Evidence map›Paper›PMID 39205152›Full record

ArticleViruses2024

Elucidating the Immune Response to SARS-CoV-2: Natural Infection versus Covaxin/Covishield Vaccination in a South Indian Population.

Agalya Vanamudhu, Renuka Devi Arumugam, Arul Nancy, Nandhini Selvaraj, Kadar Moiden, Syed Hissar, Uma Devi Ranganathan, Ramalingam Bethunaickan, Subash Babu, Nathella Pavan Kumar

Abstract read
In one paragraph

Article in Viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Agalya VanamudhuDepartment of Immunology, ICMR, National Institute for Research in Tuberculosis, Chennai 600031, India.
Renuka Devi ArumugamDepartment of Immunology, ICMR, National Institute for Research in Tuberculosis, Chennai 600031, India.
Arul NancyNational Institutes of Health, National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai 600031, India.
Nandhini SelvarajNational Institutes of Health, National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai 600031, India.
Kadar MoidenNational Institutes of Health, National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai 600031, India.
Syed HissarDepartment of Immunology, ICMR, National Institute for Research in Tuberculosis, Chennai 600031, India.ORCID 0000-0003-0905-1552
Uma Devi RanganathanDepartment of Immunology, ICMR, National Institute for Research in Tuberculosis, Chennai 600031, India.
Ramalingam BethunaickanDepartment of Immunology, ICMR, National Institute for Research in Tuberculosis, Chennai 600031, India.ORCID 0000-0003-4595-5233
Subash BabuNational Institutes of Health, National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai 600031, India.
Nathella Pavan KumarDepartment of Immunology, ICMR, National Institute for Research in Tuberculosis, Chennai 600031, India.

Funding

Indian Council of Medical Research VIR/COVID-19/13/2021/ECD-I
6 · The paper itself

Abstract

A natural infection or a vaccination can initially prime the immune system to form immunological memory. The immunity engendered by vaccination against COVID-19 versus natural infection with SARS-CoV-2 has not been well studied in the Indian population. In this study, we compared the immunity conferred by COVID-19 vaccines to naturally acquired immunity to SARS-CoV-2 in a South Indian population. We examined binding and neutralizing antibody (NAb) levels against the ancestral and variant lineages and assessed the ex vivo cellular parameters of memory T cells, memory B cells, and monocytes and finally measured the circulating cytokine response. COVID-19 vaccination stimulates heightened levels of IgG antibodies against the original strain of SARS-CoV-2, as well as increased binding to the spike protein and neutralizing antibody levels. This enhanced response extends to variant lineages such as B.1.617.2 (Delta, India), B.1.1.529 (Omicron, India), B.1.351 (Beta, South Africa), and B.1.1.7 (Alpha, UK). COVID-19 vaccination differs from SARS-CoV-2 infection by having increased frequencies of classical memory B cells, activated memory B and plasma cells, CD4/CD8 T cells of effector memory, effector cells, stem cell-like memory T cells, and classical and intermediate monocytes and diminished frequencies of CD4/CD8 T cells of central memory and non-classical monocytes in vaccinated individuals in comparison to those with natural infection. Thus, COVID-19 vaccination is characterized by enhanced humoral responses and robust activation of innate and memory T cell responses in comparison to natural infection in a South Indian population.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCOVID-19COVID-19 VaccinesSARS-CoV-2AdultCytokinesFemaleHumansImmunoglobulin GImmunologic MemoryIndiaMaleMemory B CellsMemory T CellsMiddle AgedAntibodies, NeutralizingAntibodies, ViralBBV152 COVID-19 vaccineCOVID-19 VaccinesCytokinesImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines, InactivatedB cellsCovaxinCOVID-19Covishieldmonocytes and cytokinesSARS-CoV-2T cells

Identifiers

PMID39205152
PMCPMC11360806

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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.