Evidence map›Paper›PMID 26409284›Full record

ReviewClinical infectious diseases : an official publication of the Infectious Diseases Society of America2015

T-Cell Therapy: Options for Infectious Diseases.

Shreemanta K Parida, Thomas Poiret, Liu Zhenjiang, Qingda Meng, Jan Heyckendorf, Christoph Lange, Aditya S Ambati, Martin V Rao, Davide Valentini, Giovanni Ferrara and 4 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 48 citations in OpenAlex.

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  15. mRNA: A Novel Avenue to Antibody Therapy?Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Review
  16. Improving T Cell Receptor On-Target Specificity via Structure-Guided Design.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  17. Review
  18. mRNA as novel technology for passive immunotherapy.Cellular and molecular life sciences : CMLS · 2019
    Review
  19. Article
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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

14 authors at 4 institutions in 4 countries.

Shreemanta K ParidaTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet.
Thomas PoiretTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet Centre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Solna, Sweden.
Liu ZhenjiangTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet.
Qingda MengTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet.
Jan HeyckendorfDivision of Clinical Infectious Diseases, German Center for Infection Research, Research Center Borstel.
Christoph LangeDivision of Clinical Infectious Diseases, German Center for Infection Research, Research Center Borstel International Health/Infectious Diseases, University of Lübeck, Germany Department of Medicine, Karolinska Institutet.
Aditya S AmbatiTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet Centre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Solna, Sweden Department of Medicine, Karolinska Institutet.
Martin V RaoTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet.
Davide ValentiniTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet Centre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Solna, Sweden.
Giovanni FerraraDepartment of Medicine, Karolinska Institutet.
Elena RangelovaPancreatic Surgery Unit, Division of Surgery, Department of Clinical Science, Intervention and Technology.
Ernest DodooTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet Department of Neurosurgery, Karolinska University Hospital, Stockholm, Sweden.
Alimuddin ZumlaDepartment of Infection, Division of Infection and Immunity, Centre for Clinical Microbiology, University College London National Institute for Health Research Biomedical Research Centre, University College London Hospitals, United Kingdom.
Markus MaeurerTherapeutic Immunology Division, Department of Laboratory Medicine, Karolinska Institutet Centre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Solna, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SEGerman Center for Infection Research · DEUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of drug-resistant tuberculosis is challenging tuberculosis control worldwide. In the absence of an effective vaccine to prevent primary infection with Mycobacterium tuberculosis and tuberculosis disease, host-directed therapies may offer therapeutic options, particularly for patients with multidrug-resistant and extensively drug-resistant tuberculosis where prognosis is often limited. CD8(+) and CD4(+) T cells mediate antigen-specific adaptive cellular immune responses. Their use in precision immunotherapy in clinical conditions, especially in treating cancer as well as for prevention of life-threatening viral infections in allogeneic transplant recipients, demonstrated safety and clinical efficacy. We review key achievements in T-cell therapy, including the use of recombinant immune recognition molecules (eg, T-cell receptors and CD19 chimeric antigen receptors), and discuss its potential in the clinical management of patients with drug-resistant and refractory tuberculosis failing conventional therapy.

Indexed as

Adoptive TransferCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytokinesExtensively Drug-Resistant TuberculosisHumansImmunity, CellularMycobacterium tuberculosisReceptors, Antigen, T-CellRecombinant Fusion ProteinsT-LymphocytesTuberculosis, Multidrug-ResistantCytokinesReceptors, Antigen, T-CellRecombinant Fusion Proteinsadoptive cell therapyCARhost-directed therapyMtbT-cells

Identifiers

PMID26409284
PMCPMC4583575
OpenAlexW1755519748

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.