Evidence map›Paper›PMID 33692784›Full record

ArticleFrontiers in immunology2021

Phenotypic Characterization of CD4

Jordana Batista Santana, Tarcísio Vila Verde Santana de Almeida, Diego Mota Lopes, Brady Page, Sergio Costa Oliveira, Irismá Souza, Luís Eduardo Viana Silva Ribeiro, Néstor Adrián Guerrero Gutiérrez, Edgar M Carvalho, Luciana Santos Cardoso

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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 at 6 institutions in 2 countries.

Jordana Batista SantanaServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Tarcísio Vila Verde Santana de AlmeidaServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Diego Mota LopesServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Brady PageMassachusetts General Hospital, Boston, MA, United States.
Sergio Costa OliveiraDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Irismá SouzaInstituto de Saúde Irismá Souza, Gandu, Brazil.
Luís Eduardo Viana Silva RibeiroServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Néstor Adrián Guerrero GutiérrezServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Edgar M CarvalhoServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Luciana Santos CardosoServiço de Imunologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Brazil.
Complexo Hospitalar Universitário Professor Edgard Santos · BRUniversidade Federal da Bahia · BRInstituto de Saúde · BRInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais · BRMassachusetts General Hospital · USUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schistosomiasis is a parasitic disease that affects about 166 million people around the world. It is estimated that 5%-10% of individuals with schistosomiasis develop severe forms of the disease, which are characterized by pulmonary hypertension, ascites, periportal fibrosis, and other significant complications. The chronic phase of the disease is associated with a Th2 type immune response, but evidence also suggests there are roles for Th1 and Th17 in the development of severe disease. The aim of this study was to evaluate the CD4

Indexed as

AnimalsBiomarkersCD4-Positive T-LymphocytesCytokinesDisease SusceptibilityFemaleFibrosisHumansLeukocytes, MononuclearMaleSchistosomaSchistosomiasisT-Lymphocyte SubsetsBiomarkersCytokinesCD4+ T lymphocytesfibrosisperiportal fibrosisSchistosoma mansonischistosomiasis

Identifiers

PMID33692784
PMCPMC7937650
OpenAlexW3132268136

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.