4.7 Article

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

期刊

CLINICAL INFECTIOUS DISEASES
卷 73, 期 7, 页码 E1973-E1981

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa1530

关键词

HIV; HIV latency; anti-PD-1; anti-CTLA-4

资金

  1. American Foundation for AIDS Research (amfAR) [109226-58-RGRL]
  2. Australian National Health and Medical Research Council (NHMRC) [GNT1149990]
  3. Australian Centre for HIV and Hepatitis Research (ACH2)
  4. National Institutes of Health [UM1AI126611]
  5. NCI [UM1 CA121947]
  6. public health service [CA239583, DE018304]
  7. National Cancer Institute [5K23CA177321-05]

向作者/读者索取更多资源

The study tested the combination of anti-PD-1 and anti-CTLA-4 therapy in HIV-infected individuals with cancer, finding that the combination therapy increased HIV RNA levels and potentially eliminated cells containing replication-competent HIV.
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 replicationcompetent HIV.

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