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Commentary Free access | 10.1172/JCI91916
1UCSF, San Francisco, California, USA.
2Case Western Reserve University, Cleveland, Ohio, USA.
Address correspondence to: Steven G. Deeks, 995 Potrero Avenue, San Francisco, California 94114, USA. Phone: 415.476.4082, ext. 404; E-mail: Steven.Deeks@ucsf.edu.
Find articles by Deeks, S. in: JCI | PubMed | Google Scholar |
1UCSF, San Francisco, California, USA.
2Case Western Reserve University, Cleveland, Ohio, USA.
Address correspondence to: Steven G. Deeks, 995 Potrero Avenue, San Francisco, California 94114, USA. Phone: 415.476.4082, ext. 404; E-mail: Steven.Deeks@ucsf.edu.
Find articles by Odorizzi, P. in: JCI | PubMed | Google Scholar
1UCSF, San Francisco, California, USA.
2Case Western Reserve University, Cleveland, Ohio, USA.
Address correspondence to: Steven G. Deeks, 995 Potrero Avenue, San Francisco, California 94114, USA. Phone: 415.476.4082, ext. 404; E-mail: Steven.Deeks@ucsf.edu.
Find articles by Sekaly, R. in: JCI | PubMed | Google Scholar
Published December 12, 2016 - More info
Chronic immune activation, immunosuppression, and T cell exhaustion are hallmarks of HIV infection, yet the mechanisms driving these processes are unclear. Chronic activation can be a driving force in immune exhaustion, and type I interferons (IFN-I) are emerging as critical components underlying ongoing activation in HIV infection. Here, we have tested the effect of blocking IFN-I signaling on T cell responses and virus replication in a murine model of chronic HIV infection. Using HIV-infected humanized mice, we demonstrated that in vivo blockade of IFN-I signaling during chronic HIV infection diminished HIV-driven immune activation, decreased T cell exhaustion marker expression, restored HIV-specific CD8 T cell function, and led to decreased viral replication. Antiretroviral therapy (ART) in combination with IFN-I blockade accelerated viral suppression, further decreased viral loads, and reduced the persistently infected HIV reservoir compared with ART treatment alone. Our data suggest that blocking IFN-I signaling in conjunction with ART treatment can restore immune function and may reduce viral reservoirs during chronic HIV infection, providing validation for IFN-I blockade as a potential therapy for HIV infection.
Anjie Zhen, Valerie Rezek, Cindy Youn, Brianna Lam, Nelson Chang, Jonathan Rick, Mayra Carrillo, Heather Martin, Saro Kasparian, Philip Syed, Nicholas Rice, David G. Brooks, Scott G. Kitchen
Despite the efficient suppression of HIV-1 replication that can be achieved with combined antiretroviral therapy (cART), low levels of type I interferon (IFN-I) signaling persist in some individuals. This sustained signaling may impede immune recovery and foster viral persistence. Here we report studies using a monoclonal antibody to block IFN-α/β receptor (IFNAR) signaling in humanized mice (hu-mice) that were persistently infected with HIV-1. We discovered that effective cART restored the number of human immune cells in HIV-1–infected hu-mice but did not rescue their immune hyperactivation and dysfunction. IFNAR blockade fully reversed HIV-1–induced immune hyperactivation and rescued anti–HIV-1 immune responses in T cells from HIV-1–infected hu-mice. Finally, we found that IFNAR blockade in the presence of cART reduced the size of HIV-1 reservoirs in lymphoid tissues and delayed HIV-1 rebound after cART cessation in the HIV-1–infected hu-mice. We conclude that low levels of IFN-I signaling contribute to HIV-1–associated immune dysfunction and foster HIV-1 persistence in cART-treated hosts. Our results suggest that blocking IFNAR may provide a potential strategy to enhance immune recovery and reduce HIV-1 reservoirs in individuals with sustained elevations in IFN-I signaling during suppressive cART.
Liang Cheng, Jianping Ma, Jingyun Li, Dan Li, Guangming Li, Feng Li, Qing Zhang, Haisheng Yu, Fumihiko Yasui, Chaobaihui Ye, Li-Chung Tsao, Zhiyuan Hu, Lishan Su, Liguo Zhang
While antiretroviral therapy (ART) has improved the quality of life and increased the life span of many HIV-infected individuals, this therapeutic strategy has several limitations, including a lack of efficacy in fully restoring immune function and a requirement for life-long treatment. Two studies in this issue of the JCI use a humanized mouse model and demonstrate that type I interferon (IFN) is induced early during HIV infection and that type I IFN–associated gene signatures persist, even during ART. Importantly, blockade of type I IFN improved immune function, reduced the HIV reservoir, and caused a delay in viral rebound after ART interruption. Together, these two studies support further evaluation of IFN blockade as a supplement to ART.
Those HIV-infected individuals who are able to access, tolerate, and adhere to combination antiretroviral therapy (ART) can expect to have a near-normal life span, particularly if ART is initiated during acute infection, before the virus causes significant damage to the immune system. Despite the success of ART, there are two well-recognized limitations of current strategies. First, due to resource limitations and/or treatment toxicities, many of the 37 million HIV-infected individuals worldwide are unable to remain on therapy indefinitely. Second, the vast majority of individuals who start therapy do so during more advance stages of the disease, after extensive damage to the immune system has already occurred. Chronic immune dysfunction during ART has been associated with the development of a number of non-AIDS-related complications, including cardiovascular disease and cancer. As lifetime treatment poses a variety of challenges, there is intense interest in developing therapeutic interventions that result in sustained control of the virus in the absence of therapy (a remission or cure; ref. 1). There is also great interest in therapies that reverse the chronic inflammation that appears to be central to development of immune dysfunction and non-AIDS morbidity. Therapies that address both of these recognized limitations would be particularly exciting advances.
Long-term treatment of HIV infection results in a state of chronic inflammation. Multiple factors contribute to this inflammatory state, including HIV production, irreversible loss of mucosal integrity and exposure to microbes, and an excess burden of other chronic pathogens, particularly CMV. Central to each of these inflammation-inducing pathways is the sustained upregulation of type I interferons (IFNs), which in turn triggers the transcription of a multitude of IFN-stimulated genes (ISGs) that regulate the function of T cells and other components of the immune system. During acute infection, the type I IFN signaling is clearly beneficial. Indeed, experimental inhibition of type I IFN during acute SIV infection causes poor virus control, accelerated loss of immune function, and death (2). During chronic infection, the impact of IFN signaling is less clear. Although chronic IFN signaling likely contributes to virus control, the reshaping of the adaptive immune system can be harmful. During chronic HIV infection, higher levels of type I IFN signaling are correlated with immune activation (3, 4), poor treatment-related immune reconstitution (5–7), and disease progression (8, 9). Chronic ISG signaling is also a consistent signature of blunted CD4+ T cell homeostasis during ART (6, 7, 10–12). Multiple mechanisms likely underlie these negative effects, including increased T cell apoptosis (12), activation-induced cell death (5, 13), blunted thymopoiesis (14), and increased production of a number of immunosuppressive pathways, including those mediated by indoleamine (2,3)-dioxygenase, IL-10, TGF-β, and PD-1.
This so-called “IFN paradox” has been beautifully illustrated in the lymphocytic choriomeningitis virus murine mouse model (15), in which inhibition of type I IFN prevents virus clearance during acute infection but accelerates long-term control during chronic infection. In this model, long-term viral control is mediated by decreased immune activation, decreased PD-1/PD-L1 activity, restored lymphoid architecture, and improved CD4+ T cell function (16, 17).
Two articles in this issue highlight the dual consequences of type I IFN signaling on HIV pathogenesis (18, 19). Both studies have taken advantage of a well-validated mouse model, in which explanted human bone marrow, fetal liver, and thymic tissue are cotransplanted into immunocompromised mice, leading to reconstitution of a humanized immune system. As the CD4+ T cells are human derived, it is possible to infect these mice with HIV and then treat them with ART. Both groups demonstrated that HIV infection results in upregulation of ISGs, high levels of T cell activation, and high levels of T cell dysfunction. Moreover, these effects persisted even during ART; therefore, this model recapitulates many of the major attributes of HIV pathogenesis.
Zhen et al. and Cheng et al. demonstrated that blockade of the IFN receptor during the chronic phase of infection reduces the levels of T cell activation, reduces expression of the inhibitory receptors PD-1 and TIM-3, and improves cytokine production by CD8+ T cells (18, 19). Interestingly, IFN blockade during chronic infection also resulted in lower levels of HIV replication, presumably due to improved CD8+ T cell function and/or reduced frequencies of activated CD4+ T cells, which are the preferred target cell for spreading HIV.
Perhaps the most fascinating observations from these studies are that type I IFN blockade during ART administration markedly reduced the frequency of cells harboring replication-competent HIV, the so-called “reservoir” (18, 19), and caused a delayed rebound of viremia after ART was discontinued (19). The mechanism(s) that underlie these effects, however, are not clear from these mouse studies. Based in part on a series of observations that have been made in humans by our group and others, we propose that the beneficial effect of IFN blockade on the reservoir could be due to at least three mechanisms (20, 21). First, as CD4+ T cell activation drives virus production and propagation of infection, it may be that reduced T cell activation following IFN receptor blockade decreases the pool of cells that are actively producing virus and/or that are susceptible to infection, leading to reduced virus spread. Second, as CD4+ T cell proliferation (both antigen driven and homeostatic) and long-term survival both contribute to HIV reservoir persistence, it is reasonable to postulate that IFN blockade–mediated alterations in these pathways would lead to gradual depletion of the reservoir over time. Finally, and we believe most importantly, IFN blockade–mediated improvements in CD8+ T cell function would be expected to result in accelerated clearance of virus-producing cells during ART and improved control after ART interruption. Concurrent with this, temporary increases in viral load (viral load blipping) following IFN blockade suggest a release of pathways that actively suppress low-level replication and/or latency, which, in conjunction with improved CD8+ T cell function, may lead to a successful “shock-and-kill” approach.
Chronic type I IFN signaling is central to the pathogenesis of a number of other diseases, including systemic lupus erythematosus, rheumatoid arthritis, and perhaps cancer. This has led to the development of several clinical interventions that include the use of antibodies to block IFNs and their downstream target genes to treat these autoimmune diseases (22). Emerging phase II/III clinical trial data suggest that these pathways can be inhibited therapeutically in an effective and safe manner (23, 24). Should these agents continue to show a favorable safety profile, we believe that efforts should be made to move these interventions into the HIV cure arena. Based on the work by Cheng et al. (19) and Zhen et al. (18), one might predict that administration of an antibody that blocks the type I IFN signaling in ART-suppressed HIV disease might (a) improve immunity by decreasing immune hyperactivation, decreasing expression of PD-1 and other negative regulators, and enhancing CD8+ T cell functionality; (b) curb non-AIDS morbidities associated with chronic inflammation; and (c) decrease the size and/or stability of the HIV reservoir. Collectively, these effects would lead to accelerated clearance of virus-producing cells during ART. The timing and duration of administration of IFN blockade will be critical in moving this approach forward in the clinic, as the level of viral suppression induced by ART, the degree of CD4+ T cell recovery, and the severity of CD8+ T cell exhaustion will be critical cofactors. Combination strategies to further enhance CD8+ T cell functionality or improve T cell migration into HIV “sanctuaries” may synergize to provide an even more robust “cure” strategy. Ultimately, this approach has the potential to improve control of HIV in the absence of ART and further the goal of developing a cure for HIV.
The investigators acknowledge the Delaney AIDS Research Enterprise (DARE) collaboration (UM1AI126611) and the amfAR Institute for HIV Cure Research (amfAR 109301).
Address correspondence to: Steven G. Deeks, 995 Potrero Avenue, San Francisco, California 94114, USA. Phone: 415.476.4082, ext. 404; E-mail: Steven.Deeks@ucsf.edu.
Conflict of interest: S.G. Deeks receives research support from Merck, Gilead, and ViiV Healthcare.
Reference information: J Clin Invest. 2017;127(1):103–105. doi:10.1172/JCI91916.
See the related articles at Targeting type I interferon–mediated activation restores immune function in chronic HIV infection and Blocking type I interferon signaling enhances T cell recovery and reduces HIV-1 reservoirs.