Evidence map›Paper›PMID 34835067›Full record

ArticleViruses2021

Robust and Persistent B- and T-Cell Responses after COVID-19 in Immunocompetent and Solid Organ Transplant Recipient Patients.

Federica Zavaglio, Vanessa Frangipane, Monica Morosini, Elisa Gabanti, Paola Zelini, Josè Camilla Sammartino, Alessandro Ferrari, Marilena Gregorini, Teresa Rampino, Annalia Asti and 12 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 26% of its field
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. COVID-19 and solid organ transplantation: Finding the right balance.Transplantation reviews (Orlando, Fla.) · 2022
    Pooled it
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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

22 authors at 3 institutions in 1 country.

Federica ZavaglioUnit of Microbiology and Virology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0001-5471-1711
Vanessa FrangipaneResearch Laboratory of Lung Diseases, Section of Cell Biology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0002-3194-8027
Monica MorosiniResearch Laboratory of Lung Diseases, Section of Cell Biology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0001-6516-1751
Elisa GabantiUnit of Microbiology and Virology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Paola ZeliniObstetrics and Gynecology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0002-4913-0012
Josè Camilla SammartinoUnit of Microbiology and Virology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0003-3707-3118
Alessandro FerrariUnit of Microbiology and Virology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Marilena GregoriniUnit of Nephrology, Dialysis and Transplantation, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Teresa RampinoUnit of Nephrology, Dialysis and Transplantation, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Annalia AstiUnit of Nephrology, Dialysis and Transplantation, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Elena SeminariInfectious Diseases Clinic, University of Pavia and IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0001-5246-928X
Angela Di MatteoInfectious Diseases Clinic, University of Pavia and IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Barbara CattadoriCardiac Surgery, Department of Intensive Medicine, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Carlo PellegriniCardiac Surgery, Department of Intensive Medicine, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0002-5908-5219
Stelvio TonelloImmunoreumatology Laboratory, Center for Translational Research on Autoimmune and Allergic Disease-CAAD, University of Piemonte Orientale, 28100 Novara, Italy.ORCID 0000-0002-0836-0890
Venkata Ramana MallelaImmunorheumatology Unit, Division of Internal Medicine, "Maggiore della Carità" Univerisity Hospital, 28100 Novara, Italy.ORCID 0000-0001-9664-481X
Rosalba MinisiniInternal Medicine Laboratory, Department of Translational Medicine, University of Piemonte Orientale, 28100 Novara, Italy.ORCID 0000-0002-7548-9731
Manuela RizziImmunorheumatology Unit, Division of Internal Medicine, "Maggiore della Carità" Univerisity Hospital, 28100 Novara, Italy.
Pier Paolo SainaghiImmunoreumatology Laboratory, Center for Translational Research on Autoimmune and Allergic Disease-CAAD, University of Piemonte Orientale, 28100 Novara, Italy.ORCID 0000-0001-8322-9158
Federica MeloniResearch Laboratory of Lung Diseases, Section of Cell Biology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Daniele LilleriUnit of Microbiology and Virology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.ORCID 0000-0001-7747-7622
Fausto BaldantiUnit of Microbiology and Virology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.
Policlinico San Matteo Fondazione · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversity of Pavia · IT

Funding

Fondazione Cariplo CoVIM, no. 2020-1374Ministero della Salute BIAS no. 2020-12371760
6 · The paper itself

Abstract

The development and persistence of SARS-CoV-2-specific immune response in immunocompetent (IC) and immunocompromised patients is crucial for long-term protection. Immune response to SARS-CoV-2 infection was analysed in 57 IC and 15 solid organ transplanted (TX) patients. Antibody responses were determined by ELISA and neutralization assay. T-cell response was determined by stimulation with peptide pools of the Spike, Envelope, Membrane, and Nucleocapsid proteins with a 20-h Activation Induced Marker (AIM) and 7-day lymphoproliferative assays. Antibody response was detected at similar levels in IC and TX patients. Anti-Spike IgG, IgA and neutralizing antibodies persisted for at least one year, while anti-Nucleocapsid IgG declined earlier. Patients with pneumonia developed higher antibody levels than patients with mild symptoms. Similarly, both rapid and proliferative T-cell responses were detected within the first two months after infection at comparable levels in IC and TX patients, and were higher in patients with pneumonia. T-cell response persisted for at least one year in both IC and TX patients. Spike, Membrane, and Nucleocapsid proteins elicited the major CD4

Indexed as

Immunocompromised HostOrgan TransplantationTransplant RecipientsAdultAgedAged, 80 and overAntibodies, NeutralizingAntibodies, ViralB-LymphocytesCell ProliferationCOVID-19FemaleHumansMaleMemory T CellsMiddle AgedAntibodies, NeutralizingAntibodies, Viralantibody responseCOVID-19cytokinesimmunocompetent patientsmembrane proteinnucleocapsid proteinSARS-CoV-2spike proteinT-cell responsetransplanted patients

Identifiers

PMID34835067
PMCPMC8621286
OpenAlexW3211848522

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.