Evidence map›Paper›PMID 34196737›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2021

Effect of lysed and non-lysed sickle red cells on the activation of NLRP3 inflammasome and LTB4 production by mononuclear cells.

Thassila N Pitanga, Sânzio S Santana, Dalila L Zanette, Caroline C Guarda, Rayra P Santiago, Vitor V Maffili, Jonilson B Lima, Graziele Q Carvalho, Jaime R Filho, Junia R D Ferreira and 7 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Ferroptosis as an emerging target in sickle cell disease.Current research in toxicology · 2024
    Article
  3. Inflammasomes-New Contributors to Blood Diseases.International journal of molecular sciences · 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

17 authors at 7 institutions in 1 country.

Thassila N Pitanga *Instituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Sânzio S Santana *Instituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Dalila L ZanetteFundação Oswaldo Cruz, Instituto Carlos Chagas (ICC-FIOCRUZ/PR), Curitiba, Paraná, Brazil.
Caroline C GuardaInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Rayra P SantiagoInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Vitor V MaffiliInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Jonilson B LimaUniversidade Federal do Oeste da Bahia (UFOB), Barreiras, Bahia, Brazil.
Graziele Q CarvalhoInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Jaime R FilhoInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Junia R D FerreiraUniversidade Federal da Bahia (UFBA), Salvador, Bahia, Brazil.
Milena M AleluiaUniversidade Estadual de Santa Cruz (UESC), Ilhéus, Bahia, Brazil.
Valma M L NascimentoFundação de Hematologia e Hemoterapia da Bahia (HEMOBA), Salvador, Bahia, Brazil.
Magda O S CarvalhoHospital Universitário Professor Edgard Santos (HUPES), UFBA, Salvador, Bahia, Brazil.
Isa M LyraHospital Universitário Professor Edgard Santos (HUPES), UFBA, Salvador, Bahia, Brazil.
Valéria M BorgesInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Ricardo R OliveiraInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil.
Marilda S GoncalvesInstituto Gonçalo Moniz, FIOCRUZ Bahia, Fundação Oswaldo Cruz / FIOCRUZ, Rua Waldemar Falcão, n. 121, Candeal, Salvador, Bahia, 40296710, Brazil. marilda.goncalves@fiocruz.br.ORCID http://orcid.org/0000-0003-3000-1437
Fundação Oswaldo Cruz · BRComplexo Hospitalar Universitário Professor Edgard Santos · BRUniversidade Católica do Salvador · BRUniversidade Federal da Bahia · BRFundação Carlos Chagas · BRUniversidade Estadual de Santa Cruz · BRUniversidade Federal do Oeste da Bahia · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 311888/2013-5Fundação de Amparo à Pesquisa do Estado da Bahia 1431040053063Fundação de Amparo à Pesquisa do Estado da Bahia 3626/2013Fundação de Amparo à Pesquisa do Estado da Bahia 9073/2007MCD/CNPq/MS-SCTIE-DECIT 409800/2006-6PPSUS/FAPESB 020/2013 EFP00007295
6 · The paper itself

Abstract

OBJECTIVE AND

designThis study tested the hypothesis that sickle red blood cell (SS-RBC) can induce inflammasome NLRP3 components gene expression in peripheral blood mononuclear cells (PBMCs) as well as interleukin-1β (IL-1β) and leukotriene B4 (LTB4) production. Additionally, we investigated the effect of hydroxyurea (HU) treatment in these inflammatory markers.

methodsPBMCs from healthy donors (AA-PBMC) were challenged with intact and lysed RBCs from SCA patients (SS-RBC) and from healthy volunteers (AA-RBC). NLRP3, IL-1β, IL-18 and Caspase-1 gene expression levels were assessed by quantitative PCR (qPCR). IL-1β protein levels and LTB4 were measured by ELISA.

resultsWe observed that lysed SS-RBC induced the expression of inflammasome NLRP3 components, but this increase was more prominent for CASP1 and IL18 expression levels. Moreover, we observed that intact SS-RBC induced higher production of IL-1β and LTB4 than lysed SS-RBC. Although SCA patients treated with HU have a reduction in NLRP3 gene expression and LTB4 production, this treatment did not modulate the expression of other inflammasome components or IL-1β production.

conclusionsThus, our data suggest that caspase-1, IL-1β and IL-18 may contribute to the inflammatory status observed in SCA and that HU treatment may not interfere in this inflammatory pathway.

Indexed as

AdolescentAnemia, Sickle CellAntisickling AgentsCaspase 1Cells, CulturedChildErythrocytesHumansHydroxyureaInflammasomesInterleukin-18Interleukin-1betaLeukocytes, MononuclearLeukotriene B4NLR Family, Pyrin Domain-Containing 3 ProteinAntisickling AgentsCaspase 1HydroxyureaIL1B protein, humanInflammasomesInterleukin-18Interleukin-1betaLeukotriene B4NLR Family, Pyrin Domain-Containing 3 ProteinhemeHemolysisHydroxyureaNLRP3-inflammasomeSickle cell anemia

Identifiers

PMID34196737
OpenAlexW3173294917

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.