-54753-6
PMID:39604409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11603298/
Abstract

The details of the pediatric immune system that supports induction of antibodies capable of neutralizing geographically-diverse or heterologous HIV-1 is currently unclear. Here we explore the pediatric immune environment in neonatal macaque undergoing Simian-HIV infection. Simian-HIV infection of 11 pairs of therapy-naive dams and infant rhesus macaques for 24 months results in heterologous HIV-1 neutralizing antibodies in 64% of young macaques compared to 18% of adult macaques. Heterologous HIV-1 neutralizing antibodies emerge by 12 months post-infection in young macaques, in association with lower expression of immunosuppressive genes, fewer germinal center CD4 + T regulatory cells, and a lower ratio of CD4 + T follicular regulatory to helper cells. Antibodies from peripheral blood B cells in two young macaques following SHIV infection neutralize 13% of 119 heterologous HIV-1 strains and map to regions of canonical broadly neutralizing antibody epitopes on the envelope surface protein. Here we show that pediatric immunity to SHIV infection in a macaque model may inform vaccine strategies to induce effective HIV-1 neutralizing antibodies in infants and children prior to viral exposure.

摘要

目前尚不清楚支持诱导能够中和地理上不同或异源 HIV-1 的抗体的儿科免疫系统的细节。在这里,我们探索了在感染 HIV 的新生猕猴中儿科免疫环境。11 对未经治疗的母婴和婴儿恒河猴接受猴免疫缺陷病毒(SHIV)感染 24 个月后,与 18%的成年猕猴相比,64%的幼猴体内出现了异源 HIV-1 中和抗体。在感染后 12 个月,幼猴体内出现了异源 HIV-1 中和抗体,与免疫抑制基因表达降低、生发中心 CD4+T 调节细胞减少以及滤泡辅助性 T 细胞与滤泡调节性 T 细胞的比例降低有关。SHIV 感染后,两名幼猴外周血 B 细胞中的抗体可中和 119 株异源 HIV-1 株中的 13%,并定位于包膜表面蛋白上的经典广泛中和抗体表位区域。在这里,我们表明,猕猴模型中对 SHIV 感染的儿科免疫可能为在病毒暴露之前诱导婴儿和儿童体内有效 HIV-1 中和抗体的疫苗策略提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/b878456d915c/41467_2024_54753_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/43ef0bb399e7/41467_2024_54753_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/31f9034c3a48/41467_2024_54753_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/fd698a2ed167/41467_2024_54753_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/e9343fc91180/41467_2024_54753_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/c83509b56ce7/41467_2024_54753_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/419ecc95f311/41467_2024_54753_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/b878456d915c/41467_2024_54753_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/43ef0bb399e7/41467_2024_54753_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/7bd8bfa1beae/41467_2024_54753_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/31f9034c3a48/41467_2024_54753_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/fd698a2ed167/41467_2024_54753_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/e9343fc91180/41467_2024_54753_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/c83509b56ce7/41467_2024_54753_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/419ecc95f311/41467_2024_54753_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e284/11603298/b878456d915c/41467_2024_54753_Fig8_HTML.jpg

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