Evidence map›Paper›PMID 34649116›Full record

ArticleInternational immunopharmacology2021

Serology-based therapeutic strategy in SARS-CoV-2-infected patients.

Ricardo Garcia-Muñoz, Giovanna Farfán-Quiroga, Noemí Ruiz-de-Lobera, Jesus Feliu, Judith Anton-Remirez, Maria José Nájera Irazu, Valentín Lisa Catón, José Antonio Oteo-Revuelta

Open access · greenAbstract read
In one paragraph

Article in International immunopharmacology, 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
0.2field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Immunotherapy and CRISPR Cas Systems: Potential Cure of COVID-19?Drug design, development and therapy · 2022
    Review
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

8 authors at 2 institutions in 1 country.

Ricardo Garcia-MuñozHematology Department, Hospital San Pedro, Logroño, La Rioja. C/Piqueras 98, PC 26006, Spain. Electronic address: rgmunoz@riojasalud.es.
Giovanna Farfán-QuirogaHematology Department, Hospital San Pedro, Logroño, La Rioja. C/Piqueras 98, PC 26006, Spain. Electronic address: gfarfan@riojasalud.es.
Noemí Ruiz-de-LoberaEmergency Department, Hospital San Pedro, Logroño, La Rioja. C/Piqueras 98, PC 26006, Spain. Electronic address: nrlobera@riojasalud.es.
Jesus FeliuHematology Department, Hospital San Pedro, Logroño, La Rioja. C/Piqueras 98, PC 26006, Spain. Electronic address: jfeliusa@yahoo.es.
Judith Anton-RemirezDepartment of Physical Medicine and Rehabilitation. Complejo Hospitalario de Navarra, Pamplona, Spain. Electronic address: jarenero@outlook.es.
Maria José Nájera IrazuHematology Department, Hospital San Pedro, Logroño, La Rioja. C/Piqueras 98, PC 26006, Spain. Electronic address: mjnajera@riojasalud.es.
Valentín Lisa CatónEmergency Department, Hospital San Pedro, Logroño, La Rioja, Spain. Electronic address: vlisa@riojasalud.es.
José Antonio Oteo-RevueltaInfectious Diseases Department, Hospital San Pedro, Logroño, La Rioja. C/Piqueras 98, PC 26006, Spain. Electronic address: jaoteo@riojasalud.es.
Hospital San Pedro · ESComplejo Hospitalario de Navarra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 infection can be a life-threatening disease. The optimal treatment of patients is not yet standardized. We use a serology-based therapeutic strategy based on the presence of antibodies against the SARS-CoV-2 virus, in which patients with positive serology receive aggressive anti-inflammatory treatment with high-dose dexamethasone and/or tocilizumab and patients with negative serology receive early convalescent plasma therapy. We also analyze the immunological impact of this therapy in the recovery of T cells, B cells and NK cells during hospitalization in a COVID-19 infectious ward. Our results suggest that aggressive therapy with early administration of convalescent plasma and high-dose dexamethasone may be of benefit in patients with SARS-CoV-2 infection and might avoid progression of lung damage or need of admission in intensive care. This strategy did not impair immune responses against SARS-CoV-2, as 93% of the patients generated antibodies against the virus. Independently of previous immunological status of the patients, serology-guided therapy might benefit even patients with a high CIRS-G score, immunosuppressed or medically debilitated individuals and elderly patients. T cell disturbances were most frequent in patients who required high-dose dexamethasone, and B cell depletion was most frequent in patients who received tocilizumab. Early passive immunotherapy with convalescent plasma does not affect lymphoid recovery.

Indexed as

AdultAgedAged, 80 and overAntibodies, ViralAnti-Inflammatory AgentsB-LymphocytesCOVID-19COVID-19 Drug TreatmentCOVID-19 SerotherapyDexamethasoneFemaleGlucocorticoidsHumansImmunization, PassiveImmunoglobulin GImmunoglobulin MAntibodies, ViralAnti-Inflammatory AgentsDexamethasoneGlucocorticoidsImmunoglobulin GImmunoglobulin MDexamethasoneLymphocytePlasmaSARS-CoV-2Tocilizumab

Identifiers

PMID34649116
PMCPMC8491979
OpenAlexW3203172695

What OpenQuestion holds

Textmetadata
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.