Evidence map›Paper›PMID 26141012›Full record

ReviewVaccine2015

Humoral immune responses to Streptococcus pneumoniae in the setting of HIV-1 infection.

Lumin Zhang, Zihai Li, Zhuang Wan, Andrew Kilby, J Michael Kilby, Wei Jiang

Open access · greenAbstract readReview
In one paragraph

Review in Vaccine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
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  9. Article
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  11. Article
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  13. Nasopharyngeal Exposure toJournal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  14. Frontiers in immunology · 2018
    Review
  15. Article
  16. 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

6 authors at 1 institution in 1 country.

Lumin ZhangDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, United States.
Zihai LiDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, United States.
Zhuang WanHollings Cancer Center, Medical University of South Carolina, Charleston, SC 29425, United States.
Andrew KilbyDivision of Infectious Diseases, Department of Medicine, Medical University of South Carolina, Charleston, SC 29425, United States.
J Michael KilbyDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, United States; Division of Infectious Diseases, Department of Medicine, Medical University of South Carolina, Charleston, SC 29425, United States.
Wei JiangDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, United States; Division of Infectious Diseases, Department of Medicine, Medical University of South Carolina, Charleston, SC 29425, United States. Electronic address: jianw@musc.edu.
Medical University of South Carolina · US

Funding

Patient Resource CoreP60AR062755 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GILKESON, GARY S · 2012 to 2016
$5.8M
Roles and Mechanisms of gp96 in Chaperoning Innate ImmunityR01AI070603 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LI, ZIHAI · 2007 to 2016
$3.8M
Synergistic effect of HIV virions and bacterial LPS on memory B cell apoptosisR01AI091526 · NIAID · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI JIANG, WEI · 2011 to 2015
$1.4M
NIAID NIH HHS R01 AI070603NIAID NIH HHS R01 AI091526NIAMS NIH HHS P60 AR062755NIAMS NIH HHS P60AR062755PHS HHS NIAID91526
6 · The paper itself

Abstract

Streptococcus pneumoniae (pneumococcus) remains one of the most commonly identified causes of bacterial infection in the general population, and the risk is 30-100 fold higher in HIV-infected individuals. Both innate and adaptive host immune responses to pneumococcal infection are important against pathogen invasion. Pneumococcal-specific IgA antibody (Ab) is key to control infection at the mucosal sites. Ab responses against pneumococcal infection by B cells can be generated through T cell-dependent or T cell-independent pathways. Depletion of CD4+ T cells is a hallmark of immunodeficiency in HIV infection and this defect also contributes to B cell dysfunction, which predisposes to infections such as the pneumococcus. Two pneumococcal vaccines have been demonstrated to have potential benefits for HIV-infected patients. One is a T cell dependent 13-valent pneumococcal conjugate vaccine (PCV13); the other is a T cell independent 23-valent pneumococcal polysaccharide vaccine (PPV23). However, many questions remain unknown regarding these two vaccines in the clinical setting in HIV disease. Here we review the latest research regarding B cell immune responses against pneumococcal antigens, whether derived from potentially invading pathogens or vaccinations, in the setting of HIV-1 infection.

Indexed as

Immunity, HumoralB-LymphocytesHIV-1HIV InfectionsHumansPneumococcal InfectionsPneumococcal VaccinesStreptococcus pneumoniae13-valent pneumococcal vaccine23-valent pneumococcal capsular polysaccharide vaccinePneumococcal VaccinesB cellsHIVHumoral immune responsesStreptococcus pneumoniae

Identifiers

PMID26141012
PMCPMC4547882
OpenAlexW779908845

What OpenQuestion holds

Textmetadata
LicenceTDM
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.