Evidence map›Paper›PMID 33688691›Full record

ArticlemedRxiv : the preprint server for health sciences2021

Longitudinal Analysis Reveals Distinct Antibody and Memory B Cell Responses in SARS-CoV2 Naïve and Recovered Individuals Following mRNA Vaccination.

Rishi R Goel, Sokratis A Apostolidis, Mark M Painter, Divij Mathew, Ajinkya Pattekar, Oliva Kuthuru, Sigrid Gouma, Leticia Kuri-Cervantes, Wenzhao Meng, Sharon Adamski and 16 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 2 institutions in 1 country.

Rishi R GoelInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Sokratis A ApostolidisInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Mark M PainterInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Divij MathewInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Ajinkya PattekarImmune Health™, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Oliva KuthuruInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Sigrid GoumaDepartment of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Leticia Kuri-CervantesInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Wenzhao MengInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Sharon AdamskiImmune Health™, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Amy E BaxterInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Josephine R GilesInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Madison E WeirickDepartment of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Christopher M McAllisterDepartment of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Amanda HicksImmune Health™, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Scott KorteImmune Health™, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Jeanette DoughertyInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Sherea LongInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Kurt D'AndreaImmune Health™, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Jacob T HamiltonImmune Health™, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Eline T Luning PrakInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Michael R BettsInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Paul BatesDepartment of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Scott E HensleyDepartment of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Allison R GreenplateInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
E John WherryInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
University of Pennsylvania · USParker Institute for Cancer Immunotherapy · US

Funding

Virology CoreU19AI082630 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG, GEORG Michael LAUER · 2009 to 2026
$48.1M
IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
Training Program/Rheumatic DiseasesT32AR076951 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI EDWARD M BEHRENS, Peter A Merkel · 2020 to 2026
$2.6M
Cellular and transcriptional control of exhausted CD8 T cells lineage dynamicsR01AI105343 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI WHERRY, E. JOHN · 2014 to 2017
$1.6M
The Penn-StARR Program for Research in ResidencyR38HL143613 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI KLEIN, PETER S · 2018 to 2021
$1.4M
NCI NIH HHS T32 CA009140NHLBI NIH HHS R38 HL143613NIAID NIH HHS R01 AI105343NIAID NIH HHS U19 AI082630NIAMS NIH HHS T32 AR076951
6 · The paper itself

Abstract

Novel mRNA vaccines for SARS-CoV2 have been authorized for emergency use and are currently being administered to millions of individuals worldwide. Despite their efficacy in clinical trials, there is limited data on vaccine-induced immune responses in individuals with a prior SARS-CoV2 infection compared to SARS-CoV2 naïve subjects. Moreover, how mRNA vaccines impact the development of antibodies as well as memory B cells in COVID-19 experienced versus COVID-19 naïve subjects remains poorly understood. In this study, we evaluated antibody responses and antigen-specific memory B cell responses over time in 33 SARS-CoV2 naïve and 11 SARS-CoV2 recovered subjects. mRNA vaccination induced significant antibody and memory B cell responses against full-length SARS-CoV2 spike protein and the spike receptor binding domain (RBD). SARS-CoV2 naïve individuals benefitted from both doses of mRNA vaccine with additional increases in antibodies and memory B cells following booster immunization. In contrast, SARS-CoV2 recovered individuals had a significant immune response after the first dose with no increase in circulating antibodies or antigen-specific memory B cells after the second dose. Moreover, the magnitude of the memory B cell response induced by vaccination was lower in older individuals, revealing an age-dependence to mRNA vaccine-induced B cell memory. Side effects also tended to associate with post-boost antibody levels, but not with post-boost memory B cells, suggesting that side effect severity may be a surrogate of short-term antibody responses. The frequency of pre-vaccine antigen-specific memory B cells in SARS-CoV2 recovered individuals strongly correlated with post-vaccine antibody levels, supporting a key role for memory B cells in humoral recall responses to SARS-CoV2. This observation may have relevance for future booster vaccines and for responses to viral variants that partially escape pre-existing antibodies and require new humoral responses to be generated from memory B cells. Finally, post-boost antibody levels were not correlated with post-boost memory responses in SARS-CoV2 naïve individuals, indicating that short-term antibody levels and memory B cells are complementary immunological endpoints that should be examined in tandem when evaluating vaccine response. Together, our data provide evidence of both serological response and immunological memory following mRNA vaccination that is distinct based on prior SARS-CoV2 exposure. These findings may inform vaccine distribution in a resource-limited setting.

Identifiers

PMID33688691
PMCPMC7941668
OpenAlexW3134094901

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.