Evidence map›Paper›PMID 38779686›Full record

ArticleFrontiers in immunology2024

HIV immunological non-responders are characterized by extensive immunosenescence and impaired lymphocyte cytokine production capacity.

Wilhelm A J W Vos, Adriana Navas, Elise M G Meeder, Marc J T Blaauw, Albert L Groenendijk, Louise E van Eekeren, Twan Otten, Nadira Vadaq, Vasiliki Matzaraki, Bram van Cranenbroek and 8 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

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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

18 authors.

Wilhelm A J W VosDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Adriana NavasDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Elise M G MeederDepartment of Psychiatry, Radboudumc, Radboud University, Nijmegen, Netherlands.
Marc J T BlaauwDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Albert L GroenendijkDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Louise E van EekerenDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Twan OttenDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Nadira VadaqDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Vasiliki MatzarakiDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Bram van CranenbroekDepartment of Laboratory Medicine, Laboratory for Medical Immunology, Radboud University Medical Center, Nijmegen, Netherlands.
Kees BrinkmanDepartment of Internal Medicine and Infectious Diseases, OLVG, Amsterdam, Netherlands.
Jan van LunzenDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Leo A B JoostenDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Mihai G NeteaDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Willem L BlokDepartment of Internal Medicine and Infectious Diseases, OLVG, Amsterdam, Netherlands.
Andre J A M van der VenDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
Hans J P M KoenenDepartment of Laboratory Medicine, Laboratory for Medical Immunology, Radboud University Medical Center, Nijmegen, Netherlands.
Janneke E StalenhoefDepartment of Internal Medicine and Infectious Diseases, OLVG, Amsterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Immunological non-responders (INR) are people living with HIV (PLHIV) who fail to fully restore CD4+ T-cell counts despite complete viral suppression with antiretroviral therapy (ART). INR are at higher risk for non-HIV related morbidity and mortality. Previous research suggest persistent qualitative defects. Methods: The 2000HIV study (clinical trials NTC03994835) enrolled 1895 PLHIV, divided in a discovery and validation cohort. PLHIV with CD4 T-cell count <350 cells/mm Results: The discovery cohort consisted of 62 INR and 1224 IR, the validation cohort of 26 INR and 243 IR. INR were older, had more advanced HIV disease before starting ART and had more frequently a history of non-AIDS related malignancy. INR had lower absolute CD4+ T-cell numbers in all subsets. Activated (HLA-DR+, CD38+) and exhausted (PD1+) subpopulations were proportionally increased in CD4 T-cells. Monocyte and granulocyte immunophenotypes were comparable. INR lymphocytes produced less IL-22, IFN-γ, IL-10 and IL-17 to stimuli. In contrast, monocyte cytokine production did not differ. The proportions of CD4+CD38+HLA-DR+ and CD4+PD1+ subpopulations showed an inversed correlation to lymphocyte cytokine production. Conclusions: INR compared to IR have hyperactivated and exhausted CD4+ T-cells in combination with lymphocyte functional impairment, while innate immune responses were comparable. Our data provide a rationale to consider the use of anti-PD1 therapy in INR.

Indexed as

CytokinesHIV InfectionsImmunosenescenceAdultAnti-HIV AgentsCD4 Lymphocyte CountCD4-Positive T-LymphocytesFemaleHIV-1HumansImmunophenotypingMaleMiddle AgedViral LoadAnti-HIV AgentsCytokinescytokine productionflow cytometryimmune restorationimmunological non-respondersimmunosenescencePD1

Identifiers

PMID38779686
PMCPMC11109418

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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.