Evidence map›Paper›PMID 28566085›Full record

ArticleInfectious diseases of poverty2017

Prevalence of autoantibodies against cellular antigens in patients with HIV and leprosy coinfection in the Amazon region.

Clea Nazaré Carneiro Bichara, Carlos David Araújo Bichara, Camila Tostes, Marinete Marins Povoa, Juarez Antonio Simões Quaresma, Marília Brasil Xavier

Open access · goldAbstract read
In one paragraph

Article in Infectious diseases of poverty, 2017. 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
0.3field-weighted citation impact, top 42% 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, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Peripheral nerve abnormality in HIV leprosy patients.PLoS neglected tropical diseases · 2018
    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

6 authors at 3 institutions in 1 country.

Clea Nazaré Carneiro BicharaCenter of Biological and Health Sciences, State University of Para, Campus II - CCBS, Rua Perebebui n° 2623, Marco, Belem, PA, 66087-670, Brazil. cleabichara@ig.com.br.
Carlos David Araújo BicharaCenter of Biological and Health Sciences, State University of Para, Campus II - CCBS, Rua Perebebui n° 2623, Marco, Belem, PA, 66087-670, Brazil.
Camila TostesCenter of Biological and Health Sciences, State University of Para, Campus II - CCBS, Rua Perebebui n° 2623, Marco, Belem, PA, 66087-670, Brazil.
Marinete Marins PovoaEvandro Chagas Institute, Ministry of Health, Ananindeua, PA, Brazil.
Juarez Antonio Simões QuaresmaCenter of Biological and Health Sciences, State University of Para, Campus II - CCBS, Rua Perebebui n° 2623, Marco, Belem, PA, 66087-670, Brazil.
Marília Brasil XavierCenter of Biological and Health Sciences, State University of Para, Campus II - CCBS, Rua Perebebui n° 2623, Marco, Belem, PA, 66087-670, Brazil.
Universidade do Estado do Pará · BRInstituto Evandro Chagas · BRUniversidade Federal do Pará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfectious agents can activate self-reactive T cells. In general, infections trigger various mechanisms, including a lack of auto-tolerance, induction of costimulatory molecules on antigen presenting cells, and molecular simulation, in addition to cross-reactions between microbial antigens and self-antigens. HIV and leprosy coinfections lead to self-immunity with the production of autoantibodies. However, not enough data on the immune behaviour associated with this coinfection are available. Therefore, this study focused on the detection of autoantibodies against cellular antigens (AACA) in individuals with HIV and leprosy coinfection in the Amazon region.

methodsPatients were distributed into four groups according to their infections: (i) coinfection with HIV and leprosy (n = 23), (ii) infection with leprosy (n = 33), (iii) infection with HIV/AIDS (n = 25), and (iv) healthy blood donor controls (n = 100). AACA were identified by indirect immunofluorescence and the samples were tested using a commercial diagnosis kit containing the antinuclear antibody HEp-2.

resultsMorphologically, all stages of cell division were assessed in addition to the morphological features associated with the nuclear matrix, nucleolus, mitotic spindle, and cytoplasm. There was a high prevalence of AACA in the coinfection group (47.8%, n = 11) when compared with the control group of healthy blood donors (2.0%). The results showed predominantly cytoplasmic staining in all groups analysed, and no difference was observed between the presence or absence of AACA and the leprosy forms (paucibacillary and multibacillary) in the coinfection group.

conclusionsThe results of this study show that despite the tendency of coinfected patients to have higher levels of autoantibodies, no correlation was observed between clinical and laboratorial variables and morbidity associated with HIV and leprosy coinfections or the levels of AACA in the serum of coinfected patients. These data are important to elucidate this complex relationship between HIV and leprosy and thus improve the follow-up of these patients.

Indexed as

AdultAutoantibodiesBrazilCoinfectionFemaleHIV InfectionsHumansLeprosyMalePrevalenceYoung AdultAutoantibodiesAmazon regionAutoantibodiesHIVImmunologyLeprosy

Identifiers

PMID28566085
PMCPMC5452639
OpenAlexW2604487879

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.