Evidence map›Paper›PMID 41983147›Full record

Trial reportOpen forum infectious diseases2026

A Single Dose Study of Pembrolizumab in People With HIV Infection Who are Immunologic Nonresponders.

Janaki Kuruppu, Julia B Purdy, Cheryl Pauls, Daniel C Rogan, Jana Blazkova, Lela Kardava, Adeline B Sewack, Michael A Proschan, Stephen A Migueles, Mark Connors and 10 more

Abstract readClinical Trial
In one paragraph

Trial report in Open forum infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Janaki KuruppuCritical Care Medicine Department, National Institute of Health Clinical Center, Bethesda, Maryland, USA.
Julia B PurdyCritical Care Medicine Department, National Institute of Health Clinical Center, Bethesda, Maryland, USA.
Cheryl PaulsDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Daniel C RoganDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Jana BlazkovaDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Lela KardavaDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Adeline B SewackDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Michael A ProschanOffice of Biostatistics Research, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA.
Stephen A MiguelesDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-6062-8022
Mark ConnorsDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-2108-8705
Jonathan D WebberDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Tyler MeeksDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Paulina A PrzygonskaDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Joseph W AdelsbergerAIDS Monitoring Laboratory, Leidos Biomedical Research, Inc, Frederick, Maryland, USA.
Jeanette HigginsAIDS Monitoring Laboratory, Leidos Biomedical Research, Inc, Frederick, Maryland, USA.
Adam RupertAIDS Monitoring Laboratory, Leidos Biomedical Research, Inc, Frederick, Maryland, USA.
Susan L MoirDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Tae-Wook ChunDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
H Clifford LaneDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Joseph A KovacsCritical Care Medicine Department, National Institute of Health Clinical Center, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-5191-9880

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · 2019 to 2025
$3932.6M
NIH HHS 75N91019D00024
6 · The paper itself

Abstract

Background: Some people with HIV (PWH) have a poor immunologic response to antiretroviral therapy (ART). Such immunologic nonresponders are at increased risk for HIV and non-HIV related complications. Immune exhaustion may contribute to poor immune reconstitution, and blockade of PD-1, an immune checkpoint molecule, may thus be beneficial. Method: We undertook a phase 1, 3:1 randomized, placebo-controlled trial of a single 200 mg dose of pembrolizumab in PWH with CD4+ T-cell counts between 100 and 350 cells/mm Results: Of the 7 enrolled participants, 6 received pembrolizumab and 1 received placebo. The only grade 3 event, ophthalmic zoster, developed in the placebo recipient. There were no autoimmune events requiring corticosteroid therapy. CD4+ and CD8+ T-cell counts were stable over time, though both showed increased CD38 and HLA-DR expression. PD-1 expression declined from a baseline of 60.4% (SD, 7.4%) to a nadir of 0.8%-23.5% for CD4+ T cells, and from 45.2% (SD, 9.4%) to 0.1%-23.2% for CD8+ T cells. There were no significant changes in viral killing, plasma viral loads or proviral DNA levels. Conclusions: A single dose of pembrolizumab may be safely administered to PWH who are immunologic nonresponders.

Indexed as

HIVimmunologic nonresponderPD-1pembrolizumab

Identifiers

PMID41983147
PMCPMC13075952

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.