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Commentary Free access | 10.1172/JCI135905

The gift of a lifetime: analysis of HIV at autopsy

Frank Maldarelli

HIV Dynamics and Replication Program, National Cancer Institute (NCI), NIH, Ft. Detrick, Maryland, USA.

Address correspondence to: Frank Maldarelli, HIV Dynamics and Replication Program, NCI, NIH, 1050 Boyles St., Fort Detrick, Frederick, Maryland 21702, USA. Phone: 301.846.5611; Email: fmalli@mail.nih.gov.

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Published February 24, 2020 - More info

Published in Volume 130, Issue 4 on April 1, 2020
J Clin Invest. 2020;130(4):1611–1614. https://doi.org/10.1172/JCI135905.
© 2020 American Society for Clinical Investigation
Published February 24, 2020 - Version history
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HIV persists throughout deep tissues with repopulation from multiple anatomical sources
Antoine Chaillon, … , Bram Vrancken, Davey M. Smith
Antoine Chaillon, … , Bram Vrancken, Davey M. Smith
Clinical Research and Public Health AIDS/HIV Infectious disease

HIV persists throughout deep tissues with repopulation from multiple anatomical sources

Abstract

BACKGROUND Understanding HIV dynamics across the human body is important for cure efforts. This goal has been hampered by technical difficulties and the challenge of obtaining fresh tissues.METHODS This observational study evaluated 6 individuals with HIV (n = 4 with viral suppression using antiretroviral [ART] therapy; n = 2 with rebound viremia after stopping ART), who provided serial blood samples before death and their bodies for rapid autopsy. HIV reservoirs were characterized by digital droplet PCR, single-genome amplification, and sequencing of full-length (FL) envelope HIV. Phylogeographic methods were used to reconstruct HIV spread, and generalized linear models were tested for viral factors associated with dispersal.RESULTS Across participants, HIV DNA levels varied from approximately 0 to 659 copies/106 cells (IQR: 22.9–126.5). A total of 605 intact FL env sequences were recovered in antemortem blood cells and across 28 tissues (IQR: 5–9). Sequence analysis showed (a) the emergence of large, identical, intact HIV RNA populations in blood after cessation of therapy, which repopulated tissues throughout the body; (b) that multiple sites acted as hubs for HIV dissemination but that blood and lymphoid tissues were the main source; (c) that viral exchanges occurred within brain areas and across the blood-brain barrier; and (d) that migration was associated with low HIV divergence between sites and greater diversity at the recipient site.CONCLUSION HIV reservoirs persisted in all deep tissues, and blood was the main source of dispersal. This may explain why eliminating HIV susceptibility in circulating T cells via bone marrow transplants allowed some individuals with HIV to experience therapy-free remission, even though deeper tissue reservoirs were not targeted.TRIAL REGISTRATION Not applicable.FUNDING NIH grants P01 AI31385, P30 AI036214, AI131971-01, AI120009AI036214, HD094646, AI027763, AI134295, and AI68636.

Authors

Antoine Chaillon, Sara Gianella, Simon Dellicour, Stephen A. Rawlings, Timothy E. Schlub, Michelli Faria De Oliveira, Caroline Ignacio, Magali Porrachia, Bram Vrancken, Davey M. Smith

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Abstract

Currently, the incidence of HIV infection exceeds the death rate from HIV, and as a result, the prevalence of individuals living with the infection continues to increase. A critical limitation preventing the development of curative strategies is the lack of knowledge regarding mechanisms that allow HIV-infected cells to persist in individuals during combination antiviral therapy (ART). In this issue of the JCI, Chaillon and coworkers assessed HIV-infected cells from various anatomic compartments obtained through a rapid autopsy program of individuals undergoing long-term ART. This study, made possible with strong community collaboration, provides new insights on the potential locations of reservoirs of HIV-infected cells that persist during therapy.

The Last Gift

HIV currently infects over 37 million individuals worldwide (1). Although advances in the use of combination antiretroviral therapy (ART) have resulted in substantial improvements in morbidity and mortality from HIV infection, as the HIV epidemic has matured, new challenges have arisen. Adverse side effects from ART, the presence of ongoing immune activation contributing to comorbid disease, and the potential for the emergence of resistance to ART all contribute to decreased quality of life for infected individuals. As such, the current state of the epidemic remains unacceptable, and new approaches to cure HIV are a public health imperative.

There are now several examples of individuals who have been cured of HIV as the result of bone marrow transplantation for comorbid neoplasms, demonstrating that eradication is possible (2, 3). There are also examples of individuals who have controlled viremia without ART, either naturally (4, 5) or after a period of suppression of viremia with ART (4, 6). New studies to develop feasible and scalable strategies to cure or control HIV without ART represent fundamental research priorities. Strong commitments from governmental and private organizations support initiatives that are highly collaborative (e.g., AIDS Clinical Treatment Groups, Cure Collaboratories) and that directly engage communities of affected individuals have established a solid foundation to approach HIV eradication. The Last Gift autopsy program is one example of such a collaboration. In this issue of the JCI, Chaillon and colleagues explored HIV-infected cells in anatomic compartments obtained from six individuals who underwent a rapid autopsy procedure under the Last Gift protocol (7).

Cycles of HIV infection

HIV replication is rapid and error prone, and left untreated, infected cells produce genetically diverse viral populations that are widely distributed throughout the body. Although HIV infects cells of lymphoid and myeloid origin, highly activated lymphocytes comprise the vast majority of HIV-infected cells (>99.9%) responsible for virus production. These cells are relatively short lived and are eliminated within days of infection. Since replication is error prone and most infected cells carry a defective virus due to mutations and/or deletions, a relatively small proportion of infected cells contain proviruses that can produce infectious HIV. Ongoing cycles of infection provide a constant source of newly infected cells to maintain a relatively stable level of steady-state viremia. A small fraction of infected cells that revert to a resting state are not eliminated and may persist for prolonged periods (8). In addition, HIV infects cells of myeloid origin, including macrophages (9) and microglial cells (10) that may also persist for prolonged periods in a tissue-specific manner.

The introduction of combination therapy completely blocks HIV replication, interrupts ongoing virus transmission, and disrupts the balance established by cycles of HIV infection, virus production, and cell elimination (11). Short-lived infected cells are eliminated and not replaced, and viremia declines 10–100 fold during the first weeks of ART. HIV viremia continues to decline after this initial phase, but more slowly, indicating that the cells responsible for residual viremia have longer half-lives. Analysis of plasma HIV decay kinetics revealed that cells producing residual viremia have half-lives of roughly 14 days, 39 weeks, and 110 weeks (12, 13). Following decay, a low but detectable level of viremia remains in most patients despite years of ART. Levels of HIV DNA are also reduced, although the declines (10- to 30-fold) are less substantial than noted plasma RNA reductions (14, 15). Remaining infected cells include cells with infectious proviruses, which represent an important target for eradications and can produce viral RNA and protein that are possible sources of ongoing immune activation in individuals undergoing ART (16, 17). As a result, understanding the mechanism of persistence of all infected cells during ART is a topic of intense interest. Following ART induction, a number of studies have failed to find evidence of active HIV replication cycles even within tissues (18–22). Rather, cells infected by HIV prior to the introduction of ART persist during prolonged treatment and undergo clonal expansion (23–27). Clones arise early after HIV infection is established and persist and expand after ART is initiated (28). As a result, HIV is maintained during ART by cycles of cell replication, not cycles of virus replication.

Much of what has been learned regarding HIV cell populations, viral decay kinetics, persistence, and clonal expansion has been brought to light by analysis of plasma and peripheral blood lymphocytes, which contain only a small fraction (circa 2%) of infected cells. Information regarding the anatomic distribution of infected cells during prolonged ART is essential to understand the formation and maintenance of reservoirs of HIV-infected cells. Studies of tissues have identified HIV-infected cells, including clones, in lymphoid tissue as well as in pathologic tissue in individuals with comorbid neoplasms (26, 29), and putative clonal sequences could be detected in diverse tissues including lymphoid and CNS (21). Combined with longitudinal sampling of blood prior to expiration, such studies revealed that analysis of HIV-infected cells in tissues represents an archive of the history of HIV infection. In effect, autopsy-derived samples represent the “gift of a lifetime” of HIV infection in an individual; analysis of such tissues represents a compelling approach to investigate HIV persistence.

Tracking HIV infection across tissues

In this issue of the JCI, Chaillon et al. (7) obtained tissues from six individuals undergoing long-term ART as part of the Last Gift protocol, in which autopsies were performed within six hours of death. The study participants had significant comorbidities, and several chose to discontinue ART prior to death and had detectable viremia at the time of autopsy. Samples were obtained from 28 different tissues, including CNS tissue. The authors quantified HIV DNA in tissues and used endpoint dilution, single-genome sequencing to obtain a set (median of 7) of full-length HIV envelope DNA sequences from each tissue. Sequences were analyzed to determine phylogenetic and genetic relationships, and bioinformatic approaches were used to track how infected cells dispersed and migrated across tissues (7).

HIV DNA was detected in most tissues (7). Levels of HIV DNA in CNS tissue were low but detectable, consistent with previous findings that infection of the CNS occurs (30) and persists during therapy (31). All HIV DNA populations within individuals were highly related, but evidence of compartmentalization within tissues could be detected. In general, HIV DNA populations were genetically diverse, but Chaillon et al. also identified populations of proviruses in different tissues that were identical in sequence; in the setting of a genetically diverse population, repeated recovery of identical sequences suggests that these proviruses are members of a clone. These putative clonal members were detected in a number of tissues and provide useful insights into how infected cells are distributed in individuals (Figure 1) (7). Recently, Patro et al. (32) demonstrated that proviruses with nearly identical sequences may actually have different integration sites and may result from infection of identical viruses within different cells. Bioinformatic analyses are available to provide probabilities that identical sequences are clonal, and additional studies including integration site analysis will be necessary to identify authentic clones. In addition, correlations with primate studies, in which defined, “barcoded” viruses used for infection can permit precise tracking in anatomic locations (33), will shed additional insight on in vivo viral dissemination.

Reservoirs of HIV-infected cells persist during ART.Figure 1

Reservoirs of HIV-infected cells persist during ART. Cells infected with genetically diverse HIV variants including clones of cells are present throughout infected individuals even after prolonged ART. GALT, gut-associated lymphoid tissue.

Notably, several of the study volunteers discontinued ART prior to death, and tissue analysis at autopsy revealed infected cells at multiple anatomical locations. Detailed bioinformatic analyses suggested that these locations can serve as hubs for viral dissemination as active replication cycles resume, and that these hubs are the source of rebound viremia after ART is discontinued (7). With single time-point analyses, it is often difficult to determine whether virus-infected cells in tissues are the origin or the destination of these newly infected cells; the patterns of dissemination and dispersal in tissues were complex in these study subjects. In addition, it is not clear what proportion of infected cells were producing HIV RNA. Previous studies have demonstrated heterogeneity in the levels of RNA production, including in members of individual clones (34). Since the rapid autopsy strategy is likely to preserve HIV RNA, comparing HIV RNA from these tissues with stored specimens will permit detailed analyses of source and dispersal of HIV-infected cells and evaluation of new hypotheses. For instance, Abrahams and coworkers (35) performed longitudinal studies of HIV prior to and following ART introduction and proposed that the HIV variants induced from the latent reservoir after years of ART were most closely related to variants circulating at the time of ART initiation. Further characterization of HIV in the participants who discontinued therapy in the present study may yield useful information regarding the distribution of replication-competent HIV in tissues.

Autopsy study limitations

Autopsy studies pose new challenges and limitations. As described by J. Coffin, analysis of HIV in tissues is “solid-state virology” and, by its nature, carries concerns that are not encountered in studies of plasma or peripheral blood lymphocytes. Recovering single genomes of HIV from tissues as large as liver or as small as seminal vesicles is subject to potential sampling bias. Tissues taken at autopsy may contain varying amounts of residual blood, which itself may contain infected cells, thereby confounding tissue analysis. Additionally, the effect of comorbid diseases on the distribution of infected cells remains uncertain; for instance, one participant with pancreatic cancer in the present study showed the highest concentrations of HIV-infected cells in the pancreas (7). Future studies integrating solid-state virology with clinical data will make for a comprehensive analysis of these tissues.

As Chaillon et al. point out, a principal limitation of this and similar studies of disease pathogenesis is the overall paucity of individuals undergoing autopsy (7). For HIV research, this situation may be changing. The Last Gift program and other autopsy protocols provides an opportunity for individuals who may have been longstanding volunteers in other studies to offer an additional measure of participation; Last Gift enrollees have also described an additional sense of purpose (35). Similar sentiments have been voiced by participants in other HIV studies with autopsy options, such as those at the NIH Clinical Center. There are obvious and serious ethical concerns regarding recruitment for any autopsy protocol (36), but, in fact, investigators have learned that for HIV studies, the study participants themselves are often the first to raise the possibility of postmortem examinations. It is not surprising that the generation of HIV-infected individuals who have participated in research for many years would again lead the investigators, and be first to volunteer. As such, clinical investigators can consider discussions of autopsies as part of a routine evaluation in the appropriate study participants. On several levels, therefore, autopsies represent the gift of a lifetime.

Acknowledgments

We are grateful to the study participants and their families who make autopsy studies possible. We thank J. Coffin and S. Hughes for insightful discussions and the members of the Clinical Retrovirology Section of the HIV Dynamics and Replication Program, NCI, for helpful suggestions.

Address correspondence to: Frank Maldarelli, HIV Dynamics and Replication Program, NCI, NIH, 1050 Boyles St., Fort Detrick, Frederick, Maryland 21702, USA. Phone: 301.846.5611; Email: fmalli@mail.nih.gov.

Footnotes

Conflict of interest: The author has declared that no conflict of interest exists.

Copyright: © 2020, American Society for Clinical Investigation.

Reference information: J Clin Invest. 2020;130(4):1611–1614. https://doi.org/10.1172/JCI135905.

See the related article at HIV persists throughout deep tissues with repopulation from multiple anatomical sources.

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Version history
  • Version 1 (February 24, 2020): Electronic publication
  • Version 2 (April 1, 2020): Print issue publication
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