Evidence map›Paper›PMID 41562622›Full record

ArticleMicrobiology spectrum2026

Impaired neutralizing antibody responses against the BA1.1, BA.2, and BA.5 Omicron SARS-CoV-2 subvariants in hospitalized adults infected with pre-Omicron variants in Argentina.

J Sachithanandham, I A Sitaras, R A Albertini, R H Capra, J Marquez, G B Sadino-Vallve, P R Gargantini, P R Cortes, N E Ponce, A van de Guchte and 11 more

Abstract read
In one paragraph

Article in Microbiology spectrum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

J SachithanandhamW. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.ORCID 0000-0001-7086-2990
I A SitarasW. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.ORCID 0000-0003-0161-8024
R A AlbertiniInstituto Universitario de Ciencias Biomédicas de Córdoba (IUCBC), Córdoba, Argentina.
R H CapraInstituto Universitario de Ciencias Biomédicas de Córdoba (IUCBC), Córdoba, Argentina.
J MarquezClínica Universitaria Reina Fabiola, Universidad Católica de Córdoba, Córdoba, Argentina.
G B Sadino-VallveClínica Universitaria Reina Fabiola, Universidad Católica de Córdoba, Córdoba, Argentina.ORCID 0009-0003-9335-7438
P R GargantiniClínica Universitaria Reina Fabiola, Universidad Católica de Córdoba, Córdoba, Argentina.ORCID 0000-0001-5884-8387
P R CortesCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.ORCID 0000-0003-1668-7911
N E PonceCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.ORCID 0000-0002-7052-5086
A van de GuchteDepartment of Genetics and Genomics Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID 0000-0002-0771-3842
A S Gonzalez-ReicheDepartment of Genetics and Genomics Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID 0000-0003-3583-4497
N B OliveroCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.
V E ZappiaCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.
M Hernandez-MorfaCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.ORCID 0000-0003-0603-2612
A Echenique-NunezCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.
M Nunez-FernandezCentro de Química Aplicada, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.
L Raya-PlasenciaCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.
H van BakelDepartment of Genetics and Genomics Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID 0000-0002-1376-6916
A PekoszW. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.ORCID 0000-0003-3248-1761
D R PerezDepartment of Population Health, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.ORCID 0000-0002-6569-5689
J EcheniqueCentro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Córdoba, Argentina.ORCID 0000-0003-2638-0577

Funding

Agencia Nacional de Promoción Científica y Tecnológica IP-COVID 19-240NIAID-CEIRS 15B HHSN272201400008CNIAID-CEIRS CHHS N7593021C00045Secretaría de Ciencia y Tecnología (Secyt) - Universidad Nacional de Córdoba SECYT-UNC 2020
6 · The paper itself

Abstract

Infection with SARS-CoV-2 variants typically confers protective humoral immunity. Yet, the Omicron variant demonstrates a considerable capacity to evade immune responses in individuals previously infected with other SARS-CoV-2 strains. This has prompted investigation into Omicron's potential resistance to neutralizing antibodies elicited by natural infection or vaccination. Importantly, the molecular mechanisms underlying this cross-protection have been investigated; however, they are not yet fully elucidated. In this study, we investigated the neutralization capacity of convalescent sera from COVID-19 patients in Córdoba City, Argentina, offering insights into immune responses against various SARS-CoV-2 variants. We analyzed samples from hospitalized patients infected with the Lambda and Gamma variants during the pandemic's second wave from May to August 2021. These patients showed strong neutralization against Gamma, moderate activity against the B.1 and Delta variants, a weak response to Omicron BA.2, and extremely poor cross-neutralization against the Omicron BA.1.1 and BA.5 subvariants. Additionally, we examined convalescent sera from ambulatory patients during the fourth COVID-19 wave, from May to July 2022, when various Omicron variants predominated. Consistent with the hospitalized cohort, the highest neutralizing activity was observed against the Gamma variant, with moderate responses against B.1 and Delta, and low activity against Omicron subvariants. These findings highlight the critical need for region-specific studies of neutralizing responses to inform the development of future SARS-CoV-2 vaccine formulations.IMPORTANCEInvestigating the neutralizing capacity of sera obtained from COVID-19 patients infected with distinct viral variants-in this case, a comparison between pre-Omicron and Omicron strains-is essential for elucidating mechanisms of immune evasion, cross-protective immunity, and the efficacy of vaccines. Variations in neutralization profiles provide critical insights that inform the development of updated vaccines and booster immunization strategies, particularly given the pronounced immune escape characteristics exhibited by the Omicron variant. Furthermore, it is imperative to examine geographic heterogeneity, as regional differences in variant prevalence, vaccine types, and public health interventions contribute to diverse immune profiles. Conducting such investigations is critical for informing the development of tailored public health policies, facilitating the identification of immunological susceptibilities and resilience within distinct populations. This understanding is essential for improving preparedness in response to the emergence of new SARS-CoV-2 variants.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCOVID-19SARS-CoV-2AdultAgedArgentinaFemaleHumansMaleMiddle AgedNeutralization TestsAntibodies, NeutralizingAntibodies, ViralantibodycomorbiditiesDeltaGammaneutralizing antibodiesOmicronpre-OmicronSARS-CoV-2vaccinevariants of concern

Identifiers

PMID41562622
PMCPMC12955416

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.