Impact of Anti-PD-1 and Anti-CTLA-4 on the Human Immunodeficiency Virus (HIV) Reservoir in People Living With HIV With Cancer on Antiretroviral Therapy: The AIDS Malignancy Consortium 095 Study.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
05 10 2021
Historique:
received: 22 07 2020
pubmed: 8 3 2021
medline: 21 10 2021
entrez: 7 3 2021
Statut: ppublish

Résumé

Antibodies to programmed cell death 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) may perturb human immunodeficiency virus (HIV) persistence during antiretroviral therapy (ART) by reversing HIV latency and/or boosting HIV-specific immunity, leading to clearance of infected cells. We tested this hypothesis in a clinical trial of anti-PD-1 alone or in combination with anti-CTLA-4 in people living with HIV (PLWH) and cancer. This was a substudy of the AIDS Malignancy Consortium 095 Study. ART-suppressed PLWH with advanced malignancies were assigned to nivolumab (anti-PD-1) with or without ipilimumab (anti-CTLA-4). In samples obtained preinfusion and 1 and 7 days after the first and fourth doses of immune checkpoint blockade (ICB), we quantified cell-associated unspliced (CA-US) HIV RNA and HIV DNA. Plasma HIV RNA was quantified during the first treatment cycle. Quantitative viral outgrowth assay (QVOA) to estimate the frequency of replication-competent HIV was performed before and after ICB for participants with samples available. Of 40 participants, 33 received nivolumab and 7 nivolumab plus ipilimumab. Whereas CA-US HIV RNA did not change with nivolumab monotherapy, we detected a median 1.44-fold increase (interquartile range, 1.16-1.89) after the first dose of nivolumab and ipilimumab combination therapy (P = .031). There was no decrease in the frequency of cells containing replication-competent HIV, but in the 2 individuals on combination ICB for whom we had longitudinal QVOA, we detected decreases of 97% and 64% compared to baseline. Anti-PD-1 alone showed no effect on HIV latency or the latent HIV reservoir, but the combination of anti-PD-1 and anti-CTL-4 induced a modest increase in CA-US HIV RNA and may potentially eliminate cells containing replication-competent HIV. NCT02408861.

Sections du résumé

BACKGROUND
Antibodies to programmed cell death 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) may perturb human immunodeficiency virus (HIV) persistence during antiretroviral therapy (ART) by reversing HIV latency and/or boosting HIV-specific immunity, leading to clearance of infected cells. We tested this hypothesis in a clinical trial of anti-PD-1 alone or in combination with anti-CTLA-4 in people living with HIV (PLWH) and cancer.
METHODS
This was a substudy of the AIDS Malignancy Consortium 095 Study. ART-suppressed PLWH with advanced malignancies were assigned to nivolumab (anti-PD-1) with or without ipilimumab (anti-CTLA-4). In samples obtained preinfusion and 1 and 7 days after the first and fourth doses of immune checkpoint blockade (ICB), we quantified cell-associated unspliced (CA-US) HIV RNA and HIV DNA. Plasma HIV RNA was quantified during the first treatment cycle. Quantitative viral outgrowth assay (QVOA) to estimate the frequency of replication-competent HIV was performed before and after ICB for participants with samples available.
RESULTS
Of 40 participants, 33 received nivolumab and 7 nivolumab plus ipilimumab. Whereas CA-US HIV RNA did not change with nivolumab monotherapy, we detected a median 1.44-fold increase (interquartile range, 1.16-1.89) after the first dose of nivolumab and ipilimumab combination therapy (P = .031). There was no decrease in the frequency of cells containing replication-competent HIV, but in the 2 individuals on combination ICB for whom we had longitudinal QVOA, we detected decreases of 97% and 64% compared to baseline.
CONCLUSIONS
Anti-PD-1 alone showed no effect on HIV latency or the latent HIV reservoir, but the combination of anti-PD-1 and anti-CTL-4 induced a modest increase in CA-US HIV RNA and may potentially eliminate cells containing replication-competent HIV.
CLINICAL TRIALS REGISTRATION
NCT02408861.

Identifiants

pubmed: 33677480
pii: 6156773
doi: 10.1093/cid/ciaa1530
pmc: PMC8492152
doi:

Substances chimiques

CTLA-4 Antigen 0
Programmed Cell Death 1 Receptor 0

Banques de données

ClinicalTrials.gov
['NCT02408861']

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1973-e1981

Subventions

Organisme : American Foundation for AIDS Research
ID : 109226-58-RGRL
Organisme : Australian National Health and Medical Research Council
ID : GNT1149990
Organisme : NIDCR NIH HHS
ID : R01 DE018304
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA121947
Pays : United States
Organisme : Australian Centre for HIV and Hepatitis Research
Organisme : NCI NIH HHS
ID : R01 CA228172
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA121947
Pays : United States

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Thomas A Rasmussen (TA)

The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia.

Lakshmi Rajdev (L)

Department of Haematology and Oncology, Lennox Hill Hospital, New York, New York, USA.

Ajantha Rhodes (A)

The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia.

Ashanti Dantanarayana (A)

The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia.

Surekha Tennakoon (S)

The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia.

Socheata Chea (S)

The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia.

Tim Spelman (T)

The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia.

Shelly Lensing (S)

Department of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

Rachel Rutishauser (R)

Department of Medicine, University of California, San Francisco, San Francisco, California, USA.

Sonia Bakkour (S)

Vitalant Research Institute and Department of Laboratory Medicine, University of California, San Francisco, San Francisco, California, USA.

Michael Busch (M)

Vitalant Research Institute and Department of Laboratory Medicine, University of California, San Francisco, San Francisco, California, USA.

Janet D Siliciano (JD)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Robert F Siliciano (RF)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Mark H Einstein (MH)

Department of Obstetrics, Gynecology, and Reproductive Health, Rutgers New Jersey Medical School, Newark, New Jersey, USA.

Dirk P Dittmer (DP)

Lineberger Comprehensive Cancer Center and Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Elizabeth Chiao (E)

Baylor College of Medicine, Houston, Texas, USA.

Steven G Deeks (SG)

Department of Medicine, University of California, San Francisco, San Francisco, California, USA.

Christine Durand (C)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Sharon R Lewin (SR)

The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital, Melbourne, Australia.
Department of Infectious Diseases, Alfred Hospital and Monash University, Melbourne, Australia.
Victorian Infectious Diseases Service, The Royal Melbourne Hospital, Melbourne, Australia.

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