Evidence map›Paper›PMID 25883389›Full record

ArticleThe Journal of infectious diseases2015

The T-Cell Inhibitory Molecule Butyrophilin-Like 2 Is Up-regulated in Mild Plasmodium falciparum Infection and Is Protective During Experimental Cerebral Malaria.

Krishanthi S Subramaniam, Emily Spaulding, Emil Ivan, Eugene Mutimura, Ryung S Kim, Xikui Liu, Chen Dong, Catherine M Feintuch, Xingxing Zhang, Kathryn Anastos and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The Current Status of Enteric Fever Diagnostics and Implications for Disease Control.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  10. Article
  11. Review
  12. Accelerator or Brake: Immune Regulators in Malaria.Frontiers in cellular and infection microbiology · 2020
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. 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

12 authors at 4 institutions in 3 countries.

Krishanthi S SubramaniamDepartments of Microbiology and Immunology.
Emily SpauldingDepartments of Microbiology and Immunology.
Emil IvanDepartment of Biomedical Laboratory Sciences, College of Medicine and Health Sciences, University of Rwanda.
Eugene MutimuraRegional Alliance for Sustainable Development, Kigali.
Ryung S KimEpidemiology and Population Health.
Xikui LiuDepartment of Immunology, University of Texas MD Anderson Cancer Center, Houston.
Chen DongDepartment of Immunology, University of Texas MD Anderson Cancer Center, Houston.
Catherine M FeintuchDepartments of Microbiology and Immunology.
Xingxing ZhangDepartments of Microbiology and Immunology.
Kathryn AnastosMedicine, Albert Einstein College of Medicine, Bronx, New York.
Gregoire LauvauDepartments of Microbiology and Immunology.
Johanna P DailyDepartments of Microbiology and Immunology Medicine, Albert Einstein College of Medicine, Bronx, New York.
Albert Einstein College of Medicine · USThe University of Texas MD Anderson Cancer Center · USCentre de recherche en Epidémiologie et Santé des Populations · FRUniversity of Rwanda · RW

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI ALYSON B MOADEL · 1985 to 2026
$111.2M
Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
Tumor-expressed immune checkpoint B7x-mediated resistance to anti-CTLA-4 therapy.R01CA175495 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2014 to 2025
$5.1M
Geographic Medicine and Emerging InfectionsT32AI070117 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WEISS, LOUIS M. · 2008 to 2023
$5.1M
SERINE PROTEINASES IN APICOMPLEXAN PARASITESR01AI046985 · NIAID · YESHIVA UNIVERSITY · PI KIM, KAMI · 2000 to 2009
$2.7M
Mechanisms and Therapies of B7x and B7-H3 in T1DR01DK100525 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2015 to 2019
$1.9M
Host immune response to malaria infectionRC1AI086224 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DAILY, JOHANNA PATRICIA · 2010 to 2010
$500k
Early cellular sensing of blood stage Plasmodium Parasites by Innate Immune CellsR21AI122801 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI LAUVAU, GREGOIRE STEPHANE · 2016 to 2017
$459k
NCATS NIH HHS UL1 TR001073NCI NIH HHS P30 CA013330NCI NIH HHS R01 CA175495NIAID NIH HHS 1RC1AI086224NIAID NIH HHS R01 AI046985NIAID NIH HHS R21 AI122801NIAID NIH HHS RC1 AI086224NIAID NIH HHS T32AI046985NIAID NIH HHS T32 AI070117NIDDK NIH HHS R01 DK100525
6 · The paper itself

Abstract

Plasmodium falciparum infection can result in severe disease that is associated with elevated inflammation and vital organ dysfunction; however, malaria-endemic residents gain protection from lethal outcomes and manifest only mild symptoms during infection. To characterize host responses associated with this more effective antimalarial response, we characterized whole-blood transcriptional profiles in Rwandan adults during a mild malaria episode and compared them with findings from a convalescence sample. We observed transcriptional up-regulation in many pathways, including type I interferon, interferon γ, complement activation, and nitric oxide during malaria infection, which provide benchmarks of mild disease physiology. Transcripts encoding negative regulators of T-cell activation, such as programmed death ligand 1 (PD-L1), programmed death 1 ligand 2 (PD-L2), and the butyrophilin family member butyrophilin-like 2 (BTNL2) were also increased. To support an important functional role for BTNL2 during malaria infection, we studied chimeric mice reconstituted with BTNL2(-/-) or wild-type hematopoietic cells that were inoculated with Plasmodium berghei ANKA, a murine model of cerebral malaria. We found that BTNL2(-/-) chimeric mice had a significant decrease in survival compared with wild-type counterparts. Collectively these data characterize the immune responses associated with mild malaria and uncover a novel role for BTNL2 in the host response to malaria.

Indexed as

AdultAnimalsB7-H1 AntigenButyrophilinsComplement ActivationEndemic DiseasesFemaleHumansInterferon-gammaInterferon Type ILymphocyte ActivationMalariaMalaria, CerebralMalaria, FalciparumMaleMembrane GlycoproteinsB7-H1 AntigenButyrophilinsInterferon-gammaInterferon Type IMembrane GlycoproteinsNitric Oxideantibody responsesatypical memory B cellsBTNL2experimental cerebral malariaimmune responsemalariamild malariamouse modelPlasmodium bergheiPlasmodium falciparumRwanda HIV

Identifiers

PMID25883389
PMCPMC4577049
OpenAlexW2118172611

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.