Immunological memory to COVID-19 vaccines in immunocompromised and immunocompetent children.

IF 4.8 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2025-02-17 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1527573
Constanza Russo, Adrián Otero, Macarena Uranga, Vanesa Seery, Silvina Raiden, Silvia Algieri, Norberto De Carli, Mauricio Borda, María F Albistur, Lourdes Heinitz, María Marcó Del Pont, Martina Pardini, Guillermina Budano, Laura Alvarez, Nancy Simaz, Claudia Merhar, María C Quintana, Cecilia Garbini, Luisa Aedo Portela, Misael Salcedo Pereira, Fernando Ferrero, Jorge Geffner, Lourdes Arruvito
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Abstract

Background: Most children in Argentina received only the initial COVID-19 vaccine series, with presumed hybrid immunity after multiple Omicron waves. However, the durability of immune memory, particularly in immunocompromised (IC) children, remains poorly studied.

Methods: A cohort of IC (n=45) and healthy children (HC, n=79) was assessed between 13 to 17 months after receiving two or three doses of BBIBP-CorV and/or BNT162b2. Plasma anti-spike IgG, neutralizing activity and antigen-specific CD4+ and CD8+ T cells against Wuhan and Omicron BA.5 variants were assessed.

Results: Most children remained seropositive after two vaccine doses, but compared with HC, IC exhibited lower neutralizing titers against both Wuhan and Omicron BA.5, particularly those vaccinated with BBIBP-CorV. Even after three vaccine doses, IC showed weaker neutralizing antibody response, CD8+ T cell responses and lower IFN-γ production compared with HC. Integrated analysis of neutralizing antibodies, memory CD4+, and CD8+ T cells revealed a weak immune memory among IC with an important compromise in memory CD8+ T cell responses.

Conclusions: Immunity can last up to 17 months, but reduced effectiveness against new variants highlights the need for updated COVID-19 vaccines, especially for IC children. Additional efforts are essential to enhance vaccination coverage and protect this vulnerable population.

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免疫功能低下和免疫功能正常儿童对COVID-19疫苗的免疫记忆
背景:阿根廷的大多数儿童只接种了最初的COVID-19疫苗系列,在多次欧米克隆波后推定为混合免疫。然而,免疫记忆的持久性,特别是在免疫功能低下(IC)儿童中,研究仍然很少。方法:在接受2剂或3剂BBIBP-CorV和/或BNT162b2后13至17个月,对IC (n=45)和健康儿童(HC, n=79)进行队列评估。评估血浆抗刺突IgG、中和活性和抗原特异性CD4+和CD8+ T细胞对武汉和欧米克隆BA.5变异的影响。结果:大多数儿童在两次疫苗接种后仍呈血清阳性,但与HC相比,IC对武汉和欧米克隆BA.5的中和效价较低,特别是接种了BBIBP-CorV的儿童。即使在三次疫苗剂量后,与HC相比,IC表现出较弱的中和抗体反应、CD8+ T细胞反应和较低的IFN-γ产生。对中和抗体、记忆性CD4+和CD8+ T细胞的综合分析显示,IC中的免疫记忆较弱,记忆性CD8+ T细胞反应也有重要的妥协。结论:免疫可以持续长达17个月,但对新变体的有效性降低,这表明需要更新COVID-19疫苗,特别是对IC儿童。必须进一步努力提高疫苗接种覆盖率并保护这一脆弱人群。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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