The Mtb-HIV syndemic interaction: why treating M. tuberculosis infection may be crucial for HIV-1 eradication

Accelerated tuberculosis and AIDS progression seen in HIV-1 and Mycobacterium tuberculosis (Mtb)-coinfected individuals indicates the important interaction between these syndemic pathogens. The immunological interaction between HIV-1 and Mtb has been largely defined by how the virus exacerbates tuberculosis disease pathogenesis. Understanding of the mechanisms by which pre-existing or subsequent Mtb infection may favor the replication, persistence and progression of HIV, is less characterized. We present a rationale for the critical consideration of ‘latent’ Mtb infection in HIV-1 prevention and cure strategies. In support of this position, we review evidence of the effect of Mtb infection on HIV-1 acquisition, replication and persistence. We propose that ‘latent’ Mtb infection may have considerable impact on HIV-1 pathogenesis and the continuing HIV-1 epidemic in sub-Saharan Africa.

of Mtb arising from the Euro-American Lineage 4 LAM clade ( Figure 1F) [18]. Given the inflammatory phenotype of Mtb strains have been associated with differing capacity to induce HIV-1 replication in peripheral blood cells, in vitro [21,22], the prevalence of varying strain types within a population may further exacerbate HIV-1 progression. From the expansion of the syndemic during the 1990s, the rate of coinfection has continued to increase. Globally, in 2000, given the estimate of a third of the world with LTBI [23], an estimated 0.36% of the world's population was Mtb-HIV-1 coinfected [17]. However, this rate varied significantly between regions, with HIV-1 high-burden countries in Africa noting coinfection rates of 1-8% ( Figure 1E) [17]. A recent meta-analysis of global Mtb exposure assessed by interferon gamma release assays (IGRA) and tuberculin skin test (TST) reactivity rates, between 2005 and 2018, which supported a reduction in the global LTBI prevalence to a quarter of the world's population, excluded an analysis of those HIV-coinfected [24]. Therefore, more recent global estimates of latent Mtb-HIV coinfection cannot be presented. However, this study demonstrated a strong correlation between TB case incidence and community level LTBI prevalence.
Together, these data indicate that the HIV-1 epidemic has continued to expand, despite ART rollout, in countries with the highest prevalence of non-HIV associated TB and that high rates of LTBI exist in countries with high TB case load. Given that HIV-1 coinfection is not associated with significantly increased TB transmission, we therefore forward a reverse causality hypothesis between Mtb and HIV-1 infection, whereby high rates of LTBI in a community contribute to exacerbating the HIV-1 epidemic.
Those that are HIV-1 infected are at increased risk of both reactivation of latent TB infection, during early HIV-1 and rapid progression following new Mtb infection, with greater risk of extrapulmonary TB as immune deficiency progresses [25,26]. ART decreases the incidence of TB among HIV-1 infected patients in countries with low or high TB incidence. A meta-analysis of nine observational cohort studies in which 37,879 patients were   (A) Source: UNAIDS World Bank, OurWorldInData.org/hiv-aids/ [15,16]. (B) Reproduced with permission from [9]. (C) Reproduced with permission from [17] C American Medical Association (2003). All rights reserved. (D) Reproduced with permission from [10]. (E) Tabulated data extracted from [17] are replotted. Reproduced with permission from [17]  enrolled showed that ART reduced the incidence of TB by 67% [27], with an estimated prevention of 1.9 million HIV-TB cases by ART in 12 African countries, between 2003 and 2016 [7].
While there has been increased effort to control HIV-related TB in areas of high HIV-1 transmission, there has been less consideration regarding the impact of high community prevalence of LTBI on the HIV-1 epidemic With increased HIV-1 replication at tissue sites of Mtb infection and due to a higher proinflammatory environment and cellular activation, HIV-1 will progress faster into AIDS (red) and potential TB disease. TB will coincide with a secondary viremia peak and further expansion of infected cells with integrated DNA. Following ART initiation, a larger pool of reservoir cells harboring HIV-1 and higher immune activation status has the potential to result in more frequent blips in viremia above the level of clinical detection (thin line), following viral suppression and tissue-specific HIV-1 reservoirs persisting with cell-to-cell spread, rather than a slow reduction in cells harboring integrated viral DNA. ART: Antiretroviral therapy; Mtb: Mycobacterium tuberculosis; TB: Tuberculosis.
in Africa, which has the potential to impact early HIV-1 progression following viral acquisition. Furthermore, continual community exposure to Mtb and recurrent infection could compound the increased risk of HIV-1 progression. If Mtb infection, therefore, has the potential to exacerbate HIV-1 acquisition and progression, latent Mtb elimination in HIV-1 high-burden settings may be an important factor to consider for HIV-1 prevention, treatment and cure strategies.

Is Mtb or HIV-1 the greater syndemic driver?
Active TB is a primary precipitate of AIDS progression [28]. Multiple prospective and retrospective studies demonstrate that peripheral HIV-1 RNA concentration (viral load [VL]) increases 1-2 log-fold in those HIV-1 infected at the time of TB diagnosis, and that HIV-1 VL decreases in some individuals, following successful TB treatment ( Figure 2) [28][29][30][31]. This supports the posit that the inflammatory state during active TB enhances viral replication, which is reduced following successful TB treatment and resolution of the TB-associated proinflammatory microenvironment. As such, HIV-1 VL has been demonstrated to significantly correlate with Mtb-induced plasma and pleural fluid cytokine levels in TB patients [31][32][33].
In a case-control study of persons living with HIV-1 with similar levels of immune suppression (absolute CD4 counts), TB cases had a higher incidence of other new AIDS-defining opportunistic infections (OI) and reduced survival, supporting the case that TB potentiates AIDS progression and HIV-1 induced morbidity and mortality [34]. As an AIDS defining illness in persons living with HIV, TB is unique compared with other OI in that the increased risk for TB can occur before significant CD4 depletion [31] and at a log lower HIV-1 VL than other OI [28,35]. This suggests that Mtb infection imparts a broader dysfunction on immune cells in HIV-1, than merely CD4 depletion, leading to much earlier HIV-1 disease progression than other opportunistic pathogens. While the contribution of TB disease to HIV-1 progression is unrefuted, the contribution of LTBI to AIDS development has been little explored in the literature, based solely on plasma VL and CD4 changes [36]. Recent studies investigating Mtbinduced immune activation and changes in the inflammatory mileu at infected sites potentially provide support for a larger contribution of LTBI to HIV-1 progression than is currently acknowledged [37].
The dramatic increase in incidence of TB and TB-associated mortality following the expansion of the HIV-1 epidemic has shifted the focus of the research and medical community to understanding and intervening in HIV-associated TB progression. HIV-1 coinfection complicates and worsens TB outcomes. The early development of TB in HIV-1-infected individuals has been linked to a propensity of HIV-1 to infect activated Mtb-specific T-cells, leading to preferential depletion and alteration of the phenotype and function of TB adaptive immunity in the lungs [38][39][40][41][42]. This early T-cell depletion has been suggested to cause TB granuloma disorganization, loss of Mtb containment and thus increased Mtb dissemination, resulting in higher prevalence of extrapulmonary TB [43]. In some respects, HIV-1 causes a disease more similar to primary progression in infants [44]. T-cell depletion also decreases sensitivity to diagnose Mtb sensitization, based on antigen-specific T-cell assays [45]. The exacerbation of TB severity and mortality by HIV-1, concomitantly reducing TB transmission is, however, counterintuitive to a syndemic benefit between these pathogens. HIV-1 in effect causes a 'dead end' for the bacilli. Conversely, if Mtb infection increases HIV-1 replication, and thus risk of transmission, is Mtb rather a greater benefit to the HIV-1 epidemic than HIV-1 is to Mtb?

Acquisition of infection
Latent Mtb infection LTBI represents the circumstances where individuals maintain Mtb infection by a delicately controlled innate and adaptive immune cell interaction, controlling Mtb replication, but preventing immune exacerbation [46,47]. Latently infected individuals represent the largest reservoir for potential reactivation and transmission. Inhaled Mtb bacilli are encapsulated by a collection of immunological cells, including infected and recruited alveolar macrophages, neutrophils, differentiated monocyte-derived macrophages (MDM), epithelioid cells and multinucleated giant cells, Langhans giant cells, surrounded by T and B lymphocytes and other non-classical innate cells, which organize themselves into granulomas [48].
Formation of the Mtb granuloma during latent infection is associated with a strong localized and systemic proinflammatory response. Bacterial activation of surface toll-like receptors on phagocytes induces TNF, IFN-γ, IL-1β, IL-6, IL-12, IL-10 and TGF-β, activating phagocyte and recruited T-cell functions ( Figure 3) [46,47]. A major systemic component in serum before disease onset are proteins CXCL9-10, CCL5, CCL2 and CXCL8, predominantly recruiting T-cells, monocytes and neutrophils, respectively, to the site of Mtb infection [49].
Granulomas benefit the host by containing and restricting mycobacteria, ultimately preventing dissemination. Studies using transparent zebrafish infected with Mycobacterium marinum, to model early stages of mycobacterial infection, showed the formation of epithelioid granulomas prior to activation of the adaptive immune response, coinciding with wide bacterial expansion [50]. These findings suggest that granuloma formation may also be used by bacteria to increase infection and dissemination. T and B cells recruited to help form the granuloma are primed in the lymph nodes (LN) by migrating dendritic cells (DCs) presenting Mtb antigen [51,52]. However, it has also been suggested that Mtb-infected neutrophils and DC will traffic live Mtb to LN, setting up the LN as a site of Mtb reservoir during latency [53,54]. Live Mtb bacilli have been isolated from lung granulomas of individuals with clinically inactive TB, demonstrating the ability of viable organism to persist during latent infection [55] and multiscale modeling predicts Mtb populations are highly dynamic during latent infection responding to the host inflammatory environment, countering the idea that all latent Mtb resides in a dormant nonreplicating state [56,57].

HIV-1 acquisition Crossing the primary barrier
HIV-1 is transmitted via infected bodily fluids, including seminal and vaginal fluids during sexual intercourse; blood during transfusions or blood contact between broken skin and wounds; intravenous drug use and from mother to child (in utero, during delivery or through breastfeeding). HIV-1 can cross the outer epithelial lining of skin tissue, which acts as the primary physical barrier to infection. Parts of the body covered by mucosal membranes, 'wet skin', including genital and rectal tissues, are particularly vulnerable to HIV-1 infection and are primary sites of mucosal infection. HIV-1 crosses the mucosal epithelial barrier through capture by DCs, transcytosis through the intraepithelial layer, attachment to Langerhans cells and CD4 + T-cells and/or the disruption of the mucosal membrane integrity by HIV-1 envelope glycoprotein 120 (Gp120) (reviewed in [58]).

Viral entry into cells
Viral attachment requires high affinity binding of HIV-1 Gp120 to the host CD4 receptor. HIV-1 interacts with either coreceptor C-C chemokine receptor 5 (CCR5) or C-X-C chemokine receptor 4 (CXCR4), forming a heterodimer with CD4, facilitating viral entry ( Figure 3). The HIV-1 envelope Gp41 subunit protein then  facilitates viral fusion and injects itself into the target cell membrane. Studies show that mutated coreceptors and/or coreceptor inhibitors lead to reduced HIV-1 infectivity [59][60][61]. Strains which predominantly infect using CCR5 are referred to as R5-tropic, strains which use CXCR4 are called X4-tropic, and dual-tropic R5/X4 strains infect cells expressing either coreceptor [62]. Transmitted viral strains are predominantly R5-tropic while X4 strains are seldom observed in early infection [63]. Within an infected individual, the viral population may shift from R5 to X4 over time, as it evolves in the natural course of infection, and this switch correlates with subsequent rapid disease progression [62]. Frontline mucosal-resident T lymphocytes, tissue macrophages and DCs are primary targets for HIV-1 infection. Of these, primary mucosal CD4 + T lymphocytes are the predominant target, due to their high surface expression of CD4, showing increased susceptibility to infection in vitro as well as increased levels of viral replication. Increased surface expression of CCR5 and T-cell activation status also contribute to the preferential infection of these cells [64]. HIV-1 infects monocytes and macrophages due to their high CCR5 and moderate CD4 surface expression [64,65]. HIV-1-infected tissue-resident and MDM can fuse with CD4 + T-cells enabling direct viral transmission between these cells [66].
Following HIV-1 entry into host cells, the viral reverse transcriptase enzyme converts RNA to cDNA and ultimately double-stranded DNA, which is translocated to the nucleus, where the virally encoded integrase facilitates viral DNA integration into the host genome [67]. Once integrated, the virus uses the host cellular machinery and energy to transcribe viral mRNA for packaging into new viral particles and for synthesis of its protein components. The viral protease enzyme cleaves polypeptides needed for assembly of new virions, which bud off the cell membrane through exosome transport ( Figure 3, reviewed in [68]).
Several host chemokines that are natural agonists of CCR5 may act as HIV-1 antagonists during HIV-1 infection, by blocking Gp120 interaction with CCR5. C-C chemokines CCL3 (MIP1α), CCL4 (MIP1β) and CCL5 elicit a dose-dependent inhibition of HIV-1 Gag p24 release from peripheral blood mononuclear cells (PBMCs) [69]. These chemokines specifically inhibit the infection of R5-tropic HIV-1 strains, suggesting that the mechanism of action is via impeded viral entry [70]. Paradoxically, these chemokines increase replication of X4-tropic viruses. Experiments with PBMC, depleted of CD8 + T-cells and infected with a X4 HIV-1 strain, in the presence of supplemented CCL5, exhibited an increased cellular reverse transcriptase activity, compared with untreated PBMC. This suggests that CCL5 may induce viral replication in X4-infected cells [71]. Patients with high plasma CCL5 concentration also show higher levels of plasma X4 HIV-1 RNA copies [72]. These observations suggest that C-C chemokines may be important early in blocking R5 HIV-1 infection, but detrimental to the host as the viral infection progresses and more X4-tropic viruses emerge.

Establishing HIV-1 infection
Following transmission, the founding HIV-1 variant/s rapidly expand and spread beyond the site of infection to other parts of the body via the bloodstream and lymphatic vessels that lie within the mucous membrane tissue. Rapid homing of the virus to the gut-associated lymphoid tissue, facilitated by the integrin α4β7 gut homing receptor has been demonstrated to play a major role in the early expansion of HIV-1 within an infected individual as this anatomical site harbors high levels of CD4 + CCR5 + T-cells (reviewed in [73]). A larger, self-propagating viral pool is then established and can cause systemic infection in secondary lymphoid tissue sites [74].
An 'eclipse phase', a period of approximately 10 days during which viral RNA is undetectable in the plasma, precedes the detection of viral antigen [75,76]. Peak viremia is reached at approximately 2 weeks postinfection [77], followed by significant VL reduction to a resting steady state, otherwise referred to as the viral 'set point,' and the onset of the chronic phase of infection ( Figure 2) [78]. This set point may vary up to 1000-fold between patients, with a higher set point 6 months after seroconversion as well as the decline in CD4 counts being early predictors of rate of disease [79][80][81]. However, a change in VL is less predictive in the years preceding AIDS onset, while the pattern of CD4 decline is predictive [82]. Thus, a higher VL immediately following infection and greater declines on CD4 T-cells are important defining features of the severity of outcome of infection [83].

Enhancers of HIV-1 acquisition, expansion & replication
Multiple factors have been characterized that enhance the ability of HIV-1 to both establish infection and replicate within the infected host cell. Increased inflammatory cytokine levels at the genital mucosa, potentially linked to an existing sexually transmitted infection, have been associated with increased risk of HIV-1 acquisition [84] and expanding the transmission bottleneck [85]. These cytokines facilitate recruitment and activation of cells targeted by HIV-1. Inflammation at this site has also been associated with creating an environment that is more permissive to infection by less infectious viral variants [86].
The mode of infection has also been linked to the rate of HIV-1 expansion at the site of infection and dissemination into secondary lymphoid tissues. Cell-to-cell transmission, facilitated through viral synapses, is proven to be a significantly more effective means of viral expansion than cell-free virus-mediated spread [87]. This is the case for spread of HIV-1 from T lymphocytes to MDM, and from infected macrophages to other permissive cells [88]. Migration of HIV-1-infected antigen-presenting cells (APCs) particularly to the LN and associated tissue increases the chance of infecting resident macrophages and T lymphocytes, thus further spreading HIV-1 infection [89]. Receptor tropism is also associated with expansion of HIV-1 within a host whereby X4-tropic viruses, more prevalent in late stages of infection, expand more rapidly as they infect a broader range of cells and have enhanced pathogenicity [90,91].

Mtb infection creates an expanded cellular niche susceptible to HIV-1 infection
In vitro infection of CD8 + T-cell-depleted LN lymphocytes and PBMC isolated from HIV-1-infected individuals with and without LTBI, indicated HIV-1 replication was only induced in cells isolated from those with LTBI, hypothesized as a consequence of the preferential infection of activated Mtb antigen-specific T-cells by HIV-1 [29]. Mtb infection may favor HIV-1 infection by increasing the density of viral entry coreceptors, CCR5 and CXCR4, on the surface of CD4 + Mtb antigen-specific T-cells and various myeloid populations [100][101][102]. The recruitment of such T-cells to the site of HIV-1 acquisition would result in the establishment of a larger pool of virus, expanded viral reservoirs and consequently, a higher viral set point during the acute phase of infection. As HIV-1 is not incredibly efficient at establishing infection, creating an environment with a diversity of cells with increased viral receptor density would benefit the virus [103].
Clinical evidence to support the early recruitment of circulating Mtb-specific T-cells to genital mucosa is difficult to obtain, although their circulating abundance and higher chemokine receptor density would support this likelihood. Clearly, their peripheral circulation would have direct relevance to increased HIV-1 acquisition following intravenous exposure.
Increased density of HIV-1 coreceptors on Mtb-specific T-cells is not the sole mechanism by which LTBI may enhance HIV-1 acquisition and established infection. Blood from pulmonary TB patients had significantly increased CCR5 + T-cells, as well as increased CXCR4 + and CCR5 + monocytes [100]. T-cells isolated from PBMC stimulated with mycobacterial species M. bovis BCG and Mtb are also more susceptible to R5 and X4 HIV-1 infection, compared with unstimulated T-cells or cells infected with M. smegmatis. This effect is abrogated by TLR2 silencing in PBMC, supporting the concept that monocyte/macrophage proinflammatory cytokine production during Mtb infection enhances bystander T-cell HIV-1 susceptibility [104]. Mtb-specific CD4 T-cells, CD27 + CD57 -, also show increased susceptibility to HIV-1 infection, correlating with reduced CCL4 secretion, hypothesized to facilitate greater CCR5-Gp120 interaction [105].
Early studies of newly diagnosed HIV-1 and TB-HIV-1 patients indicated that HIV-TB exacerbates immune activation, with elevated HLA-DR expression on CD4 + and CD8 + T-cells, correlating with elevated expression of Fc receptors I and III on peripheral monocytes [106]. Recently, in whole blood transcriptomic analyses, elevated Fc Gamma Receptor signaling and classic complement activation were the greatest predictors of subclinical TB infection and risk of TB progression in ART naive HIV-1-infected individuals with LTBI [107]. More complex multiparameter flow cytometry of antigen-specific T-cells also indicated that TB-HIV-1 patients, compared with TB only, have a higher frequency of IFN-γ producing Mtb-specific CD4 + and CD8 + T-cells with elevated activation markers HLA-DR and CD38 and higher TNF production. By contrast, IFN-γ producing CMV-specific T-cells show no elevated activation. This indicated that immune activation in HIV-1 is specific to Mtb antigen-specific T-cells, and not nonspecific activation of any antigen-specific T-cell [108,109]. These findings support the hypothesis that Mtb infection creates a larger circulating pool of innate and adaptive immune cells susceptible to HIV-1 infection, which can increase both risk of HIV-1 infection, quicker expansion of infection during acute infection and thus enhanced HIV-1 progression during chronic infection.

Mtb impact on HIV-1 viral replication & set point
LTBI may increase HIV-1 viral set point, leading to an increase in the severity of HIV-1 disease in TB endemic regions [80]. This hypothesis is supported by multiple lines of evidence including that infection with Mtb increases HIV-1 risk of infection [101,104] and the rate of replication both in vivo [31,110] and in vitro [21,22]. Mathematical modeling predicts that coinfected patients have a VL set point 27% greater than HIV-only infected patients [111]. With the support of their model, the authors argue that a high VL set point increases the risk and timing of coinfected persons progressing to AIDS, by 2 years.
It has long been known that coinfection of the same cell by Mtb is not necessary to induce HIV-1 replication in PBMC [112]. In 1997, Nakata et al. investigated the in vivo effect of coinfection with Mtb using bronchoalveolar lavage (BAL) fluid from HIV-1-coinfected TB patients compared with individuals with no lung disease, demonstrating a striking increase in HIV-1 VL in BAL from Mtb-infected lung segments. In each patient tested, the amount of HIV-1 RNA was greater in the infected lung segment versus the uninfected segment, suggesting that local inflammation increased HIV-1 replication and VL. BAL fluid levels of HIV-1 were also increased in all patients compared with plasma levels [113]. In 2001, Toossi et al. first showed increased HIV-1 replication at sites of active Mtb infection in pleural fluid from pleural TB patients. Increased replication was associated with increased TNF and CCL2 expression, decreased amounts of HIV-1 entry blocking C-C chemokines (CCL3, CCL4, CCL5) and upregulation of CCR5 on pleural fluid mononuclear cells [114]. Such a suppression of CCR5 ligands, with concomitant CCR5 increase, would increase the propensity for R5-ropic virus infection. While these observations were made in fluid isolated from TB patients, the impact on HIV-1 at the local site of Mtb infection, supports the hypothesis that such a relationship would occur in any tissue site where HIV-1 and replicating Mtb coexist, prior to the development of symptomatic TB disease.
Later studies implicated the proinflammatory cytokine milieu in enhancing replication of HIV-1 through hTF activation of the LTR [115]. Alveolar macrophages isolated from TB patient BAL, compared with noninflamed lungs from healthy controls, have downregulated expression of the inhibitory C/EBPβ isoform and increase expression of the C/EBP-activating isoform, facilitating increased HIV-1 replication [116]. In an in vitro PBMC coinfection model, HIV-1 replication had a magnitude-dependent cytokine-induced increase, relative to the strain of infecting Mtb [22]. Coinfection with the proinflammatory Mtb Lineage 4 strain CDC1551 significantly increased supernatant HIV-1 Gag p24 protein concentrations, compared with infection with Lineage 2 HN878, a less inflammatory strain which produces the cell wall phenolic glycopid [22]. This strain difference was abrogated by deletion of phenolic glycopid from HN878 [22] or by silencing the expression of NFAT5 induced by CDC1551 [21]. Silencing of the TLR downstream adapters, MyD88, IRAK1 and TRAF6, in human monocytes also inhibited Mtb-induced NFAT5 expression and HIV-1 replication during CDC1551 coinfection [21]. ZNF134 has recently been identified as a novel HIV-1 LTR activator, which is induced to a greater extent during mycobacterial infection compared with HIV-1, and PBMC from TB patients demonstrate high levels of ZNF134 expression, even in the absence of HIV-1 [117]. These studies demonstrate that Mtb cell wall components activate hTFs via TLR signalling, inducing HIV-1 replication. Importantly, Mtb culture filtrate proteins or purified cell wall mannose-capped LAM can independently activate HIV-1 LTR transcription, in the absence of live bacilli. This suggests bacterial products within the granuloma milieu could activate HIV-1 transcription in bystander Mtb-uninfected cells [118]. Coinfection within the same cell is thus neither required, nor likely the predominant effect via which Mtb affects HIV-1 replication and infection within the same individual.
In further support of this, coinfection with Mtb may also contribute to elevated levels of systemic immune activation, which will potentiate HIV-1 disease pathogenesis. Macrophage and T-cell-specific soluble cellular markers of immune activation, sCD27, sCD163, IL1RA and sCD14, are found at increased levels in pleural fluid versus plasma, and even higher in TB patients coinfected with HIV-1 [119]. Soluble monocyte activation markers, sCD14, IL-6, CXCL10 and CRP, are elevated in coinfected patients with active but not latent infection. However, the same HIV-1-infected individuals were found to have elevated lymphocyte activation with higher surface expression of CD38 and HLA-DR on CD4 + and CD8 + T-cells when latently Mtb infected, increasing the propensity of HIV-1 for T-cell infection [37].

HIV-1 immune evasion & viral spread Cytolytic T-cell responses & ADCC
The success of HIV-1 infection is governed by early immune evasion and ineffective viral clearance. Natural killer (NK) cell and HIV-specific CD8 + T-cell responses arise shortly after infection and are pivotal in the outcome of infection [120]. CD8 + T-cell responses have been proposed to play a role in reducing peak viremia to a stable state set point VL [121]. However, due to the error prone HIV-1 reverse transcriptase that misincorporates nucleotide bases into the viral genome [122], these responses are rapidly (within weeks) escaped through selection of amino acid mutations in HLA-presented epitopes [123]. Likewise, evidence of escape from NK cell responses have been reported [124]. Antibody responses confer even less benefit to control of HIV-1. Those that are able to neutralize the virus arise somewhat later in infection (months) [125,126] and are likewise rapidly escaped through mutations in the viral envelope.
Exploitation and evasion of these immune-targeted responses enables the virus to replicate and persist despite the host's best efforts to eradicate HIV-1. Viral accessory proteins, Vif, Nef, Vpu and Vpr, modify the hostile host cell environment and facilitate viral escape from cell-mediated and innate immune responses, through a variety of mechanisms (reviewed in [127]). Viral protein-induced CD4 + T-cell apoptosis and cell death of bystander cells, potentially induced by both host factors (e.g., TNF, Fas ligand and TRAIL) and various HIV-1 factors (Tat, Vpr and Nef ), disable CD4 + T-cell secretion of inflammatory cytokines and impact their action on APC [128,129].
Antibody-dependent cellular cytotoxicity (ADCC) is a highly effective host control mechanism mediated predominately by NK cell activation of cytolytic T lymphocytes (CTLs). The intricate activating and inhibiting receptor combination presented by NK subsets facilitates a highly coordinated response to sensed ligands and CTL activation. Nef proteins downregulate surface expression of the NK ADDC-activating receptor NKG2D, reducing ADCC susceptibility [130]. Similarly, HIV-1 proteins reduce surface expression of CD4 and presentation of CD4-Env epitopes, to evade ADCC [131,132].
HIV-1 has also been shown to modulate the expression of MHC Class I and II proteins [133]. HIV-1 infected cells can avoid the CTL response and subsequent killing by Nef-mediated downregulation of surface MHC I [134]. MHC II restricted peptide presentation to specific T-cells is inhibited by Nef, reducing the activity of CD4 + T-helper cells required for control of viral infection [133].

While CD8 and NK cells play an important role in ADCC and CTL-mediated killing of HIV-1-infected cells, their role in
Mtb control is far less defined or as studied as CD4 + T-cells. NK cells are found in human TB granulomas and their ability to produce IFN-γ and TNF during in vitro Mtb infection varies by blood donor KIR genotype [135]. NK cells from TB patients during disease have reduced IFN-γ and degranulation, compared with post-treatment, suggesting Mtb infection that progresses to disease impairs NK function [136]; this would benefit HIV-1 escape from CTL killing. As macrophage cross-priming via MHC-I optimizes CTL responses, Mtb-induced impairment of cross-presentation [137] may further contribute to CTL evasion.
A recent study identified distinct PPD-specific Fc Gamma antibody profiles between latent Mtb infected and active TB patients [138], yet there were no uninfected controls (controlling for other mycobacteria) or post-treatment responses to determine whether the difference arose during TB disease or in those at risk of developing the disease when Mtb infected. Antibody differences were associated with PPD-specific reduced NK cell-mediated ADCC, degranulation (CD107a) and CCL4 and IFN-γ secretion in those with active TB [138]. How Mtb infection may truly impair ADCC and CTL-mediated HIV-1 killing in vivo during LTBI is far from elucidated and requires greater investigation.

Viral reservoirs & latency Cellular targets of latent HIV-1
Despite the unquestionable success of ART to reduce viral replication and improve the quality of life of HIVinfected people, HIV-1 continues to persist latently within infected host cells and tissues, in the absence of viral replication [139][140][141][142]. This may be caused by unsuppressed low levels of HIV-1 replication within drug-privileged anatomical sites, but has predominantly been characterized in cells harboring integrated, transcriptionally silent viral genomes. The large majority of these integrated viral genomes are defective and harbor internal deletions or are hypermutated [143,144]. These persistent quiescent cells can escape host-targeted killing by immune responses and drug targeting, as current drug regimens target stages of the life cycle prior to or postviral integration. Quiescentinfected cells can re-enter a productive HIV-1 life cycle in response to various stimuli, including antigen-specific T-cell activation and inflammatory cytokine induction in the tissue microenvironment (reviewed in [142]).
A pool of latently HIV-1-infected cells is established during the early stages of HIV-1 infection, when infected patients are untreated. Despite initiation of ART as early as 3 days postinfection, this pool is established [145] and is highly stable and long-lived [140,146], owing largely to maintenance through homeostatic proliferation [147]. These cells may originate from infected and activated HIV-1 antigen-specific cells that differentiate into long-lived resting memory T-cells or may be directly established in inactivated resting CD4 + T-cells. As HIV-1 exhibits a narrow tropism for CD4 + T-cells, this pool of cells represents a large, if not the largest, viral reservoir in an infected host [139,148]. Two different sets of resting CD4 + T-cells exist: the naive and the memory CD4 + T-cells. Naive cells can carry HIV-1 DNA and replication competent HIV; however, their frequency of infection is usually much lower than that of the memory CD4 + T-cells [142].
There is mounting evidence that other nonconventional viral reservoirs exist within the host (reviewed in [149][150][151]). Tissue macrophages and/or monocytes enable viral persistence by harboring viral particles and relocating them to inaccessible immune-privileged sites, where they can evade the host and ART restriction. At the same time, macrophage functioning is impaired by HIV-1 proteins (eg. Nef, Gag, Tat and Env) permitting a unique environment for HIV-1 to persist [152]. Unlike the apoptotic cascade induced in activated CD4 + T-cells; in macrophages, HIV-1 blocks apoptosis, prolonging survival, through degradation of the host long noncoding RNA lincRNA-p21. This prevents activation of its apoptotic partner hnRNP-K, removing lincRNA-p21 inhibition of the prosurvival MAP2K1 [153]. It is estimated that HIV-1 proviral DNA is present in less than 1% of monocytes [154].
Other studies indicate approximately 50 per 10 6 LN macrophages are infected [155]. Infectious HIV-1 has also been detected in circulating monocytes from patients initiated on ART for extended periods. Importantly, undetectable amounts of HIV-1 RNA are produced under basal conditions, but viral reactivation can occur following coinfection with opportunistic infections [156].

Tissue targets of latent HIV-1
Several organs serve as viral tissue reservoirs that enable the persistence of HIV-1 infection in the presence of ART [148]. The LN and lymphoid tissues are major tissue reservoirs of HIV-1, enabling viral replication, production and persistence and the storage of viral particles within immune complexes [157,158]. Replication-competent virus has been recovered in cells isolated from LN of virally suppressed patients. Both naive and central memory T-cells (TCM) are selectively retained in the LN, due to their homing receptor expression and DCs also accumulate in the LN, all with the potential to aid in viral expansion (reviewed in [159]). Central memory peripheral T follicular helper (Tfh) cells, in particular those PD1 + CXCR3 -, were identified as the major circulating T-cell reservoir, also being highly susceptible to HIV-1 infection. Frequencies of activated HLADR + CD38 + CD4 + T-cells correlate with the level of viral induction in peripheral Tfh cells, suggesting systemic immune activation contributes to reservoir maintenance and functionality [158].
Other lymphoid organs such as the spleen, thymus and bone marrow have also been implicated as potential HIV-1 reservoirs (reviewed in [160]). Bone marrow, as a secondary lymphoid organ and site of haematopoiesis, contains progenitor cells that are not only long-lived, but divide and thus can act as replicating nodes, producing progeny with integrated HIV-1 DNA. In ART-naive individuals, HIV-1 has been identified in bone marrow CD133 + hematopoetic stem cells, mesenchymal stem cells, macrophages and memory CD4 + T-cells. CD4 + Tcells expressing the surface receptor CCR6, a marker of Th17 cells with homing capacity to the gut, are highly sensitive to HIV-1 infection. This also implicates the gut as a potential HIV-1 reservoir [161,162].
The lungs are very active immunological effector sites constantly being exposed to viral and bacterial airborne pathogens and represent potential HIV-1 lymphoid reservoirs. The lungs have features that render them ideal 'sanctuaries' for HIV-1 persistence. Cell-to-cell viral spread may be promoted by the proximity of millions of alveoli that provide a large surface area for persistence and an abundance of macrophages and DCs. Alveolar macrophages that are abundant in the lung spaces provide an ideal niche for persistent HIV-1 due to their resistance to HIV-induced apoptosis [163]. Mtb has also been shown to increase the surface expression of CXCR4 on alveolar macrophages, thus enhancing their susceptibility to X4 HIV-1 [101].
Differing levels of HIV-1 within the lungs, in comparison to peripheral blood, have been documented. In ART naive individuals HIV-1 has successfully been isolated from lung cell-free BAL fluid, CD4 + and CD8 + T-cells and alveolar macrophages [150,164]. Alveolar macrophage infection is associated with weakened phagocytic functioning; and HIV-1 RNA and DNA have also been detected in these macrophages from ART-initiated patients [165,166]. During ART, macrophages within sanctuary sites may, therefore, be a source of persistent HIV-1 viremia, although their role here remains controversial [167].

Mtb contribution to HIV-1 reservoir abundance & activation
Pulmonary TB patients have increased CCR5 + CD4 + T-cells in the BAL fluid and lower respiratory tract when compared with healthy controls or non-TB lung disease controls [102]. Comparing blood and BAL cellular compart- There was a positive correlation with absolute number of CD4 + and CD8 + T-cells in the BAL and BAL VL, while an inverse relationship was found in the periphery with plasma VL and CD4 + T-cells. Three quarters of BAL CD4 + T-cells were positive for CCR5 and thus potential targets of HIV-1 infection [42]. Given the efficiency of direct cell-to-cell viral transmission [88], the TB granuloma provides an ideal permissive environment for HIV-1 infection and spread due to its tightly packed cellular architecture. Mtb has been shown to exacerbate HIV-1 infection by increasing viral transfer between cells, using tunneling nanotubes formed from IL-10-stimulated macrophages [168]. HIV-1 infection of LN-migrating Mtb-infected macrophages and DCs also has the potential to enhance the lymphatic spread of HIV-1 during ART [169]. It could be hypothesized that Mtb infection stimulates trafficking of HIV-1-infected peripheral circulating monocytes or HIV-infected CD4 + T-cells from the LN to the site of Mtb infection, thereby providing quiescent HIV-1-infected cells new tissue-resident target cells, and exposure to a proinflammatory tissue environment, to reactivate viral replication. Alternatively, trafficking Mtbinfected cells may coinfect a HIV-1-infected lymphatic microenvironment, resulting in recruitment of activated peripheral monocytes and T-cells to the LN, delivering a pool of HIV-1 susceptible cells to the HIV-1-infected environment (Table 1). These potential kinetic movements need in vivo validation.
During latent infection, Mtb has been identified in circulating human CD34 + peripheral hematopoetic stem cells and CD127 + bone marrow mesenchymal stem cells [170], suggesting that bone marrow may also be a reservoir for Mtb [171] as well as HIV-1. Enhanced recruitment of Mtb-specific T-cells to the bone marrow would create another niche for viral expansion and replication. During early ART reconstitution, the strongest correlate of restored Mtb immunity is an expanded CD27 + TCM response, the predominant T-cell reservoir for HIV-1 [172]. Thus, the coexistence of latent Mtb and HIV-1 reservoirs in the same tissue microenvironments has the potential for expanded HIV-1 infection and cell-to-cell spread during ART.
Extrapulmonary TB is much more common in HIV-1-infected individuals, and this occurs at sites where HIV-1 reservoirs are predominately found, particularly, LN, brain and cerebrospinal fluid, kidneys, liver, spleen and bone marrow, whilst some HIV-1 lymphoid reservoirs (thymus, gut-associated lymphoid tissue) are less common sites of TB (reviewed in [173,174]). With the exception of T-cell populations in the LN; macrophages, DC, astrocytes, microglia and epithelial cells are the commonly identified HIV-1 reservoir cells in these tissues and autopsy studies demonstrate Mtb DNA presence in these cells in latent infection [171,175]. The order of pathogen arrival in these sites is unclear and likely to exist in both directions, in any one individual.
Inflammatory DCs and MDM are capable of carrying Mtb from the granuloma to LN [176,177]. Neutrophils are also able to participate by harboring and transporting viable Mtb, which can be subsequently phagocytosed by tissue macrophages after transport [178]. Pre-existence of Mtb in these lymphoid sites would have the propensity to favor viral expansion once HIV-1 arrives in the LN.
Conversely, CD16 + monocytes that are found in greater frequency in Mtb infection [179] are susceptible to HIV-1 infection [180] and show increased transmigration from bone marrow, especially to the CNS, during HIV-1 infection [181]. Activated monocytes could, therefore, traffic HIV-1 to peripheral Mtb-infected sites, along a CCL2 gradient, thus setting up a peripheral site of coinfection. We postulate that pre-existence of Mtb in tissues that are common HIV-1 sanctuaries, as well as increased transmigration of HIV-infected APC to sites of LTBI both contribute to the higher frequency of extrapulmonary TB progression in HIV-infected individuals.

Defining coinfection dynamics in HIV/Mtb animal models
In the majority of clinical studies, determining the sequence of coinfection and dynamic changes during HIV-1 progression at diverse anatomical sites is difficult to determine, although critical to the understanding of the key effectors of Mtb infection on HIV-1 progression. Whether Mtb has a greater effect on HIV-1 acquisition risk or progression, and whether enhanced HIV-1 expansion is restricted to Mtb granulomas or extends to more diverse HIV-infected anatomical sites and tissue reservoirs, are key questions to inform any strategy designed to reduce the effect of Mtb on HIV-1 infection and progression.
Nonhuman primate (NHP) and bone marrow, liver and thymus (BLT)-humanized mice animal models allow researchers to build more detailed understanding of disease progression dynamics and the sequence of immune perturbations during coinfection, which clinical studies cannot answer. HIV-1 and Mtb coinfection models allow specific examination of pathogen strain, dose and duration, which reduces some variability observed in human studies. It also allows simultaneous investigation in plasma and tissues, including lung granulomas, LN, spleen and other extrapulmonary sites. Although no animal model completely recapitulates all aspects of any human disease, NHP studies of simian immunodeficiency virus (SIV) and Mtb closely resemble the full spectrum of both diseases (reviewed in [182,183]).

Variable impact of Mtb coinfection on SIV replication within plasma of coinfected NHP
NHP are unique in that they are one of the only animals who develop TB similar to humans, whilst also being a natural host of an immune deficiency virus (SIV) related to HIV. As an animal model of coinfection, they facilitate plasma sampling examined over an entire course of infection. SIV levels within plasma, over the course of disease, have been found to be similar within NHP with coinfected latent Mtb (CDC1551 or Erdman lab-adapted strains) infection compared with NHP infected with SIV alone [184][185][186]. There was no difference noted in peak viremia within coinfected and SIV-only infected macaques [185]. Interestingly, when SIV was used as a secondary infection to reactivate LTBI, no difference in SIV replication within the periphery was observed [186,187], suggesting that plasma viral set point did not change when TB was reactivated. Similarly, plasma SIV replication generally did not change within SIV-infected NHP from set point when Mtb infection followed SIV [188][189][190]. Taken together, these data suggest that Mtb and disease status do not change SIV replication within plasma. However, these observations counter human prospective HIV-TB cohorts [25] and it must be noted that lab-adapted SIV strains may not reflect naturally circulating strains or responses [191].
Studies examining infection with the live-attenuated TB vaccine M. bovis BCG and SIV coinfection found that NHP infected with BCG required fewer low-dose oral exposures of SIV to become SIV infected than their BCG naive counterparts [192], suggesting that BCG infection increased the number of SIV-susceptible cells and risk of SIV acquisition. BCG-infected NHP also developed a higher peak viral RNA count compared with uninfected NHP [192]. Similarly, SIV-infected NHP that were inoculated with BCG experienced a transient spike in plasma VL after 1-2 weeks [193]. Although these studies run counter to the Mtb/SIV coinfection studies, they demonstrate how mycobacteria have the capacity to increase SIV replication and set point and there may be significant interactions related to NHP and pathogen diversity in the models used [191,194].

Disease status & Mtb presence within tissue changes SIV or HIV-1 replication within coinfected animal models
One of the most significant benefits of HIV/Mtb coinfection animal models is the ability to examine viral replication and integration within a variety of Mtb-infected tissues. Within Mtb and SIV-coinfected NHP, SIV replication has been identified in lung granulomas [184][185][186][187] and thoracic LN [186]. This demonstrates that SIV replication ubiquitously occurs within a variety of tissues of coinfected NHP, but does not quantify how these tissues change SIV replication.
When quantifying the impact of change in VL during latent Mtb (CDC1551) progression to TB, a higher abundance of SIV RNA was observed within lung tissue of Mtb-infected NHP who progressed to TB disease following SIV infection, compared with coinfected NHP that did not reactivate following SIV infection [187]. Likewise, lung tissue from SIV/Mtb-coinfected NHP with active TB contained more SIV DNA than coinfected NHP with LTBI. Whether this relates only to tissue with granulomas is unclear from the published methodology [185]. This study also identified the colocalization of SIV RNA and Mtb bacilli within CD68 + macrophages, suggesting that macrophages might provide an opportunity for direct interaction between both pathogens. These data suggest that lung tissue from NHP with TB disease might behave as active reservoirs of SIV because they contain more CD4 + T-cells with integrated viral DNA and SIV replication and coinfectable macrophages than NHP with controlled LTBI. One potential difference between HIV-1 and SIV is the suggestion that macrophages are more readily infected with SIV and genetic differences between these two viruses may impact the relevance of macrophage SIV infection in NHP models to human macrophages [195].
NHP with active TB also contain more Mtb growth than ones with LTBI [196]. Investigating a correlation between Mtb and SIV abundance between disease states found no correlation between Mtb CFU growth and total SIV RNA [186] or SIV p28 protein [184] within the same lung tissue sections. Together, these studies provide a crude bulk level analysis, indicating at the tissue level, there is some evidence that inflammation during TB disease progression increases SIV replication and integration at the site of disease, while there is little direct correlation to pathogen abundance. These studies are far from conclusive, as they do not compare pathogen abundance at a single cell or single granuloma level. They also only quantitate live Mtb and not the presence of other bacterial products, nonreplicating Mtb, or the cytokine milieu induced at the local Mtb infection site and how these correlate with SIV infection and activation status. BLT-humanized mice have also been used to study the interaction between HIV-1 and Mtb in vivo. A higher frequency of HIV-1 Gag p24:CD4 + T-cell ratio was observed within lung interstitial tissue compared with spleen within HIV/Mtb-coinfected BLT-humanized mice [197]. Although the cellular composition within lung and spleen differ, this study suggests that CD4 + T-cells within Mtb diseased lung tissue are more susceptible to HIV-1 than CD4 + T-cells within spleen. Similarly, HIV-1 Gag p24 abundance within lung tissue of Mtb-coinfected BLT mice demonstrated a weak but positive correlation between Mtb CFU growth [198]. These humanized mice studies provide further evidence that HIV-1 can preferentially replicate within Mtb-infected lung tissue and that there exists increased recruitment of T-cells that have a higher susceptibility of infection either before or after reaching the infected lung.

Implications of latent Mtb treatment on HIV-1 prevention & cure strategies
Latent Mtb treatment is currently recommended for individuals who are frequently exposed to active TB disease, at high risk of progressing to active TB disease or immunocompromized (e.g., HIV-infected). In high TB burden countries, the WHO recommends HIV-1-infected individuals are given 6-9 months or continuous isoniazid prevention therapy (IPT) for LTBI, while initiating ART or if not yet received. However, only an estimated 49% of HIV-1-infected individuals were reported to have initiated TB preventative therapy in 2018 [4]. The first 12-month trial of IPT at ART initiation resulted in a median reduction in TB by 37% over 2 years, although the greatest reduction in risk occurred during the 12 months while receiving IPT; there was a gradual increase thereafter, rather than a rapid increase, with IPT still protective from TB at 2 years [199]. Shorter, 6 month courses are associated with faster loss of benefit [200]. The fast spike after only 6 months of IPT may reflect insufficient clearance of latent Mtb, and a continual contribution of Mtb to faster HIV-1 progression.
Although the WHO recommends short-course (6-9 months) IPT at ART initiation for people living in high TB transmission countries, as there is no evidence that repeat treatment offers further protection, there are no recommendations for repeat IPT in the WHO guidelines. This is despite the fact that repeat exposure to Mtb in high incidence settings is likely occurring. If concurrent Mtb infection, irrespective of TB progression, potentiates HIV-1 progression and risk of transmission through increasing VL, then repeat IPT or alternative shorter course prophylaxis could benefit those living with HIV-1 at risk of Mtb reexposure.
Perhaps of most importance to HIV-1 eradication, is if Mtb infection is shown to impact the abundance, activation status and microenvironment of HIV-1 reservoir cells, this may have significant implications for the design and efficacy of cure strategies for those on long-term ART. The leading cure approach is the 'Shock and Kill' technique aimed at activating all quiescent HIV-1-infected cells, in order to leverage CTL and ADCC-mediated killing (reviewed in [201]). Thus, the impact of Mtb infection of inhibiting CTL targeting of HIV-1 infection is a critical question requiring more research. The second option 'Lock and Block' is the opposite, aimed at preventing HIV-1 from ever being activated [202]. The potential impact of Mtb infection activating viral reservoirs, during this approach, is more evident and should be taken into consideration in future study designs for such HIV-1 cure strategies.

Conclusion
We have considered findings from epidemiological studies of TB-HIV coevolution, human and animal in vivo and in vitro studies in order to systematically assess the potential impact of Mtb infection, prior to TB development, on the progression and risk of HIV-1 infection. We acknowledge that potential confounders may exist when characterizing direct links between Mtb-HIV-1 coinfection and HIV-1 disease progression. These include behavioral and socioeconomic drivers of infection with either pathogen in communities where prevalence and incidence rates of both are high. We have not exhaustively covered the effects of treatment for either pathogen nor the immune environment induced by infection with either pathogen that could play a role in disease exacerbation. Although animal studies are sparse, compared with clinical studies, they demonstrate that SIV and HIV-1 do infect Mtbdiseased tissue and exist in close proximity, increasing the probability that HIV-1 replication is directly affected in Mtb-infected human tissues.
The interaction between these pathogens is complex and interweaved. It is likely that in any one individual, all modes and dynamics of coinfection may exist at any one time. While the TB granuloma may be the site where an HIV-1-infected T-cell first encounters Mtb, the LN may be the site where an Mtb-infected DC first encounters HIV-1. Conversely, if Mtb exists in the LN prior to HIV-1 infection, then the LN may be the first site a migrating HIV-infected T-cell encounters Mtb. The likely impact of coinfection may not necessarily be reliant on the order of events, and who gets where first, but rather their interaction within a shared microenvironment once there, which both pathogens are levering to ensure their longevity and transmission to future hosts.

Future perspective
The early era of HIV-TB research, focused on the role of Mtb coinfection on HIV-1 replication and immune cell susceptibility to infection. As we progress into an era of life-long ART, studies evaluating the impact of Mtb on the establishment, size and maintenance of the HIV-1 reservoir are of interest to determine the effect of LTBI on HIV-1 eradication. New multiomic single-cell technologies, including single-cell sequencing, RNA flow-FISH cytometry and whole tissue laser scanning microscopy could provide unprecedented sensitivity to assess the presence and metabolic state of both pathogens and the relative contribution of their spatial interaction within various microenvironments. Such studies using clinical samples could be augmented by animal models examining how Mtb changes HIV-1 replication in close proximity and if lung granulomas and peripheral sites of coinfection are HIV-1 reservoirs in vivo. Using a BLT mouse model, it is possible to block HIV-1 dissemination by limiting T-cell recirculation, through hindering the movement of migratory T-cells from LNs into efferent lymph [203]. Utilization of such in vivo manipulation of T-cell recruitment during LTBI could help dissect the contribution of recruitment to Mtb-infected sites and LN dissemination in HIV-1 progression and reservoir expansion.
Answers to the following questions will provide further insight into whether Mtb coinfection changes the dynamics of HIV-1 reservoirs and decreases the barrier to success of HIV-1 cure strategies:  The authors state that they have obtained appropriate institutional review board approval or have followed the principles outlined in the Declaration of Helsinki for all human or animal experimental investigations. In addition, for investigations involving human subjects, informed consent has been obtained from the participants involved.

Open access
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Evolution of the world's deadliest syndemic infection
• There was a significantly high incidence of tuberculosis (TB) in sub-Saharan Africa before the HIV-1 epidemic caused up to a tenfold increase in TB incidence. Africa now accounts for 71% of all HIV-TB cases and 84% of coinfection deaths.

Defining coinfection dynamics in animal models
• Nonhuman primate (NHP) and bone marrow, liver and thymus (BLT)-humanized mice models allow researchers to build a more detailed understanding of disease progression dynamics, which clinical studies cannot answer. • Conflicting results of the impact of Mtb on simian immunodeficiency virus (SIV)/HIV-1 replication exist between different animal models, which may relate to the diversity and interaction between NHP and pathogens used. • Tissue level analyses in NHP coinfection provide some evidence that inflammation during TB progression increases SIV replication and integration at the site of disease, with less correlation to total pathogen abundance. • BLT mice provide evidence that HIV-1 can preferentially replicate within Mtb infected lung tissue and there exists increased recruitment of T-cells, which have a higher susceptibility to HIV-1 infection either before or after reaching the Mtb-infected lung.

Implications of latent Mtb treatment on HIV-1 prevention & cure strategies
• 'Shock and Kill' is aimed at activating all quiescent HIV-1-infected cells, in order to leverage CTL and antibody-dependent cellular cytotoxicity-mediated killing. The impact of Mtb infection on inhibiting CTL targeting of HIV-1 infection is a critical question requiring more research. • 'Lock and Block' aims to prevent HIV-1 from ever being activated. The potential impact of Mtb infection activating viral reservoirs during this approach is more evident and should be taken into consideration in future study designs.