Evidence map›Paper›PMID 32828803›Full record

ArticleBiochemical pharmacology2020

Cytotoxic cell populations developed during treatment with tyrosine kinase inhibitors protect autologous CD4+ T cells from HIV-1 infection.

Lorena Vigón, Sara Rodríguez-Mora, Alejandro Luna, Virginia Sandonís, Elena Mateos, Guiomar Bautista, Juan Luis Steegmann, Nuria Climent, Montserrat Plana, Pilar Pérez-Romero and 6 more

Abstract read
In one paragraph

Article in Biochemical pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Sustained antiviral response againstFrontiers in pharmacology · 2024
    Article
  2. Review
  3. Article
  4. Review
  5. Gene Expression Risk Scores for COVID-19 Illness Severity.The Journal of infectious diseases · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Gene Expression Risk Scores for COVID-19 Illness Severity.bioRxiv : the preprint server for biology · 2021
    Article
  10. 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.

Lorena VigónAIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Sara Rodríguez-MoraAIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Alejandro LunaClinical Hematology Service, Hospital Universitario Ramón y Cajal, YRICIS, Madrid, Spain.
Virginia SandonísViral Isolation and Detection, CIBER Epidemiology and Public Health (CNM, ISCIII), Madrid, Spain.
Elena MateosAIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Guiomar BautistaClinical Hematology Service, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Juan Luis SteegmannHematology and Hemotherapy Service, Hospital Universitario de La Princesa, Madrid, Spain.
Nuria ClimentRetrovirology and Viral Immunopathology Laboratory, AIDS Research Group, Hospital Clínic, IDIBAPS, Barcelona, Spain.
Montserrat PlanaRetrovirology and Viral Immunopathology Laboratory, AIDS Research Group, Hospital Clínic, IDIBAPS, Barcelona, Spain.
Pilar Pérez-RomeroViral Isolation and Detection, CIBER Epidemiology and Public Health (CNM, ISCIII), Madrid, Spain.
Fernando de OrySerology Service, CIBER Epidemiology and Public Health (CNM, ISCIII), Madrid, Spain.
José AlcamíAIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Valentín García-GutierrezClinical Hematology Service, Hospital Universitario Ramón y Cajal, YRICIS, Madrid, Spain.
Vicente PlanellesMicrobiology and Immunology Lab, University of Utah, Salt Lake City, USA.
María Rosa López-HuertasAIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain. Electronic address: mrlhuertas@isciii.es.
Mayte CoirasAIDS Immunopathology Unit, National Center of Microbiology (CNM), Instituto de Salud Carlos III (ISCIII), Madrid, Spain. Electronic address: mcoiras@isciii.es.

Funding

Tyrosine Kinase inhibition: The New Front in HIV Cure EffortsR01AI143567 · NIAID · UNIVERSITY OF UTAH · PI COIRAS, MAYTE, PLANELLES, VICENTE · 2019 to 2023
$2.3M
NIAID NIH HHS R01 AI143567
6 · The paper itself

Abstract

Tyrosine kinase inhibitors (TKIs) are successfully used in clinic to treat chronic myeloid leukemia (CML). Our group previously described that CD4+ T cells from patients with CML on treatment with TKIs such as dasatinib were resistant to HIV-1 infection ex vivo. The main mechanism for this antiviral activity was primarily based on the inhibition of SAMHD1 phosphorylation, which preserves the activity against HIV-1 of this innate immune factor. Approximately 50% CML patients who achieved a deep molecular response (DMR) may safely withdraw TKI treatment without molecular recurrence. Therefore, it has been speculated that TKIs may induce a potent antileukemic response that is maintained in most patients even one year after treatment interruption (TI). Subsequent to in vitro T-cell activation, we observed that SAMHD1 was phosphorylated in CD4+ T cells from CML patients who withdrew TKI treatment more than one year earlier, which indicated that these cells were now susceptible to HIV-1 infection. Importantly, these patients were seronegative for HIV-1 and seropositive for cytomegalovirus (CMV), but without CMV viremia. Although activated CD4+ T cells from CML patients on TI were apparently permissive to HIV-1 infection ex vivo, the frequency of proviral integration was reduced more than 12-fold on average when these cells were infected ex vivo in comparison with cells isolated from untreated, healthy donors. This reduced susceptibility to infection could be related to an enhanced NK-dependent cytotoxic activity, which was increased 8-fold on average when CD4+ T cells were infected ex vivo with HIV-1 in the presence of autologous NK cells. Enhanced cytotoxic activity was also observed in CD8 + T cells from these patients, which showed 8-fold increased expression of TCRγδ and more than 18-fold increased production of IFNγ upon activation with CMV peptides. In conclusion, treatment with TKIs induced a potent antileukemic response that may also have antiviral effects against HIV-1 and CMV, suggesting that transient use of TKIs in HIV-infected patients could develop a sustained antiviral response that would potentially interfere with HIV-1 reservoir dynamics.

Indexed as

AdultAgedAged, 80 and overAntiviral AgentsCD4-Positive T-LymphocytesCytoprotectionFemaleHIV-1HIV InfectionsHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedProtein Kinase InhibitorsAntiviral AgentsProtein Kinase InhibitorsChronic myeloid leukemiaHIV-1SAMHD1Src tyrosine kinasesViral reservoir

Identifiers

PMID32828803
PMCPMC7686055

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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.