在巴西亚马逊地区,HLA II 类的 DRB1 位点等位基因与 HIV-1/Epstein-Barr 病毒双重感染的不同血清学特征中的免疫反应调节有关

Leonn Mendes Soares Pereira, Eliane dos Santos França, I. B. Costa, Igor Tenório Lima, Erika Vanessa Oliveira Jorge, Patrícia Jeanne de Souza Mendonça Mattos, Amaury Bentes Cunha Freire, Francisco Lúzio de Paula Ramos, T. F. Monteiro, O. Macêdo, Rita Catarina Medeiros Sousa, F. B. Freitas, I. B. Costa, A. Vallinoto
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引用次数: 0

摘要

Epstein-Barr 病毒(EBV)感染涉及不同的临床和血清学特征。我们招募了 19 名原发感染患者、90 名血清学转归患者和 467 名既往感染过 EBV 的患者,原发感染患者中 100%合并有 HIV-1 感染,其他血清学转归患者中约 70%合并有 HIV-1 感染。EBV 病毒载量通过实时 PCR 进行定量,T 淋巴细胞定量和细胞因子水平分析通过流式细胞术进行,HLA 位点基因分型通过 PCR-SSO 进行。DRB1*09等位基因与原发性感染相关(p:0.0477),等位基因携带者的EBV病毒载量(p:0.0485)、CD8(+)T淋巴细胞计数(p:0.0206)、双阳性T淋巴细胞计数(p:0.0093)、IL-4水平(p:0.0464)和TNF水平(p:0.0161)均有变化。该等位基因在艾滋病毒合并感染者中也很常见(p:0.0023),并与 log10 HIV 病毒载量(p:0.0176)和 CD8(+)T 淋巴细胞计数(p:0.0285)有关。在原发性感染中,log10 HIV 病毒载量较高(p:0.0060),与 EBV 病毒载量成正比(p:0.0412)。DRB1*03 等位基因与血清学转换(p:0.0477)、EBV 病毒载量(p:0.0015)、CD4(+)T 淋巴细胞计数(p:0.0112)、CD8(+)T 淋巴细胞计数(p:0.0260)、双阴性 T 淋巴细胞计数(p:0.0540)、IL-4 水平(p:0.0478)和 IL-6 水平(p:0.0175)相关。在血清学转换组中,log10 HIV 病毒载量较高(p:0.0060),但与 EBV 病毒载量无关(p:0.1214)。既往感染与 DRB1*16 等位基因有关(p:0.0477),携带者显示 IgG 水平(p:0.0020)、CD4(+)T 淋巴细胞计数(p:0.0116)和提示性 CD8(+)T 计数改变(p:0.0602)。我们的研究结果表明,HLA II 类等位基因可能与合并感染 HIV-1 的患者对 Epstein-Barr 病毒感染的免疫反应血清学特征的调节有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DRB1 locus alleles of HLA class II are associated with modulation of the immune response in different serological profiles of HIV-1/Epstein-Barr virus coinfection in the Brazilian Amazon region
Epstein–Barr virus (EBV) infection involves distinct clinical and serological profiles. We evaluated the frequency of alleles of locus DRB1 of HLA class II in different serological profiles of EBV infection among HIV-1 infected patients.We recruited 19 patients with primary infection, 90 with serological transition and 467 with past infection by EBV, HIV-1 co-infection was 100% in primary infection and approximately 70% in other serological profiles. EBV viral load was quantified by real-time PCR, T lymphocyte quantification and cytokine level analysis were performed by flow cytometry, and HLA locus genotyping was performed by PCR-SSO.The DRB1*09 allele was associated with primary infection (p: 0.0477), and carriers of the allele showed changes in EBV viral load (p: 0.0485), CD8(+) T lymphocyte counts (p: 0.0206), double-positive T lymphocyte counts (p: 0.0093), IL-4 levels (p: 0.0464) and TNF levels (p: 0.0161). This allele was also frequent in HIV-coinfected individuals (p: 0.0023) and was related to the log10 HIV viral load (p: 0.0176) and CD8(+) T lymphocyte count (p: 0.0285). In primary infection, the log10 HIV viral load was high (p: 0.0060) and directly proportional to the EBV viral load (p: 0.0412). The DRB1*03 allele correlated with serological transition (p: 0.0477), EBV viral load (p: 0.0015), CD4(+) T lymphocyte count (p: 0.0112), CD8(+) T lymphocyte count (p: 0.0260), double-negative T lymphocyte count (p: 0.0540), IL-4 levels (p: 0.0478) and IL-6 levels (p: 0.0175). In the serological transition group, the log10 HIV viral load was high (p: 0.0060), but it was not associated with the EBV viral load (p: 0.1214). Past infection was related to the DRB1*16 allele (p: 0.0477), with carriers displaying IgG levels (p: 0.0020), CD4(+) T lymphocyte counts (p: 0.0116) and suggestive CD8(+) T count alterations (p: 0.0602). The DRB01*16 allele was also common in HIV-1 patients with past EBV infection (p: 0.0192); however, the allele was not associated with clinical markers of HIV-1 infection.Our results suggest that HLA class II alleles may be associated with the modulation of the serological profiles of the immune response to Epstein-Barr virus infection in patients coinfected with HIV-1.
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