Evidence map›Paper›PMID 21595736›Full record

ArticleScandinavian journal of immunology2011

Evaluation of the microbicidal activity and cytokines/chemokines profile released by neutrophils from HTLV-1-infected individuals.

Caroline A Bezerra, Thiago M Cardoso, Angela Giudice, Aurélia F Porto, Silvane B Santos, Edgar M Carvalho, Olívia Bacellar

Open access · bronzeAbstract read
In one paragraph

Article in Scandinavian journal of immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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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

7 authors at 3 institutions in 1 country.

Caroline A BezerraServiço de Imunologia, Hospital Universitário Prof. Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, BrazilUniversidade Federal de Sergipe, Aracaju, Sergipe, BrazilInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais (INCT-DT/CNPQ), Salvador, Bahia, Brazil.
Thiago M CardosoServiço de Imunologia, Hospital Universitário Prof. Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, BrazilUniversidade Federal de Sergipe, Aracaju, Sergipe, BrazilInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais (INCT-DT/CNPQ), Salvador, Bahia, Brazil.
Angela GiudiceServiço de Imunologia, Hospital Universitário Prof. Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, BrazilUniversidade Federal de Sergipe, Aracaju, Sergipe, BrazilInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais (INCT-DT/CNPQ), Salvador, Bahia, Brazil.
Aurélia F PortoServiço de Imunologia, Hospital Universitário Prof. Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, BrazilUniversidade Federal de Sergipe, Aracaju, Sergipe, BrazilInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais (INCT-DT/CNPQ), Salvador, Bahia, Brazil.
Silvane B SantosServiço de Imunologia, Hospital Universitário Prof. Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, BrazilUniversidade Federal de Sergipe, Aracaju, Sergipe, BrazilInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais (INCT-DT/CNPQ), Salvador, Bahia, Brazil.
Edgar M CarvalhoServiço de Imunologia, Hospital Universitário Prof. Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, BrazilUniversidade Federal de Sergipe, Aracaju, Sergipe, BrazilInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais (INCT-DT/CNPQ), Salvador, Bahia, Brazil.
Olívia BacellarServiço de Imunologia, Hospital Universitário Prof. Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, BrazilUniversidade Federal de Sergipe, Aracaju, Sergipe, BrazilInstituto Nacional de Ciência e Tecnologia de Doenças Tropicais (INCT-DT/CNPQ), Salvador, Bahia, Brazil.
Complexo Hospitalar Universitário Professor Edgard Santos · BRUniversidade Federal da Bahia · BRUniversidade Federal de Sergipe · BR

Funding

The role of Leishmania braziliensis strain polymorphism on disease outcome and ..P50AI030639 · NIAID · FEDERAL UNIVERSITY OF BAHIA · PI CARVALHO, EDGAR M · 1991 to 2023
$9.1M
NIAID NIH HHS AI-30639NIAID NIH HHS P50 AI030639
6 · The paper itself

Abstract

Human T cell lymphotropic virus type-1 (HTLV-1) induces activation and spontaneous proliferation of T cells with production of type-1 pro-inflammatory cytokines. It modifies the immune response to other antigens and increases susceptibility to infectious diseases. However, little is known about innate immunity in HTLV-1 infection. HTLV-1-infected individuals have higher spontaneous neutrophil activation than HTLV-1-seronegative individuals, as shown by the nitroblue tetrazolium (NBT) assay. This study was conducted to evaluate neutrophil function in HTLV-1-infected individuals. Participants in the study included 18 HTLV-1-infected individuals and 14 HTLV-1-seronegative controls. We evaluated the ability of neutrophils (PMNs) to control a parasite infection, to produce peroxynitrite, cytokines and chemokines and to express activation markers in cultures when stimulated with LPS or infected with Leishmania. When compared with the control group, there was no difference in the percentage of PMNs infected with Leishmania or in the number of amastigotes/100 PMNs in HTLV-1-infected individuals. The microbicidal activity of the PMNs and the levels of CXCL8 and CCL4 released by these cells did not show a difference between HTLV-1-infected individuals and the control group. In both the HTLV-1 group and the control group, infection with Leishmania or stimulation of PMNs led to cellular activation. These observations suggest that neutrophils from HTLV-1-infected individuals have preserved their ability to become activated and to produce chemokines and peroxynitrite after stimulation and that the susceptibility to infection by intracellular Leishmania amazonensis in HTLV-1-infected individuals does not depend on impairment of neutrophil function.

Indexed as

Antigens, CDCell Adhesion MoleculesChemokinesCytokinesFemaleGPI-Linked ProteinsHTLV-I InfectionsHumansImmunity, InnateLeishmania mexicanaLipopolysaccharidesL-SelectinMaleNeutrophil ActivationNeutrophilsPeroxynitrous AcidAntigens, CDCEACAM8 protein, humanCell Adhesion MoleculesChemokinesCytokinesGPI-Linked ProteinsLipopolysaccharidesL-SelectinPeroxynitrous Acid

Identifiers

PMID21595736
PMCPMC3153872
OpenAlexW1577525918

What OpenQuestion holds

Textmetadata
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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.