Booster Vaccination Against SARS-CoV-2 Induces Potent Immune Responses in People With Human Immunodeficiency Virus.

Booster Vaccination Against SARS-CoV-2 Induces Potent Immune Responses in People With Human Immunodeficiency Virus.
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DOI:
10.1093/cid/ciac796
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发表时间:
2023-01-13
期刊:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
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接受抗逆转录病毒治疗(ART)的人类免疫缺陷病毒(HIV)感染者CD4 t细胞计数良好,在接种严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)疫苗后产生有效的免疫反应。关于长期反应和加强剂量影响的数据很少。成年艾滋病毒感染者被纳入一项单臂开放标签研究。两剂ChAdOx1 nCoV-19疫苗接种12个月后,再接种第三剂异源疫苗。参与者ART检测不到病毒血症,CD4细胞计数为350个/µL。通过抗刺突免疫球蛋白G (IgG)酶联免疫吸附试验(ELISA)、MesoScale Discovery (MSD)抗刺突平台、ACE-2抑制、激活诱导标记(AIM)试验和t细胞增殖检测对祖先菌株和相关变异株的免疫应答。总共有54名参与者接受了2剂ChAdOx1 nCoV-19。43人在第一次注射后1年接受第三次注射(42人使用BNT162b2, 1人使用mRNA-1273)。第三次给药后,抗sars - cov -2总刺突IgG滴度(MSD)、ACE-2抑制和IgG ELISA结果均显著高于第182天滴度(P < 0.0001)。AIM检测的针对SARS-CoV-2 S1和S2肽库的SARS-CoV-2特异性CD4+ t细胞反应在第三次疫苗接种后与第一次接种后6个月相比显著增加,增强后对SARS-CoV-2 S1和S2的增殖性CD4+和CD8+ t细胞反应显著增加。对Alpha、Beta、Gamma和Delta变体的反应有所提高,尽管对Omicron的反应程度较低。在接受第三剂疫苗的PWH中,B细胞和t细胞免疫力显著增加,包括对已知的关注变体(VOCs)的免疫力。接受抗逆转录病毒治疗(ART)且CD4 t细胞计数良好的人类免疫缺陷病毒(HIV)患者在接种第三剂严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)疫苗后产生有效的交叉变异免疫反应。
People with human immunodeficiency virus (HIV) on antiretroviral therapy (ART) with good CD4 T-cell counts make effective immune responses following vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). There are few data on longer term responses and the impact of a booster dose. Adults with HIV were enrolled into a single arm open label study. Two doses of ChAdOx1 nCoV-19 were followed 12 months later by a third heterologous vaccine dose. Participants had undetectable viraemia on ART and CD4 counts >350 cells/µL. Immune responses to the ancestral strain and variants of concern were measured by anti-spike immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA), MesoScale Discovery (MSD) anti-spike platform, ACE-2 inhibition, activation induced marker (AIM) assay, and T-cell proliferation. In total, 54 participants received 2 doses of ChAdOx1 nCoV-19. 43 received a third dose (42 with BNT162b2; 1 with mRNA-1273) 1 year after the first dose. After the third dose, total anti-SARS-CoV-2 spike IgG titers (MSD), ACE-2 inhibition, and IgG ELISA results were significantly higher compared to Day 182 titers (P < .0001 for all 3). SARS-CoV-2 specific CD4+ T-cell responses measured by AIM against SARS-CoV-2 S1 and S2 peptide pools were significantly increased after a third vaccine compared to 6 months after a first dose, with significant increases in proliferative CD4+ and CD8+ T-cell responses to SARS-CoV-2 S1 and S2 after boosting. Responses to Alpha, Beta, Gamma, and Delta variants were boosted, although to a lesser extent for Omicron. In PWH receiving a third vaccine dose, there were significant increases in B- and T-cell immunity, including to known variants of concern (VOCs). People with human immunodeficiency virus (HIV) on antiretroviral therapy (ART) with good CD4 T-cell counts make effective cross variant immune responses following third dose vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
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影响因子: --
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