Evidence map›Paper›PMID 32420917›Full record

ReviewThe Journal of clinical investigation2020

Therapies for tuberculosis and AIDS: myeloid-derived suppressor cells in focus.

Anca Dorhoi, Leigh A Kotzé, Jay A Berzofsky, Yongjun Sui, Dmitry I Gabrilovich, Ankita Garg, Richard Hafner, Shabaana A Khader, Ulrich E Schaible, Stefan He Kaufmann and 6 more

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. CXCR6Frontiers in immunology · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Towards a map of the immune system manipulation network byFrontiers in cellular and infection microbiology · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. MedComm · 2023
    Review
  16. Review
  17. Review
  18. Article
  19. Suppressive myeloid cells in SARS-CoV-2 andFrontiers in immunology · 2023
    Article
  20. 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

16 authors at 13 institutions in 4 countries.

Anca DorhoiInstitute of Immunology, Friedrich-Loeffler-Institute, Greifswald-Insel Riems, Germany.
Leigh A KotzéCentre for Tuberculosis Research, South African Medical Research Council, Cape Town, South Africa.
Jay A BerzofskyVaccine Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Yongjun SuiVaccine Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Dmitry I GabrilovichWistar Institute, Philadelphia, Pennsylvania, USA.
Ankita GargDepartment of Infectious Diseases, University of Georgia, Athens, Georgia, USA.
Richard HafnerDivision of AIDS, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
Shabaana A KhaderDepartment of Molecular Microbiology, Washington University in St. Louis, St. Louis, Missouri, USA.
Ulrich E SchaibleCellular Microbiology, Priority Program Infections.
Stefan He KaufmannMax Planck Institute for Infection Biology, Berlin, Germany.
Gerhard WalzlCentre for Tuberculosis Research, South African Medical Research Council, Cape Town, South Africa.
Manfred B LutzInstitute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
Robert N MahonDivision of AIDS, Columbus Technologies & Services Inc., Contractor to National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
Suzanne Ostrand-RosenbergDepartment of Pathology and Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
William BishaiCenter for Tuberculosis Research, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Nelita du PlessisCentre for Tuberculosis Research, South African Medical Research Council, Cape Town, South Africa.
South African Medical Research Council · ZANational Cancer Institute · USColumbus Technologies and Services (United States) · USFriedrich-Loeffler-Institut · DEGerman Center for Infection Research · DEHuntsman Cancer Institute · USInstitute for Advanced Study · USJohns Hopkins University · USNational Institute of Allergy and Infectious Diseases · USThe Wistar Institute · USUniversity of Georgia · USUniversity of Würzburg · DEWashington University in St. Louis · US

Funding

Vaccine and immunotherapy strategies for cancer and viruses causing cancerZIASC004020 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI BERZOFSKY, JAY A · 2009 to 2025
$51.8M
Mycobacterium tuberculosis Survival Regulatory GenesR01AI037856 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BISHAI, WILLIAM RAMSES · 1997 to 2020
$7.2M
Targeted cell-depleting immunotherapy for TB and HIVR01AI152688 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BISHAI, WILLIAM RAMSES · 2020 to 2024
$3.4M
Aberrant immune activation in the tuberculosis granuloma: a pivotal role in necrosisR01HL133190 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BISHAI, WILLIAM RAMSES, KRAMNIK, IGOR · 2016 to 2019
$3.0M
Targeted Immunotherapy for Tuberculosis and HIV co-infectionR21AI130595 · NIAID · JOHNS HOPKINS UNIVERSITY · PI BISHAI, WILLIAM RAMSES · 2017 to 2018
$449k
Role of Myeloid Derived Suppressor Cells in Mycobacterium tuberculosis(Mtb)Reactivation in HIV-Mtb co-infected IndividualsR21AI127132 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GARG, ANKITA · 2016 to 2017
$412k
NHLBI NIH HHS R01 HL133190NIAID NIH HHS HHSN272201600001CNIAID NIH HHS HHSN272201600001GNIAID NIH HHS R01 AI037856NIAID NIH HHS R01 AI152688NIAID NIH HHS R21 AI127132NIAID NIH HHS R21 AI130595
6 · The paper itself

Abstract

The critical role of suppressive myeloid cells in immune regulation has come to the forefront in cancer research, with myeloid-derived suppressor cells (MDSCs) as a main oncology immunotherapeutic target. Recent improvement and standardization of criteria classifying tumor-induced MDSCs have led to unified descriptions and also promoted MDSC research in tuberculosis (TB) and AIDS. Despite convincing evidence on the induction of MDSCs by pathogen-derived molecules and inflammatory mediators in TB and AIDS, very little attention has been given to their therapeutic modulation or roles in vaccination in these diseases. Clinical manifestations in TB are consequences of complex host-pathogen interactions and are substantially affected by HIV infection. Here we summarize the current understanding and knowledge gaps regarding the role of MDSCs in HIV and Mycobacterium tuberculosis (co)infections. We discuss key scientific priorities to enable application of this knowledge to the development of novel strategies to improve vaccine efficacy and/or implementation of enhanced treatment approaches. Building on recent findings and potential for cross-fertilization between oncology and infection biology, we highlight current challenges and untapped opportunities for translating new advances in MDSC research into clinical applications for TB and AIDS.

Indexed as

Acquired Immunodeficiency SyndromeTuberculosisHIV-1HumansMycobacterium tuberculosisMyeloid-Derived Suppressor Cells

Identifiers

PMID32420917
PMCPMC7260010
OpenAlexW3024889823

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.